2-ethoxyethanol, 2-ethoxyethanol acetate, 2-methoxyethanol, and 2-methoxyethanol acetate; Proposed Significant New Use Rule, 9902-9909 [05-3911]
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Federal Register / Vol. 70, No. 39 / Tuesday, March 1, 2005 / Proposed Rules
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 721
[OPPT–2004–0111; FRL–7692–8]
RIN 2070–AJ12
2-ethoxyethanol, 2-ethoxyethanol
acetate, 2-methoxyethanol, and 2methoxyethanol acetate; Proposed
Significant New Use Rule
Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
AGENCY:
SUMMARY: EPA is proposing a significant
new use rule (SNUR) under section
5(a)(2) of the Toxic Substances Control
Act (TSCA) which would require
persons to notify EPA at least 90 days
before commencing the manufacture,
import, or processing of 2-ethoxyethanol
(CAS No. 110–80–5) (2-EE), 2ethoxyethanol acetate (CAS No. 111–
15–9) (2-EEA), 2-methoxyethanol (CAS
No. 109–86–4) (2-ME), or 2methoxyethanol acetate (CAS No. 110–
49–6) (2-MEA) for domestic use in a
consumer product or the manufacture or
import of 2-MEA at levels greater than
10,000 pounds per year. EPA believes
that this action is necessary because
these chemicals may be hazardous to
human health and their use in a
consumer product may result in human
exposure. The required notice would
provide EPA with the opportunity to
evaluate intended new uses and
associated activities, and if necessary,
prohibit or limit those uses and
activities before they occur.
DATES: Comments, identified by docket
identification (ID) number OPPT–2004–
0111, must be received on or before May
2, 2005.
ADDRESSES: Submit your comments,
identified by docket ID number OPPT–
2004–0111, by one of the following
methods:
• Federal eRulemaking Portal: https://
www.regulations.gov/. Follow the online instructions for submitting
comments.
• Agency Website: https://
www.epa.gov/edocket/. EDOCKET,
EPA’s electronic public docket and
comment system, is EPA’s preferred
method for receiving comments. Follow
the on-line instructions for submitting
comments.
• E-mail: oppt.ncic@epa.gov.
• Mail: Document Control Office
(DCO) (7407M), Office of Pollution
Prevention and Toxics (OPPT),
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001.
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• Hand Delivery: OPPT Document
Control Office, EPA East Bldg., Rm.
6428, 1201 Constitution Ave., NW.,
Washington, DC. Attention: Docket ID
number OPPT–2004–0111. The DCO is
open from 8 a.m. to 4 p.m., Monday
through Friday, excluding legal
holidays. The telephone number for the
DCO is (202) 564–8930. Such deliveries
are only accepted during the Docket’s
normal hours of operation, and special
arrangements should be made for
deliveries of boxed information.
Instructions: Direct your comments to
docket ID number OPPT–2004–0111.
EPA’s policy is that all comments
received will be included in the public
docket without change and may be
made available on-line at https://
www.epa.gov/edocket/, including any
personal information provided, unless
the comment includes information
claimed to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Do not submit information that you
consider to be CBI or otherwise
protected through EDOCKET,
regulations.gov, or e-mail. The EPA
EDOCKET and the regulations.gov
websites are ‘‘anonymous access’’
systems, which means EPA will not
know your identity or contact
information unless you provide it in the
body of your comment. If you send an
e-mail comment directly to EPA without
going through EDOCKET or
regulations.gov, your e-mail address
will be automatically captured and
included as part of the comment that is
placed in the public docket and made
available on the Internet. If you submit
an electronic comment, EPA
recommends that you include your
name and other contact information in
the body of your comment and with any
disk or CD ROM you submit. If EPA
cannot read your comment due to
technical difficulties and cannot contact
you for clarification, EPA may not be
able to consider your comment.
Electronic files should avoid the use of
special characters, any form of
encryption, and be free of any defects or
viruses. For additional information
about EPA’s public docket, visit
EDOCKET on-line or see the Federal
Register of May 31, 2002 (67 FR 38102)
(FRL–7181–7).
Docket: All documents in the docket
are listed in the EDOCKET index at
https://www.epa.gov/edocket/. Although
listed in the index, some information is
not publicly available, i.e., CBI or other
information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
is not placed on the Internet and will be
publicly available only in hard copy
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form. Publicly available docket
materials are available either
electronically in EDOCKET or in hard
copy at the OPPT Docket, EPA Docket
Center, EPA West, Rm. B102, 1301
Constitution Ave., NW., Washington,
DC. The Public Reading Room is open
from 8:30 a.m. to 4:30 p.m., Monday
through Friday, excluding legal
holidays. The EPA Docket Center
Reading Room telephone number is
(202) 566–1744, and the telephone
number for the OPPT Docket, which is
located in the EPA Docket Center, is
(202) 566–0280.
FOR FURTHER INFORMATION CONTACT: For
general information contact: Colby
Lintner, Regulatory Coordinator,
Environmental Assistance Division
(7408M), Office of Pollution Prevention
and Toxics, Environmental Protection
Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460–0001; telephone
number: (202) 554–1404; e-mail address:
TSCA-Hotline@epa.gov.
For technical information contact:
Amy Breedlove, Chemical Control
Division (7405M), Office of Pollution
Prevention and Toxics, Environmental
Protection Agency, 1200 Pennsylvania
Ave., NW., Washington, DC 20460–
0001; telephone number: (202) 564–
9823; e-mail address:
breedlove.amy@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action Apply to Me?
You may be potentially affected by
this action if you manufacture, import,
or process 2-EE (CAS No. 110–80–5), 2EEA (CAS No. 111–15–9), 2-ME (CAS
No. 109–86–4), or 2-MEA (CAS No.
110–49–6) for use in consumer products
or manufacture or import 2-MEA (CAS
No. 110–49–6) at levels greater than
10,000 pounds per year.
Persons who intend to import any
chemical substance governed by a final
SNUR are subject to the TSCA section
13 (15 U.S.C. 2612) import certification
requirements, and to the regulations
codified at 19 CFR 12.118 through
12.127 and 127.28. Those persons must
certify that they are in compliance with
the SNUR requirements (see TSCA
section 13 (15 U.S.C. 2612) and 19 CFR
12.118 through 12.127 and 127.28). The
EPA policy in support of import
certification appears at 40 CFR part 707,
subpart B. In addition, any persons who
export or intend to export a chemical
substance that is the subject of this
proposed rule on or after March 31,
2005 are subject to the export
notification provisions of TSCA section
12(b) (15 U.S.C. 2611(b)) (see 40 CFR
721.20), and must comply with the
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export notification requirements in 40
CFR part 707, subpart D. Potentially
affected entities may include, but are
not limited to:
• Manufacturers (defined by statute to
include importers) and processors of 2EE, 2-EEA, 2-ME, and 2-MEA (NAICS
325 and 324110), e.g., chemical
manufacturing and petroleum refineries.
This listing is not intended to be
exhaustive, but rather provides a guide
for readers regarding entities likely to be
affected by this action. Other types of
entities not listed in this unit could also
be affected. The North American
Industrial Classification System
(NAICS) codes have been provided to
assist you and others in determining
whether this action might apply to
certain entities. To determine whether
you or your business may be affected by
this action, you should carefully
examine the applicability provisions in
40 CFR 721.5 for SNUR-related
obligations. If you have any questions
regarding the applicability of this action
to a particular entity, consult the
technical person listed under FOR
FURTHER INFORMATION CONTACT.
B. How Can I Access Electronic Copies
of this Document and Other Related
Information?
In addition to using EDOCKET (http:/
/www.epa.gov/edocket), you may access
this Federal Register document
electronically through the EPA Internet
under the ‘‘Federal Register’’ listings at
https://www.epa.gov/fedrgstr/. A
frequently updated electronic version of
40 CFR part 721 is available on E-CFR
Beta Site Two at https://
www.gpoaccess.gov/ecfr/.
C. What Should I Consider as I Prepare
My Comments for EPA?
1. Submitting CBI. Do not submit this
information to EPA through EDOCKET,
regulations.gov, or e-mail. Clearly mark
the part or all of the information that
you claim to be CBI. For CBI
information in a disk or CD ROM that
you mail to EPA, mark the outside of the
disk or CD ROM as CBI and then
identify electronically within the disk or
CD ROM the specific information that is
claimed as CBI. In addition to one
complete version of the comment that
includes information claimed as CBI, a
copy of the comment that does not
contain the information claimed as CBI
must be submitted for inclusion in the
public docket. Information so marked
will not be disclosed except in
accordance with procedures set forth in
40 CFR part 2.
2. Tips for preparing your comments.
When submitting comments, remember
to:
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i. Identify the rulemaking by docket
ID number and other identifying
information (subject heading, Federal
Register date, and page number).
ii. Follow directions. The Agency may
ask you to respond to specific questions
or organize comments by referencing a
Code of Federal Regulations (CFR) part
or section number.
iii. Explain why you agree or disagree;
suggest alternatives and substitute
language for your requested changes.
iv. Describe any assumptions and
provide any technical information and/
or data that you used.
v. If you estimate potential costs or
burdens, explain how you arrived at
your estimate in sufficient detail to
allow for it to be reproduced.
vi. Provide specific examples to
illustrate your concerns, and suggest
alternatives.
vii. Explain your views as clearly as
possible, avoiding the use of profanity
or personal threats.
viii. Make sure to submit your
comments by the comment period
deadline identified.
II. Background
A. What Action is the Agency Taking?
EPA is proposing to designate the
manufacture, import, or processing of 2EE (CAS No. 110–80–5), 2-EEA (CAS
No. 111–15–9), 2-ME (CAS No. 109–86–
4), and 2-MEA (CAS No. 110–49–6) for
domestic use in consumer products as a
significant new use, as well as the
manufacture or import of 2-MEA (CAS
No. 110–49–6) at levels greater than
10,000 pounds per year. ‘‘Consumer
product’’ is defined at 40 CFR 721.3 as
‘‘a chemical substance that is directly,
or as part of a mixture, sold or made
available to consumers for their use in
or around a permanent or temporary
household or residence, in or around a
school, or in recreation.’’ This proposed
rule would require persons intending to
manufacture or import 2-MEA at levels
greater than 10,000 pounds per year as
well as those intending to manufacture,
import, or process 2-EE, 2-EEA, 2-ME, or
2-MEA for domestic use in a consumer
product to submit a Significant New Use
Notice (SNUN) to EPA at least 90 days
before such manufacture, import, or
processing.
B. What is the Agency’s Authority for
Taking this Action?
Section 5(a)(2) of TSCA (15 U.S.C.
2604(a)(2)) authorizes EPA to determine
that a use of a chemical substance is a
‘‘significant new use.’’ EPA must make
this determination by rule after
considering all relevant factors,
including those listed in TSCA section
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5(a)(2). Once EPA determines that a use
of a chemical substance is a significant
new use, and promulgates a SNUR,
section 5(a)(1)(B) of TSCA requires
persons to submit a SNUN to EPA at
least 90 days before commencement of
manufacture, import, or processing of
the chemical substance for that use.
C. What is the Applicability of the
General Regulatory Provisions?
General regulatory provisions for
SNURs appear under subpart A of 40
CFR part 721. These provisions describe
persons subject to the rule,
recordkeeping requirements, and
exemptions to reporting requirements.
Provisions relating to user fees appear at
40 CFR part 700. Persons subject to the
rule, when finalized, would be required
to comply with the same notice
requirements and EPA regulatory
procedures as submitters of
premanufacture notices (PMNs) under
section 5(a)(1)(A) of TSCA. In particular,
these requirements include the
information submission requirements of
TSCA section 5(b) and 5(d)(1), the
exemptions authorized by TSCA section
5(h)(1), (2), (3), and (5), and the
regulations at 40 CFR part 720. Receipt
of a SNUN by EPA may trigger
regulatory action under TSCA sections
5(e), 5(f), 6, or 7, if appropriate, to
control the activities on which it has
received the SNUN. If EPA does not take
action, EPA is required under TSCA
section 5(g) to explain in the Federal
Register its reasons for not taking
action.
Persons who intend to export a
substance identified in a proposed or
final SNUR are subject to the export
notification provisions of TSCA section
12(b). The regulations that interpret
TSCA section 12(b) appear at 40 CFR
part 707, subpart D. Persons who intend
to import a chemical substance
identified in a final SNUR are subject to
the TSCA section 13 import certification
requirements, which are codified at 19
CFR sections 12.118 through 12.127 and
section 127.28. Such persons must
certify that they are in compliance with
TSCA requirements. The EPA policy
relating to import certification appears
at 40 CFR part 707, subpart B.
III. Summary of this Proposed Rule
A. Why is EPA Taking this Action?
1. Background. On January 24, 1984,
EPA published an Advance Notice of
Proposed Rulemaking (ANPRM) (49 FR
2921) which stated that EPA
determined, based on animal studies,
that adverse reproductive and
developmental effects are associated
with the subject glycol ethers, i.e., 2-EE,
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2-EEA, 2-ME, and 2-MEA, at
concentrations to which humans may be
exposed. (Ref. 1). EPA was considering
the regulatory options available under
TSCA section 6 to control any
unreasonable risks from these
chemicals. It solicited comments on the
appropriateness of imposing a partial or
total ban on these chemicals. EPA had
also consulted with the Occupational
Safety and Health Administration
(OSHA) and the Consumer Product
Safety Commission (CPSC) on possible
actions under their legal authorities.
Later, in October 1984, the Agency
concluded that these chemicals may
pose a significant hazard to humans
(Ref. 2). However, by 1986, EPA’s
investigation of risks to consumers had
led the Agency to conclude that the
current information would not support
an unreasonable risk finding for
consumer use. This conclusion was
based on the fact that because of
wholesale switching to substitute
solvents, EPA had not been able to
identify manufacturers who were
currently using these glycol ethers in
their consumer products. EPA stated
that it would continue to consult with
the CPSC pursuant to section 9(d) of
TSCA to resolve outstanding issues,
particularly to clarify whether these
glycol ethers were being used in
consumer products (Ref. 3).
Additionally, EPA stated it was satisfied
that any risks from the substitutes were
less than those presented by 2-EE, 2EEA, 2-ME, or 2-MEA, and that use of
substitutes would reduce overall risks to
humans (Ref. 4).
On May 20, 1986 (51 FR 18488), EPA
issued a report to OSHA, under section
9(a) of TSCA, stating that EPA had a
reasonable basis to conclude that the
risk of injury to worker health from
exposure to 2-EE, 2-EEA, 2-ME, and 2MEA during their manufacturing,
processing, and use is unreasonable and
that this risk may be prevented or
reduced sufficiently by OSHA
regulatory action (Ref. 3).
2. Initial regulatory response by
OSHA. OSHA published its response on
December 11, 1986 (51 FR 44699),
stating that it had preliminarily
concluded that occupational exposures
to 2-EE, 2-EEA, 2-ME, and 2-MEA at the
current OSHA permissible exposure
limits (PELs) may present significant
risks to the health of workers (Ref. 5).
On April 2, 1987 (52 FR 10586), OSHA
published an ANPRM under section 6(b)
of the Occupational Safety and Health
Act of 1970 (29 U.S.C. 654), announcing
its intention to proceed to rulemaking to
reduce occupational exposure to 2-EE,
2-EEA, 2-ME, and 2-MEA (Ref. 6). On
March 23, 1993 (58 FR 15526), OSHA
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published a proposed rule that would
reduce the chemicals’ PELs and provide
other protective measures for the
approximately 46,000 workers exposed
to the substances (Ref. 7). After
publishing the 1993 proposal, OSHA
held informal public hearings on the
proposal, and the record closed in
March 1994 (Ref. 8).
3. EPA regulatory activities in the
1990’s. In the period immediately after
OSHA published its proposed rule,
EPA, on July 27, 1993 (58 FR 40262)
(Ref. 9), promulgated a TSCA section 4
test rule to require neurotoxicity testing
of 2-EE (among other chemical
substances). The required testing was
based on suggestive evidence of
neurotoxicity involving the alteration of
motor performance and avoidance
conditioning in the offspring of rats
exposed to 100 and 200 parts per
million (ppm) (Refs. 10 and 11), as well
as substantial occupational and
consumer exposure, and substantial
environmental release (Ref. 12). After
publication of that rule, however, the
producers of 2-EE told EPA that there
were no consumer uses of 2-EE (Ref. 13).
Given this information, and because
OSHA was continuing to work toward
revising the PELs for glycol ethers, EPA
believed that exposure to 2-EE was not
substantial and revoked the TSCA
section 4 testing requirements for 2-EE
in a settlement agreement with
producers in 1994 (Ref. 13). The
settlement agreement required that the
Chemical Manufacturers Association
(now the American Chemistry Council
(ACC)) and the manufacturers and
processors of these chemicals perform
certain neurotoxicity and
pharmacokinetics testing on 7 of the 10
chemicals subject to the final
neurotoxicity test rule (Ref. 14). This
revocation was also reflected in the
January 23, 1995 Federal Register (60
FR 4514) (FRL–4924–7) (Ref. 15). At the
time that EPA was considering revoking
the testing requirements in the section
4 rule, the Agency also believed it
would be prudent to provide some
mechanism to monitor the possible reemergence of the consumer use of 2-EE.
Therefore, in the same notice in which
it proposed to revoke the testing
requirements of 2-EE (59 FR 33187, June
27, 1994) (Ref. 14), EPA announced its
intention to propose and promulgate a
SNUR. The parties to the settlement
agreement supported such a SNUR (Ref.
13).
4. Final OSHA regulatory actions.
OSHA reopened the record on August 8,
2002 seeking comment on how the
substances were being used in the
workplace, including their level of
production, and the industries and
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processes in which they were used (Ref.
16). Based on the information submitted
during this comment period, OSHA
determined that a major decline in the
production of the substances was
apparent and that their use in several
key industry sectors has been
eliminated or is in the process of being
phased out. Additionally, OSHA
determined that where these substances
were still being manufactured, their
production was virtually limited to
‘‘closed systems’’ and average exposures
already were at or below the proposed
PEL (Ref. 8). OSHA concluded that the
proposed rule was no longer necessary
and withdrew its proposed Glycol
Ethers rule on December 31, 2003 (Ref.
8).
B. What are the Uses and Production
Levels of these Chemicals?
The chemical substances 2-EE, 2-EEA,
2-ME, and 2-MEA, are considered
members of a broad class of chemicals
known as ethylene glycol ethers. As
with other glycol ethers, 2-EE, 2-EEA, 2ME, and 2-MEA are colorless,
flammable liquids which are compatible
with a broad range of resins and can be
mixed with both organic solvents and
water. They have relatively low vapor
pressures, high boiling points, low
evaporation rates and high flash points.
Due to these physical characteristics, 2EE, 2-EEA, 2-ME, and 2-MEA are
potentially useful in a wide variety of
applications, particularly as solvents
(Ref. 7). They have been used in many
industrial and consumer products, but
concerns for their health effects have
caused these uses to be severely
curtailed in recent years.
U.S. production of 2-EE peaked at
200.7 million pounds in 1980 and had
decreased to 118 million pounds by
1999. U.S. consumption of 2-EE
(including consumption to manufacture
2-EEA) was 175 million pounds in 1980,
and down to 53 million pounds in 1999,
of which, 52 of the 53 million pounds
was used to manufacture 2-EEA. U.S.
consumption of 2-EE for uses other than
acetate production was less than 1
million pounds. Production and/or
imports of 2-EE were below 100 million
pounds based on data collected for the
2002 TSCA section 8(a) Inventory
Update Rule (IUR) (see 40 CFR part 710)
(Ref. 17).
U.S. production of 2-EEA dropped
from 136.7 million pounds in 1984 to 72
million pounds in 1999. In 1999, all but
one million of those pounds were
exported. Data collected for the 2002
IUR show production and/or import
levels of less than 100 million pounds
(Ref. 17).
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U.S. production of 2-ME, which
peaked at 97.3 million pounds in 1980,
was down to 55 million pounds by 1999
(at which time most 2-ME produced was
exported). U.S. consumption, still 50 to
53 million pounds in the early 1990’s,
had declined to approximately 3 million
pounds in 1999. 2002 IUR data show
that production and/or import was less
than 50 million pounds (Ref. 17).
U.S. production of 2-MEA in 1991
was estimated to be 0.5 million pounds.
There were no reports of 2-MEA
production or import under the IUR in
1994, 1998, and 2002 (Ref. 17).
Therefore, EPA is proposing that
persons intending to manufacture or
import 2-MEA at levels greater than
10,000 pounds per year as well as
persons intending to manufacture,
import, or process 2-EE, 2-EEA, 2-ME, or
2-MEA for domestic use in a consumer
product to submit a SNUN to EPA at
least 90 days before such manufacture,
import, or processing.
Production of the E-series glycol
ethers, i.e., ethanol based glycol ethers
and their acetates, had been declining or
has ceased and EPA believes there is no
ongoing use of these chemicals in
consumer products in the U.S. In
response to a proposed TSCA section 4
test rule, manufacturers of 2-EE told
EPA that there was no consumer use of
2-EE (Ref. 13). In 2004, a representative
for the Ethylene Glycol Ethers Panel of
the ACC confirmed that concerns over
the toxicity of E-series glycol ethers has
subsequently resulted in the elimination
of E-series glycol ethers from all
consumer products in the 1980’s and
the development of alternatives to 2-ME,
2-EE, and 2-EEA (Ref. 18).
C. What are the Potential Routes of
Exposure?
Despite the diminished potential for
human exposure due to the decline in
production and use in industrial
products and the termination of the
chemicals’ use in consumer products as
discussed in Unit III.B., EPA believes
there may still be some potential for
human exposure to 2-EE, 2-EEA, 2-ME,
and 2-MEA. Their physical
characteristics discussed in Unit III.B.
make them useful in a variety of
applications, particularly as solvents.
‘‘A major route of exposure is the skin.
The ubiquity of solvents and the casual
approach [of consumers] to their use
almost assure skin contact with liquid
solvents.’’ (Ref. 19). Also, as members of
the ethylene series (‘‘E-series’’ used in
Unit III.B.) of glycol ethers, 2-EE, 2-EEA,
2-ME, and 2-MEA are well absorbed
from the skin. They are so readily
absorbed through the skin that the
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dermal to oral 50% lethal dose (LD50)
ratio is approximately one (Ref 19).
Although 2-EE, 2-EEA, 2-ME, and 2MEA are not highly volatile, high vapor
concentrations can be generated under
the conditions of solvent use. When
glycol ether vapors enter the lungs they
can readily diffuse across respiratory
membranes and enter the bloodstream
(Ref. 19).
D. What are the Potential Sources of
Exposure?
EPA believes that 2-EE, 2-ME, 2-MEA,
and 2-EEA are currently used only in
industrial products. EPA also believes
that the documented decline in
production volumes of 2-EE, 2-EEA, 2ME, and 2-MEA discussed in Unit III.B.
has probably already reduced the
potential for occupational exposure.
OSHA reported in late 2003 that
production, use, and exposure to these
glycol ethers has ceased or is virtually
limited to closed system production
where there is little opportunity for
worker exposure. Exposure levels in
those operations already are at or below
the proposed PELs. In addition, use of
these glycol ethers has largely been
replaced by less-toxic substitutes, such
as E-series butyl glycol ethers, other
ethylene glycol ethers, propylene glycol
ethers, and other types of solvents (Ref.
8). A decline in environmental release
of 2-EE is reflected in Toxics Release
Inventory (TRI) data from the years 1987
through 1996 which indicates a steady
decline from 2,770,113 pounds in 1987
to 192,468 pounds in 1996 (Ref. 20) to
103,513 pounds in 2001 (Ref. 17).
EPA has found evidence which
suggests that 2-EE, as well as 2-ME, 2MEA, and 2-EEA, are not currently used
in consumer products (Ref. 17), and the
manufacturers of 2-EE which were
parties to the 1994 settlement agreement
told EPA that, to the best of their
knowledge, there were, at that time, no
consumer uses of 2-EE (Refs. 9 and 13).
The ACC also reported in 2001, citing
the SRI Chemical Economics Handbook
as its source, that the remaining
domestic consumption of 2-EE is in
non-consumer solvents for paints,
coatings, and other industrial uses; the
only remaining domestic use of 2-EEA
is in machinery and equipment paints
and coatings; and the only remaining
use of 2-ME, other than as a chemical
intermediate, is as a jet fuel deicer. No
information on current uses of 2-MEA
was identified (Ref. 17).
E. What are the Health Effects of these
Chemicals?
Toxicity studies in rats, rabbits, mice,
and monkeys via inhalation, dermal,
and oral exposure, have shown clearly
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and consistently that 2-EE and 2-ME can
cause adverse hematologic,
reproductive, and developmental
effects. These effects include decreased
white and red blood cell counts,
decreased hemoglobin, decreased
fertility, decreased sperm count,
decreased testes size and weight,
increased resorptions, increased fetal
malformations, and behavioral and
neurochemical alterations in the
neonate (Refs. 7 and 2).
Although data on workers is often
compromised by confounding exposure
to other solvents, studies of workers
exposed to 2-ME and 2-EE have
documented adverse effects on the
hematologic and male reproductive
systems. Blood effects observed among
the exposed workers include bone
marrow injury, reduced red and white
blood cell counts, and anemia, while the
major reproductive effect observed is
reduced sperm count (Ref. 7). Thus,
although the human data have their
limitations, there is evidence of certain
adverse effects in humans exposed to 2EE and 2-ME and this evidence is
consistent with a strong body of
evidence of the same or similar effects
in experimental animals.
Animal studies with 2-EEA and 2MEA have shown that these acetates
induce adverse reproductive,
developmental, and hematological
effects similar to those ascribed to their
parent glycol ethers, 2-EE and 2-ME.
These studies confirm the findings of
metabolic studies which indicate that 2ME, 2-EE, and their acetates follow
similar metabolic pathways, producing
the same metabolites, which are the
active agents most likely responsible for
the observed effects (Ref. 7).
IV. Determining a Significant New Use
Section 5(a)(2) of TSCA provides that
EPA’s determination that a use of a
chemical substance is a significant new
use must be made after consideration of
all relevant factors including:
• The projected volume of
manufacturing and processing of a
chemical substance.
• The extent to which a use changes
the type or form of exposure of human
beings or the environment to a chemical
substance.
• The extent to which a use increases
the magnitude and duration of exposure
of human beings or the environment to
a chemical substance.
• The reasonably anticipated manner
and methods of manufacturing,
processing, distribution in commerce,
and disposal of a chemical substance.
EPA construes the statute to allow
consideration of any other relevant
factors, in addition to those enumerated
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in section 5(a)(2)(A) through (D) of
TSCA.
To determine what would constitute a
significant new use of 2-EE, 2-EEA, 2ME, and 2-MEA, EPA considered
relevant information about the toxicity
of the substances, likely exposures/
releases associated with possible uses,
and the four factors listed in section
5(a)(2) of TSCA.
The latest information available to
EPA indicates that there is no ongoing
domestic use of 2-EE, 2-EEA, 2-ME, or
2-MEA in consumer products. EPA
believes that the renewed use of 2-EE,
2-EEA, 2-ME, or 2-MEA in a consumer
product would increase the magnitude
and duration of exposure. Considering
the health concerns for 2-EE, 2-EEA, 2ME, and 2-MEA, EPA believes that
individuals could suffer adverse effects
from their use in consumer products.
Thus, EPA is proposing to designate
‘‘domestic use in a consumer product’’
as well as the manufacture or import of
2-MEA at levels greater than 10,000
pounds per year as a significant new use
of 2-EE, 2-EEA, 2-ME, and 2-MEA.
Based on these considerations, EPA is
pursuing the following objectives with
regard to the use of 2-EE, 2-EEA, 2-ME,
and 2-MEA in consumer products:
• EPA wants to ensure that it would
receive notice of any person’s intent to
manufacture or import 2-MEA at levels
greater than 10,000 pounds per year or
intending to manufacture, import, or
process 2-EE, 2-EEA, 2-ME, and 2-MEA
for domestic use in a consumer product
before that activity begins.
• EPA wants to ensure that it would
have the opportunity to review and
evaluate data submitted in a SNUN
before the notice submitter begins
manufacturing, importing, or processing
2-EE, 2-EEA, 2-ME, and 2-MEA for
domestic use in a consumer product or
manufacturing or importing 2-MEA at
levels greater than 10,000 pounds per
year.
• EPA wants to ensure that it would
be able to regulate prospective
manufacturers, importers, or processors
of 2-EE, 2-EEA, 2-ME, and 2-MEA before
use of any of these chemicals in a
consumer product occurs, provided that
the degree of potential risk is sufficient
to warrant such regulation.
As noted in Unit III.B., the production
of the chemicals included in this SNUR
have declined significantly over time.
EPA is not aware of current domestic
consumer uses for the chemicals, and
substitutes are available. The Agency
will use information submitted pursuant
to the Inventory Update Rule (40 CFR
part 710) to track the production
volumes and uses of these chemicals. If
needed, EPA may pursue additional
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regulatory actions as appropriate under
TSCA sections 4, 5, 6, or 8.
V. Test Data and Other Information
EPA recognizes that section 5 of
TSCA does not require the development
of any particular test data before
submission of a SNUN. Persons are
required only to submit test data in their
possession or control and to describe
any other data known to or reasonably
ascertainable by them (15 U.S.C.
2604(d); 40 CFR 721.25).
However, SNUN submitters should be
aware that EPA will be better able to
evaluate SNUNs which provide detailed
information on:
• Human exposure and
environmental releases that may result
from the significant new use of the
chemical substances.
• Potential benefits of the chemical
substances.
• Information on risks posed by the
chemical substances relative to risks
posed by potential substitutes.
Submitters should consider including
with a SNUN any other available studies
on the chemical substances or studies
on analogous substances which may
demonstrate that the significant new
uses being reported are unlikely to
present an unreasonable risk.
In view of the potential risks posed by
these chemicals, EPA would
recommend that potential SNUN
submitters include data that would
permit a reasoned evaluation of risks
posed by these chemicals. EPA
encourages persons to consult with the
Agency before submitting a SNUN for
these substances. As part of this
optional pre-notice consultation, EPA
would discuss specific data it believes
are necessary to evaluate a significant
new use. A SNUN submitted without
sufficient data to reasonably evaluate
risks posed by a significant new use of
2-EE, 2-EEA, 2-ME, and/or 2-MEA may
increase the likelihood that EPA will
take action under TSCA section 5(e) to
prohibit or limit activities associated
with these chemicals. EPA recommends
that potential SNUN submitters contact
the Agency early enough that they will
be able to conduct any appropriate tests.
VI. Recordkeeping Requirements
In addition to the recordkeeping
requirements of 40 CFR 721.40 which
require persons subject to a SNUR to
retain documentation of information
contained in a SNUN, EPA is proposing
to require the recordkeeping
requirements in 40 CFR 721.125 (a), (b),
and (c) in this SNUR. Section 721.125(a)
requires records documenting
manufacture and importation volume
and dates; § 721.125(b) documents
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volumes purchased in the U.S. by
processors, the names and addresses of
suppliers, and the dates of purchase;
and § 721.125(c) requires records
documenting the names and addresses
(including shipment destination
address, if different) of all persons
outside the site of manufacture,
importation, or processing to whom the
manufacturer, importer, or processor
directly sells or transfers the substance,
the date, and the quantity of each sale
or transfer. EPA is also proposing to
require the maintenance of records
documenting the compliance with the
significant new use of domestic use in
a consumer product or the manufacture
or import of 2-MEA at levels greater
than 10,000 pounds per year. For the
significant new use of 2-MEA
manufacture or import at levels greater
than 10,000 pounds per year, records
required by § 721.125(a) would be
sufficient. For the significant new use of
domestic use in a consumer product,
required documentation must
demonstrate compliance with the
significant new use, i.e.,: 1) That 2-EE,
2-EEA, 2-ME or 2-MEA were not
manufactured, imported, or processed
for use in a consumer product; and, 2)
that, where no significant new use
notice is filed, any recipients of these
chemicals either (a) were notified of the
SNUR and its provisions by the
manufacturer, importer, or processor, (b)
knew of the SNUR independently, or (c)
cannot undertake the significant new
use. See 40 CFR 720.5(a)(2). These
records will enable EPA to determine
compliance with the SNUR.
VII. SNUN Submissions
SNUNs should be mailed to the
Environmental Protection Agency,
OPPT Document Control Office
(7407M), 1200 Pennsylvania Ave., NW.,
Washington, DC 20460–0001.
Information must be submitted in the
form and manner set forth in EPA Form
No. 7710–25. This form is available
from the Environmental Assistance
Division (7408M), OPPT, Environmental
Protection Agency, 1200 Pennsylvania
Ave., NW., Washington, DC 20460–0001
(see 40 CFR 721.25(a) and
720.40(a)(2)(i)).
VIII. Alternatives
Before proposing this SNUR, EPA
considered promulgating a TSCA
section 8(a) reporting rule for 2-EE, 2EEA, 2-ME, and 2-MEA. Under such a
rule, EPA could generally require any
person to report information to the
Agency when they intend to
manufacture, import, or process 2-EE, 2EEA, 2-ME, or 2-MEA. However, in the
case of these particular substances, the
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use of TSCA section 8(a) rather than
SNUR authority would have several
drawbacks. First, EPA would not be able
to take immediate follow-up regulatory
action under TSCA sections 5(e) or 5(f)
to prohibit or limit the activity before it
begins. In addition, EPA may not
receive important information from
small businesses, because such firms
generally are exempt from TSCA section
8(a) reporting requirements. In view of
the level of health concerns for 2-EE, 2EEA, 2-ME, and 2-MEA, EPA believes
that a TSCA section 8(a) rule for these
substances would not meet EPA’s
regulatory objectives.
Currently 2-EE, 2-EEA, 2-ME, and 2MEA are not subject to any other
Federal regulation which would notify
the Federal Government of activities
that might result in adverse exposures
associated with the proposed significant
new uses, or provide a mechanism that
could protect against potentially adverse
exposures associated with those uses
before they occur.
IX. Applicability of Rule to Uses
Occurring Before Effective Date of the
Final Rule
As discussed in the Federal Register
of April 24, 1990 (55 FR 17376), EPA
believes that the intent of TSCA section
5(a)(1)(B) is best served by designating
a use as a significant new use as of the
date of publication of the proposed
SNUR rather than as of the effective date
of the final rule. If uses begun after
publication of the proposed SNUR were
considered to be ongoing rather than
new, it would be difficult for EPA to
establish SNUR notice requirements,
because any person could defeat the
SNUR by initiating the proposed
significant new use before the rule
became final.
Any person who, after publication of
this proposed SNUR, begins to
manufacture, import, or process 2-EE, 2EEA, 2-ME, or 2-MEA for a proposed
significant new use must stop such
activity before the effective date of the
final rule. Persons who cease those
activities will have to meet all SNUR
notice requirements and wait until the
end of the notice review period,
including all extensions, before
engaging in any activities designated as
significant new uses. If, however,
persons who begin to manufacture,
import, or process any of these
chemicals between the proposal and the
effective date of the final SNUR meet
the conditions of advance compliance as
codified at 40 CFR 721.45(h), those
persons would be considered to have
met the requirements of the final SNUR
for those activities.
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X. Economic Analysis
XI. References
EPA has evaluated the potential costs
of establishing SNUR reporting
requirements for potential
manufacturers, importers, and
processors of the chemical substances
included in this proposed rule. While
there is no precise way to calculate the
total annual cost of compliance with the
final rule, given the uncertainties
related to predicting the number of
SNUN’s that would be submitted as a
result of this SNUR, EPA estimates that
the cost for preparing and submitting a
SNUN is $7,174, including a $2,500 user
fee required by 40 CFR part
700.45(b)(2)(iii) (Ref. 18). Small
businesses with annual sales of less
than $40 million when combined with
those of the parent company (if any) are
subject to a reduced user fee of $100 (40
CFR part 700.45(b)(1)). Based on past
experience with SNURs and the low
number of SNUNs which are submitted
on an annual basis, EPA believes that
there will be few, if any, SNUNs
submitted as a result of this SNUR. The
costs of submission of SNUNs will not
be incurred by any company unless a
company decides to pursue a significant
new use as defined in this SNUR.
Furthermore, while the expense of a
notice and the uncertainty of possible
EPA regulation may discourage certain
innovations, that impact would be
limited because such factors are
unlikely to discourage an innovation
that has high potential value. EPA’s
complete economic analysis is available
in the public docket for this proposed
rule (Ref. 18).
Under section 12(b) of TSCA,
exporters must notify EPA if they export
or intend to export a chemical substance
or mixture for which a rule has been
proposed or promulgated under section
5 or 6. Notice must be provided for the
first export or intended export to a
particular country in a calendar year. In
an economic analysis of an amendment
to the rules implementing TSCA section
12(b), EPA estimated that the one-time
cost of preparing and submitting an
export notification was $62.60 in 1992,
or $93.02 when inflated to 2003 dollars
by a factor of approximately 1.5, from
the Employment Cost Index for White
Collar Occupations. The total costs of
export notification will vary per
chemical, depending on the number of
required notifications (i.e., number of
countries to which the chemical is
exported). EPA is unable to make any
estimate of the likely number of export
notifications for chemicals covered in
this SNUR (Ref. 17).
The public docket for this action,
OPPT–2004–0111, currently includes
the following documents:
1. USEPA. ‘‘2-Methoxyethanol and 2Ethoxyethanol and their Acetates;
Initiation of Regulatory Investigation,
Advance Notice of Proposed
Rulemaking.’’ 49 FR 2921. (January 24,
1984).
2. USEPA. ‘‘Glycol Ethers Health
Effects Assessment.’’ Intra-agency
memorandum from M.S. Ottley to Harry
Teitelbaum, Existing Chemicals
Assessment Division. (October 31,
1984).
3. U.S. Environmental Protection
Agency (USEPA). ‘‘Toxic and Hazardous
Substances Control; 2-Methoxyethanol,
2-Ethoxyethanol and their Acetates;
Referral For Additional Action.’’ TSCA
section 9 referral to OSHA. 51 FR 18488.
(May 20, 1986).
4. USEPA. ‘‘Substitutes for 2Ethoxyethanol (2-EE), 2-Methoxyethanol
(2-ME) and their Acetates.’’ Intra-agency
memorandum from Harry Teitelbaum,
Risk Management Branch to Joseph
Merenda, Existing Chemicals
Assessment Division. (March 15, 1984).
5. OSHA. ‘‘Occupational Exposure to
2-Methoxyethanol, 2-Ethoxyethanol and
Their Acetates; Response to the
Environmental Protection Agency under
section 9(a) of the Toxic Substances
Control Act.’’ 51 FR 44699. (December
11, 1986).
6. OSHA. ‘‘Occupational Exposure to
2-Methoxyethanol, 2-Ethoxyethanol and
Their Acetates; Advance Notice of
Proposed Rulemaking.’’ 52 FR 10586.
(April 2, 1987).
7. Occupational Health and Safety
Administration (OSHA). ‘‘Occupational
Exposure to 2-Methoxyethanol, 2Ethoxyethanol and their Acetates
(Glycol Ethers); Proposed Rule.’’ 58 FR
15526 (March 23, 1993).
8. OSHA. ‘‘Occupational Exposure to
2-Methoxyethanol, 2-Ethoxyethanol and
Their Acetates (Glycol Ethers);
Withdrawal of Proposed Rule.’’
68:75475–75476. (December 31, 2003).
9. USEPA. ‘‘Multi-substance Rule for
the Testing of Neurotoxicity; Final
Rule.’’ 58 FR 40262. (July 27, 1993).
10. Nelson, B.K., Brightwell, W.S.,
Setzer, J.V., Taylor, B.J., Hornung, R.W.
and O’Donohue, T.L. ‘‘Ethoxyethanol
Behavioral Teratology in Rats.’’
Neurotoxicology. 2:231–249. (1981).
11. Nelson, B.K., Brightwell, W.S. and
Setzer, J.V. ‘‘Prenatal Interaction
Between Ethanol and the Industrial
Solvent 2-Ethoxyethanol in Rats;
Maternal and Behavioral Teratogenic
Effects.’’ Neurobehavioral Toxicology
and Teratology. 4:387–394. (1982).
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12. USEPA. ‘‘Multi-substance Rule for
the Testing of Neurotoxicity; Proposed
Rule.’’ 56 FR 9105. (March 4, 1991).
13. United States Court of Appeals for
the Fifth Circuit. Settlement Agreement
between Environmental Protection
Agency and petitioners (Chemical
Manufacturers Association et al.), No.
93–5381. (April 28, 1994).
14. USEPA. ‘‘Proposed Revocation of
Final Multi-substance Rule for the
Testing of Neurotoxicity; Proposed
Rule.’’ 59 FR 33187 (June 27, 1994).
15. USEPA. ‘‘Revocation of Final
Multi-substance Rule for the Testing of
Neurotoxicity.’’ 60 FR 4514. (January 23,
1995).
16. OSHA. ‘‘Occupational Exposure to
2-Methoxyethanol, 2-Ethoxyethanol and
Their Acetates (Glycol Ethers).’’ 67 FR
51524. (August 8, 2002).
17. USEPA, 2004. ‘‘Economic
Analysis of Expedited Significant New
Use Rules for Four Glycol Ethers.’’
Washington, DC: U.S. EPA/OPPT/EETD/
EPAB, October 27, 2004.
18. ACC, 2004. Personal
Communication Between American
Chemistry Council, Ethylene Glycol
Ethers Panel representative and Jason
Sacks, Abt Associates Inc. May 10, 2004.
19. Casarett and Doull’s Toxicology.
Editors: Klaassen, C.D., Amdur, M.O.,
and Doull J. Chapter 20: Toxic Effects of
Solvents and Vapors. Pages 636–638
and 656–658, 3rd Edition. (1986).
20. USEPA. Toxic Release Inventory
(TRI). Total annual environmental
releases of 2-ethoxyethanol for the years
1987 through 1996. TRI printouts. (April
26, 1994, May 6, 1994, May 19, 1998,
and May 28, 1998).
XII. Statutory and Executive Order
Reviews
A. Executive Order 12866: Regulatory
Planning and Review
Under Executive Order 12866,
entitled Regulatory Planning and
Review (58 FR 51735, October 4, 1993),
the Office of Management and Budget
(OMB) has determined that proposed or
final SNURs are not a ‘‘significant
regulatory action’’ subject to review by
OMB, because they do not meet the
criteria in section 3(f) of the Executive
Order.
B. Paperwork Reduction Act
According to the Paperwork
Reduction Act (PRA), 44 U.S.C. 3501 et
seq., an Agency may not conduct or
sponsor, and a person is not required to
respond to a collection of information
that requires OMB approval under the
PRA, unless it has been approved by
OMB and displays a currently valid
OMB control number. The OMB control
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numbers for EPA’s regulations in title 40
of the CFR, after appearing in the
Federal Register, are listed in 40 CFR
part 9, and included on the related
collection instrument or form, if
applicable.
The information collection
requirements related to this action have
already been approved by OMB
pursuant to the PRA under OMB control
number 2070–0038 (EPA ICR No. 1188).
This action would not impose any
burden requiring additional OMB
approval. If an entity were to submit a
SNUN to the Agency, the annual burden
is estimated to average 105 hours per
submission. This burden estimate
includes the time needed to review
instructions, search existing data
sources, gather and maintain the data
needed, and complete, review, and
submit the required SNUN.
Send any comments about the
accuracy of the burden estimate, and
any suggested methods for minimizing
respondent burden, including through
the use of automated collection
techniques, to the Director, Collection
Strategies Division, Office of
Environmental Information (2822T),
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001. Please remember to
include the OMB control number in any
correspondence, but do not submit any
completed forms to this address.
C. Regulatory Flexibility Act
Pursuant to section 605(b) of the
Regulatory Flexibility Act (RFA) (5
U.S.C. 601 et seq.), the Agency hereby
certifies that promulgation of this SNUR
would not have a significant adverse
economic impact on a substantial
number of small entities. The rationale
supporting this conclusion is as follows.
A SNUR applies to any person
(including small or large entities) who
intends to engage in any activity
described in the rule as a ‘‘significant
new use.’’ By definition of the word
‘‘new,’’ and based on all information
currently available to EPA, it appears
that no small or large entities presently
engage in such activity. Since a SNUR
only requires that any person who
intends to engage in such activity in the
future must first notify EPA by
submitting a SNUN, no economic
impact would even occur until someone
decides to engage in those activities.
Although some small entities may
decide to conduct such activities in the
future, EPA cannot presently determine
how many, if any, there may be.
However, EPA’s experience to date is
that, in response to the promulgation of
over 1,000 SNURs, the Agency receives
on average only 10 notices per year. Of
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those SNUNs submitted, none appear to
be from small entities in response to any
SNUR. In addition, the estimated
reporting cost for submission of a SNUN
(see Unit X.), are minimal regardless of
the size of the firm. Therefore, EPA
believes that the potential economic
impact of complying with this SNUR is
not expected to be significant or
adversely impact a substantial number
of small entities. In a SNUR that
published on June 2, 1997 (62 FR 29684)
(FRL–5597–1), the Agency presented its
general determination that proposed
and final SNURs are not expected to
have a significant economic impact on
a substantial number of small entities,
which was provided to the Chief
Counsel for Advocacy of the Small
Business Administration.
D. Unfunded Mandates Reform Act
Based on EPA’s experience with
proposing and finalizing SNURs, State,
local, and Tribal governments have not
been impacted by these rulemakings,
and EPA does not have any reasons to
believe that any State, local, or Tribal
government would be impacted by this
rulemaking. As such, EPA has
determined that this regulatory action
would not impose any enforceable duty,
contain any unfunded mandate, or
otherwise have any affect on small
governments subject to the requirements
of sections 202, 203, 204, or 205 of the
Unfunded Mandates Reform Act of 1995
(UMRA) (Public Law 104–4).
E. Executive Order 13132: Federalism
This action would not have a
substantial direct effect on States, on the
relationship between the national
government and the States, or on the
distribution of power and
responsibilities among the various
levels of government, as specified in
Executive Order 13132, entitled
Federalism (64 FR 43255, August 10,
1999).
F. Executive Order 13175: Consultation
and Coordination with Indian Tribal
Governments
This proposed rule would not have
Tribal implications because it is not
expected to have substantial direct
effects on Indian Tribes. This proposed
rule would not significantly or uniquely
affect the communities of Indian Tribal
governments, nor would it involve or
impose any requirements that affect
Indian Tribes. Accordingly, the
requirements of Executive Order 13175,
entitled Consultation and Coordination
with Indian Tribal Governments (65 FR
67249, November 6, 2000), do not apply
to this proposed rule.
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G. Executive Order 13045: Protection of
Children from Environmental Health
Risks and Safety Risks
This action is not subject to Executive
Order 13045, entitled Protection of
Children from Environmental Health
Risks and Safety Risks (62 FR 19885,
April 23, 1997), because this is not an
economically significant regulatory
action as defined by Executive Order
12866, and this action does not address
environmental health or safety risks
disproportionately affecting children.
H. Executive Order 13211: Actions that
Significantly Affect Energy Supply,
Distribution, or Use
This proposed rule is not subject to
Executive Order 13211, entitled Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution, or Use (66 FR 28355, May
22, 2001), because this action is not
expected to affect energy supply,
distribution, or use.
I. National Technology Transfer
Advancement Act
In addition, since this action does not
involve any technical standards, section
12(d) of the National Technology
Transfer and Advancement Act of 1995
(NTTAA), Public Law 104–113, section
12(d) (15 U.S.C. 272 note), does not
apply to this action.
J. Executive Order 12898: Federal
Actions to Address Environmental
Justice in Minority Populations and
Low-Income Populations
This action does not entail special
considerations of environmental justice
related issues as delineated by
Executive Order 12898, entitled Federal
Actions to Address Environmental
Justice in Minority Populations and
Low-Income Populations (59 FR 7629,
February 16, 1994).
K. Executive Order 12988: Civil Justice
Reform
In issuing this proposed rule, EPA has
taken the necessary steps to eliminate
drafting errors and ambiguity, minimize
potential litigation, and provide a clear
legal standard for affected conduct, as
required by section 3 of Executive Order
12988, entitled Civil Justice Reform (61
FR 4729, February 7, 1996).
List of Subjects in 40 CFR Part 721
Environmental protection, Chemicals,
Hazardous substances, Reporting and
recordkeeping requirements.
Dated: February 16, 2005.
Charles M. Auer,
Director, Office of Pollution Prevention and
Toxics.
Therefore, it is proposed that 40 CFR
part 721 be amended as follows:
PART 721—[AMENDED]
1. The authority citation for part 721
would continue to read as follows:
Authority: 15 U.S.C. 2604, 2607, and
2625(c).
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2. Add new § 721.10001 to subpart E
to read as follows:
§ 721.10001 2-Ethoxyethanol, 2ethoxyethanol acetate, 2-methoxyethanol,
and 2-methoxyethanol acetate.
(a) Chemical substances and
significant new uses subject to reporting.
(1) The chemical substances identified
as 2-ethoxyethanol (CAS No. 110–80–5),
2-ethoxyethanol acetate (CAS No. 111–
15–9), 2-methoxyethanol (CAS No. 109–
86–4), and 2-methoxyethanol acetate
(CAS No. 110–49–6) are subject to
reporting under this section for the
significant new use described in
paragraph (a)(2) of this section.
(2) The significant new use is
domestic use in a consumer product or
the manufacture or import of 2methoxyethanol acetate at levels greater
than 10,000 pounds per year.
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), and (c) apply to the significant
new use specified in § 721.10001. In
addition, records documenting
compliance with the significant new use
of domestic use in a consumer product
or the manufacture or import of 2methoxyethanol acetate at levels greater
than 10,000 pounds per year must be
maintained.
(2) [Reserved]
[FR Doc. 05–3911 Filed 2–28–05; 8:45 am]
BILLING CODE 6560–50–S
E:\FR\FM\01MRP1.SGM
01MRP1
Agencies
[Federal Register Volume 70, Number 39 (Tuesday, March 1, 2005)]
[Proposed Rules]
[Pages 9902-9909]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-3911]
[[Page 9902]]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 721
[OPPT-2004-0111; FRL-7692-8]
RIN 2070-AJ12
2-ethoxyethanol, 2-ethoxyethanol acetate, 2-methoxyethanol, and
2-methoxyethanol acetate; Proposed Significant New Use Rule
AGENCY: Environmental Protection Agency (EPA).
ACTION: Proposed rule.
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SUMMARY: EPA is proposing a significant new use rule (SNUR) under
section 5(a)(2) of the Toxic Substances Control Act (TSCA) which would
require persons to notify EPA at least 90 days before commencing the
manufacture, import, or processing of 2-ethoxyethanol (CAS No. 110-80-
5) (2-EE), 2-ethoxyethanol acetate (CAS No. 111-15-9) (2-EEA), 2-
methoxyethanol (CAS No. 109-86-4) (2-ME), or 2-methoxyethanol acetate
(CAS No. 110-49-6) (2-MEA) for domestic use in a consumer product or
the manufacture or import of 2-MEA at levels greater than 10,000 pounds
per year. EPA believes that this action is necessary because these
chemicals may be hazardous to human health and their use in a consumer
product may result in human exposure. The required notice would provide
EPA with the opportunity to evaluate intended new uses and associated
activities, and if necessary, prohibit or limit those uses and
activities before they occur.
DATES: Comments, identified by docket identification (ID) number OPPT-
2004-0111, must be received on or before May 2, 2005.
ADDRESSES: Submit your comments, identified by docket ID number OPPT-
2004-0111, by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov/.
Follow the on-line instructions for submitting comments.
Agency Website: https://www.epa.gov/edocket/. EDOCKET,
EPA's electronic public docket and comment system, is EPA's preferred
method for receiving comments. Follow the on-line instructions for
submitting comments.
E-mail: oppt.ncic@epa.gov.
Mail: Document Control Office (DCO) (7407M), Office of
Pollution Prevention and Toxics (OPPT), Environmental Protection
Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460-0001.
Hand Delivery: OPPT Document Control Office, EPA East
Bldg., Rm. 6428, 1201 Constitution Ave., NW., Washington, DC.
Attention: Docket ID number OPPT-2004-0111. The DCO is open from 8 a.m.
to 4 p.m., Monday through Friday, excluding legal holidays. The
telephone number for the DCO is (202) 564-8930. Such deliveries are
only accepted during the Docket's normal hours of operation, and
special arrangements should be made for deliveries of boxed
information.
Instructions: Direct your comments to docket ID number OPPT-2004-
0111. EPA's policy is that all comments received will be included in
the public docket without change and may be made available on-line at
https://www.epa.gov/edocket/, including any personal information
provided, unless the comment includes information claimed to be
Confidential Business Information (CBI) or other information whose
disclosure is restricted by statute. Do not submit information that you
consider to be CBI or otherwise protected through EDOCKET,
regulations.gov, or e-mail. The EPA EDOCKET and the regulations.gov
websites are ``anonymous access'' systems, which means EPA will not
know your identity or contact information unless you provide it in the
body of your comment. If you send an e-mail comment directly to EPA
without going through EDOCKET or regulations.gov, your e-mail address
will be automatically captured and included as part of the comment that
is placed in the public docket and made available on the Internet. If
you submit an electronic comment, EPA recommends that you include your
name and other contact information in the body of your comment and with
any disk or CD ROM you submit. If EPA cannot read your comment due to
technical difficulties and cannot contact you for clarification, EPA
may not be able to consider your comment. Electronic files should avoid
the use of special characters, any form of encryption, and be free of
any defects or viruses. For additional information about EPA's public
docket, visit EDOCKET on-line or see the Federal Register of May 31,
2002 (67 FR 38102) (FRL-7181-7).
Docket: All documents in the docket are listed in the EDOCKET index
at https://www.epa.gov/edocket/. Although listed in the index, some
information is not publicly available, i.e., CBI or other information
whose disclosure is restricted by statute. Certain other material, such
as copyrighted material, is not placed on the Internet and will be
publicly available only in hard copy form. Publicly available docket
materials are available either electronically in EDOCKET or in hard
copy at the OPPT Docket, EPA Docket Center, EPA West, Rm. B102, 1301
Constitution Ave., NW., Washington, DC. The Public Reading Room is open
from 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding legal
holidays. The EPA Docket Center Reading Room telephone number is (202)
566-1744, and the telephone number for the OPPT Docket, which is
located in the EPA Docket Center, is (202) 566-0280.
FOR FURTHER INFORMATION CONTACT: For general information contact: Colby
Lintner, Regulatory Coordinator, Environmental Assistance Division
(7408M), Office of Pollution Prevention and Toxics, Environmental
Protection Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460-
0001; telephone number: (202) 554-1404; e-mail address: TSCA-
Hotline@epa.gov.
For technical information contact: Amy Breedlove, Chemical Control
Division (7405M), Office of Pollution Prevention and Toxics,
Environmental Protection Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001; telephone number: (202) 564-9823; e-mail
address: breedlove.amy@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action Apply to Me?
You may be potentially affected by this action if you manufacture,
import, or process 2-EE (CAS No. 110-80-5), 2-EEA (CAS No. 111-15-9),
2-ME (CAS No. 109-86-4), or 2-MEA (CAS No. 110-49-6) for use in
consumer products or manufacture or import 2-MEA (CAS No. 110-49-6) at
levels greater than 10,000 pounds per year.
Persons who intend to import any chemical substance governed by a
final SNUR are subject to the TSCA section 13 (15 U.S.C. 2612) import
certification requirements, and to the regulations codified at 19 CFR
12.118 through 12.127 and 127.28. Those persons must certify that they
are in compliance with the SNUR requirements (see TSCA section 13 (15
U.S.C. 2612) and 19 CFR 12.118 through 12.127 and 127.28). The EPA
policy in support of import certification appears at 40 CFR part 707,
subpart B. In addition, any persons who export or intend to export a
chemical substance that is the subject of this proposed rule on or
after March 31, 2005 are subject to the export notification provisions
of TSCA section 12(b) (15 U.S.C. 2611(b)) (see 40 CFR 721.20), and must
comply with the
[[Page 9903]]
export notification requirements in 40 CFR part 707, subpart D.
Potentially affected entities may include, but are not limited to:
Manufacturers (defined by statute to include importers)
and processors of 2-EE, 2-EEA, 2-ME, and 2-MEA (NAICS 325 and 324110),
e.g., chemical manufacturing and petroleum refineries.
This listing is not intended to be exhaustive, but rather provides
a guide for readers regarding entities likely to be affected by this
action. Other types of entities not listed in this unit could also be
affected. The North American Industrial Classification System (NAICS)
codes have been provided to assist you and others in determining
whether this action might apply to certain entities. To determine
whether you or your business may be affected by this action, you should
carefully examine the applicability provisions in 40 CFR 721.5 for
SNUR-related obligations. If you have any questions regarding the
applicability of this action to a particular entity, consult the
technical person listed under FOR FURTHER INFORMATION CONTACT.
B. How Can I Access Electronic Copies of this Document and Other
Related Information?
In addition to using EDOCKET (https://www.epa.gov/edocket), you may
access this Federal Register document electronically through the EPA
Internet under the ``Federal Register'' listings at https://www.epa.gov/
fedrgstr/. A frequently updated electronic version of 40 CFR part 721
is available on E-CFR Beta Site Two at https://www.gpoaccess.gov/ecfr/.
C. What Should I Consider as I Prepare My Comments for EPA?
1. Submitting CBI. Do not submit this information to EPA through
EDOCKET, regulations.gov, or e-mail. Clearly mark the part or all of
the information that you claim to be CBI. For CBI information in a disk
or CD ROM that you mail to EPA, mark the outside of the disk or CD ROM
as CBI and then identify electronically within the disk or CD ROM the
specific information that is claimed as CBI. In addition to one
complete version of the comment that includes information claimed as
CBI, a copy of the comment that does not contain the information
claimed as CBI must be submitted for inclusion in the public docket.
Information so marked will not be disclosed except in accordance with
procedures set forth in 40 CFR part 2.
2. Tips for preparing your comments. When submitting comments,
remember to:
i. Identify the rulemaking by docket ID number and other
identifying information (subject heading, Federal Register date, and
page number).
ii. Follow directions. The Agency may ask you to respond to
specific questions or organize comments by referencing a Code of
Federal Regulations (CFR) part or section number.
iii. Explain why you agree or disagree; suggest alternatives and
substitute language for your requested changes.
iv. Describe any assumptions and provide any technical information
and/or data that you used.
v. If you estimate potential costs or burdens, explain how you
arrived at your estimate in sufficient detail to allow for it to be
reproduced.
vi. Provide specific examples to illustrate your concerns, and
suggest alternatives.
vii. Explain your views as clearly as possible, avoiding the use of
profanity or personal threats.
viii. Make sure to submit your comments by the comment period
deadline identified.
II. Background
A. What Action is the Agency Taking?
EPA is proposing to designate the manufacture, import, or
processing of 2-EE (CAS No. 110-80-5), 2-EEA (CAS No. 111-15-9), 2-ME
(CAS No. 109-86-4), and 2-MEA (CAS No. 110-49-6) for domestic use in
consumer products as a significant new use, as well as the manufacture
or import of 2-MEA (CAS No. 110-49-6) at levels greater than 10,000
pounds per year. ``Consumer product'' is defined at 40 CFR 721.3 as ``a
chemical substance that is directly, or as part of a mixture, sold or
made available to consumers for their use in or around a permanent or
temporary household or residence, in or around a school, or in
recreation.'' This proposed rule would require persons intending to
manufacture or import 2-MEA at levels greater than 10,000 pounds per
year as well as those intending to manufacture, import, or process 2-
EE, 2-EEA, 2-ME, or 2-MEA for domestic use in a consumer product to
submit a Significant New Use Notice (SNUN) to EPA at least 90 days
before such manufacture, import, or processing.
B. What is the Agency's Authority for Taking this Action?
Section 5(a)(2) of TSCA (15 U.S.C. 2604(a)(2)) authorizes EPA to
determine that a use of a chemical substance is a ``significant new
use.'' EPA must make this determination by rule after considering all
relevant factors, including those listed in TSCA section 5(a)(2). Once
EPA determines that a use of a chemical substance is a significant new
use, and promulgates a SNUR, section 5(a)(1)(B) of TSCA requires
persons to submit a SNUN to EPA at least 90 days before commencement of
manufacture, import, or processing of the chemical substance for that
use.
C. What is the Applicability of the General Regulatory Provisions?
General regulatory provisions for SNURs appear under subpart A of
40 CFR part 721. These provisions describe persons subject to the rule,
recordkeeping requirements, and exemptions to reporting requirements.
Provisions relating to user fees appear at 40 CFR part 700. Persons
subject to the rule, when finalized, would be required to comply with
the same notice requirements and EPA regulatory procedures as
submitters of premanufacture notices (PMNs) under section 5(a)(1)(A) of
TSCA. In particular, these requirements include the information
submission requirements of TSCA section 5(b) and 5(d)(1), the
exemptions authorized by TSCA section 5(h)(1), (2), (3), and (5), and
the regulations at 40 CFR part 720. Receipt of a SNUN by EPA may
trigger regulatory action under TSCA sections 5(e), 5(f), 6, or 7, if
appropriate, to control the activities on which it has received the
SNUN. If EPA does not take action, EPA is required under TSCA section
5(g) to explain in the Federal Register its reasons for not taking
action.
Persons who intend to export a substance identified in a proposed
or final SNUR are subject to the export notification provisions of TSCA
section 12(b). The regulations that interpret TSCA section 12(b) appear
at 40 CFR part 707, subpart D. Persons who intend to import a chemical
substance identified in a final SNUR are subject to the TSCA section 13
import certification requirements, which are codified at 19 CFR
sections 12.118 through 12.127 and section 127.28. Such persons must
certify that they are in compliance with TSCA requirements. The EPA
policy relating to import certification appears at 40 CFR part 707,
subpart B.
III. Summary of this Proposed Rule
A. Why is EPA Taking this Action?
1. Background. On January 24, 1984, EPA published an Advance Notice
of Proposed Rulemaking (ANPRM) (49 FR 2921) which stated that EPA
determined, based on animal studies, that adverse reproductive and
developmental effects are associated with the subject glycol ethers,
i.e., 2-EE,
[[Page 9904]]
2-EEA, 2-ME, and 2-MEA, at concentrations to which humans may be
exposed. (Ref. 1). EPA was considering the regulatory options available
under TSCA section 6 to control any unreasonable risks from these
chemicals. It solicited comments on the appropriateness of imposing a
partial or total ban on these chemicals. EPA had also consulted with
the Occupational Safety and Health Administration (OSHA) and the
Consumer Product Safety Commission (CPSC) on possible actions under
their legal authorities. Later, in October 1984, the Agency concluded
that these chemicals may pose a significant hazard to humans (Ref. 2).
However, by 1986, EPA's investigation of risks to consumers had led the
Agency to conclude that the current information would not support an
unreasonable risk finding for consumer use. This conclusion was based
on the fact that because of wholesale switching to substitute solvents,
EPA had not been able to identify manufacturers who were currently
using these glycol ethers in their consumer products. EPA stated that
it would continue to consult with the CPSC pursuant to section 9(d) of
TSCA to resolve outstanding issues, particularly to clarify whether
these glycol ethers were being used in consumer products (Ref. 3).
Additionally, EPA stated it was satisfied that any risks from the
substitutes were less than those presented by 2-EE, 2-EEA, 2-ME, or 2-
MEA, and that use of substitutes would reduce overall risks to humans
(Ref. 4).
On May 20, 1986 (51 FR 18488), EPA issued a report to OSHA, under
section 9(a) of TSCA, stating that EPA had a reasonable basis to
conclude that the risk of injury to worker health from exposure to 2-
EE, 2-EEA, 2-ME, and 2-MEA during their manufacturing, processing, and
use is unreasonable and that this risk may be prevented or reduced
sufficiently by OSHA regulatory action (Ref. 3).
2. Initial regulatory response by OSHA. OSHA published its response
on December 11, 1986 (51 FR 44699), stating that it had preliminarily
concluded that occupational exposures to 2-EE, 2-EEA, 2-ME, and 2-MEA
at the current OSHA permissible exposure limits (PELs) may present
significant risks to the health of workers (Ref. 5). On April 2, 1987
(52 FR 10586), OSHA published an ANPRM under section 6(b) of the
Occupational Safety and Health Act of 1970 (29 U.S.C. 654), announcing
its intention to proceed to rulemaking to reduce occupational exposure
to 2-EE, 2-EEA, 2-ME, and 2-MEA (Ref. 6). On March 23, 1993 (58 FR
15526), OSHA published a proposed rule that would reduce the chemicals'
PELs and provide other protective measures for the approximately 46,000
workers exposed to the substances (Ref. 7). After publishing the 1993
proposal, OSHA held informal public hearings on the proposal, and the
record closed in March 1994 (Ref. 8).
3. EPA regulatory activities in the 1990's. In the period
immediately after OSHA published its proposed rule, EPA, on July 27,
1993 (58 FR 40262) (Ref. 9), promulgated a TSCA section 4 test rule to
require neurotoxicity testing of 2-EE (among other chemical
substances). The required testing was based on suggestive evidence of
neurotoxicity involving the alteration of motor performance and
avoidance conditioning in the offspring of rats exposed to 100 and 200
parts per million (ppm) (Refs. 10 and 11), as well as substantial
occupational and consumer exposure, and substantial environmental
release (Ref. 12). After publication of that rule, however, the
producers of 2-EE told EPA that there were no consumer uses of 2-EE
(Ref. 13). Given this information, and because OSHA was continuing to
work toward revising the PELs for glycol ethers, EPA believed that
exposure to 2-EE was not substantial and revoked the TSCA section 4
testing requirements for 2-EE in a settlement agreement with producers
in 1994 (Ref. 13). The settlement agreement required that the Chemical
Manufacturers Association (now the American Chemistry Council (ACC))
and the manufacturers and processors of these chemicals perform certain
neurotoxicity and pharmacokinetics testing on 7 of the 10 chemicals
subject to the final neurotoxicity test rule (Ref. 14). This revocation
was also reflected in the January 23, 1995 Federal Register (60 FR
4514) (FRL-4924-7) (Ref. 15). At the time that EPA was considering
revoking the testing requirements in the section 4 rule, the Agency
also believed it would be prudent to provide some mechanism to monitor
the possible re-emergence of the consumer use of 2-EE. Therefore, in
the same notice in which it proposed to revoke the testing requirements
of 2-EE (59 FR 33187, June 27, 1994) (Ref. 14), EPA announced its
intention to propose and promulgate a SNUR. The parties to the
settlement agreement supported such a SNUR (Ref. 13).
4. Final OSHA regulatory actions. OSHA reopened the record on
August 8, 2002 seeking comment on how the substances were being used in
the workplace, including their level of production, and the industries
and processes in which they were used (Ref. 16). Based on the
information submitted during this comment period, OSHA determined that
a major decline in the production of the substances was apparent and
that their use in several key industry sectors has been eliminated or
is in the process of being phased out. Additionally, OSHA determined
that where these substances were still being manufactured, their
production was virtually limited to ``closed systems'' and average
exposures already were at or below the proposed PEL (Ref. 8). OSHA
concluded that the proposed rule was no longer necessary and withdrew
its proposed Glycol Ethers rule on December 31, 2003 (Ref. 8).
B. What are the Uses and Production Levels of these Chemicals?
The chemical substances 2-EE, 2-EEA, 2-ME, and 2-MEA, are
considered members of a broad class of chemicals known as ethylene
glycol ethers. As with other glycol ethers, 2-EE, 2-EEA, 2-ME, and 2-
MEA are colorless, flammable liquids which are compatible with a broad
range of resins and can be mixed with both organic solvents and water.
They have relatively low vapor pressures, high boiling points, low
evaporation rates and high flash points. Due to these physical
characteristics, 2-EE, 2-EEA, 2-ME, and 2-MEA are potentially useful in
a wide variety of applications, particularly as solvents (Ref. 7). They
have been used in many industrial and consumer products, but concerns
for their health effects have caused these uses to be severely
curtailed in recent years.
U.S. production of 2-EE peaked at 200.7 million pounds in 1980 and
had decreased to 118 million pounds by 1999. U.S. consumption of 2-EE
(including consumption to manufacture 2-EEA) was 175 million pounds in
1980, and down to 53 million pounds in 1999, of which, 52 of the 53
million pounds was used to manufacture 2-EEA. U.S. consumption of 2-EE
for uses other than acetate production was less than 1 million pounds.
Production and/or imports of 2-EE were below 100 million pounds based
on data collected for the 2002 TSCA section 8(a) Inventory Update Rule
(IUR) (see 40 CFR part 710) (Ref. 17).
U.S. production of 2-EEA dropped from 136.7 million pounds in 1984
to 72 million pounds in 1999. In 1999, all but one million of those
pounds were exported. Data collected for the 2002 IUR show production
and/or import levels of less than 100 million pounds (Ref. 17).
[[Page 9905]]
U.S. production of 2-ME, which peaked at 97.3 million pounds in
1980, was down to 55 million pounds by 1999 (at which time most 2-ME
produced was exported). U.S. consumption, still 50 to 53 million pounds
in the early 1990's, had declined to approximately 3 million pounds in
1999. 2002 IUR data show that production and/or import was less than 50
million pounds (Ref. 17).
U.S. production of 2-MEA in 1991 was estimated to be 0.5 million
pounds. There were no reports of 2-MEA production or import under the
IUR in 1994, 1998, and 2002 (Ref. 17). Therefore, EPA is proposing that
persons intending to manufacture or import 2-MEA at levels greater than
10,000 pounds per year as well as persons intending to manufacture,
import, or process 2-EE, 2-EEA, 2-ME, or 2-MEA for domestic use in a
consumer product to submit a SNUN to EPA at least 90 days before such
manufacture, import, or processing.
Production of the E-series glycol ethers, i.e., ethanol based
glycol ethers and their acetates, had been declining or has ceased and
EPA believes there is no ongoing use of these chemicals in consumer
products in the U.S. In response to a proposed TSCA section 4 test
rule, manufacturers of 2-EE told EPA that there was no consumer use of
2-EE (Ref. 13). In 2004, a representative for the Ethylene Glycol
Ethers Panel of the ACC confirmed that concerns over the toxicity of E-
series glycol ethers has subsequently resulted in the elimination of E-
series glycol ethers from all consumer products in the 1980's and the
development of alternatives to 2-ME, 2-EE, and 2-EEA (Ref. 18).
C. What are the Potential Routes of Exposure?
Despite the diminished potential for human exposure due to the
decline in production and use in industrial products and the
termination of the chemicals' use in consumer products as discussed in
Unit III.B., EPA believes there may still be some potential for human
exposure to 2-EE, 2-EEA, 2-ME, and 2-MEA. Their physical
characteristics discussed in Unit III.B. make them useful in a variety
of applications, particularly as solvents. ``A major route of exposure
is the skin. The ubiquity of solvents and the casual approach [of
consumers] to their use almost assure skin contact with liquid
solvents.'' (Ref. 19). Also, as members of the ethylene series (``E-
series'' used in Unit III.B.) of glycol ethers, 2-EE, 2-EEA, 2-ME, and
2-MEA are well absorbed from the skin. They are so readily absorbed
through the skin that the dermal to oral 50% lethal dose
(LD50) ratio is approximately one (Ref 19).
Although 2-EE, 2-EEA, 2-ME, and 2-MEA are not highly volatile, high
vapor concentrations can be generated under the conditions of solvent
use. When glycol ether vapors enter the lungs they can readily diffuse
across respiratory membranes and enter the bloodstream (Ref. 19).
D. What are the Potential Sources of Exposure?
EPA believes that 2-EE, 2-ME, 2-MEA, and 2-EEA are currently used
only in industrial products. EPA also believes that the documented
decline in production volumes of 2-EE, 2-EEA, 2-ME, and 2-MEA discussed
in Unit III.B. has probably already reduced the potential for
occupational exposure. OSHA reported in late 2003 that production, use,
and exposure to these glycol ethers has ceased or is virtually limited
to closed system production where there is little opportunity for
worker exposure. Exposure levels in those operations already are at or
below the proposed PELs. In addition, use of these glycol ethers has
largely been replaced by less-toxic substitutes, such as E-series butyl
glycol ethers, other ethylene glycol ethers, propylene glycol ethers,
and other types of solvents (Ref. 8). A decline in environmental
release of 2-EE is reflected in Toxics Release Inventory (TRI) data
from the years 1987 through 1996 which indicates a steady decline from
2,770,113 pounds in 1987 to 192,468 pounds in 1996 (Ref. 20) to 103,513
pounds in 2001 (Ref. 17).
EPA has found evidence which suggests that 2-EE, as well as 2-ME,
2-MEA, and 2-EEA, are not currently used in consumer products (Ref.
17), and the manufacturers of 2-EE which were parties to the 1994
settlement agreement told EPA that, to the best of their knowledge,
there were, at that time, no consumer uses of 2-EE (Refs. 9 and 13).
The ACC also reported in 2001, citing the SRI Chemical Economics
Handbook as its source, that the remaining domestic consumption of 2-EE
is in non-consumer solvents for paints, coatings, and other industrial
uses; the only remaining domestic use of 2-EEA is in machinery and
equipment paints and coatings; and the only remaining use of 2-ME,
other than as a chemical intermediate, is as a jet fuel deicer. No
information on current uses of 2-MEA was identified (Ref. 17).
E. What are the Health Effects of these Chemicals?
Toxicity studies in rats, rabbits, mice, and monkeys via
inhalation, dermal, and oral exposure, have shown clearly and
consistently that 2-EE and 2-ME can cause adverse hematologic,
reproductive, and developmental effects. These effects include
decreased white and red blood cell counts, decreased hemoglobin,
decreased fertility, decreased sperm count, decreased testes size and
weight, increased resorptions, increased fetal malformations, and
behavioral and neurochemical alterations in the neonate (Refs. 7 and
2).
Although data on workers is often compromised by confounding
exposure to other solvents, studies of workers exposed to 2-ME and 2-EE
have documented adverse effects on the hematologic and male
reproductive systems. Blood effects observed among the exposed workers
include bone marrow injury, reduced red and white blood cell counts,
and anemia, while the major reproductive effect observed is reduced
sperm count (Ref. 7). Thus, although the human data have their
limitations, there is evidence of certain adverse effects in humans
exposed to 2-EE and 2-ME and this evidence is consistent with a strong
body of evidence of the same or similar effects in experimental
animals.
Animal studies with 2-EEA and 2-MEA have shown that these acetates
induce adverse reproductive, developmental, and hematological effects
similar to those ascribed to their parent glycol ethers, 2-EE and 2-ME.
These studies confirm the findings of metabolic studies which indicate
that 2-ME, 2-EE, and their acetates follow similar metabolic pathways,
producing the same metabolites, which are the active agents most likely
responsible for the observed effects (Ref. 7).
IV. Determining a Significant New Use
Section 5(a)(2) of TSCA provides that EPA's determination that a
use of a chemical substance is a significant new use must be made after
consideration of all relevant factors including:
The projected volume of manufacturing and processing of a
chemical substance.
The extent to which a use changes the type or form of
exposure of human beings or the environment to a chemical substance.
The extent to which a use increases the magnitude and
duration of exposure of human beings or the environment to a chemical
substance.
The reasonably anticipated manner and methods of
manufacturing, processing, distribution in commerce, and disposal of a
chemical substance.
EPA construes the statute to allow consideration of any other
relevant factors, in addition to those enumerated
[[Page 9906]]
in section 5(a)(2)(A) through (D) of TSCA.
To determine what would constitute a significant new use of 2-EE,
2-EEA, 2-ME, and 2-MEA, EPA considered relevant information about the
toxicity of the substances, likely exposures/releases associated with
possible uses, and the four factors listed in section 5(a)(2) of TSCA.
The latest information available to EPA indicates that there is no
ongoing domestic use of 2-EE, 2-EEA, 2-ME, or 2-MEA in consumer
products. EPA believes that the renewed use of 2-EE, 2-EEA, 2-ME, or 2-
MEA in a consumer product would increase the magnitude and duration of
exposure. Considering the health concerns for 2-EE, 2-EEA, 2-ME, and 2-
MEA, EPA believes that individuals could suffer adverse effects from
their use in consumer products. Thus, EPA is proposing to designate
``domestic use in a consumer product'' as well as the manufacture or
import of 2-MEA at levels greater than 10,000 pounds per year as a
significant new use of 2-EE, 2-EEA, 2-ME, and 2-MEA.
Based on these considerations, EPA is pursuing the following
objectives with regard to the use of 2-EE, 2-EEA, 2-ME, and 2-MEA in
consumer products:
EPA wants to ensure that it would receive notice of any
person's intent to manufacture or import 2-MEA at levels greater than
10,000 pounds per year or intending to manufacture, import, or process
2-EE, 2-EEA, 2-ME, and 2-MEA for domestic use in a consumer product
before that activity begins.
EPA wants to ensure that it would have the opportunity to
review and evaluate data submitted in a SNUN before the notice
submitter begins manufacturing, importing, or processing 2-EE, 2-EEA,
2-ME, and 2-MEA for domestic use in a consumer product or manufacturing
or importing 2-MEA at levels greater than 10,000 pounds per year.
EPA wants to ensure that it would be able to regulate
prospective manufacturers, importers, or processors of 2-EE, 2-EEA, 2-
ME, and 2-MEA before use of any of these chemicals in a consumer
product occurs, provided that the degree of potential risk is
sufficient to warrant such regulation.
As noted in Unit III.B., the production of the chemicals included
in this SNUR have declined significantly over time. EPA is not aware of
current domestic consumer uses for the chemicals, and substitutes are
available. The Agency will use information submitted pursuant to the
Inventory Update Rule (40 CFR part 710) to track the production volumes
and uses of these chemicals. If needed, EPA may pursue additional
regulatory actions as appropriate under TSCA sections 4, 5, 6, or 8.
V. Test Data and Other Information
EPA recognizes that section 5 of TSCA does not require the
development of any particular test data before submission of a SNUN.
Persons are required only to submit test data in their possession or
control and to describe any other data known to or reasonably
ascertainable by them (15 U.S.C. 2604(d); 40 CFR 721.25).
However, SNUN submitters should be aware that EPA will be better
able to evaluate SNUNs which provide detailed information on:
Human exposure and environmental releases that may result
from the significant new use of the chemical substances.
Potential benefits of the chemical substances.
Information on risks posed by the chemical substances
relative to risks posed by potential substitutes.
Submitters should consider including with a SNUN any other
available studies on the chemical substances or studies on analogous
substances which may demonstrate that the significant new uses being
reported are unlikely to present an unreasonable risk.
In view of the potential risks posed by these chemicals, EPA would
recommend that potential SNUN submitters include data that would permit
a reasoned evaluation of risks posed by these chemicals. EPA encourages
persons to consult with the Agency before submitting a SNUN for these
substances. As part of this optional pre-notice consultation, EPA would
discuss specific data it believes are necessary to evaluate a
significant new use. A SNUN submitted without sufficient data to
reasonably evaluate risks posed by a significant new use of 2-EE, 2-
EEA, 2-ME, and/or 2-MEA may increase the likelihood that EPA will take
action under TSCA section 5(e) to prohibit or limit activities
associated with these chemicals. EPA recommends that potential SNUN
submitters contact the Agency early enough that they will be able to
conduct any appropriate tests.
VI. Recordkeeping Requirements
In addition to the recordkeeping requirements of 40 CFR 721.40
which require persons subject to a SNUR to retain documentation of
information contained in a SNUN, EPA is proposing to require the
recordkeeping requirements in 40 CFR 721.125 (a), (b), and (c) in this
SNUR. Section 721.125(a) requires records documenting manufacture and
importation volume and dates; Sec. 721.125(b) documents volumes
purchased in the U.S. by processors, the names and addresses of
suppliers, and the dates of purchase; and Sec. 721.125(c) requires
records documenting the names and addresses (including shipment
destination address, if different) of all persons outside the site of
manufacture, importation, or processing to whom the manufacturer,
importer, or processor directly sells or transfers the substance, the
date, and the quantity of each sale or transfer. EPA is also proposing
to require the maintenance of records documenting the compliance with
the significant new use of domestic use in a consumer product or the
manufacture or import of 2-MEA at levels greater than 10,000 pounds per
year. For the significant new use of 2-MEA manufacture or import at
levels greater than 10,000 pounds per year, records required by Sec.
721.125(a) would be sufficient. For the significant new use of domestic
use in a consumer product, required documentation must demonstrate
compliance with the significant new use, i.e.,: 1) That 2-EE, 2-EEA, 2-
ME or 2-MEA were not manufactured, imported, or processed for use in a
consumer product; and, 2) that, where no significant new use notice is
filed, any recipients of these chemicals either (a) were notified of
the SNUR and its provisions by the manufacturer, importer, or
processor, (b) knew of the SNUR independently, or (c) cannot undertake
the significant new use. See 40 CFR 720.5(a)(2). These records will
enable EPA to determine compliance with the SNUR.
VII. SNUN Submissions
SNUNs should be mailed to the Environmental Protection Agency, OPPT
Document Control Office (7407M), 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001. Information must be submitted in the form
and manner set forth in EPA Form No. 7710-25. This form is available
from the Environmental Assistance Division (7408M), OPPT, Environmental
Protection Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460-
0001 (see 40 CFR 721.25(a) and 720.40(a)(2)(i)).
VIII. Alternatives
Before proposing this SNUR, EPA considered promulgating a TSCA
section 8(a) reporting rule for 2-EE, 2-EEA, 2-ME, and 2-MEA. Under
such a rule, EPA could generally require any person to report
information to the Agency when they intend to manufacture, import, or
process 2-EE, 2-EEA, 2-ME, or 2-MEA. However, in the case of these
particular substances, the
[[Page 9907]]
use of TSCA section 8(a) rather than SNUR authority would have several
drawbacks. First, EPA would not be able to take immediate follow-up
regulatory action under TSCA sections 5(e) or 5(f) to prohibit or limit
the activity before it begins. In addition, EPA may not receive
important information from small businesses, because such firms
generally are exempt from TSCA section 8(a) reporting requirements. In
view of the level of health concerns for 2-EE, 2-EEA, 2-ME, and 2-MEA,
EPA believes that a TSCA section 8(a) rule for these substances would
not meet EPA's regulatory objectives.
Currently 2-EE, 2-EEA, 2-ME, and 2-MEA are not subject to any other
Federal regulation which would notify the Federal Government of
activities that might result in adverse exposures associated with the
proposed significant new uses, or provide a mechanism that could
protect against potentially adverse exposures associated with those
uses before they occur.
IX. Applicability of Rule to Uses Occurring Before Effective Date of
the Final Rule
As discussed in the Federal Register of April 24, 1990 (55 FR
17376), EPA believes that the intent of TSCA section 5(a)(1)(B) is best
served by designating a use as a significant new use as of the date of
publication of the proposed SNUR rather than as of the effective date
of the final rule. If uses begun after publication of the proposed SNUR
were considered to be ongoing rather than new, it would be difficult
for EPA to establish SNUR notice requirements, because any person could
defeat the SNUR by initiating the proposed significant new use before
the rule became final.
Any person who, after publication of this proposed SNUR, begins to
manufacture, import, or process 2-EE, 2-EEA, 2-ME, or 2-MEA for a
proposed significant new use must stop such activity before the
effective date of the final rule. Persons who cease those activities
will have to meet all SNUR notice requirements and wait until the end
of the notice review period, including all extensions, before engaging
in any activities designated as significant new uses. If, however,
persons who begin to manufacture, import, or process any of these
chemicals between the proposal and the effective date of the final SNUR
meet the conditions of advance compliance as codified at 40 CFR
721.45(h), those persons would be considered to have met the
requirements of the final SNUR for those activities.
X. Economic Analysis
EPA has evaluated the potential costs of establishing SNUR
reporting requirements for potential manufacturers, importers, and
processors of the chemical substances included in this proposed rule.
While there is no precise way to calculate the total annual cost of
compliance with the final rule, given the uncertainties related to
predicting the number of SNUN's that would be submitted as a result of
this SNUR, EPA estimates that the cost for preparing and submitting a
SNUN is $7,174, including a $2,500 user fee required by 40 CFR part
700.45(b)(2)(iii) (Ref. 18). Small businesses with annual sales of less
than $40 million when combined with those of the parent company (if
any) are subject to a reduced user fee of $100 (40 CFR part
700.45(b)(1)). Based on past experience with SNURs and the low number
of SNUNs which are submitted on an annual basis, EPA believes that
there will be few, if any, SNUNs submitted as a result of this SNUR.
The costs of submission of SNUNs will not be incurred by any company
unless a company decides to pursue a significant new use as defined in
this SNUR. Furthermore, while the expense of a notice and the
uncertainty of possible EPA regulation may discourage certain
innovations, that impact would be limited because such factors are
unlikely to discourage an innovation that has high potential value.
EPA's complete economic analysis is available in the public docket for
this proposed rule (Ref. 18).
Under section 12(b) of TSCA, exporters must notify EPA if they
export or intend to export a chemical substance or mixture for which a
rule has been proposed or promulgated under section 5 or 6. Notice must
be provided for the first export or intended export to a particular
country in a calendar year. In an economic analysis of an amendment to
the rules implementing TSCA section 12(b), EPA estimated that the one-
time cost of preparing and submitting an export notification was $62.60
in 1992, or $93.02 when inflated to 2003 dollars by a factor of
approximately 1.5, from the Employment Cost Index for White Collar
Occupations. The total costs of export notification will vary per
chemical, depending on the number of required notifications (i.e.,
number of countries to which the chemical is exported). EPA is unable
to make any estimate of the likely number of export notifications for
chemicals covered in this SNUR (Ref. 17).
XI. References
The public docket for this action, OPPT-2004-0111, currently
includes the following documents:
1. USEPA. ``2-Methoxyethanol and 2-Ethoxyethanol and their
Acetates; Initiation of Regulatory Investigation, Advance Notice of
Proposed Rulemaking.'' 49 FR 2921. (January 24, 1984).
2. USEPA. ``Glycol Ethers Health Effects Assessment.'' Intra-agency
memorandum from M.S. Ottley to Harry Teitelbaum, Existing Chemicals
Assessment Division. (October 31, 1984).
3. U.S. Environmental Protection Agency (USEPA). ``Toxic and
Hazardous Substances Control; 2-Methoxyethanol, 2-Ethoxyethanol and
their Acetates; Referral For Additional Action.'' TSCA section 9
referral to OSHA. 51 FR 18488. (May 20, 1986).
4. USEPA. ``Substitutes for 2-Ethoxyethanol (2-EE), 2-
Methoxyethanol (2-ME) and their Acetates.'' Intra-agency memorandum
from Harry Teitelbaum, Risk Management Branch to Joseph Merenda,
Existing Chemicals Assessment Division. (March 15, 1984).
5. OSHA. ``Occupational Exposure to 2-Methoxyethanol, 2-
Ethoxyethanol and Their Acetates; Response to the Environmental
Protection Agency under section 9(a) of the Toxic Substances Control
Act.'' 51 FR 44699. (December 11, 1986).
6. OSHA. ``Occupational Exposure to 2-Methoxyethanol, 2-
Ethoxyethanol and Their Acetates; Advance Notice of Proposed
Rulemaking.'' 52 FR 10586. (April 2, 1987).
7. Occupational Health and Safety Administration (OSHA).
``Occupational Exposure to 2-Methoxyethanol, 2-Ethoxyethanol and their
Acetates (Glycol Ethers); Proposed Rule.'' 58 FR 15526 (March 23,
1993).
8. OSHA. ``Occupational Exposure to 2-Methoxyethanol, 2-
Ethoxyethanol and Their Acetates (Glycol Ethers); Withdrawal of
Proposed Rule.'' 68:75475-75476. (December 31, 2003).
9. USEPA. ``Multi-substance Rule for the Testing of Neurotoxicity;
Final Rule.'' 58 FR 40262. (July 27, 1993).
10. Nelson, B.K., Brightwell, W.S., Setzer, J.V., Taylor, B.J.,
Hornung, R.W. and O'Donohue, T.L. ``Ethoxyethanol Behavioral Teratology
in Rats.'' Neurotoxicology. 2:231-249. (1981).
11. Nelson, B.K., Brightwell, W.S. and Setzer, J.V. ``Prenatal
Interaction Between Ethanol and the Industrial Solvent 2-Ethoxyethanol
in Rats; Maternal and Behavioral Teratogenic Effects.'' Neurobehavioral
Toxicology and Teratology. 4:387-394. (1982).
[[Page 9908]]
12. USEPA. ``Multi-substance Rule for the Testing of Neurotoxicity;
Proposed Rule.'' 56 FR 9105. (March 4, 1991).
13. United States Court of Appeals for the Fifth Circuit.
Settlement Agreement between Environmental Protection Agency and
petitioners (Chemical Manufacturers Association et al.), No. 93-5381.
(April 28, 1994).
14. USEPA. ``Proposed Revocation of Final Multi-substance Rule for
the Testing of Neurotoxicity; Proposed Rule.'' 59 FR 33187 (June 27,
1994).
15. USEPA. ``Revocation of Final Multi-substance Rule for the
Testing of Neurotoxicity.'' 60 FR 4514. (January 23, 1995).
16. OSHA. ``Occupational Exposure to 2-Methoxyethanol, 2-
Ethoxyethanol and Their Acetates (Glycol Ethers).'' 67 FR 51524.
(August 8, 2002).
17. USEPA, 2004. ``Economic Analysis of Expedited Significant New
Use Rules for Four Glycol Ethers.'' Washington, DC: U.S. EPA/OPPT/EETD/
EPAB, October 27, 2004.
18. ACC, 2004. Personal Communication Between American Chemistry
Council, Ethylene Glycol Ethers Panel representative and Jason Sacks,
Abt Associates Inc. May 10, 2004.
19. Casarett and Doull's Toxicology. Editors: Klaassen, C.D.,
Amdur, M.O., and Doull J. Chapter 20: Toxic Effects of Solvents and
Vapors. Pages 636-638 and 656-658, 3rd Edition. (1986).
20. USEPA. Toxic Release Inventory (TRI). Total annual
environmental releases of 2-ethoxyethanol for the years 1987 through
1996. TRI printouts. (April 26, 1994, May 6, 1994, May 19, 1998, and
May 28, 1998).
XII. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory Planning and Review
Under Executive Order 12866, entitled Regulatory Planning and
Review (58 FR 51735, October 4, 1993), the Office of Management and
Budget (OMB) has determined that proposed or final SNURs are not a
``significant regulatory action'' subject to review by OMB, because
they do not meet the criteria in section 3(f) of the Executive Order.
B. Paperwork Reduction Act
According to the Paperwork Reduction Act (PRA), 44 U.S.C. 3501 et
seq., an Agency may not conduct or sponsor, and a person is not
required to respond to a collection of information that requires OMB
approval under the PRA, unless it has been approved by OMB and displays
a currently valid OMB control number. The OMB control numbers for EPA's
regulations in title 40 of the CFR, after appearing in the Federal
Register, are listed in 40 CFR part 9, and included on the related
collection instrument or form, if applicable.
The information collection requirements related to this action have
already been approved by OMB pursuant to the PRA under OMB control
number 2070-0038 (EPA ICR No. 1188). This action would not impose any
burden requiring additional OMB approval. If an entity were to submit a
SNUN to the Agency, the annual burden is estimated to average 105 hours
per submission. This burden estimate includes the time needed to review
instructions, search existing data sources, gather and maintain the
data needed, and complete, review, and submit the required SNUN.
Send any comments about the accuracy of the burden estimate, and
any suggested methods for minimizing respondent burden, including
through the use of automated collection techniques, to the Director,
Collection Strategies Division, Office of Environmental Information
(2822T), Environmental Protection Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001. Please remember to include the OMB control
number in any correspondence, but do not submit any completed forms to
this address.
C. Regulatory Flexibility Act
Pursuant to section 605(b) of the Regulatory Flexibility Act (RFA)
(5 U.S.C. 601 et seq.), the Agency hereby certifies that promulgation
of this SNUR would not have a significant adverse economic impact on a
substantial number of small entities. The rationale supporting this
conclusion is as follows. A SNUR applies to any person (including small
or large entities) who intends to engage in any activity described in
the rule as a ``significant new use.'' By definition of the word
``new,'' and based on all information currently available to EPA, it
appears that no small or large entities presently engage in such
activity. Since a SNUR only requires that any person who intends to
engage in such activity in the future must first notify EPA by
submitting a SNUN, no economic impact would even occur until someone
decides to engage in those activities. Although some small entities may
decide to conduct such activities in the future, EPA cannot presently
determine how many, if any, there may be. However, EPA's experience to
date is that, in response to the promulgation of over 1,000 SNURs, the
Agency receives on average only 10 notices per year. Of those SNUNs
submitted, none appear to be from small entities in response to any
SNUR. In addition, the estimated reporting cost for submission of a
SNUN (see Unit X.), are minimal regardless of the size of the firm.
Therefore, EPA believes that the potential economic impact of complying
with this SNUR is not expected to be significant or adversely impact a
substantial number of small entities. In a SNUR that published on June
2, 1997 (62 FR 29684) (FRL-5597-1), the Agency presented its general
determination that proposed and final SNURs are not expected to have a
significant economic impact on a substantial number of small entities,
which was provided to the Chief Counsel for Advocacy of the Small
Business Administration.
D. Unfunded Mandates Reform Act
Based on EPA's experience with proposing and finalizing SNURs,
State, local, and Tribal governments have not been impacted by these
rulemakings, and EPA does not have any reasons to believe that any
State, local, or Tribal government would be impacted by this
rulemaking. As such, EPA has determined that this regulatory action
would not impose any enforceable duty, contain any unfunded mandate, or
otherwise have any affect on small governments subject to the
requirements of sections 202, 203, 204, or 205 of the Unfunded Mandates
Reform Act of 1995 (UMRA) (Public Law 104-4).
E. Executive Order 13132: Federalism
This action would not have a substantial direct effect on States,
on the relationship between the national government and the States, or
on the distribution of power and responsibilities among the various
levels of government, as specified in Executive Order 13132, entitled
Federalism (64 FR 43255, August 10, 1999).
F. Executive Order 13175: Consultation and Coordination with Indian
Tribal Governments
This proposed rule would not have Tribal implications because it is
not expected to have substantial direct effects on Indian Tribes. This
proposed rule would not significantly or uniquely affect the
communities of Indian Tribal governments, nor would it involve or
impose any requirements that affect Indian Tribes. Accordingly, the
requirements of Executive Order 13175, entitled Consultation and
Coordination with Indian Tribal Governments (65 FR 67249, November 6,
2000), do not apply to this proposed rule.
[[Page 9909]]
G. Executive Order 13045: Protection of Children from Environmental
Health Risks and Safety Risks
This action is not subject to Executive Order 13045, entitled
Protection of Children from Environmental Health Risks and Safety Risks
(62 FR 19885, April 23, 1997), because this is not an economically
significant regulatory action as defined by Executive Order 12866, and
this action does not address environmental health or safety risks
disproportionately affecting children.
H. Executive Order 13211: Actions that Significantly Affect Energy
Supply, Distribution, or Use
This proposed rule is not subject to Executive Order 13211,
entitled Actions Concerning Regulations That Significantly Affect
Energy Supply, Distribution, or Use (66 FR 28355, May 22, 2001),
because this action is not expected to affect energy supply,
distribution, or use.
I. National Technology Transfer Advancement Act
In addition, since this action does not involve any technical
standards, section 12(d) of the National Technology Transfer and
Advancement Act of 1995 (NTTAA), Public Law 104-113, section 12(d) (15
U.S.C. 272 note), does not apply to this action.
J. Executive Order 12898: Federal Actions to Address Environmental
Justice in Minority Populations and Low-Income Populations
This action does not entail special considerations of environmental
justice related issues as delineated by Executive Order 12898, entitled
Federal Actions to Address Environmental Justice in Minority
Populations and Low-Income Populations (59 FR 7629, February 16, 1994).
K. Executive Order 12988: Civil Justice Reform
In issuing this proposed rule, EPA has taken the necessary steps to
eliminate drafting errors and ambiguity, minimize potential litigation,
and provide a clear legal standard for affected conduct, as required by
section 3 of Executive Order 12988, entitled Civil Justice Reform (61
FR 4729, February 7, 1996).
List of Subjects in 40 CFR Part 721
Environmental protection, Chemicals, Hazardous substances,
Reporting and recordkeeping requirements.
Dated: February 16, 2005.
Charles M. Auer,
Director, Office of Pollution Prevention and Toxics.
Therefore, it is proposed that 40 CFR part 721 be amended as
follows:
PART 721--[AMENDED]
1. The authority citation for part 721 would continue to read as
follows:
Authority: 15 U.S.C. 2604, 2607, and 2625(c).
2. Add new Sec. 721.10001 to subpart E to read as follows:
Sec. 721.10001 2-Ethoxyethanol, 2-ethoxyethanol acetate, 2-
methoxyethanol, and 2-methoxyethanol acetate.
(a) Chemical substances and significant new uses subject to
reporting. (1) The chemical substances identified as 2-ethoxyethanol
(CAS No. 110-80-5), 2-ethoxyethanol acetate (CAS No. 111-15-9), 2-
methoxyethanol (CAS No. 109-86-4), and 2-methoxyethanol acetate (CAS
No. 110-49-6) are subject to reporting under this section for the
significant new use described in paragraph (a)(2) of this section.
(2) The significant new use is domestic use in a consumer product
or the manufacture or import of 2-methoxyethanol acetate at levels
greater than 10,000 pounds per year.
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), and (c) apply to the significant new use specified in
Sec. 721.10001. In addition, records documenting compliance with the
significant new use of domestic use in a consumer product or the
manufacture or import of 2-methoxyethanol acetate at levels greater
than 10,000 pounds per year must be maintained.
(2) [Reserved]
[FR Doc. 05-3911 Filed 2-28-05; 8:45 am]
BILLING CODE 6560-50-S