Polymer of 2-Ethyl-2-(Hydroxymethyl)-1,3-Propanediol, Oxirane, Methyloxirane, 1,2-Epoxyalkanes; Tolerance Exemption, 10074-10077 [E7-4083]
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10074
Federal Register / Vol. 72, No. 44 / Wednesday, March 7, 2007 / Rules and Regulations
Participant’s benefits to Spouse as the
alternate payee. Participant marries Spouse 2,
and then they divorce. Participant’s 401(k)
plan administrator subsequently receives a
domestic relations order pertaining to Spouse
2. The order assigns to Spouse 2 a portion of
Participant’s 401(k) benefits not already
allocated to Spouse 1. The second order does
not fail to be a QDRO solely because the
second order is issued after the plan
administrator has determined that an earlier
order pertaining to Spouse 1 is a QDRO.
(c) Timing. (1) Subject to paragraph
(d)(1) of this section, a domestic
relations order shall not fail to be
treated as a qualified domestic relations
order solely because of the time at
which it is issued.
(2) The rule described in paragraph
(c)(1) of this section is illustrated by the
following examples:
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Example (1). Orders issued after death.
Participant and Spouse divorce, and the
administrator of Participant’s plan receives a
domestic relations order, but the
administrator finds the order deficient and
determines that it is not a QDRO. Shortly
thereafter, Participant dies while actively
employed. A second domestic relations order
correcting the defects in the first order is
subsequently submitted to the plan. The
second order does not fail to be treated as a
QDRO solely because it is issued after the
death of the Participant.
Example (2). Orders issued after divorce.
Participant and Spouse divorce. As a result,
Spouse no longer meets the definition of
‘‘surviving spouse’’ under the terms of the
plan. Subsequently, the plan administrator
receives a domestic relations order requiring
that Spouse be treated as the Participant’s
surviving spouse for purposes of receiving a
death benefit payable under the terms of the
plan only to a participant’s surviving spouse.
The order does not fail to be treated as a
QDRO solely because, at the time it is issued,
Spouse no longer meets the definition of a
‘‘surviving spouse’’ under the terms of the
plan.
Example (3). Orders issued after annuity
starting date. Participant retires and
commences benefit payments in the form of
a straight life annuity, with respect to which
Spouse waives the surviving spousal rights
provided under the plan and section 205 of
ERISA. Participant and Spouse divorce after
Participant’s annuity starting date and
present the plan with a domestic relations
order providing for Spouse, as alternate
payee, to receive half of the benefit payments
that are made to Participant after a specified
future date. Pursuant to paragraph (c)(1) of
this section, the order does not fail to be a
QDRO solely because it is issued after the
annuity starting date.
(d) Requirements and protections. (1)
Any domestic relations order described
in this section shall be subject to the
same requirements and protections that
apply to qualified domestic relations
orders under section 206(d)(3) of ERISA.
(2) The rule described in paragraph
(d)(1) of this section is illustrated by the
following examples:
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Example (1). Type or form of benefit.
Participant and Spouse divorce, and their
divorce decree provides that the parties will
prepare a domestic relations order assigning
50 percent of Participant’s benefits under a
401(k) plan to Spouse to be paid in monthly
installments over a ten-year period. Shortly
thereafter, Participant dies while actively
employed. A domestic relations order
consistent with the decree is subsequently
submitted to the 401(k) plan; however, the
plan does not provide for ten-year
installment payments of the type described
in the order. Pursuant to paragraph (c)(1) of
this section, the order does not fail to be
treated as a QDRO solely because it is issued
after the death of Participant, but the order
would fail to be a QDRO under section
206(d)(3)(D)(i) and paragraph (d)(1) of this
section because the order requires the plan to
provide a type or form of benefit, or any
option, not otherwise provided under the
plan.
Example (2). Segregation of payable
benefits. Participant and Spouse divorce, and
the administrator of Participant’s plan
receives a domestic relations order under
which Spouse would begin to receive
benefits immediately if the order is
determined to be a QDRO. The plan
administrator separately accounts for the
amounts covered by the domestic relations
order as is required under section
206(d)(3)(H)(v) of ERISA. The plan
administrator finds the order deficient and
determines that it is not a QDRO.
Subsequently, after the expiration of the
segregation period pertaining to that order,
the plan administrator receives a second
domestic relations order relating to the same
parties under which Spouse would begin to
receive benefits immediately if the second
order is determined to be a QDRO.
Notwithstanding the expiration of the first
segregation period, the amounts covered by
the second order must be separately
accounted for by the plan administrator for
an 18-month period, in accordance with
section 206(d)(3)(H) of ERISA and paragraph
(d)(1) of this section.
Example (3). Previously assigned benefits.
Participant and Spouse divorce, and the
administrator of Participant’s 401(k) plan
receives a domestic relations order. The
administrator determines that the order is a
QDRO. The QDRO assigns a portion of
Participant’s benefits to Spouse as the
alternate payee. Participant marries Spouse 2,
and then they divorce. Participant’s 401(k)
plan administrator subsequently receives a
domestic relations order pertaining to Spouse
2. The order assigns to Spouse 2 a portion of
Participant’s 401(k) benefits already assigned
to Spouse 1. The second order does not fail
to be treated as a QDRO solely because the
second order is issued after the plan
administrator has determined that an earlier
order pertaining to Spouse 1 is a QDRO. The
second order, however, would fail to be a
QDRO under section 206(d)(3)(D)(iii) and
paragraph (d)(1) of this section because it
assigns all or a portion of Participant’s
benefits that are already assigned to Spouse
1 by the prior QDRO.
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Signed at Washington, DC, this 28th day of
February, 2007.
Bradford P. Campbell,
Acting Assistant Secretary, Employee Benefits
Security Administration, Department of
Labor.
[FR Doc. E7–3820 Filed 3–6–07; 8:45 am]
BILLING CODE 4510–29–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2006–0658; FRL–8116–9]
Polymer of 2-Ethyl-2-(Hydroxymethyl)1,3-Propanediol, Oxirane,
Methyloxirane, 1,2-Epoxyalkanes;
Tolerance Exemption
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
SUMMARY: This regulation establishes
exemptions from the requirement of a
tolerance for residues of polymer of 2ethyl-2-(hydroxymethyl)-1,3propanediol, oxirane, methyloxirane,
1,2-epoxyalkanes; when used as inert
ingredients in a pesticide chemical
formulation. BASF Corporation
submitted a petition to EPA under the
Federal Food, Drug, and Cosmetic Act
(FFDCA), as amended by the Food
Quality Protection Act of 1996 (FQPA)
requesting an exemption from the
requirement of a tolerance. This
regulation eliminates the need to
establish a maximum permissible level
for residues of polymer of 2-ethyl-2(hydroxymethyl)-1,3-propanediol,
oxirane, methyloxirane, 1,2epoxyalkanes.
This regulation is effective
March 7, 2007. Objections and requests
for hearings must be received on or
before May 7, 2007, and must be filed
in accordance with the instructions
provided in 40 CFR part 178 (see also
Unit I.C. of the SUPPLEMENTARY
INFORMATION).
ADDRESSES: EPA has established a
docket for this action under docket
identification (ID) number EPA–HQ–
OPP–2006–0658. To access the
electronic docket, go to https://
www.regulations.gov, select ‘‘Advanced
Search,’’ then ‘‘Docket Search.’’ Insert
the docket ID number where indicated
and select the ‘‘Submit’’ button. Follow
the instructions on the regulations.gov
web site to view the docket index or
access available documents. All
documents in the docket are listed in
the docket index available in
regulations.gov. Although listed in the
DATES:
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index, some information is not publicly
available, e.g., Confidential Business
Information (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 in the electronic docket at
https://www.regulations.gov, or, if only
available in hard copy, at the OPP
Regulatory Public Docket in Rm. S-4400,
One Potomac Yard (South Bldg.), 2777
S. Crystal Drive, Arlington, VA. The
Docket Facility is open from 8:30 a.m.
to 4 p.m., Monday through Friday,
excluding legal holidays. The Docket
telephone number is (703) 305–5805.
FOR FURTHER INFORMATION CONTACT:
Bipin Gandhi, Registration Division
(7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001; telephone number:
(703) 308–8380; e-mail address:
gandhi.bipin@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
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A. Does This Action Apply to Me?
You may be potentially affected by
this action if you are an agricultural
producer, food manufacturer, or
pesticide manufacturer. Potentially
affected entities may include, but are
not limited to:
• Crop production (NAICS code 111).
• Animal production (NAICS code
112).
• Food manufacturing (NAICS code
311).
• Pesticide manufacturing (NAICS
code 32532).
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. If you have any
questions regarding the applicability of
this action to a particular entity, consult
the person listed under FOR FURTHER
INFORMATION CONTACT.
B. How Can I Access Electronic Copies
of This Document?
In addition to accessing an electronic
copy of this Federal Register document
through the electronic docket at https://
www.regulations.gov, you may access
this ‘‘Federal Register’’ document
electronically through the EPA Internet
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under the ‘‘Federal Register’’ listings at
https://www.epa.gov/fedrgstr. You may
also access a frequently updated
electronic version of 40 CFR part 180
through the Government Printing
Office’s pilot e-CFR site at https://
www.gpoaccess.gov/ecfr.
C. Can I File an Objection or Hearing
Request?
Under section 408(g) of the FFDCA, as
amended by the FQPA, any person may
file an objection to any aspect of this
regulation and may also request a
hearing on those objections. The EPA
procedural regulations which govern the
submission of objections and requests
for hearings appear in 40 CFR part 178.
You must file your objection or request
a hearing on this regulation in
accordance with the instructions
provided in 40 CFR part 178. To ensure
proper receipt by EPA, you must
identify docket ID number EPA–HQ–
OPP–2006–0658 in the subject line on
the first page of your submission. All
requests must be in writing, and must be
mailed or delivered to the Hearing Clerk
on or before May 7, 2007.
In addition to filing an objection or
hearing request with the Hearing Clerk
as described in 40 CFR part 178, please
submit a copy of the filing that does not
contain any CBI for inclusion in the
public docket that is described in
ADDRESSES. Information not marked
confidential pursuant to 40 CFR part 2
may be disclosed publicly by EPA
without prior notice. Submit your
copies, identified by docket ID number
EPA–HQ–OPP–2006–0658, by one of
the following methods.
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the on-line
instructions for submitting comments.
• Mail: Office of Pesticide Programs
(OPP) Regulatory Public Docket (7502P),
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001.
• Delivery: OPP Regulatory Public
Docket (7502P), Environmental
Protection Agency, Rm. S-4400, One
Potomac Yard (South Bldg.), 2777 S.
Crystal Drive, Arlington, VA. Deliveries
are only accepted during the Docket’s
normal hours of operation (8:30 a.m. to
4 p.m., Monday through Friday,
excluding legal holidays). Special
arrangements should be made for
deliveries of boxed information. The
Docket telephone number is (703) 305–
5805.
II. Background and Statutory Findings
In the Federal Register of December
20, 2006 (71 FR 76321) (FRL–8104–4),
EPA issued a notice pursuant to section
408 of the FFDCA, 21 U.S.C. 346a, as
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amended by the FQPA (Public Law 104–
170), announcing the filing of a
pesticide petition (PP 6E7079) by BASF
Corporation, 100 Campus Drive,
Florham Park, NJ 07932. The petition
requested that 40 CFR 180.960 be
amended by establishing exemptions
from the requirement of a tolerance for
residues of polymer of 2-ethyl-2(hydroxymethyl)-1,3-propanediol,
oxirane, methyloxirane, 1,2epoxyalkanes; CAS Reg. No. 903890–
89–1 when 1,2-epoxyalkane is 1,2epoxydodecane; CAS Reg. No. 903890–
90–4 when 1,2-epoxyalkane is 1,2epoxyhexadecane; and CAS Reg. No.
893427–80–0 when 1,2-epoxyalkane is
1,2-epoxyoctadecane. That notice
included a summary of the petition
prepared by the petitioner. There were
no comments in response to the notice
of filing.
Section 408(c)(2)(A)(i) of the FFDCA
allows EPA to establish an exemption
from the requirement for a tolerance (the
legal limit for a pesticide chemical
residue in or on a food) only if EPA
determines that the tolerance is ‘‘safe.’’
Section 408(c)(2)(A)(ii) of the FFDCA
defines ‘‘safe’’ to mean that ‘‘there is a
reasonable certainty that no harm will
result from aggregate exposure to the
pesticide chemical residue, including
all anticipated dietary exposures and all
other exposures for which there is
reliable information.’’ This includes
exposure through drinking water and in
residential settings, but does not include
occupational exposure. Section
408(b)(2)(C) of the FFDCA requires EPA
to give special consideration to
exposure of infants and children to the
pesticide chemical residue in
establishing an exemption from the
requirement of a tolerance and to
‘‘ensure that there is a reasonable
certainty that no harm will result to
infants and children from aggregate
exposure to the pesticide chemical
residue * * *’’ and specifies factors
EPA is to consider in establishing an
exemption.
III. Inert Ingredient Definition
Inert ingredients are all ingredients
that are not active ingredients as defined
in 40 CFR 153.125 and include, but are
not limited to, the following types of
ingredients (except when they have a
pesticidal efficacy of their own):
Solvents such as alcohols and
hydrocarbons; surfactants such as
polyoxyethylene polymers and fatty
acids; carriers such as clay and
diatomaceous earth; thickeners such as
carrageenan and modified cellulose;
wetting, spreading, and dispersing
agents; propellants in aerosol
dispensers; microencapsulating agents;
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and emulsifiers. The term ‘‘inert’’ is not
intended to imply nontoxicity; the
ingredient may or may not be
chemically active. Generally, EPA has
exempted inert ingredients from the
requirement of a tolerance based on the
low toxicity of the individual inert
ingredients.
IV. Risk Assessment and Statutory
Findings
EPA establishes exemptions from the
requirement of a tolerance only in those
cases where it can be shown that the
risks from aggregate exposure to
pesticide chemical residues under
reasonably foreseeable circumstances
will pose no appreciable risks to human
health. In order to determine the risks
from aggregate exposure to pesticide
inert ingredients, the Agency considers
the toxicity of the inert in conjunction
with possible exposure to residues of
the inert ingredient through food,
drinking water, and through other
exposures that occur as a result of
pesticide use in residential settings. If
EPA is able to determine that a finite
tolerance is not necessary to ensure that
there is a reasonable certainty that no
harm will result from aggregate
exposure to the inert ingredient, an
exemption from the requirement of a
tolerance may be established.
Consistent with section 408(b)(2)(D)
of the FFDCA, EPA has reviewed the
available scientific data and other
relevant information in support of this
action and considered its validity,
completeness and reliability and the
relationship of this information to
human risk. EPA has also considered
available information concerning the
variability of the sensitivities of major
identifiable subgroups of consumers,
including infants and children. In the
case of certain chemical substances that
are defined as polymers, the Agency has
established a set of criteria to identify
categories of polymers that should
present minimal or no risk. The
definition of a polymer is given in 40
CFR 723.250(b). The following
exclusion criteria for identifying these
low risk polymers are described in 40
CFR 723.250(d).
1. The polymers are not cationic
polymers nor are they reasonably
anticipated to become a cationic
polymers in a natural aquatic
environment.
2. The polymers do contain as an
integral part of its composition the
atomic elements carbon, hydrogen, and
oxygen.
3. The polymers do not contain as an
integral part of its composition, except
as impurities, any element other than
those listed in 40 CFR 723.250(d)(2)(ii).
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4. The polymers are neither designed
nor can they be reasonably anticipated
to substantially degrade, decompose, or
depolymerize.
5. The polymers are manufactured or
imported from monomers and/or
reactants that are already included on
the TSCA Chemical Substance
Inventory or manufactured under an
applicable TSCA section 5 exemption.
6. The polymers are not water
absorbing polymers with a number
average molecular weight (MW) greater
than or equal to 10,000 daltons.
Additionally, the polymers, also meet
as required the following exemption
criteria specified in 40 CFR 723.250(e).
7. The polymers’ number average MW
of 16,000 to 20,000 are greater than or
equal to 10,000 daltons. The polymers
contain less than 2% oligomeric
material below MW 500 and less than
5% oligomeric material below MW
1,000.
Thus, the polymer of 2-ethyl-2(hydroxymethyl)-1,3 propanediol,
oxirane, methyloxirane, 1,2epoxyalkanes meets all the criteria for a
polymers to be considered low risk
under 40 CFR 723.250. Based on its
conformance to the above criteria, no
mammalian toxicity is anticipated from
dietary, inhalation, or dermal exposure
to polymer of 2-ethyl-2(hydroxymethyl)-1,3 propanediol,
oxirane, methyloxirane, 1,2epoxyalkanes.
V. Aggregate Exposures
For the purposes of assessing
potential exposure under this
exemption, EPA considered that
polymer of 2-ethyl-2-(hydroxymethyl)1,3 propanediol, oxirane,
methyloxirane, 1,2-epoxyalkanes could
be present in all raw and processed
agricultural commodities and drinking
water, and that non-occupational nondietary exposures were possible. The
number average MW of polymer of 2ethyl-2-(hydroxymethyl)-1,3
propanediol, oxirane, methyloxirane,
1,2-epoxyalkanes is in the range of
16,000 to 20,000 daltons. Generally, a
polymer of this size would be poorly
absorbed through the intact
gastrointestinal tract or through intact
human skin. Since polymer of 2-ethyl2-(hydroxymethyl)-1,3 propanediol,
oxirane, methyloxirane, 1,2epoxyalkanes conforms to the criteria
that identify a low risk polymer, there
are no concerns for risks associated with
any potential exposure scenarios that
are reasonably foreseeable. The Agency
has determined that a tolerance is not
necessary to protect the public health.
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VI. Cumulative Effects
Section 408 (b)(2)(D)(v) of FFDCA
requires that, when considering whether
to establish, modify, or revoke a
tolerance or tolerance exemption, the
Agency consider ‘‘available
information’’ concerning the cumulative
effects of a particular chemical’s
residues and ‘‘other substances that
have a common mechanism of toxicity.’’
EPA does not have, at this time,
available data to determine whether
polymer of 2-ethyl-2-(hydroxymethyl)1,3 propanediol, oxirane,
methyloxirane, 1,2-epoxyalkanes has a
common mechanism of toxicity with
other substances. Unlike other
pesticides for which EPA has followed
a cumulative risk approach based on a
common mechanism of toxicity, EPA
has not made a common mechanism of
toxicity finding as to polymer of 2-ethyl2-(hydroxymethyl)-1,3 propanediol,
oxirane, methyloxirane, 1,2epoxyalkanes and any other substances
and polymer of 2-ethyl-2(hydroxymethyl)-1,3 propanediol,
oxirane, methyloxirane, 1,2epoxyalkanes do not appear to produce
toxic metabolite produced by other
substances. For the purposes of this
tolerance action, therefore, EPA has not
assumed that polymer of 2-ethyl-2(hydroxymethyl)-1,3 propanediol,
oxirane, methyloxirane, 1,2epoxyalkanes have common mechanism
of toxicity with other substances. For
information regarding EPA’s efforts to
determine which chemicals have a
common mechanism of toxicity and to
evaluate the cumulative effects of such
chemicals, see the policy statements
released by EPA’s Office of Pesticide
Programs concerning common
mechanism determinations and
procedures for cumulating effects from
substances found to have a common
mechanism on EPA’s website at https://
www.epa.gov/pesticides/cumulative.
VII. Additional Safety Factor for the
Protection of Infants and Children
Section 408 of the FFDCA provides
that EPA shall apply an additional
tenfold margin of safety for infants and
children in the case of threshold effects
to account for prenatal and postnatal
toxicity and the completeness of the
data base unless EPA concludes that a
different margin of safety will be safe for
infants and children. Due to the
expected low toxicity of polymer of 2ethyl-2-(hydroxymethyl)-1,3
propanediol, oxirane, methyloxirane,
1,2-epoxyalkanes, EPA has not used a
safety factor analysis to assess the risk.
For the same reasons the additional
tenfold safety factor is unnecessary.
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VIII. Determination of Safety
Based on the conformance to the
criteria used to identify a low risk
polymer, EPA concludes that there is a
reasonable certainty of no harm to the
U.S. population, including infants and
children, from aggregate exposure to
residues of polymer of 2-ethyl-2(hydroxymethyl)-1,3 propanediol,
oxirane, methyloxirane, 1,2epoxyalkanes.
IX. Other Considerations
A. Endocrine Disruptors
There is no available evidence that
polymer of 2-ethyl-2-(hydroxymethyl)1,3 propanediol, oxirane,
methyloxirane, 1,2-epoxyalkanes are
endocrine disruptors.
B. Analytical Enforcement Methodology
An analytical method is not required
for enforcement purposes since the
Agency is establishing an exemption
from the requirement of a tolerance
without any numerical limitation.
C. International Tolerances
The Agency is not aware of any
country requiring a tolerance for
polymer of 2-ethyl-2-(hydroxymethyl)1,3 propanediol, oxirane,
methyloxirane, 1,2-epoxyalkanes nor
have any CODEX Maximum Residue
Levels (MRLs) been established for any
food crops at this time.
X. Conclusion
Accordingly, EPA finds that
exempting residues of polymer of 2ethyl-2-(hydroxymethyl)-1,3
propanediol, oxirane, methyloxirane,
1,2-epoxyalkanes from the requirement
of a tolerance will be safe.
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XI. Statutory and Executive Order
Reviews
This final rule establishes a tolerance
under section 408(d) of FFDCA in
response to a petition submitted to the
Agency. The Office of Management and
Budget (OMB) has exempted these types
of actions from review under Executive
Order 12866, entitled Regulatory
Planning and Review (58 FR 51735,
October 4, 1993). Because this rule has
been exempted from review under
Executive Order 12866, this rule is not
subject to Executive Order 13211,
Actions Concerning Regulations That
Significantly Affect Energy Supply,
Distribution, or Use (66 FR 28355, May
22, 2001) or Executive Order 13045,
entitled Protection of Children from
Environmental Health Risks and Safety
Risks (62 FR 19885, April 23, 1997).
This final rule does not contain any
information collections subject to OMB
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approval under the Paperwork
Reduction Act (PRA), 44 U.S.C. 3501 et
seq., nor does it require any special
considerations under Executive Order
12898, entitled Federal Actions to
Address Environmental Justice in
Minority Populations and Low-Income
Populations (59 FR 7629, February 16,
1994).
Since tolerances and exemptions that
are established on the basis of a petition
under section 408(d) of FFDCA, such as
the tolerance in this final rule, do not
require the issuance of a proposed rule,
the requirements of the Regulatory
Flexibility Act (RFA) (5 U.S.C. 601 et
seq.) do not apply.
This final rule directly regulates
growers, food processors, food handlers
and food retailers, not States or tribes,
nor does this action alter the
relationships or distribution of power
and responsibilities established by
Congress in the preemption provisions
of section 408(n)(4) of FFDCA. As such,
the Agency has determined that this
action will not have a substantial direct
effect on States or tribal governments,
on the relationship between the national
government and the States or tribal
governments, or on the distribution of
power and responsibilities among the
various levels of government or between
the Federal Government and Indian
tribes. Thus, the Agency has determined
that Executive Order 13132, entitled
Federalism (64 FR 43255, August 10,
1999) and Executive Order 13175,
entitled Consultation and Coordination
with Indian Tribal Governments (65 FR
67249, November 6, 2000) do not apply
to this rule. In addition, This rule does
not impose any enforceable duty or
contain any unfunded mandate as
described under Title II of the Unfunded
Mandates Reform Act of 1995 (UMRA)
(Pub. L. 104–4).
This action does not involve any
technical standards that would require
Agency consideration of voluntary
consensus standards pursuant to 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).
XII. Congressional Review Act
The Congressional Review Act, 5
U.S.C. 801 et seq., generally provides
that before a rule may take effect, the
agency promulgating the rule must
submit a rule report to each House of
the Congress and to the Comptroller
General of the United States. EPA will
submit a report containing this rule and
other required information to the U.S.
Senate, the U.S. House of
Representatives, and the Comptroller
General of the United States prior to
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publication of this rule in the Federal
Register. This rule is not a ‘‘major rule’’
as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
Dated: February 27, 2007.
Lois Rossi,
Director, Registration Division, Office of
Pesticide Programs.
Therefore, 40 CFR chapter I is
amended as follows:
I
PART 180—[AMENDED]
1. The authority citation for part 180
continues to read as follows:
I
Authority: 1 U.S.C. 321(q), 346a and 371.
2. In § 180.960 the table is amended
by adding alphabetically polymers to
read as follows:
I
§ 180.960 Polymers; exemptions from the
requirement of a tolerance.
*
*
*
*
*
Polymer
*
*
CAS No.
*
*
*
Oxirane, decyl-, reaction
products with polyethylene-polypropylene
glycol ether with
trimethylolpropane (3:1).
903890–89–1
Oxirane, hexadecyl-, reaction products with polyethylene-polypropylene
glycol ether with
trimethylolpropane (3:1).
893427–80–0
Oxirane, methyl-, polymer
with oxirane, ether with
2-ethyl-2-(hydroxymethyl)
– 1,3 - propanediol (3:1),
reaction products with
tetradecyloxirane.
903890–90–4
*
*
*
*
*
[FR Doc. E7–4083 Filed 3–6–07; 8:45 am]
BILLING CODE 6560–50–S
E:\FR\FM\07MRR1.SGM
07MRR1
Agencies
[Federal Register Volume 72, Number 44 (Wednesday, March 7, 2007)]
[Rules and Regulations]
[Pages 10074-10077]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-4083]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2006-0658; FRL-8116-9]
Polymer of 2-Ethyl-2-(Hydroxymethyl)-1,3-Propanediol, Oxirane,
Methyloxirane, 1,2-Epoxyalkanes; Tolerance Exemption
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes exemptions from the requirement of
a tolerance for residues of polymer of 2-ethyl-2-(hydroxymethyl)-1,3-
propanediol, oxirane, methyloxirane, 1,2-epoxyalkanes; when used as
inert ingredients in a pesticide chemical formulation. BASF Corporation
submitted a petition to EPA under the Federal Food, Drug, and Cosmetic
Act (FFDCA), as amended by the Food Quality Protection Act of 1996
(FQPA) requesting an exemption from the requirement of a tolerance.
This regulation eliminates the need to establish a maximum permissible
level for residues of polymer of 2-ethyl-2-(hydroxymethyl)-1,3-
propanediol, oxirane, methyloxirane, 1,2-epoxyalkanes.
DATES: This regulation is effective March 7, 2007. Objections and
requests for hearings must be received on or before May 7, 2007, and
must be filed in accordance with the instructions provided in 40 CFR
part 178 (see also Unit I.C. of the SUPPLEMENTARY INFORMATION).
ADDRESSES: EPA has established a docket for this action under docket
identification (ID) number EPA-HQ-OPP-2006-0658. To access the
electronic docket, go to https://www.regulations.gov, select ``Advanced
Search,'' then ``Docket Search.'' Insert the docket ID number where
indicated and select the ``Submit'' button. Follow the instructions on
the regulations.gov web site to view the docket index or access
available documents. All documents in the docket are listed in the
docket index available in regulations.gov. Although listed in the
[[Page 10075]]
index, some information is not publicly available, e.g., Confidential
Business Information (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 in the electronic docket at https://www.regulations.gov, or,
if only available in hard copy, at the OPP Regulatory Public Docket in
Rm. S-4400, One Potomac Yard (South Bldg.), 2777 S. Crystal Drive,
Arlington, VA. The Docket Facility is open from 8:30 a.m. to 4 p.m.,
Monday through Friday, excluding legal holidays. The Docket telephone
number is (703) 305-5805.
FOR FURTHER INFORMATION CONTACT: Bipin Gandhi, Registration Division
(7505P), Office of Pesticide Programs, Environmental Protection Agency,
1200 Pennsylvania Ave., NW., Washington, DC 20460-0001; telephone
number: (703) 308-8380; e-mail address: gandhi.bipin@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does This Action Apply to Me?
You may be potentially affected by this action if you are an
agricultural producer, food manufacturer, or pesticide manufacturer.
Potentially affected entities may include, but are not limited to:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
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. If you have any
questions regarding the applicability of this action to a particular
entity, consult the person listed under FOR FURTHER INFORMATION
CONTACT.
B. How Can I Access Electronic Copies of This Document?
In addition to accessing an electronic copy of this Federal
Register document through the electronic docket at https://
www.regulations.gov, you may access this ``Federal Register'' document
electronically through the EPA Internet under the ``Federal Register''
listings at https://www.epa.gov/fedrgstr. You may also access a
frequently updated electronic version of 40 CFR part 180 through the
Government Printing Office's pilot e-CFR site at https://
www.gpoaccess.gov/ecfr.
C. Can I File an Objection or Hearing Request?
Under section 408(g) of the FFDCA, as amended by the FQPA, any
person may file an objection to any aspect of this regulation and may
also request a hearing on those objections. The EPA procedural
regulations which govern the submission of objections and requests for
hearings appear in 40 CFR part 178. You must file your objection or
request a hearing on this regulation in accordance with the
instructions provided in 40 CFR part 178. To ensure proper receipt by
EPA, you must identify docket ID number EPA-HQ-OPP-2006-0658 in the
subject line on the first page of your submission. All requests must be
in writing, and must be mailed or delivered to the Hearing Clerk on or
before May 7, 2007.
In addition to filing an objection or hearing request with the
Hearing Clerk as described in 40 CFR part 178, please submit a copy of
the filing that does not contain any CBI for inclusion in the public
docket that is described in ADDRESSES. Information not marked
confidential pursuant to 40 CFR part 2 may be disclosed publicly by EPA
without prior notice. Submit your copies, identified by docket ID
number EPA-HQ-OPP-2006-0658, by one of the following methods.
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the on-line instructions for submitting comments.
Mail: Office of Pesticide Programs (OPP) Regulatory Public
Docket (7502P), Environmental Protection Agency, 1200 Pennsylvania
Ave., NW., Washington, DC 20460-0001.
Delivery: OPP Regulatory Public Docket (7502P),
Environmental Protection Agency, Rm. S-4400, One Potomac Yard (South
Bldg.), 2777 S. Crystal Drive, Arlington, VA. Deliveries are only
accepted during the Docket's normal hours of operation (8:30 a.m. to 4
p.m., Monday through Friday, excluding legal holidays). Special
arrangements should be made for deliveries of boxed information. The
Docket telephone number is (703) 305-5805.
II. Background and Statutory Findings
In the Federal Register of December 20, 2006 (71 FR 76321) (FRL-
8104-4), EPA issued a notice pursuant to section 408 of the FFDCA, 21
U.S.C. 346a, as amended by the FQPA (Public Law 104-170), announcing
the filing of a pesticide petition (PP 6E7079) by BASF Corporation, 100
Campus Drive, Florham Park, NJ 07932. The petition requested that 40
CFR 180.960 be amended by establishing exemptions from the requirement
of a tolerance for residues of polymer of 2-ethyl-2-(hydroxymethyl)-
1,3-propanediol, oxirane, methyloxirane, 1,2-epoxyalkanes; CAS Reg. No.
903890-89-1 when 1,2-epoxyalkane is 1,2-epoxydodecane; CAS Reg. No.
903890-90-4 when 1,2-epoxyalkane is 1,2-epoxyhexadecane; and CAS Reg.
No. 893427-80-0 when 1,2-epoxyalkane is 1,2-epoxyoctadecane. That
notice included a summary of the petition prepared by the petitioner.
There were no comments in response to the notice of filing.
Section 408(c)(2)(A)(i) of the FFDCA allows EPA to establish an
exemption from the requirement for a tolerance (the legal limit for a
pesticide chemical residue in or on a food) only if EPA determines that
the tolerance is ``safe.'' Section 408(c)(2)(A)(ii) of the FFDCA
defines ``safe'' to mean that ``there is a reasonable certainty that no
harm will result from aggregate exposure to the pesticide chemical
residue, including all anticipated dietary exposures and all other
exposures for which there is reliable information.'' This includes
exposure through drinking water and in residential settings, but does
not include occupational exposure. Section 408(b)(2)(C) of the FFDCA
requires EPA to give special consideration to exposure of infants and
children to the pesticide chemical residue in establishing an exemption
from the requirement of a tolerance and to ``ensure that there is a
reasonable certainty that no harm will result to infants and children
from aggregate exposure to the pesticide chemical residue * * *'' and
specifies factors EPA is to consider in establishing an exemption.
III. Inert Ingredient Definition
Inert ingredients are all ingredients that are not active
ingredients as defined in 40 CFR 153.125 and include, but are not
limited to, the following types of ingredients (except when they have a
pesticidal efficacy of their own): Solvents such as alcohols and
hydrocarbons; surfactants such as polyoxyethylene polymers and fatty
acids; carriers such as clay and diatomaceous earth; thickeners such as
carrageenan and modified cellulose; wetting, spreading, and dispersing
agents; propellants in aerosol dispensers; microencapsulating agents;
[[Page 10076]]
and emulsifiers. The term ``inert'' is not intended to imply
nontoxicity; the ingredient may or may not be chemically active.
Generally, EPA has exempted inert ingredients from the requirement of a
tolerance based on the low toxicity of the individual inert
ingredients.
IV. Risk Assessment and Statutory Findings
EPA establishes exemptions from the requirement of a tolerance only
in those cases where it can be shown that the risks from aggregate
exposure to pesticide chemical residues under reasonably foreseeable
circumstances will pose no appreciable risks to human health. In order
to determine the risks from aggregate exposure to pesticide inert
ingredients, the Agency considers the toxicity of the inert in
conjunction with possible exposure to residues of the inert ingredient
through food, drinking water, and through other exposures that occur as
a result of pesticide use in residential settings. If EPA is able to
determine that a finite tolerance is not necessary to ensure that there
is a reasonable certainty that no harm will result from aggregate
exposure to the inert ingredient, an exemption from the requirement of
a tolerance may be established.
Consistent with section 408(b)(2)(D) of the FFDCA, EPA has reviewed
the available scientific data and other relevant information in support
of this action and considered its validity, completeness and
reliability and the relationship of this information to human risk. EPA
has also considered available information concerning the variability of
the sensitivities of major identifiable subgroups of consumers,
including infants and children. In the case of certain chemical
substances that are defined as polymers, the Agency has established a
set of criteria to identify categories of polymers that should present
minimal or no risk. The definition of a polymer is given in 40 CFR
723.250(b). The following exclusion criteria for identifying these low
risk polymers are described in 40 CFR 723.250(d).
1. The polymers are not cationic polymers nor are they reasonably
anticipated to become a cationic polymers in a natural aquatic
environment.
2. The polymers do contain as an integral part of its composition
the atomic elements carbon, hydrogen, and oxygen.
3. The polymers do not contain as an integral part of its
composition, except as impurities, any element other than those listed
in 40 CFR 723.250(d)(2)(ii).
4. The polymers are neither designed nor can they be reasonably
anticipated to substantially degrade, decompose, or depolymerize.
5. The polymers are manufactured or imported from monomers and/or
reactants that are already included on the TSCA Chemical Substance
Inventory or manufactured under an applicable TSCA section 5 exemption.
6. The polymers are not water absorbing polymers with a number
average molecular weight (MW) greater than or equal to 10,000 daltons.
Additionally, the polymers, also meet as required the following
exemption criteria specified in 40 CFR 723.250(e).
7. The polymers' number average MW of 16,000 to 20,000 are greater
than or equal to 10,000 daltons. The polymers contain less than 2%
oligomeric material below MW 500 and less than 5% oligomeric material
below MW 1,000.
Thus, the polymer of 2-ethyl-2-(hydroxymethyl)-1,3 propanediol,
oxirane, methyloxirane, 1,2-epoxyalkanes meets all the criteria for a
polymers to be considered low risk under 40 CFR 723.250. Based on its
conformance to the above criteria, no mammalian toxicity is anticipated
from dietary, inhalation, or dermal exposure to polymer of 2-ethyl-2-
(hydroxymethyl)-1,3 propanediol, oxirane, methyloxirane, 1,2-
epoxyalkanes.
V. Aggregate Exposures
For the purposes of assessing potential exposure under this
exemption, EPA considered that polymer of 2-ethyl-2-(hydroxymethyl)-1,3
propanediol, oxirane, methyloxirane, 1,2-epoxyalkanes could be present
in all raw and processed agricultural commodities and drinking water,
and that non-occupational non-dietary exposures were possible. The
number average MW of polymer of 2-ethyl-2-(hydroxymethyl)-1,3
propanediol, oxirane, methyloxirane, 1,2-epoxyalkanes is in the range
of 16,000 to 20,000 daltons. Generally, a polymer of this size would be
poorly absorbed through the intact gastrointestinal tract or through
intact human skin. Since polymer of 2-ethyl-2-(hydroxymethyl)-1,3
propanediol, oxirane, methyloxirane, 1,2-epoxyalkanes conforms to the
criteria that identify a low risk polymer, there are no concerns for
risks associated with any potential exposure scenarios that are
reasonably foreseeable. The Agency has determined that a tolerance is
not necessary to protect the public health.
VI. Cumulative Effects
Section 408 (b)(2)(D)(v) of FFDCA requires that, when considering
whether to establish, modify, or revoke a tolerance or tolerance
exemption, the Agency consider ``available information'' concerning the
cumulative effects of a particular chemical's residues and ``other
substances that have a common mechanism of toxicity.'' EPA does not
have, at this time, available data to determine whether polymer of 2-
ethyl-2-(hydroxymethyl)-1,3 propanediol, oxirane, methyloxirane, 1,2-
epoxyalkanes has a common mechanism of toxicity with other substances.
Unlike other pesticides for which EPA has followed a cumulative risk
approach based on a common mechanism of toxicity, EPA has not made a
common mechanism of toxicity finding as to polymer of 2-ethyl-2-
(hydroxymethyl)-1,3 propanediol, oxirane, methyloxirane, 1,2-
epoxyalkanes and any other substances and polymer of 2-ethyl-2-
(hydroxymethyl)-1,3 propanediol, oxirane, methyloxirane, 1,2-
epoxyalkanes do not appear to produce toxic metabolite produced by
other substances. For the purposes of this tolerance action, therefore,
EPA has not assumed that polymer of 2-ethyl-2-(hydroxymethyl)-1,3
propanediol, oxirane, methyloxirane, 1,2-epoxyalkanes have common
mechanism of toxicity with other substances. For information regarding
EPA's efforts to determine which chemicals have a common mechanism of
toxicity and to evaluate the cumulative effects of such chemicals, see
the policy statements released by EPA's Office of Pesticide Programs
concerning common mechanism determinations and procedures for
cumulating effects from substances found to have a common mechanism on
EPA's website at https://www.epa.gov/pesticides/cumulative.
VII. Additional Safety Factor for the Protection of Infants and
Children
Section 408 of the FFDCA provides that EPA shall apply an
additional tenfold margin of safety for infants and children in the
case of threshold effects to account for prenatal and postnatal
toxicity and the completeness of the data base unless EPA concludes
that a different margin of safety will be safe for infants and
children. Due to the expected low toxicity of polymer of 2-ethyl-2-
(hydroxymethyl)-1,3 propanediol, oxirane, methyloxirane, 1,2-
epoxyalkanes, EPA has not used a safety factor analysis to assess the
risk. For the same reasons the additional tenfold safety factor is
unnecessary.
[[Page 10077]]
VIII. Determination of Safety
Based on the conformance to the criteria used to identify a low
risk polymer, EPA concludes that there is a reasonable certainty of no
harm to the U.S. population, including infants and children, from
aggregate exposure to residues of polymer of 2-ethyl-2-(hydroxymethyl)-
1,3 propanediol, oxirane, methyloxirane, 1,2-epoxyalkanes.
IX. Other Considerations
A. Endocrine Disruptors
There is no available evidence that polymer of 2-ethyl-2-
(hydroxymethyl)-1,3 propanediol, oxirane, methyloxirane, 1,2-
epoxyalkanes are endocrine disruptors.
B. Analytical Enforcement Methodology
An analytical method is not required for enforcement purposes since
the Agency is establishing an exemption from the requirement of a
tolerance without any numerical limitation.
C. International Tolerances
The Agency is not aware of any country requiring a tolerance for
polymer of 2-ethyl-2-(hydroxymethyl)-1,3 propanediol, oxirane,
methyloxirane, 1,2-epoxyalkanes nor have any CODEX Maximum Residue
Levels (MRLs) been established for any food crops at this time.
X. Conclusion
Accordingly, EPA finds that exempting residues of polymer of 2-
ethyl-2-(hydroxymethyl)-1,3 propanediol, oxirane, methyloxirane, 1,2-
epoxyalkanes from the requirement of a tolerance will be safe.
XI. Statutory and Executive Order Reviews
This final rule establishes a tolerance under section 408(d) of
FFDCA in response to a petition submitted to the Agency. The Office of
Management and Budget (OMB) has exempted these types of actions from
review under Executive Order 12866, entitled Regulatory Planning and
Review (58 FR 51735, October 4, 1993). Because this rule has been
exempted from review under Executive Order 12866, this rule is not
subject to Executive Order 13211, Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution, or Use (66 FR 28355,
May 22, 2001) or Executive Order 13045, entitled Protection of Children
from Environmental Health Risks and Safety Risks (62 FR 19885, April
23, 1997). This final rule does not contain any information collections
subject to OMB approval under the Paperwork Reduction Act (PRA), 44
U.S.C. 3501 et seq., nor does it require any special considerations
under Executive Order 12898, entitled Federal Actions to Address
Environmental Justice in Minority Populations and Low-Income
Populations (59 FR 7629, February 16, 1994).
Since tolerances and exemptions that are established on the basis
of a petition under section 408(d) of FFDCA, such as the tolerance in
this final rule, do not require the issuance of a proposed rule, the
requirements of the Regulatory Flexibility Act (RFA) (5 U.S.C. 601 et
seq.) do not apply.
This final rule directly regulates growers, food processors, food
handlers and food retailers, not States or tribes, nor does this action
alter the relationships or distribution of power and responsibilities
established by Congress in the preemption provisions of section
408(n)(4) of FFDCA. As such, the Agency has determined that this action
will not have a substantial direct effect on States or tribal
governments, on the relationship between the national government and
the States or tribal governments, or on the distribution of power and
responsibilities among the various levels of government or between the
Federal Government and Indian tribes. Thus, the Agency has determined
that Executive Order 13132, entitled Federalism (64 FR 43255, August
10, 1999) and Executive Order 13175, entitled Consultation and
Coordination with Indian Tribal Governments (65 FR 67249, November 6,
2000) do not apply to this rule. In addition, This rule does not impose
any enforceable duty or contain any unfunded mandate as described under
Title II of the Unfunded Mandates Reform Act of 1995 (UMRA) (Pub. L.
104-4).
This action does not involve any technical standards that would
require Agency consideration of voluntary consensus standards pursuant
to 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).
XII. Congressional Review Act
The Congressional Review Act, 5 U.S.C. 801 et seq., generally
provides that before a rule may take effect, the agency promulgating
the rule must submit a rule report to each House of the Congress and to
the Comptroller General of the United States. EPA will submit a report
containing this rule and other required information to the U.S. Senate,
the U.S. House of Representatives, and the Comptroller General of the
United States prior to publication of this rule in the Federal
Register. This rule is not a ``major rule'' as defined by 5 U.S.C.
804(2).
List of Subjects in 40 CFR Part 180
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Pesticides and pests, Reporting and
recordkeeping requirements.
Dated: February 27, 2007.
Lois Rossi,
Director, Registration Division, Office of Pesticide Programs.
0
Therefore, 40 CFR chapter I is amended as follows:
PART 180--[AMENDED]
0
1. The authority citation for part 180 continues to read as follows:
Authority: 1 U.S.C. 321(q), 346a and 371.
0
2. In Sec. 180.960 the table is amended by adding alphabetically
polymers to read as follows:
Sec. 180.960 Polymers; exemptions from the requirement of a
tolerance.
* * * * *
------------------------------------------------------------------------
Polymer CAS No.
------------------------------------------------------------------------
* * * * *
------------------------------------------------------------------------
Oxirane, decyl-, reaction products with 903890-89-1
polyethylene-polypropylene glycol ether
with trimethylolpropane (3:1).
------------------------------------------------------------------------
Oxirane, hexadecyl-, reaction products 893427-80-0
with polyethylene-polypropylene glycol
ether with trimethylolpropane (3:1).
------------------------------------------------------------------------
Oxirane, methyl-, polymer with oxirane, 903890-90-4
ether with 2-ethyl-2-(hydroxymethyl) -
1,3 - propanediol (3:1), reaction
products with tetradecyloxirane.
------------------------------------------------------------------------
* * * * *
------------------------------------------------------------------------
[FR Doc. E7-4083 Filed 3-6-07; 8:45 am]
BILLING CODE 6560-50-S