1-Bromopropane (1-BP); Draft Toxic Substances Control Act (TSCA) Risk Evaluation and TSCA Science Advisory Committee on Chemicals (SACC) Meetings; Notice of Availability and Public Meetings, 39830-39833 [2019-17222]
Download as PDF
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Federal Register / Vol. 84, No. 155 / Monday, August 12, 2019 / Notices
EPA case No.
Chemical identity
P–19–0072 ...........................
1-Butanol, reaction products with 2-[(2-propen-1yloxy)methyl]oxirane.
P–18–0170 ...........................
1-Propanaminium, N,N′-(oxydi-2,1-ethanediyl)bis[3chloro-2-hydroxy-N,N-dimethyl-, chloride (1:2)
(CASRN: 96320–92–2).
1H-Imidazole, 1,2,4,5-tetramethyl- (CASRN: 1739-83-9)
P–18–0011 ...........................
P–18–0239, P–18–0240 ......
(P–18–0239) N-alkyl propanamide, (P–18–0240) Nalkyl acetamide (generic names).
J–19–0019, J–19–0020 .......
Genetically modified microorganism for the production
of an enzyme substance (generic name).
P–19–0065 ...........................
2lambda5, 4lambda5, 6lambda5- 1,3,5,2,4,6
Triazatriphosphorine, 2,2,4,4,6,6—hexaphenoxy(CASRN: 1184–10–7).
Benzenedicarboxylic acid, reaction products with
isobenzofurandione and diethylene glycol (generic
name).
Alkylmultiheteroatom,2-functionalisedalkyl-2hydroxyalkyl-, polymer with alkylheteroatommultialkylfunctionalised carbomonocyleheteroatom
and multiglycidylether difunctionalised polyalkylene
glycol (generic name).
Fatty acids, polymers with alkanoic acid and substituted
carbomonocycle, peroxide-initiated, polymers with
alkanoic acid esters and substituted carbomonocycle,
ammonium salts; polymer exemption flag (generic
name).
Oxoalkylcarboxylic acid, sodium salt (generic name) .....
P–19–0012 ...........................
P–18–0404 ...........................
P–18–0260 ...........................
P–18–0125 ...........................
Authority: 15 U.S.C. 2601 et seq.
Dated: July 29, 2019.
Leo Schweer,
Chief, New Chemicals Management Branch,
Chemical Control Division, Office of Pollution
Prevention and Toxics.
[FR Doc. 2019–17151 Filed 8–9–19; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2019–0235; FRL–9997–25]
1-Bromopropane (1–BP); Draft Toxic
Substances Control Act (TSCA) Risk
Evaluation and TSCA Science
Advisory Committee on Chemicals
(SACC) Meetings; Notice of Availability
and Public Meetings
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
jspears on DSK3GMQ082PROD with NOTICES
Website link
EPA is announcing the
availability of documents and dates for
the peer review of the draft risk
evaluation for 1-Bromopropane (1–BP).
The purpose of the risk evaluations
under the Toxic Substances Control Act
(TSCA) is to determine whether a
chemical substance presents an
SUMMARY:
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https://www.epa.gov/reviewing-new-chemicals-undertoxic-substances-control-act-tsca/tsca-section-5a3cdetermination-245.
https://www.epa.gov/reviewing-new-chemicals-undertoxic-substances-control-act-tsca/tsca-section-5a3cdetermination-244.
https://www.epa.gov/reviewing-new-chemicals-undertoxic-substances-control-act-tsca/tsca-section-5a3cdetermination-243.
https://www.epa.gov/reviewing-new-chemicals-undertoxic-substances-control-act-tsca/tsca-section-5a3cdetermination-242.
https://www.epa.gov/reviewing-new-chemicals-undertoxic-substances-control-act-tsca/tsca-section-5a3cdetermination-241.
https://www.epa.gov/reviewing-new-chemicals-undertoxic-substances-control-act-tsca/tsca-section-5a3cdetermination-240.
https://www.epa.gov/reviewing-new-chemicals-undertoxic-substances-control-act-tsca/tsca-section-5a3cdetermination-239.
https://www.epa.gov/reviewing-new-chemicals-undertoxic-substances-control-act-tsca/tsca-section-5a3cdetermination-238.
https://www.epa.gov/reviewing-new-chemicals-undertoxic-substances-control-act-tsca/tsca-section-5a3cdetermination-237.
https://www.epa.gov/reviewing-new-chemicals-undertoxic-substances-control-act-tsca/tsca-section-5a3cdetermination-236
unreasonable risk of injury to health or
the environment under the conditions of
use, including an unreasonable risk to a
relevant potentially exposed or
susceptible subpopulation. EPA is also
submitting these same documents to the
TSCA Science Advisory Committee on
Chemicals (SACC) for peer review and
is announcing that there will be a 3-day
in-person meeting of the TSCA SACC to
consider and review these draft risk
evaluations. Preceding the in-person
meeting, there will be a 3-hour
preparatory virtual meeting for the
panel to consider the scope and clarity
of the draft charge questions for the peer
reviews.
DATES:
Comments: Comments on the draft
risk evaluation must be received on or
before October 11, 2019. Please submit
comments on the draft risk evaluation
by August 30, 2019 to allow the SACC
time to review and consider them before
the peer review meeting. Comments
received after August 30, 2019 will still
be provided to the SACC for their
consideration. For additional
instructions, see Unit II.A. and Unit II.B.
of the SUPPLEMENTARY INFORMATION.
Meetings: The preparatory virtual
meeting will be held on August 21,
2019, from 1 p.m. to approximately 4
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p.m. (EDT). The 3-day in-person
meeting will be held on September 10–
12, 2019 from 9:00 a.m. to
approximately 5:30 p.m. (EDT).
Virtual Meeting: The
preparatory virtual meeting will be
conducted via webcast and telephone.
Registration is open to the public and is
required to participate during the
preparatory virtual meeting. Please visit
https://www.epa.gov/tsca-peer-review
website for additional information
including how to register.
In-Person Meeting: The location of the
in-person meeting will be announced on
the TSCA SACC website at https://
www.epa.gov/TSCA-Peer-Review. The
in-person meeting may also be webcast.
Please refer to the TSCA SACC website
at https://www.epa.gov/tsca-peer-review
for information on how to access the
webcast. Please note that for the inperson meeting, the webcast is a
supplementary public process provided
only for convenience. If difficulties arise
resulting in webcasting outages, the inperson meeting will continue as
planned.
Comments. Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2019–0235, by
one of the following methods:
ADDRESSES:
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• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Do not submit electronically any
information you consider to be
Confidential Business Information (CBI)
or other information whose disclosure is
restricted by statute.
• Mail: OPPT Docket, Environmental
Protection Agency Docket Center (EPA/
DC), (28221T), 1200 Pennsylvania Ave.
NW, Washington, DC 20460–0001.
• Hand Delivery: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/contacts.html.
Additional instructions on
commenting or visiting the docket,
along with more information about
dockets generally, is available at https://
www.epa.gov/dockets.
Requests to present oral comments
and requests for special
accommodations. Submit requests for
special accommodations, or requests to
present oral comments (in-person or
over the telephone) during the webcast
and/or the public portion of the peer
review meeting to the Designated
Federal Official (DFO) listed under FOR
FURTHER INFORMATION CONTACT by the
deadline identified in the DATES section.
Comments received after the date set in
the DATES section and prior to the end
of the oral public comment period
during the meeting for each chemical
will still be provided to the SACC for
their consideration.
jspears on DSK3GMQ082PROD with NOTICES
FOR FURTHER INFORMATION CONTACT:
TSCA SACC meetings: Tamue Gibson,
DFO, Office of Science Coordination
and Policy (7201M), Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW, Washington, DC 20460–0001;
telephone number: (202) 564–7642;
email address: gibson.tamue@epa.gov.
Risk Evaluations: Dr. Stan Barone,
Office of Pollution Prevention and
Toxics (7403M), Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW, Washington, DC 20460–0001;
telephone number: 202–564–1169;
email address: barone.stan@epa.gov.
Special accommodations for the
SACC meeting: For information on
access or services for individuals with
disabilities, and to request
accommodation of a disability, please
contact the DFO listed under FOR
FURTHER INFORMATION CONTACT at least
10 days prior to the meeting to give EPA
as much time as possible to process
your request.
SUPPLEMENTARY INFORMATION:
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I. General Information
A. Does this action apply to me?
This action is directed to the public
in general. This action may be of
interest to persons who are or may be
required to conduct testing and risk
evaluations of chemical substances
under the TSCA, 15 U.S.C. 2601 et seq.
Since other entities may also be
interested in these risk evaluations, the
EPA has not attempted to describe all
the specific entities that may be affected
by this action.
B. What action is the EPA taking?
EPA is announcing the availability of
and seeking public comment on the
draft risk evaluation for 1Bromopropane (1–BP). EPA is seeking
public comment on all aspects of the
draft risk evaluation, including any
conclusions, findings, and
determinations, and the submission of
any additional information that might
be relevant to the science underlying the
risk evaluation and the outcome of the
systematic review associated with the
chemical. This 60-day comment period
on the draft risk evaluations satisfies
TSCA section 6(b)(4)(H), which requires
EPA to ‘‘provide no less than 30 days
public notice and an opportunity for
comment on a draft risk evaluation prior
to publishing a final risk evaluation’’
and 40 CFR 702.49(a), which states that
‘‘EPA will publish a draft risk
evaluation in the Federal Register, open
a docket to facilitate receipt of public
comment, and provide no less than a 60day comment period, during which time
the public may submit comment on
EPA’s draft risk evaluation.’’ In addition
to any new comments on the draft risk
evaluation, the public should resubmit
or clearly identify any previously filed
comments, modified as appropriate, that
are relevant to the draft risk evaluation
and that the submitter feels have not
been addressed. EPA does not intend to
respond to comments submitted prior to
the release of the draft risk evaluation
unless they are clearly identified in
comments on the draft risk evaluation.
EPA is also submitting these same
documents to the TSCA SACC for peer
review and announcing the meetings for
the peer review panel. All comments
submitted to the dockets for
consideration by the TSCA SACC by the
deadline identified in the DATES section
will be provided to the TSCA SACC
peer review panel, which will have the
opportunity to consider the comments
during its discussions.
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39831
C. What is the EPA’s authority for taking
this action?
TSCA section 6, 15 U.S.C. 2605,
requires EPA to conduct risk
evaluations to ‘‘determine whether a
chemical substance presents an
unreasonable risk of injury to health or
the environment, without consideration
of costs or other nonrisk factors,
including an unreasonable risk to a
potentially exposed or susceptible
subpopulation identified as relevant to
the risk evaluation by the
Administrator, under the conditions of
use.’’ 15 U.S.C. 2605(b)(4)(A). TSCA
sections 6(b)(4)(A) through (H)
enumerate the deadlines and minimum
requirements applicable to this process,
including provisions that direct which
chemical substances must undergo
evaluation, the development of criteria
for manufacturer-requested evaluations,
the minimum components of an EPA
risk evaluation, and the timelines for
public comment and completion of the
risk evaluation. The law also requires
that EPA operate in a manner that is
consistent with the best available
science and make decisions based on
the weight of the scientific evidence. 15
U.S.C. 2625(h) and (i).
The statute identifies the minimum
components EPA must include in all
chemical substance risk evaluations. For
each risk evaluation, EPA must publish
a document that outlines the scope of
the risk evaluation to be conducted,
which includes the hazards, exposures,
conditions of use, and the potentially
exposed or susceptible subpopulations
that EPA expects to consider. 15 U.S.C.
2605(b)(4)(D). The statute further
provides that each risk evaluation must
also: (1) Integrate and assess available
information on hazards and exposure
for the conditions of use of the chemical
substance, including information on
specific risks of injury to health or the
environment and information on
relevant potentially exposed or
susceptible subpopulations; (2) describe
whether aggregate or sentinel exposures
were considered and the basis for that
consideration; (3) take into account,
where relevant, the likely duration,
intensity, frequency, and number of
exposures under the conditions of use;
and (4) describe the weight of the
scientific evidence for the identified
hazards and exposure. 15 U.S.C.
2605(b)(4)(F)(i)–(ii) and (iv)–(v). Each
risk evaluation must not consider costs
or other nonrisk factors. 15 U.S.C.
2605(b)(4)(F)(iii).
The statute requires that the risk
evaluation process last no longer than
three years, with a possible additional
six-month extension. 15 U.S.C.
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2605(b)(4)(G). The statute also requires
that the EPA allow for no less than a 30day public comment period on the draft
risk evaluation, prior to publishing a
final risk evaluation. 15 U.S.C.
2605(b)(4)(H).
jspears on DSK3GMQ082PROD with NOTICES
II. TSCA SACC Meetings
The focus of the public meeting is to
peer review EPA’s draft risk evaluation
of 1–BP. After the peer review process,
EPA will consider peer reviewer
comments and recommendations and
public comments, in finalizing the risk
evaluation. The draft risk evaluation
contains: discussion of chemistry and
physical-chemical properties;
characterization of conditions of use;
environmental fate and transport
assessment; human health exposures;
environmental hazard assessment; risk
characterization; risk determination;
and a detailed description of the
systematic review process developed by
the Office of Pollution Prevention and
Toxics to search, screen, and evaluate
scientific literature for use in the risk
evaluation process.
A. How may I participate in the inperson meeting?
You may participate in the in person
meeting by following the instructions in
this unit. To ensure proper receipt by
EPA, it is imperative that you identify
the corresponding docket ID number for
1–BP (EPA–HQ–OPPT–2019–0235) in
the subject line on the first page of your
request.
1. Written comments. To provide
TSCA SACC the time necessary to
consider and review your comments,
written comments must be submitted by
the date set in the DATES section and
using the instructions in the ADDRESSES
section and Unit II.C. Comments
received after the date set in the DATES
section and prior to the end of the oral
public comment period during the
meeting for each chemical will still be
provided to the SACC for their
consideration.
2. Oral comments. In order to be
included on the meeting agenda, submit
your request to make brief oral
comments to the TSCA SACC during the
in-person meeting to the DFO listed
under FOR FURTHER INFORMATION
CONTACT on or before the date outlined
in the DATES section. The request should
identify the name of the individual
making the presentation, the
organization (if any) the individual will
represent, and any requirements for
audiovisual equipment. Oral comments
before TSCA SACC during the in-person
meeting are limited to approximately 5
minutes unless prior arrangements have
been made. In addition, each speaker
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should bring 30 copies of his or her
comments and presentation for
distribution by the DFO to the TSCA
SACC at the meeting.
3. Seating at the meeting. Seating at
the meeting will be open and on a firstcome basis.
B. How may I participate in the
preparatory virtual meeting?
Registration for the August 21, 2019,
preparatory virtual meeting is required.
To participate by listening or making a
comment during this meeting, please
visit:https://www.epa.gov/tsca-peerreview website to register. Registration
online will be confirmed by email that
will include the webcast meeting link
and audio teleconference information.
1. Written comments. Written
comments for consideration during the
preparatory virtual meeting should be
submitted, using the instructions in
ADDRESSES and Unit II.C., on or before
August 20, 2019.
2. Oral comments. Requests to make
brief oral comments to the TSCA SACC
during the preparatory virtual meeting
should be submitted when registering
online or with the DFO listed under FOR
FURTHER INFORMATION CONTACT on or
before noon on August 20, 2019. Oral
comments before TSCA SACC during
the preparatory webcast are limited to
approximately 5 minutes due to the
time constraints of this webcast.
3. Webcast. The preparatory virtual
meeting will be webcast only and will
be open to the public. Please refer to the
TSCA SACC website at https://
www.epa.gov/tsca-peer-review for
information on how to access the
webcast. Registration is required.
C. What should I consider as I prepare
my comments for EPA?
1. Submitting CBI. Do not submit CBI
to EPA through regulations.gov or email.
If your comments contain any
information that you consider to be CBI
or otherwise protected, please contact
the DFO listed under FOR FURTHER
INFORMATION CONTACT to obtain special
instructions before submitting your
comments.
2. Tips for preparing your comments.
When preparing and submitting your
comments, see the commenting tips at
https://www.epa.gov/dockets/
comments.html.
III. Background
A. What is EPA’s risk evaluation process
for existing chemicals under TSCA?
The risk evaluation process is the
second step in EPA’s existing chemical
process under TSCA, following
prioritization and before risk
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management. As this chemical is part of
the first ten chemical substances
undergoing risk evaluation, the
chemical substance was not required to
go through prioritization (81 FR 91927,
December 19, 2016) (FRL–9956–47). The
purpose of risk evaluation is to
determine whether a chemical
substance presents an unreasonable risk
of injury to health or the environment,
under the conditions of use, including
an unreasonable risk to a relevant
potentially exposed or susceptible
subpopulation. As part of this process,
EPA must evaluate both hazard and
exposure, not consider costs or other
nonrisk factors, use scientific
information and approaches in a
manner that is consistent with the
requirements in TSCA for the best
available science, and ensure decisions
are based on the weight-of-scientificevidence.
The specific risk evaluation process
that EPA has established by rule to
implement the statutory process is set
out in 40 CFR part 702 and summarized
on EPA’s website at https://
www.epa.gov/assessing-and-managingchemicals-under-tsca/risk-evaluationsexisting-chemicals-under-tsca. As
explained in the preamble to EPA’s final
rule on procedures for risk evaluation
(82 FR 33726, July 20, 2017) (FRL–
9964–38), the specific regulatory
process set out in 40 CFR part 702,
subpart B will be followed for the first
ten chemical substances undergoing risk
evaluation to the maximum extent
practicable.
B. What is 1-Bromopropane?
1-Bromopropane (1–BP) is primarily
used as a solvent cleaner in vapor and
immersion degreasing operations to
clean optics, electronics and metals, and
it has also been reported to be used as
a solvent vehicle in industries using
spray adhesives such as those used in
foam cushion manufacturing.
Information from the 2016 Chemical
Data Reporting (CDR) for 1–BP indicates
the reported production volume is 25.9
million lbs/year (manufacture and
import).
Information about the problem
formulation and scope phases of the risk
evaluation for this chemical is available
at https://www.epa.gov/assessing-andmanaging-chemicals-under-tsca/riskevaluation-1-bromopropane-1-bp.
C. What is the purpose of the TSCA
SACC?
The TSCA SACC was established by
EPA in 2016 and operates in accordance
with the Federal Advisory Committee
Act (FACA), 5 U.S.C. Appendix 2 et seq.
The SACC supports activities under
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TSCA, the Pollution Prevention Act
(PPA), 42 U.S.C. 13101 et seq., and other
applicable statutes. The TSCA SACC
provides expert independent scientific
advice and recommendations to the EPA
on the scientific and technical aspects of
risk assessments, methodologies, and
pollution prevention measures and
approaches for chemicals regulated
under TSCA.
The TSCA SACC is comprised of
experts in: Toxicology; human health
and environmental risk assessment;
exposure assessment; and related
sciences (e.g., synthetic biology,
pharmacology, biotechnology,
nanotechnology, biochemistry,
biostatistics, PBPK modeling,
computational toxicology,
epidemiology, environmental fate, and
environmental engineering and
sustainability). The TSCA SACC
currently consists of 24 members. When
needed, the committee will be assisted
in their reviews by ad hoc participants
with specific expertise in the topics
under consideration.
D. TSCA SACC Documents and Meeting
Minutes
EPA’s background paper, related
supporting materials, and draft charge
questions to TSCA SACC are available
on the TSCA SACC website and in the
docket established for the specific
chemical. In addition, the EPA will
provide additional background
documents (e.g., TSCA SACC members
participating in this meeting and the
meeting agenda) as the materials
become available. You may obtain
electronic copies of these documents,
and certain other related documents that
might be available, at https://
www.regulations.gov and the TSCA
SACC website at https://www.epa.gov/
tsca-peer-review.
TSCA SACC will prepare meeting
minutes summarizing its
recommendations to the EPA. The
meeting minutes will be posted on the
TSCA SACC website and in the relevant
docket.
jspears on DSK3GMQ082PROD with NOTICES
Authority: 15 U.S.C. 2601 et seq.; 5 U.S.C.
Appendix 2 et seq.
Dated: August 5, 2019.
Andrew R. Wheeler,
Administrator.
[FR Doc. 2019–17222 Filed 8–9–19; 8:45 am]
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ENVIRONMENTAL PROTECTION
AGENCY
39833
SUPPLEMENTARY INFORMATION:
I. General Information
[EPA–HQ–OPP–2019–0448; FRL–9997–71]
A. Does this action apply to me?
Nominations to the Federal Insecticide,
Fungicide, and Rodenticide Act
Scientific Advisory Panel; Request for
Comments
This action is directed to the public
in general. This action may, however, be
of interest to persons who are or may be
required to conduct testing of chemical
substances under the Federal Food,
Drug, and Cosmetic Act (FFDCA) and
FIFRA. Given other entities may also be
interested, the Agency has not
attempted to describe all the specific
entities that may be affected by this
action. If you have any questions
regarding the applicability of this action
to a particular entity, consult the DFO
listed under FOR FURTHER INFORMATION
CONTACT.
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
This notice provides the
names, addresses, and professional
affiliations of persons recently
nominated to serve on the Scientific
Advisory Panel (SAP) established under
section 25(d) of the Federal Insecticide,
Fungicide, and Rodenticide Act
(FIFRA). The Panel was created on
November 28, 1975, and made a
permanent Panel by amendment to
FIFRA, dated October 25, 1988. The
Agency, at this time, anticipates
selecting three new members to serve on
the panel because of membership terms
that will expire during the next year.
Public comments on the current
nominations are invited, as these
comments will be used to assist the
Agency in selecting the new members
for the chartered Scientific Advisory
Panel.
SUMMARY:
Comments identified by docket
ID number EPA–HQ–OPP–2019–0448,
must be received on or before
September 11, 2019.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPP–2019–0448, by
one of the following methods:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
online instructions for submitting
comments. Do not electronically submit
any information you consider to be
Confidential Business Information (CBI)
or information whose disclosure is
restricted by statute.
• Mail: OPP Docket, Environmental
Protection Agency Docket Center (EPA/
DC), (28221T), 1200 Pennsylvania Ave.
NW, Washington, DC 20460–0001.
• Hand Delivery: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/contacts.html.
FOR FURTHER INFORMATION CONTACT:
Steven Knott, M.S., Designated Federal
Officer (DFO), Office of Science
Coordination and Policy (7201M),
Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC
20460–0001; telephone number: (202)
564–0103; email address: knott.steven@
epa.gov.
DATES:
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B. What should I consider as I prepare
my comments for EPA?
1. Submitting CBI. Do not submit CBI
information to EPA through
regulations.gov or email. If your
comments contain any information that
you consider to be CBI or otherwise
protected, please contact the DFO listed
under FOR FURTHER INFORMATION
CONTACT to obtain special instructions
before submitting your comments.
2. Tips for preparing your comments.
When preparing and submitting your
comments, see the commenting tips at
https://www.epa.gov/dockets/
comments.html.
II. Background
The FIFRA SAP serves as a scientific
peer review mechanism of EPA’s Office
of Chemical Safety and Pollution
Prevention (OCSPP) and is structured to
provide independent scientific advice,
information, and recommendations to
the EPA Administrator on pesticides
and pesticide-related issues as to the
impact of regulatory actions on health
and the environment. The FIFRA SAP is
a federal advisory committee
established in 1975 under FIFRA that
operates in accordance with
requirements of the Federal Advisory
Committee Act (5 U.S.C. Appendix).
The FIFRA SAP is composed of a
permanent panel consisting of seven
members who are appointed by the EPA
Administrator from nominees provided
by the National Institutes of Health
(NIH) and the National Science
Foundation (NSF). FIFRA established a
Science Review Board (SRB) consisting
of at least 60 scientists who are available
to the FIFRA SAP on an ad hoc basis to
assist in reviews conducted by the
FIFRA SAP. As a scientific peer review
mechanism, the FIFRA SAP provides
comments, evaluations, and
recommendations to improve the
E:\FR\FM\12AUN1.SGM
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Agencies
[Federal Register Volume 84, Number 155 (Monday, August 12, 2019)]
[Notices]
[Pages 39830-39833]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-17222]
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ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2019-0235; FRL-9997-25]
1-Bromopropane (1-BP); Draft Toxic Substances Control Act (TSCA)
Risk Evaluation and TSCA Science Advisory Committee on Chemicals (SACC)
Meetings; Notice of Availability and Public Meetings
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
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SUMMARY: EPA is announcing the availability of documents and dates for
the peer review of the draft risk evaluation for 1-Bromopropane (1-BP).
The purpose of the risk evaluations under the Toxic Substances Control
Act (TSCA) is to determine whether a chemical substance presents an
unreasonable risk of injury to health or the environment under the
conditions of use, including an unreasonable risk to a relevant
potentially exposed or susceptible subpopulation. EPA is also
submitting these same documents to the TSCA Science Advisory Committee
on Chemicals (SACC) for peer review and is announcing that there will
be a 3-day in-person meeting of the TSCA SACC to consider and review
these draft risk evaluations. Preceding the in-person meeting, there
will be a 3-hour preparatory virtual meeting for the panel to consider
the scope and clarity of the draft charge questions for the peer
reviews.
DATES:
Comments: Comments on the draft risk evaluation must be received on
or before October 11, 2019. Please submit comments on the draft risk
evaluation by August 30, 2019 to allow the SACC time to review and
consider them before the peer review meeting. Comments received after
August 30, 2019 will still be provided to the SACC for their
consideration. For additional instructions, see Unit II.A. and Unit
II.B. of the SUPPLEMENTARY INFORMATION.
Meetings: The preparatory virtual meeting will be held on August
21, 2019, from 1 p.m. to approximately 4 p.m. (EDT). The 3-day in-
person meeting will be held on September 10-12, 2019 from 9:00 a.m. to
approximately 5:30 p.m. (EDT).
ADDRESSES: Virtual Meeting: The preparatory virtual meeting will be
conducted via webcast and telephone. Registration is open to the public
and is required to participate during the preparatory virtual meeting.
Please visit https://www.epa.gov/tsca-peer-review website for
additional information including how to register.
In-Person Meeting: The location of the in-person meeting will be
announced on the TSCA SACC website at https://www.epa.gov/TSCA-Peer-Review. The in-person meeting may also be webcast. Please refer to the
TSCA SACC website at https://www.epa.gov/tsca-peer-review for
information on how to access the webcast. Please note that for the in-
person meeting, the webcast is a supplementary public process provided
only for convenience. If difficulties arise resulting in webcasting
outages, the in-person meeting will continue as planned.
Comments. Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2019-0235, by one of the following methods:
[[Page 39831]]
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the online instructions for submitting comments. Do not submit
electronically any information you consider to be Confidential Business
Information (CBI) or other information whose disclosure is restricted
by statute.
Mail: OPPT Docket, Environmental Protection Agency Docket
Center (EPA/DC), (28221T), 1200 Pennsylvania Ave. NW, Washington, DC
20460-0001.
Hand Delivery: To make special arrangements for hand
delivery or delivery of boxed information, please follow the
instructions at https://www.epa.gov/dockets/contacts.html.
Additional instructions on commenting or visiting the docket, along
with more information about dockets generally, is available at https://www.epa.gov/dockets.
Requests to present oral comments and requests for special
accommodations. Submit requests for special accommodations, or requests
to present oral comments (in-person or over the telephone) during the
webcast and/or the public portion of the peer review meeting to the
Designated Federal Official (DFO) listed under FOR FURTHER INFORMATION
CONTACT by the deadline identified in the DATES section. Comments
received after the date set in the DATES section and prior to the end
of the oral public comment period during the meeting for each chemical
will still be provided to the SACC for their consideration.
FOR FURTHER INFORMATION CONTACT: TSCA SACC meetings: Tamue Gibson, DFO,
Office of Science Coordination and Policy (7201M), Environmental
Protection Agency, 1200 Pennsylvania Ave. NW, Washington, DC 20460-
0001; telephone number: (202) 564-7642; email address:
[email protected].
Risk Evaluations: Dr. Stan Barone, Office of Pollution Prevention
and Toxics (7403M), Environmental Protection Agency, 1200 Pennsylvania
Ave. NW, Washington, DC 20460-0001; telephone number: 202-564-1169;
email address: [email protected].
Special accommodations for the SACC meeting: For information on
access or services for individuals with disabilities, and to request
accommodation of a disability, please contact the DFO listed under FOR
FURTHER INFORMATION CONTACT at least 10 days prior to the meeting to
give EPA as much time as possible to process your request.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
This action is directed to the public in general. This action may
be of interest to persons who are or may be required to conduct testing
and risk evaluations of chemical substances under the TSCA, 15 U.S.C.
2601 et seq. Since other entities may also be interested in these risk
evaluations, the EPA has not attempted to describe all the specific
entities that may be affected by this action.
B. What action is the EPA taking?
EPA is announcing the availability of and seeking public comment on
the draft risk evaluation for 1-Bromopropane (1-BP). EPA is seeking
public comment on all aspects of the draft risk evaluation, including
any conclusions, findings, and determinations, and the submission of
any additional information that might be relevant to the science
underlying the risk evaluation and the outcome of the systematic review
associated with the chemical. This 60-day comment period on the draft
risk evaluations satisfies TSCA section 6(b)(4)(H), which requires EPA
to ``provide no less than 30 days public notice and an opportunity for
comment on a draft risk evaluation prior to publishing a final risk
evaluation'' and 40 CFR 702.49(a), which states that ``EPA will publish
a draft risk evaluation in the Federal Register, open a docket to
facilitate receipt of public comment, and provide no less than a 60-day
comment period, during which time the public may submit comment on
EPA's draft risk evaluation.'' In addition to any new comments on the
draft risk evaluation, the public should resubmit or clearly identify
any previously filed comments, modified as appropriate, that are
relevant to the draft risk evaluation and that the submitter feels have
not been addressed. EPA does not intend to respond to comments
submitted prior to the release of the draft risk evaluation unless they
are clearly identified in comments on the draft risk evaluation.
EPA is also submitting these same documents to the TSCA SACC for
peer review and announcing the meetings for the peer review panel. All
comments submitted to the dockets for consideration by the TSCA SACC by
the deadline identified in the DATES section will be provided to the
TSCA SACC peer review panel, which will have the opportunity to
consider the comments during its discussions.
C. What is the EPA's authority for taking this action?
TSCA section 6, 15 U.S.C. 2605, requires EPA to conduct risk
evaluations to ``determine whether a chemical substance presents an
unreasonable risk of injury to health or the environment, without
consideration of costs or other nonrisk factors, including an
unreasonable risk to a potentially exposed or susceptible subpopulation
identified as relevant to the risk evaluation by the Administrator,
under the conditions of use.'' 15 U.S.C. 2605(b)(4)(A). TSCA sections
6(b)(4)(A) through (H) enumerate the deadlines and minimum requirements
applicable to this process, including provisions that direct which
chemical substances must undergo evaluation, the development of
criteria for manufacturer-requested evaluations, the minimum components
of an EPA risk evaluation, and the timelines for public comment and
completion of the risk evaluation. The law also requires that EPA
operate in a manner that is consistent with the best available science
and make decisions based on the weight of the scientific evidence. 15
U.S.C. 2625(h) and (i).
The statute identifies the minimum components EPA must include in
all chemical substance risk evaluations. For each risk evaluation, EPA
must publish a document that outlines the scope of the risk evaluation
to be conducted, which includes the hazards, exposures, conditions of
use, and the potentially exposed or susceptible subpopulations that EPA
expects to consider. 15 U.S.C. 2605(b)(4)(D). The statute further
provides that each risk evaluation must also: (1) Integrate and assess
available information on hazards and exposure for the conditions of use
of the chemical substance, including information on specific risks of
injury to health or the environment and information on relevant
potentially exposed or susceptible subpopulations; (2) describe whether
aggregate or sentinel exposures were considered and the basis for that
consideration; (3) take into account, where relevant, the likely
duration, intensity, frequency, and number of exposures under the
conditions of use; and (4) describe the weight of the scientific
evidence for the identified hazards and exposure. 15 U.S.C.
2605(b)(4)(F)(i)-(ii) and (iv)-(v). Each risk evaluation must not
consider costs or other nonrisk factors. 15 U.S.C. 2605(b)(4)(F)(iii).
The statute requires that the risk evaluation process last no
longer than three years, with a possible additional six-month
extension. 15 U.S.C.
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2605(b)(4)(G). The statute also requires that the EPA allow for no less
than a 30-day public comment period on the draft risk evaluation, prior
to publishing a final risk evaluation. 15 U.S.C. 2605(b)(4)(H).
II. TSCA SACC Meetings
The focus of the public meeting is to peer review EPA's draft risk
evaluation of 1-BP. After the peer review process, EPA will consider
peer reviewer comments and recommendations and public comments, in
finalizing the risk evaluation. The draft risk evaluation contains:
discussion of chemistry and physical-chemical properties;
characterization of conditions of use; environmental fate and transport
assessment; human health exposures; environmental hazard assessment;
risk characterization; risk determination; and a detailed description
of the systematic review process developed by the Office of Pollution
Prevention and Toxics to search, screen, and evaluate scientific
literature for use in the risk evaluation process.
A. How may I participate in the in-person meeting?
You may participate in the in person meeting by following the
instructions in this unit. To ensure proper receipt by EPA, it is
imperative that you identify the corresponding docket ID number for 1-
BP (EPA-HQ-OPPT-2019-0235) in the subject line on the first page of
your request.
1. Written comments. To provide TSCA SACC the time necessary to
consider and review your comments, written comments must be submitted
by the date set in the DATES section and using the instructions in the
ADDRESSES section and Unit II.C. Comments received after the date set
in the DATES section and prior to the end of the oral public comment
period during the meeting for each chemical will still be provided to
the SACC for their consideration.
2. Oral comments. In order to be included on the meeting agenda,
submit your request to make brief oral comments to the TSCA SACC during
the in-person meeting to the DFO listed under FOR FURTHER INFORMATION
CONTACT on or before the date outlined in the DATES section. The
request should identify the name of the individual making the
presentation, the organization (if any) the individual will represent,
and any requirements for audiovisual equipment. Oral comments before
TSCA SACC during the in-person meeting are limited to approximately 5
minutes unless prior arrangements have been made. In addition, each
speaker should bring 30 copies of his or her comments and presentation
for distribution by the DFO to the TSCA SACC at the meeting.
3. Seating at the meeting. Seating at the meeting will be open and
on a first-come basis.
B. How may I participate in the preparatory virtual meeting?
Registration for the August 21, 2019, preparatory virtual meeting
is required. To participate by listening or making a comment during
this meeting, please visit:https://www.epa.gov/tsca-peer-review website
to register. Registration online will be confirmed by email that will
include the webcast meeting link and audio teleconference information.
1. Written comments. Written comments for consideration during the
preparatory virtual meeting should be submitted, using the instructions
in ADDRESSES and Unit II.C., on or before August 20, 2019.
2. Oral comments. Requests to make brief oral comments to the TSCA
SACC during the preparatory virtual meeting should be submitted when
registering online or with the DFO listed under FOR FURTHER INFORMATION
CONTACT on or before noon on August 20, 2019. Oral comments before TSCA
SACC during the preparatory webcast are limited to approximately 5
minutes due to the time constraints of this webcast.
3. Webcast. The preparatory virtual meeting will be webcast only
and will be open to the public. Please refer to the TSCA SACC website
at https://www.epa.gov/tsca-peer-review for information on how to access
the webcast. Registration is required.
C. What should I consider as I prepare my comments for EPA?
1. Submitting CBI. Do not submit CBI to EPA through regulations.gov
or email. If your comments contain any information that you consider to
be CBI or otherwise protected, please contact the DFO listed under FOR
FURTHER INFORMATION CONTACT to obtain special instructions before
submitting your comments.
2. Tips for preparing your comments. When preparing and submitting
your comments, see the commenting tips at https://www.epa.gov/dockets/comments.html.
III. Background
A. What is EPA's risk evaluation process for existing chemicals under
TSCA?
The risk evaluation process is the second step in EPA's existing
chemical process under TSCA, following prioritization and before risk
management. As this chemical is part of the first ten chemical
substances undergoing risk evaluation, the chemical substance was not
required to go through prioritization (81 FR 91927, December 19, 2016)
(FRL-9956-47). The purpose of risk evaluation is to determine whether a
chemical substance presents an unreasonable risk of injury to health or
the environment, under the conditions of use, including an unreasonable
risk to a relevant potentially exposed or susceptible subpopulation. As
part of this process, EPA must evaluate both hazard and exposure, not
consider costs or other nonrisk factors, use scientific information and
approaches in a manner that is consistent with the requirements in TSCA
for the best available science, and ensure decisions are based on the
weight-of-scientific-evidence.
The specific risk evaluation process that EPA has established by
rule to implement the statutory process is set out in 40 CFR part 702
and summarized on EPA's website at https://www.epa.gov/assessing-and-managing-chemicals-under-tsca/risk-evaluations-existing-chemicals-under-tsca. As explained in the preamble to EPA's final rule on
procedures for risk evaluation (82 FR 33726, July 20, 2017) (FRL-9964-
38), the specific regulatory process set out in 40 CFR part 702,
subpart B will be followed for the first ten chemical substances
undergoing risk evaluation to the maximum extent practicable.
B. What is 1-Bromopropane?
1-Bromopropane (1-BP) is primarily used as a solvent cleaner in
vapor and immersion degreasing operations to clean optics, electronics
and metals, and it has also been reported to be used as a solvent
vehicle in industries using spray adhesives such as those used in foam
cushion manufacturing. Information from the 2016 Chemical Data
Reporting (CDR) for 1-BP indicates the reported production volume is
25.9 million lbs/year (manufacture and import).
Information about the problem formulation and scope phases of the
risk evaluation for this chemical is available at https://www.epa.gov/assessing-and-managing-chemicals-under-tsca/risk-evaluation-1-bromopropane-1-bp.
C. What is the purpose of the TSCA SACC?
The TSCA SACC was established by EPA in 2016 and operates in
accordance with the Federal Advisory Committee Act (FACA), 5 U.S.C.
Appendix 2 et seq. The SACC supports activities under
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TSCA, the Pollution Prevention Act (PPA), 42 U.S.C. 13101 et seq., and
other applicable statutes. The TSCA SACC provides expert independent
scientific advice and recommendations to the EPA on the scientific and
technical aspects of risk assessments, methodologies, and pollution
prevention measures and approaches for chemicals regulated under TSCA.
The TSCA SACC is comprised of experts in: Toxicology; human health
and environmental risk assessment; exposure assessment; and related
sciences (e.g., synthetic biology, pharmacology, biotechnology,
nanotechnology, biochemistry, biostatistics, PBPK modeling,
computational toxicology, epidemiology, environmental fate, and
environmental engineering and sustainability). The TSCA SACC currently
consists of 24 members. When needed, the committee will be assisted in
their reviews by ad hoc participants with specific expertise in the
topics under consideration.
D. TSCA SACC Documents and Meeting Minutes
EPA's background paper, related supporting materials, and draft
charge questions to TSCA SACC are available on the TSCA SACC website
and in the docket established for the specific chemical. In addition,
the EPA will provide additional background documents (e.g., TSCA SACC
members participating in this meeting and the meeting agenda) as the
materials become available. You may obtain electronic copies of these
documents, and certain other related documents that might be available,
at https://www.regulations.gov and the TSCA SACC website at https://www.epa.gov/tsca-peer-review.
TSCA SACC will prepare meeting minutes summarizing its
recommendations to the EPA. The meeting minutes will be posted on the
TSCA SACC website and in the relevant docket.
Authority: 15 U.S.C. 2601 et seq.; 5 U.S.C. Appendix 2 et seq.
Dated: August 5, 2019.
Andrew R. Wheeler,
Administrator.
[FR Doc. 2019-17222 Filed 8-9-19; 8:45 am]
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