Di-isodecyl Phthalate (DIDP) and Di-isononyl Phthalate (DINP); Science Advisory Committee on Chemicals (SACC) Peer Review of Draft Documents; Notice of SACC Meeting; Availability; and Request for Comment, 43847-43850 [2024-10999]
Download as PDF
Federal Register / Vol. 89, No. 98 / Monday, May 20, 2024 / Notices
power beyond WAPA’s P–DP
transmission system. WAPA may assist
new contractors in obtaining third-party
transmission arrangements for delivery
of firm power allocated during the
forthcoming marketing period. WAPA
will determine the use of its
transmission resources concurrently
with further development of the
products and services under this
Proposed 2028 Plan. A list of designated
delivery points will be provided with
the Call for Resource Pool Applications.
WAPA will market surplus transmission
capacity on P–DP under WAPA’s Open
Access Transmission Tariff and other
applicable arrangements.
Legal Authorities
WAPA developed this Proposed 2028
Plan in accordance with its power
marketing authorities pursuant to the
Department of Energy Organization Act
(42 U.S.C. 7101, et seq.); the
Reclamation Act of June 17, 1902 (32
Stat. 388), as amended and
supplemented by subsequent
enactments, particularly section 9(c) of
the Reclamation Project Act of 1939 (43
U.S.C. 485(c)); and other acts
specifically applicable to P–DP.
Procedural Requirements
Review Under the Paperwork Reduction
Act
In accordance with the Paperwork
Reduction Act of 1980 (44 U.S.C. 3501,
et seq.), WAPA has received approval
from the Office of Management and
Budget for the collection of customer
information under control number
1910–5136.
lotter on DSK11XQN23PROD with NOTICES1
Environmental Compliance
WAPA has determined this action fits
within the following categorical
exclusions listed in appendix B to
subpart D of 10 CFR part 1021: B4.1
(Contracts, policies, and marketing and
allocation plans for electric power) and
B4.4 (Power marketing services and
activities). Categorically excluded
projects and activities do not require
preparation of either an environmental
impact statement or an environmental
assessment.9A copy of the categorical
exclusion determination is available on
WAPA’s website under the 2024
accordion menu at www.wapa.gov/
about-wapa/regions/dsw/environment.
9 The determination was done in compliance with
NEPA (42 U.S.C. 4321–4347); the Council on
Environmental Quality Regulations for
implementing NEPA (40 CFR parts 1500–1508); and
DOE NEPA Implementing Procedures and
Guidelines (10 CFR part 1021).
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Determination Under Executive Order
12866
WAPA has an exemption from
centralized regulatory review under
Executive Order 12866; accordingly, no
clearance of this notice by the Office of
Management and Budget is required.
Signing Authority
This document of the Department of
Energy was signed on May 13, 2024, by
Tracey A. LeBeau, Administrator,
Western Area Power Administration.
For administrative purposes only, and
in compliance with requirements of the
Office of the Federal Register, the
undersigned DOE Federal Register
Liaison Officer has been authorized to
sign and submit the document in
electronic format for publication, as an
official document of the Department of
Energy. This administrative process in
no way alters the legal effect of this
document upon publication in the
Federal Register.
Signed in Washington, DC, on May 15,
2024.
Treena V. Garrett,
Federal Register Liaison Officer, U.S.
Department of Energy.
43847
documents and public comments for
peer review.
DATES:
Virtual Preparatory Public Meeting
Comments: Submit written comments
on the scope and clarity of the charge
questions on or before noon (12:00 p.m.
EDT) on July 19, 2024.
Registration: To request time to
present oral comments, you must
register by noon (12:00 p.m. EDT) on
July 19, 2024. For those not making oral
comments, registration will remain open
through the end of the meeting on July
19, 2024.
Meeting date: July 23, 2024, 1 p.m. to
4 p.m. (EDT).
Virtual Peer Review Public Meeting
Comments: Submit comments on or
before July 19, 2024.
Registration: To request time to
present oral comments, you must
register by noon, July 26, 2024. For
those not making oral comments,
registration will remain open through
the end of the meeting.
Meeting dates: July 30–August 2,
2024, 10 a.m. to 5 p.m. (EDT).
[FR Doc. 2024–10997 Filed 5–17–24; 8:45 am]
Special Accommodations
BILLING CODE 6450–01–P
To allow sufficient time for EPA to
process your request before the
applicable meeting, please submit your
requests at least ten business days in
advance of the meeting.
See unit III. of SUPPLEMENTARY
INFORMATION.
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2024–0073; FRL–11760–
02–OCSPP]
Di-isodecyl Phthalate (DIDP) and Diisononyl Phthalate (DINP); Science
Advisory Committee on Chemicals
(SACC) Peer Review of Draft
Documents; Notice of SACC Meeting;
Availability; and Request for Comment
ACTION:
Notice.
The Environmental Protection
Agency (EPA or ‘‘Agency’’) is
announcing the availability of and
soliciting public comment on the draft
manufacturer-requested risk evaluation
for Di-isodecyl Phthalate (DIDP) and the
draft physical chemical, fate, and hazard
assessments for Di-isononyl Phthalate
(DINP) prepared under the Toxic
Substances Control Act (TSCA). The
draft documents will also be submitted
to the Science Advisory Committee on
Chemicals (SACC) for peer review. EPA
is also announcing that there will be
two virtual public meetings of the
SACC: On July 23, 2024, for the SACC
to consider the scope and clarity of the
draft charge questions for the peer
review; and on July 30–August 2, 2024,
for the SACC to consider the draft
SUMMARY:
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ADDRESSES:
Comments: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2024–0073,
through the Federal eRulemaking Portal
at 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. Additional
instructions on commenting and visiting
the docket is available at https://
www.epa.gov/dockets.
Meeting registration: For information
and instructions on how to register and
access these virtual public meetings,
please refer to the SACC website at
https://www.epa.gov/tsca-peer-review.
After registering, you will receive the
webcast and streaming service meeting
links and audio teleconference
information.
Special accommodation requests: To
request accommodation for a disability,
please contact the Designated Federal
Official (DFO) listed under FOR FURTHER
INFORMATION CONTACT.
E:\FR\FM\20MYN1.SGM
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43848
Federal Register / Vol. 89, No. 98 / Monday, May 20, 2024 / Notices
FOR FURTHER INFORMATION CONTACT:
SACC peer review: The Designated
Federal Official (DFO) is Dr. Alaa
Kamel, Mission Support Division
(7602M), Office of Program Support,
Office of Chemical Safety and Pollution
Prevention, Environmental Protection
Agency; telephone number: (202) 564–
5336 or SACC main office number: (202)
564–8450; email address: kamel.alaa@
epa.gov.
Draft documents: Todd Coleman,
Existing Chemicals Risk Management
Division (7404M), Office of Pollution
Prevention and Toxics, Office of
Chemical Safety and Pollution
Prevention, Environmental Protection
Agency; telephone number: (202) 564–
1208; email address: coleman.todd@
epa.gov.
SUPPLEMENTARY INFORMATION:
I. Executive Summary
A. What action is the Agency taking?
EPA is announcing the availability of
and soliciting public comment on the
draft risk evaluation for DIDP and the
draft physical chemical, fate, and hazard
assessments for DINP. EPA is also
announcing a virtual peer review public
meeting on July 30-August 2, 2024, for
the SACC to consider and review the
draft documents. A virtual preparatory
public meeting will be held on July 23,
2024, for the SACC to consider and ask
questions regarding the scope and
clarity of the draft charge questions.
This document provides instructions for
accessing the materials, submitting
written comments, and registering to
provide oral comments and attend the
public meetings.
lotter on DSK11XQN23PROD with NOTICES1
B. What is the Agency’s authority for
taking this action?
EPA established the SACC in 2016 in
accordance with the TSCA, 15 U.S.C.
2625(o), to provide independent advice
and expert consultation with respect to
the scientific and technical aspects of
issues relating to the implementation of
TSCA. The SACC operates in
accordance with the Federal Advisory
Committee Act (FACA), 5 U.S.C. 10, and
supports activities under TSCA, 15
U.S.C. 2601 et seq., the Pollution
Prevention Act (PPA), 42 U.S.C. 13101
et seq., and other applicable statutes.
C. Does this action apply to me?
This action is directed to the public
in general and may be of particular
interest to those involved in the
manufacture, processing, distribution,
and disposal of the subject chemical
substance, and/or those interested in the
assessment of risks involving chemical
substances and mixtures regulated
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under TSCA (including members of atrisk communities, non-governmental
organizations (NGOs), Federal, State,
and local officials). Since other entities
may also be interested, the Agency has
not attempted to describe all the specific
entities that may be interested.
D. What should I consider as I submit
my comments to EPA?
1. Submitting CBI. Do not submit CBI
to EPA through email or https://
www.regulations.gov. If you wish to
include CBI in your comment, please
contact the DFO listed under FOR
FURTHER INFORMATION CONTACT to obtain
special instructions before submitting
that information.
2. Tips for preparing your comments.
When preparing and submitting your
comments, see https://www.epa.gov/
dockets/commenting-epa-dockets. See
also the instructions in unit III.C.
E. How can I stay informed about SACC
activities?
You may subscribe to the following
listserv for alerts regarding this and
other SACC-related activities: https://
public.govdelivery.com/accounts/
USAEPAOPPT/subscriber/new?topic_
id=USAEPAOPPT_101.
II. Background
A. What is the purpose of the SACC?
The SACC provides independent
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 SACC is composed of
experts in toxicology; environmental
risk assessment; exposure assessment;
and related sciences (e.g., synthetic
biology, pharmacology, biotechnology,
nanotechnology, biochemistry,
biostatistics, physiologically based
pharmacokinetic (PBPK) modeling,
computational toxicology,
epidemiology, environmental fate, and
environmental engineering and
sustainability). The SACC currently
consists of 18 members. When needed,
the committee will be assisted by ad hoc
reviewers with specific expertise in the
topics under consideration.
B. Why is EPA conducting these risk
evaluations?
TSCA requires EPA to conduct risk
evaluations on prioritized chemical
substances and allows chemical
manufacturers to request an EPAconducted risk evaluation of a chemical
substance (or category of chemical
substances) using the procedures
established in 40 CFR 702.37. TSCA
also identifies the minimum
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components EPA must include in all
chemical substance risk evaluations.
EPA received manufacturer requests to
conduct risk evaluations for DIDP and
DINP, both as categories of chemical
substances, and subsequently granted
and initiated risk evaluations for both of
them. The purpose of conducting risk
evaluations is to determine whether a
chemical substance presents an
unreasonable risk to human health or
the environment under the Conditions
of Use (COUs). These evaluations
include assessing unreasonable risks to
relevant potentially exposed or
susceptible subpopulations. As part of
this process EPA: (1) Integrates hazard
and exposure assessments using the best
available science that is reasonably
available to assure decisions are based
on the weight of the scientific evidence,
and (2) Conducts peer review for risk
evaluation approaches that have not
been previously peer reviewed. For
more information about the three stages
of EPA’s process for ensuring the safety
of existing chemicals (i.e., prioritization,
risk evaluation, and risk management),
go to https://www.epa.gov/assessingand-managing-chemicals-under-tsca/
how-epa-evaluates-safety-existingchemicals.
C. Why is EPA evaluating the risks from
DIDP and DINP?
On May 24, 2019, EPA received
requests to conduct risk evaluations for
DIDP and DINP from ExxonMobil
Chemical Company, Evonik
Corporation, and Teknor Apex, through
the American Chemistry Council’s High
Phthalates Panel (ACC HPP). In
December 2019, EPA notified ACC HPP
that the Agency had granted their
manufacturer requested risk
evaluations.
DIDP is a common chemical name for
the category of chemical substances that
includes the following substances: 1,2benzenedicarboxylic acid, 1,2diisodecyl ester (CASRN 26761–40–0)
and 1,2-benzenedicarboxylic acid, diC9-11-branched alkyl esters, C10-rich
(CASRN 68515–49–1). Both CASRNs
contain mainly C10 dialkyl phthalate
esters.
DINP is a common chemical name for
the category of chemical substances that
includes the following substances: 1,2benzenedicarboxylic acid, 1,2-isononyl
ester (CASRN 28553–12–0) and 1,2benzenedicarboxylic acid, di-C9-11branched alkyl esters, C9-rich (CASRN
68515–48–0). Both CASRNs contain
mainly C9 dialkyl phthalate esters. Both
DIDP and DINP are primarily used as a
plasticizer in polyvinyl chloride (PVC)
in consumer, commercial, and
industrial applications.
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Federal Register / Vol. 89, No. 98 / Monday, May 20, 2024 / Notices
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DIDP and DINP are both structurally
phthalates, and therefore many aspects
of physical-chemical (p-chem)
properties and exposure (to humans and
ecological species) are similar,
described further in the draft physical
chemical and fate assessments for both
chemical substances. Because of the
similar exposure and physical chemical
properties of DIDP and DINP, EPA is
developing these individual risk
evaluations in parallel, and similarly the
SACC peer review of the methods and
novel analyses for the draft risk
evaluations will occur concurrently.
Both DIDP and DINP have extremely
low water solubility and will be
preferentially sorbed into sediments,
soils, and suspended solids in surface
water and wastewater. Both are
expected to be persistent in anaerobic
environments. Under indoor settings,
DIDP and DINP are expected to partition
to airborne particles and are expected to
have extended lifetime compared to
outdoor settings.
For both DIDP and DINP, liver and
developmental toxicity are indicated as
the most sensitive and robust noncancer hazards. However, these two
phthalates differ in several important
respects regarding their human health
hazard profiles. For DIDP, the
developmental toxicity is not
characterized by androgen insufficiency,
and data are insufficient to determine
the carcinogenicity. For DINP,
developmental toxicity results in
androgen insufficiency (phthalate
syndrome), and the effects on the liver
include cancer. Therefore, because of
these hazard differences, EPA is
requesting peer review on the draft
hazard assessment of DINP ahead of
issuing the risk evaluation of DINP.
D. What is the topic of the planned
SACC peer review?
EPA is submitting the draft risk
evaluation of DIDP, draft physical
chemical, fate, and hazard assessments
of DINP, and associated supporting
documents to the SACC for peer review,
along with the public comments
received. The draft risk evaluation for
DIDP includes analyses of physical
chemical properties, the fate and
transport in the environment, exposure
to workers, consumers and general
population including potentially
exposed or susceptible subpopulations
(PESS), releases to the environment,
environmental hazard and risk
characterization for terrestrial and
aquatic species, and human health
hazard and risk characterization for
workers, consumers, and the general
population. The draft assessments of
DINP includes analyses of physical
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19:14 May 17, 2024
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chemical properties, the fate and
transport in the environment,
environmental hazard for terrestrial and
aquatic species, human health noncancer hazards, and human health
cancer hazards.
EPA is not developing charge
questions for all aspects of the draft
documents but is instead focusing its
charge to the SACC on specific scientific
areas that need peer review. Many of the
methods and analyses used in these
evaluations are not novel and have been
reviewed in the development of the
tools, used in various agency work
products or in previous TSCA
assessments (e.g., systematic review,
consumer exposure model (CEM),
American Meteorological Society
(AMS)/EPA Regulatory Model
(AERMOD), point source calculator
(PSC), etc.). Also, EPA is not soliciting
comments on uses of these phthalates
that are outside the scope of TSCA (e.g.,
personal care products, cosmetics, food
contact materials, medical devices);
those uses will be addressed as
appropriate within the cumulative risk
assessment.
As a result of the similarities in
conditions of use, chemical properties,
and data availability between DIDP and
DINP, the methods and approaches used
to assess DIDP apply to DINP.
Nonetheless, these two chemicals differ
most in their human health hazard
profiles and therefore SACC is requested
to review these novel analyses for DINP.
Any relevant recommendations from
this SACC review on DIDP will be also
considered in the development of the
final risk evaluations for both DIDP and
DINP. By taking the DIDP risk
evaluation and DINP hazard
assessments to peer review in this
manner, EPA will obtain the necessary
independent review and advice for the
DINP risk evaluation.
EPA continues to work on risk
evaluations of additional high-priority
substance phthalates, in addition to the
cumulative risk assessment (CRA) for
the phthalates. The subsequent five
individual risk evaluations and the CRA
are not part of this peer review but will
be brought to the SACC for peer review
at a future date.
III. Public Meeting of the SACC
A. What is the purpose of the virtual
peer review public meeting(s)?
EPA is planning two virtual public
meetings: (1) A preparatory public
meeting for the SACC to consider and
ask questions regarding the scope and
clarity of the draft charge questions; and
(2) a public meeting for the SACC to
consider and review the draft
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43849
documents. These public meetings are
part of the SACC peer review of the
Agency’s methods and novel analyses
for the draft evaluations of the risks
from the phthalates DIDP and DINP to
inform risk management decisions
under TSCA. EPA expects to ask the
SACC to consider and review this DIDP
draft risk evaluation and DINP
assessments. The agenda for these
meetings will be posted in the docket
and the SACC website.
To participate in these virtual public
meetings, you must register online to
receive the webcast and streaming
service meeting links and audio
teleconference information for each
meeting. Online registration will be
available beginning approximately one
month prior to the meeting, and remain
open through the end of the meeting. To
make oral comments during one of these
meetings, follow the instructions in unit
III.C.
Recommendations from this SACC
review and public comments will be
considered in the development of the
final risk evaluation for DIDP and DINP.
The Agency will be seeking SACC
review of its data analyses and
methodologies relevant to human health
hazard and exposure analyses that have
not been previously peer reviewed.
B. How can I access the documents?
The manufacturer-requested draft risk
evaluation for DIDP, draft assessments
for DINP, and related documents,
including background documents,
related supporting materials, and draft
charge questions, are available in the
docket. As additional background
materials become available, EPA will
include those additional background
materials (e.g., SACC members and
consultants participating in this meeting
and the meeting agenda) in the docket
and through links on the SACC website
at https://www.epa.gov/tsca-peerreview.
After the public meeting, the SACC
will prepare the meeting minutes and a
final report document summarizing its
recommendations to the EPA, which
will also be available in the docket and
through the SACC website.
C. How can I provide comments?
To ensure proper receipt of
comments, it is imperative that you
identify docket ID No. EPA–HQ–OPPT–
2024–0073 in the subject line on the
first page of your comments and follow
the instructions in this document.
1. Written comments. Submit written
comments by the deadlines set in the
DATES section of this document and as
described in the ADDRESSES section of
this document.
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Federal Register / Vol. 89, No. 98 / Monday, May 20, 2024 / Notices
2. Oral comments. To request time to
present oral comments during one of the
virtual public meetings, you must
register online by the deadlines set in
the DATES section of this document. Oral
comments during the virtual public
meetings are limited to 5 minutes. In
addition, each speaker should submit a
written copy of their oral comments and
any supporting materials (e.g.,
presentation slides) to the DFO prior to
the meetings for distribution to the
SACC.
Authority: 15 U.S.C. 2625(o); 5 U.S.C.
10.
Dated: May 15, 2024.
Michal Freedhoff,
Assistant Administrator, Office of Chemical
Safety and Pollution Prevention.
[FR Doc. 2024–10999 Filed 5–17–24; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2017–0720; FRL–11906–01–
OCSPP]
Pesticide Registration Review; Draft
Human Health and/or Ecological Risk
Assessments for Several Pesticides;
Notice of Availability
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
This notice announces the
availability of EPA’s draft human health
and/or ecological risk assessments for
the registration review of 3-Iodo-2propynyl butylcarbamate (IPBC) and
Pyrimethanil. EPA is opening a 60-day
public comment period for these risk
assessments.
DATES: Comments must be received on
or before July 19, 2024.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPP–2017–0720,
through the Federal eRulemaking Portal
at https://www.regulations.gov. Follow
the online instructions for submitting
comments. Do not submit electronically
any information you consider to be
SUMMARY:
Confidential Business Information (CBI)
or other information whose disclosure is
restricted by statute. Additional
instructions on commenting and visiting
the docket, along with more information
about dockets generally, is available at
https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
For pesticide specific information
contact: The Chemical Review Manager
for the pesticide of interest identified in
table 1 of unit I.
For general questions on the
registration review program, contact:
Melanie Biscoe, Pesticide Re-Evaluation
Division (7508P), Office of Pesticide
Programs, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW,
Washington, DC 20460–0001; telephone
number: (202) 566–0701; email address:
biscoe.melanie@epa.gov.
SUPPLEMENTARY INFORMATION:
I. Purpose of This Notice
Pursuant to 40 CFR 155.53(c), this
notice announces the availability of
EPA’s human health and/or ecological
risk assessments for the pesticides
shown in table 1 and opens a 60-day
public comment period on the risk
assessments.
lotter on DSK11XQN23PROD with NOTICES1
TABLE 1—DRAFT RISK ASSESSMENTS BEING MADE AVAILABLE FOR PUBLIC COMMENT
Registration review case name and No.
Docket ID No.
Chemical review manager and contact information
3-Iodo-2-propynyl butylcarbamate (IPBC);
Case Number 2725.
Pyrimethanil; Case Number 7059 .....................
EPA–HQ–OPP–2011–0420 .............................
Areej Jahangir, jahangir.areej@epa.gov, (202)
566–1577.
Christian Bongard, bongard.christian@
epa.gov, (202) 566–2248.
II. Background
EPA is conducting its registration
review of the chemicals listed in table
1 of unit I pursuant to the Federal
Insecticide, Fungicide, and Rodenticide
Act (FIFRA) section 3(g) (7 U.S.C.
136(g)) and the Procedural Regulations
for Registration Review at 40 CFR part
155, subpart C. FIFRA section 3(g)
provides, among other things, that
pesticide registrations are to be
reviewed every 15 years. Consistent
with 40 CFR 155.57, in its final
registration review decision, EPA will
ultimately determine whether a
pesticide continues to meet the
registration standard in FIFRA section
3(c)(5) (7 U.S.C. 136a(c)(5)).
As part of the registration review
process, the Agency has completed draft
human health and/or ecological risk
assessments for all pesticides listed in
table 1 of unit I. Pursuant to 40 CFR
155.53(c), EPA generally provides for at
least a 30-day public comment period
on draft human health and/or ecological
risk assessments during registration
review. This comment period is
intended to provide an opportunity for
public input on the Agency’s
assessment of the human health and/or
ecological risks posed by use of these
pesticides.
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EPA–HQ–OPP–2019–0380 .............................
III. What should I consider as I prepare
a comment for EPA?
Does this action apply to me?
This notice is directed to the public
in general and may be of interest to a
wide range of stakeholders including
environmental, human health, farm
worker, and agricultural advocates; the
chemical industry; pesticide users; and
members of the public interested in the
sale, distribution, or use of pesticides.
Since others also may 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
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to a particular entity, consult the
Chemical Review Manager identified in
table 1 in unit I. In submitting a
comment to EPA, please consider the
following:
1. Submitting CBI. Do not submit this
information to EPA through
regulations.gov or email. Clearly mark
the part or all of the information that
you claim to be CBI. For CBI
information in a disk or CD–ROM that
you mail to EPA, mark the outside of the
disk or CD–ROM as CBI and then
identify electronically within the disk or
CD–ROM the specific information that
is claimed as CBI. In addition to one
complete version of the comment that
includes information claimed as CBI, a
copy of the comment that does not
contain the information claimed as CBI
must be submitted for inclusion in the
public docket. Information so marked
will not be disclosed except in
accordance with procedures set forth in
40 CFR part 2.
E:\FR\FM\20MYN1.SGM
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Agencies
[Federal Register Volume 89, Number 98 (Monday, May 20, 2024)]
[Notices]
[Pages 43847-43850]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-10999]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2024-0073; FRL-11760-02-OCSPP]
Di-isodecyl Phthalate (DIDP) and Di-isononyl Phthalate (DINP);
Science Advisory Committee on Chemicals (SACC) Peer Review of Draft
Documents; Notice of SACC Meeting; Availability; and Request for
Comment
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Environmental Protection Agency (EPA or ``Agency'') is
announcing the availability of and soliciting public comment on the
draft manufacturer-requested risk evaluation for Di-isodecyl Phthalate
(DIDP) and the draft physical chemical, fate, and hazard assessments
for Di-isononyl Phthalate (DINP) prepared under the Toxic Substances
Control Act (TSCA). The draft documents will also be submitted to the
Science Advisory Committee on Chemicals (SACC) for peer review. EPA is
also announcing that there will be two virtual public meetings of the
SACC: On July 23, 2024, for the SACC to consider the scope and clarity
of the draft charge questions for the peer review; and on July 30-
August 2, 2024, for the SACC to consider the draft documents and public
comments for peer review.
DATES:
Virtual Preparatory Public Meeting
Comments: Submit written comments on the scope and clarity of the
charge questions on or before noon (12:00 p.m. EDT) on July 19, 2024.
Registration: To request time to present oral comments, you must
register by noon (12:00 p.m. EDT) on July 19, 2024. For those not
making oral comments, registration will remain open through the end of
the meeting on July 19, 2024.
Meeting date: July 23, 2024, 1 p.m. to 4 p.m. (EDT).
Virtual Peer Review Public Meeting
Comments: Submit comments on or before July 19, 2024.
Registration: To request time to present oral comments, you must
register by noon, July 26, 2024. For those not making oral comments,
registration will remain open through the end of the meeting.
Meeting dates: July 30-August 2, 2024, 10 a.m. to 5 p.m. (EDT).
Special Accommodations
To allow sufficient time for EPA to process your request before the
applicable meeting, please submit your requests at least ten business
days in advance of the meeting.
See unit III. of SUPPLEMENTARY INFORMATION.
ADDRESSES:
Comments: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2024-0073, through the Federal eRulemaking
Portal at 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. Additional
instructions on commenting and visiting the docket is available at
https://www.epa.gov/dockets.
Meeting registration: For information and instructions on how to
register and access these virtual public meetings, please refer to the
SACC website at https://www.epa.gov/tsca-peer-review. After
registering, you will receive the webcast and streaming service meeting
links and audio teleconference information.
Special accommodation requests: To request accommodation for a
disability, please contact the Designated Federal Official (DFO) listed
under FOR FURTHER INFORMATION CONTACT.
[[Page 43848]]
FOR FURTHER INFORMATION CONTACT:
SACC peer review: The Designated Federal Official (DFO) is Dr. Alaa
Kamel, Mission Support Division (7602M), Office of Program Support,
Office of Chemical Safety and Pollution Prevention, Environmental
Protection Agency; telephone number: (202) 564-5336 or SACC main office
number: (202) 564-8450; email address: [email protected].
Draft documents: Todd Coleman, Existing Chemicals Risk Management
Division (7404M), Office of Pollution Prevention and Toxics, Office of
Chemical Safety and Pollution Prevention, Environmental Protection
Agency; telephone number: (202) 564-1208; email address:
[email protected].
SUPPLEMENTARY INFORMATION:
I. Executive Summary
A. What action is the Agency taking?
EPA is announcing the availability of and soliciting public comment
on the draft risk evaluation for DIDP and the draft physical chemical,
fate, and hazard assessments for DINP. EPA is also announcing a virtual
peer review public meeting on July 30-August 2, 2024, for the SACC to
consider and review the draft documents. A virtual preparatory public
meeting will be held on July 23, 2024, for the SACC to consider and ask
questions regarding the scope and clarity of the draft charge
questions. This document provides instructions for accessing the
materials, submitting written comments, and registering to provide oral
comments and attend the public meetings.
B. What is the Agency's authority for taking this action?
EPA established the SACC in 2016 in accordance with the TSCA, 15
U.S.C. 2625(o), to provide independent advice and expert consultation
with respect to the scientific and technical aspects of issues relating
to the implementation of TSCA. The SACC operates in accordance with the
Federal Advisory Committee Act (FACA), 5 U.S.C. 10, and supports
activities under TSCA, 15 U.S.C. 2601 et seq., the Pollution Prevention
Act (PPA), 42 U.S.C. 13101 et seq., and other applicable statutes.
C. Does this action apply to me?
This action is directed to the public in general and may be of
particular interest to those involved in the manufacture, processing,
distribution, and disposal of the subject chemical substance, and/or
those interested in the assessment of risks involving chemical
substances and mixtures regulated under TSCA (including members of at-
risk communities, non-governmental organizations (NGOs), Federal,
State, and local officials). Since other entities may also be
interested, the Agency has not attempted to describe all the specific
entities that may be interested.
D. What should I consider as I submit my comments to EPA?
1. Submitting CBI. Do not submit CBI to EPA through email or
https://www.regulations.gov. If you wish to include CBI in your
comment, please contact the DFO listed under FOR FURTHER INFORMATION
CONTACT to obtain special instructions before submitting that
information.
2. Tips for preparing your comments. When preparing and submitting
your comments, see https://www.epa.gov/dockets/commenting-epa-dockets.
See also the instructions in unit III.C.
E. How can I stay informed about SACC activities?
You may subscribe to the following listserv for alerts regarding
this and other SACC-related activities: https://public.govdelivery.com/accounts/USAEPAOPPT/subscriber/new?topic_id=USAEPAOPPT_101.
II. Background
A. What is the purpose of the SACC?
The SACC provides independent 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 SACC is composed of experts in
toxicology; environmental risk assessment; exposure assessment; and
related sciences (e.g., synthetic biology, pharmacology, biotechnology,
nanotechnology, biochemistry, biostatistics, physiologically based
pharmacokinetic (PBPK) modeling, computational toxicology,
epidemiology, environmental fate, and environmental engineering and
sustainability). The SACC currently consists of 18 members. When
needed, the committee will be assisted by ad hoc reviewers with
specific expertise in the topics under consideration.
B. Why is EPA conducting these risk evaluations?
TSCA requires EPA to conduct risk evaluations on prioritized
chemical substances and allows chemical manufacturers to request an
EPA-conducted risk evaluation of a chemical substance (or category of
chemical substances) using the procedures established in 40 CFR 702.37.
TSCA also identifies the minimum components EPA must include in all
chemical substance risk evaluations. EPA received manufacturer requests
to conduct risk evaluations for DIDP and DINP, both as categories of
chemical substances, and subsequently granted and initiated risk
evaluations for both of them. The purpose of conducting risk
evaluations is to determine whether a chemical substance presents an
unreasonable risk to human health or the environment under the
Conditions of Use (COUs). These evaluations include assessing
unreasonable risks to relevant potentially exposed or susceptible
subpopulations. As part of this process EPA: (1) Integrates hazard and
exposure assessments using the best available science that is
reasonably available to assure decisions are based on the weight of the
scientific evidence, and (2) Conducts peer review for risk evaluation
approaches that have not been previously peer reviewed. For more
information about the three stages of EPA's process for ensuring the
safety of existing chemicals (i.e., prioritization, risk evaluation,
and risk management), go to https://www.epa.gov/assessing-and-managing-chemicals-under-tsca/how-epa-evaluates-safety-existing-chemicals.
C. Why is EPA evaluating the risks from DIDP and DINP?
On May 24, 2019, EPA received requests to conduct risk evaluations
for DIDP and DINP from ExxonMobil Chemical Company, Evonik Corporation,
and Teknor Apex, through the American Chemistry Council's High
Phthalates Panel (ACC HPP). In December 2019, EPA notified ACC HPP that
the Agency had granted their manufacturer requested risk evaluations.
DIDP is a common chemical name for the category of chemical
substances that includes the following substances: 1,2-
benzenedicarboxylic acid, 1,2-diisodecyl ester (CASRN 26761-40-0) and
1,2-benzenedicarboxylic acid, di-C9-11-branched alkyl esters, C10-rich
(CASRN 68515-49-1). Both CASRNs contain mainly C10 dialkyl phthalate
esters.
DINP is a common chemical name for the category of chemical
substances that includes the following substances: 1,2-
benzenedicarboxylic acid, 1,2-isononyl ester (CASRN 28553-12-0) and
1,2-benzenedicarboxylic acid, di-C9-11-branched alkyl esters, C9-rich
(CASRN 68515-48-0). Both CASRNs contain mainly C9 dialkyl phthalate
esters. Both DIDP and DINP are primarily used as a plasticizer in
polyvinyl chloride (PVC) in consumer, commercial, and industrial
applications.
[[Page 43849]]
DIDP and DINP are both structurally phthalates, and therefore many
aspects of physical-chemical (p-chem) properties and exposure (to
humans and ecological species) are similar, described further in the
draft physical chemical and fate assessments for both chemical
substances. Because of the similar exposure and physical chemical
properties of DIDP and DINP, EPA is developing these individual risk
evaluations in parallel, and similarly the SACC peer review of the
methods and novel analyses for the draft risk evaluations will occur
concurrently. Both DIDP and DINP have extremely low water solubility
and will be preferentially sorbed into sediments, soils, and suspended
solids in surface water and wastewater. Both are expected to be
persistent in anaerobic environments. Under indoor settings, DIDP and
DINP are expected to partition to airborne particles and are expected
to have extended lifetime compared to outdoor settings.
For both DIDP and DINP, liver and developmental toxicity are
indicated as the most sensitive and robust non-cancer hazards. However,
these two phthalates differ in several important respects regarding
their human health hazard profiles. For DIDP, the developmental
toxicity is not characterized by androgen insufficiency, and data are
insufficient to determine the carcinogenicity. For DINP, developmental
toxicity results in androgen insufficiency (phthalate syndrome), and
the effects on the liver include cancer. Therefore, because of these
hazard differences, EPA is requesting peer review on the draft hazard
assessment of DINP ahead of issuing the risk evaluation of DINP.
D. What is the topic of the planned SACC peer review?
EPA is submitting the draft risk evaluation of DIDP, draft physical
chemical, fate, and hazard assessments of DINP, and associated
supporting documents to the SACC for peer review, along with the public
comments received. The draft risk evaluation for DIDP includes analyses
of physical chemical properties, the fate and transport in the
environment, exposure to workers, consumers and general population
including potentially exposed or susceptible subpopulations (PESS),
releases to the environment, environmental hazard and risk
characterization for terrestrial and aquatic species, and human health
hazard and risk characterization for workers, consumers, and the
general population. The draft assessments of DINP includes analyses of
physical chemical properties, the fate and transport in the
environment, environmental hazard for terrestrial and aquatic species,
human health non-cancer hazards, and human health cancer hazards.
EPA is not developing charge questions for all aspects of the draft
documents but is instead focusing its charge to the SACC on specific
scientific areas that need peer review. Many of the methods and
analyses used in these evaluations are not novel and have been reviewed
in the development of the tools, used in various agency work products
or in previous TSCA assessments (e.g., systematic review, consumer
exposure model (CEM), American Meteorological Society (AMS)/EPA
Regulatory Model (AERMOD), point source calculator (PSC), etc.). Also,
EPA is not soliciting comments on uses of these phthalates that are
outside the scope of TSCA (e.g., personal care products, cosmetics,
food contact materials, medical devices); those uses will be addressed
as appropriate within the cumulative risk assessment.
As a result of the similarities in conditions of use, chemical
properties, and data availability between DIDP and DINP, the methods
and approaches used to assess DIDP apply to DINP. Nonetheless, these
two chemicals differ most in their human health hazard profiles and
therefore SACC is requested to review these novel analyses for DINP.
Any relevant recommendations from this SACC review on DIDP will be also
considered in the development of the final risk evaluations for both
DIDP and DINP. By taking the DIDP risk evaluation and DINP hazard
assessments to peer review in this manner, EPA will obtain the
necessary independent review and advice for the DINP risk evaluation.
EPA continues to work on risk evaluations of additional high-
priority substance phthalates, in addition to the cumulative risk
assessment (CRA) for the phthalates. The subsequent five individual
risk evaluations and the CRA are not part of this peer review but will
be brought to the SACC for peer review at a future date.
III. Public Meeting of the SACC
A. What is the purpose of the virtual peer review public meeting(s)?
EPA is planning two virtual public meetings: (1) A preparatory
public meeting for the SACC to consider and ask questions regarding the
scope and clarity of the draft charge questions; and (2) a public
meeting for the SACC to consider and review the draft documents. These
public meetings are part of the SACC peer review of the Agency's
methods and novel analyses for the draft evaluations of the risks from
the phthalates DIDP and DINP to inform risk management decisions under
TSCA. EPA expects to ask the SACC to consider and review this DIDP
draft risk evaluation and DINP assessments. The agenda for these
meetings will be posted in the docket and the SACC website.
To participate in these virtual public meetings, you must register
online to receive the webcast and streaming service meeting links and
audio teleconference information for each meeting. Online registration
will be available beginning approximately one month prior to the
meeting, and remain open through the end of the meeting. To make oral
comments during one of these meetings, follow the instructions in unit
III.C.
Recommendations from this SACC review and public comments will be
considered in the development of the final risk evaluation for DIDP and
DINP. The Agency will be seeking SACC review of its data analyses and
methodologies relevant to human health hazard and exposure analyses
that have not been previously peer reviewed.
B. How can I access the documents?
The manufacturer-requested draft risk evaluation for DIDP, draft
assessments for DINP, and related documents, including background
documents, related supporting materials, and draft charge questions,
are available in the docket. As additional background materials become
available, EPA will include those additional background materials
(e.g., SACC members and consultants participating in this meeting and
the meeting agenda) in the docket and through links on the SACC website
at https://www.epa.gov/tsca-peer-review.
After the public meeting, the SACC will prepare the meeting minutes
and a final report document summarizing its recommendations to the EPA,
which will also be available in the docket and through the SACC
website.
C. How can I provide comments?
To ensure proper receipt of comments, it is imperative that you
identify docket ID No. EPA-HQ-OPPT-2024-0073 in the subject line on the
first page of your comments and follow the instructions in this
document.
1. Written comments. Submit written comments by the deadlines set
in the DATES section of this document and as described in the ADDRESSES
section of this document.
[[Page 43850]]
2. Oral comments. To request time to present oral comments during
one of the virtual public meetings, you must register online by the
deadlines set in the DATES section of this document. Oral comments
during the virtual public meetings are limited to 5 minutes. In
addition, each speaker should submit a written copy of their oral
comments and any supporting materials (e.g., presentation slides) to
the DFO prior to the meetings for distribution to the SACC.
Authority: 15 U.S.C. 2625(o); 5 U.S.C. 10.
Dated: May 15, 2024.
Michal Freedhoff,
Assistant Administrator, Office of Chemical Safety and Pollution
Prevention.
[FR Doc. 2024-10999 Filed 5-17-24; 8:45 am]
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