Di-isodecyl Phthalate (DIDP); Draft Scope of the Risk Evaluation to be Conducted Under the Toxic Substances Control Act (TSCA); Notice of Availability and Request for Comments, 76077-76078 [2020-26203]

Download as PDF Federal Register / Vol. 85, No. 229 / Friday, November 27, 2020 / Notices Dated: November 19, 2020. David Gray, Acting Regional Administrator, Region 6. ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–OPPT–2018–0435; FRL–10017– 14] [FR Doc. 2020–26038 Filed 11–25–20; 8:45 am] BILLING CODE 6560–50–P Di-isodecyl Phthalate (DIDP); Draft Scope of the Risk Evaluation to be Conducted Under the Toxic Substances Control Act (TSCA); Notice of Availability and Request for Comments ENVIRONMENTAL PROTECTION AGENCY [ER–FRL–9054–1] Environmental Protection Agency (EPA). ACTION: Notice. AGENCY: Environmental Impact Statements; Notice of Availability Responsible Agency: Office of Federal Activities, General Information 202– 564–5632 or https://www.epa.gov/nepa. Weekly receipt of Environmental Impact Statements (EIS) Filed November 16, 2020 10 a.m. EST Through November 20, 2020 10 a.m. EST Pursuant to 40 CFR 1506.9. Notice: Section 309(a) of the Clean Air Act requires that EPA make public its comments on EISs issued by other Federal agencies. EPA’s comment letters on EISs are available at: https:// cdxnodengn.epa.gov/cdx-enepa-public/ action/eis/search. jbell on DSKJLSW7X2PROD with NOTICES EIS No. 20200238, Draft, USFS, OR, Stella Restoration Project, Comment Period Ends: 01/12/2021, Contact: Elizabeth Bly 541–560–3465. EIS No. 20200239, Draft, USCG, TX, Texas Gulflink Deepwater Port License Application, Comment Period Ends: 01/11/2021, Contact: Brad McKitrick 202–372–1443. EIS No. 20200240, Final, USFWS, REG, Regulations Governing Take of Migratory Birds, Review Period Ends: 12/28/2020, Contact: Lesley Kordella 703–963–1729. EIS No. 20200241, Final, BLM, PRO, Final Programmatic EIS for Fuels Reduction and Rangeland Restoration in the Great Basin, Review Period Ends: 12/28/2020, Contact: Shannon Bassista 208–373–3845. EIS No. 20200242, Draft, USACE, VA, Surry To Skiffes Creek To Whealton Transmission Project, Comment Period Ends: 01/11/2021, Contact: Randy Steffey 757–201–7579. Dated: November 20, 2020. Cindy S. Barger, Director, NEPA Compliance Division, Office of Federal Activities. [FR Doc. 2020–26179 Filed 11–25–20; 8:45 am] BILLING CODE 6560–50–P VerDate Sep<11>2014 19:29 Nov 25, 2020 Jkt 253001 The Environmental Protection Agency (EPA) is announcing the availability of and soliciting public comment on the draft scope document for the risk evaluation to be conducted for di-isodecyl phthalate (DIDP) (1,2benzenedicarboxylic acid, 1,2diisodecyl ester and 1,2benzenedicarboxylic acid, di-C9-11branched alkyl esters, C10-rich; Chemical Abstracts Service Registry Number (CASRN) 26761–40–0 and CASRN 68515–49–1), a category of chemical substances for which EPA received a manufacturer request for risk evaluation. The draft scope document for this category of chemical substances includes the conditions of use, hazards, exposures, and the potentially exposed or susceptible subpopulations EPA plans to consider in conducting the risk evaluation for this category of chemical substances. EPA is also asking the public to provide additional data or information that could be useful to the Agency in finalizing the scope of the risk evaluation. DATES: Comments must be received on or before January 11, 2021. ADDRESSES: Submit your comments, identified by docket identification (ID) number EPA–HQ–OPPT–2018–0435, 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. To make special arrangements for hand delivery or delivery of boxed information, please follow the instructions at https:// www.epa.gov/dockets/contacts.html. Due to the public health concerns related to COVID–19, the EPA Docket Center (EPA/DC) and Reading Room is closed to visitors with limited exceptions. The staff continues to provide remote customer service via email, phone, and webform. For the latest status information on EPA/DC SUMMARY: PO 00000 Frm 00074 Fmt 4703 Sfmt 4703 76077 services and docket access, visit https:// www.epa.gov/dockets. FOR FURTHER INFORMATION CONTACT: For technical information contact: Collin Beachum, Existing Chemical Risk Assessment Division (Mailcode E205– 02), Office of Pollution Prevention and Toxics, Environmental Protection Agency, 109 T.W. Alexander Drive, RTP, NC 27711; telephone number: (919) 541–7554; email address: beachum.collin@epa.gov. For general information contact: The TSCA-Hotline, ABVI-Goodwill, 422 South Clinton Ave., Rochester, NY 14620; telephone number: (202) 554– 1404; email address: TSCA-Hotline@ epa.gov. SUPPLEMENTARY INFORMATION: I. General Information A. Does this action apply to me? This action is directed to the public in general and may be of interest to entities that manufacture (including import) a chemical substance regulated under TSCA (e.g., entities identified under North American Industrial Classification System (NAICS) codes 325 and 324110). The action may also be of interest to chemical processors, distributors in commerce, and users; non-governmental organizations in the environmental and public health sectors; state and local government agencies; and members of the public. Since other entities may also be interested, the Agency has not attempted to describe all the specific entities and corresponding NAICS codes for entities that may be interested in or affected by this action. B. What is the Agency’s authority for taking this action? The draft scope document is issued pursuant to TSCA section 6(b) and EPA’s implementing regulations at 40 CFR 702.41(c)(7). C. What action is the Agency taking? EPA is publishing the draft scope of the risk evaluation for DIDP under TSCA. Through the risk evaluation process, EPA will determine whether the category of chemical substances presents an unreasonable risk of injury to health or the environment under the conditions of use, as determined by the Administrator, in accordance with TSCA section 6(b)(4). II. Background TSCA allows chemical manufacturers to request an EPA-conducted risk evaluation of a chemical under 40 CFR 702.37. On May 24, 2019, EPA received a manufacturer request for a risk E:\FR\FM\27NON1.SGM 27NON1 76078 Federal Register / Vol. 85, No. 229 / Friday, November 27, 2020 / Notices jbell on DSKJLSW7X2PROD with NOTICES evaluation of DIDP. On December 20, 2019, the Agency granted the request, and subsequently initiated the scoping process for a risk evaluation for this category of chemical substances. The purpose of a risk evaluation is to determine whether a chemical substance, or group of chemical substances, presents an unreasonable risk to health or the environment, under the conditions of use, including an unreasonable risk to a relevant potentially exposed or susceptible subpopulation (15 U.S.C. 2605(b)(4)(A)). As part of this process, EPA must evaluate both hazards and exposures for the conditions of use; describe whether aggregate or sentinel exposures were considered and the basis for consideration; not consider costs or other nonrisk factors; take into account where relevant, likely duration, intensity, frequency, and number of exposures and describe the weight of the scientific evidence for hazards and exposures (15 U.S.C. 2605(b)(4)(F)). This process will culminate in a determination of whether or not the category of chemical substances presents an unreasonable risk of injury to health or the environment under the conditions of use (15 U.S.C. 2605(b)(4)(A); 40 CFR 702.47). III. Draft Scope of the Risk Evaluation for Di-isodecyl phthalate (DIDP) The category of chemical substances for which EPA is publishing the draft scope of the risk evaluation includes the following chemical 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). The draft scope of the risk evaluation for this category of chemical substances includes the conditions of use, hazards, exposures, and the potentially exposed or susceptible subpopulations EPA plans to consider in the risk evaluation (15 U.S.C. 2605(b)(4)(D)). Development of the scope is the first step of a risk evaluation. The draft scope of the risk evaluation will include the following components (40 CFR 702.41(c)): • The conditions of use, as determined by the Administrator, that EPA plans to consider in the risk evaluation. • The potentially exposed populations that EPA plans to evaluate; the ecological receptors that EPA plans to evaluate; and the hazards to health and the environment that EPA plans to evaluate. • A description of the reasonably available information and the science VerDate Sep<11>2014 19:29 Nov 25, 2020 Jkt 253001 approaches that the Agency plans to use. • A conceptual model that will describe the actual or predicted relationships between the chemical substance, the conditions of use within the scope of the evaluation and the receptors, either human or environmental, with consideration of the life cycle of the chemical substance—from manufacturing, processing, distribution in commerce, use, to release or disposal—and identification of human and ecological health hazards EPA plans to evaluate for the exposure scenarios EPA plans to evaluate. • An analysis plan, which will identify the approaches and methods EPA plans to use to assess exposure, hazards, and risk, including associated uncertainty and variability, as well as a strategy for using reasonably available information and best available science approaches. • A plan for peer review. EPA encourages commenters to provide information they believe might be missing or may further inform the risk evaluation. EPA will publish a notice in the Federal Register announcing the availability of the final scope within three months of publishing the draft scope. IV. References The following is a listing of the documents that are specifically referenced in this Federal Register notice. The docket for this action includes these documents and other information considered by EPA, including documents that are referenced within the documents that are included in the docket. For assistance in locating these referenced documents, please consult the technical person listed under FOR FURTHER INFORMATION CONTACT. 1. EPA. Di-isodecyl Phthalate (DIDP) (1,2-Benzene-dicarboxylic acid, 1,2diisodecyl ester); Manufacturer Request for Risk Evaluation Under the Toxic Substances Control Act (TSCA); Notice of Availability and Request for Comments. Federal Register. (84 FR 42914, August 30, 2019) (FRL–9998–26). (Authority: 15 U.S.C. 2601 et seq.) Andrew Wheeler, Administrator. [FR Doc. 2020–26203 Filed 11–25–20; 8:45 am] BILLING CODE 6560–50–P PO 00000 Frm 00075 Fmt 4703 Sfmt 4703 DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [Document Identifier: CMS–10292 and CMS– R–65] Agency Information Collection Activities: Proposed Collection; Comment Request Centers for Medicare & Medicaid Services, Health and Human Services (HHS). ACTION: Notice. AGENCY: The Centers for Medicare & Medicaid Services (CMS) is announcing an opportunity for the public to comment on CMS’ intention to collect information from the public. Under the Paperwork Reduction Act of 1995 (the PRA), federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information (including each proposed extension or reinstatement of an existing collection of information) and to allow 60 days for public comment on the proposed action. Interested persons are invited to send comments regarding our burden estimates or any other aspect of this collection of information, including the necessity and utility of the proposed information collection for the proper performance of the agency’s functions, the accuracy of the estimated burden, ways to enhance the quality, utility, and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden. DATES: Comments must be received by January 26, 2021. ADDRESSES: When commenting, please reference the document identifier or OMB control number. To be assured consideration, comments and recommendations must be submitted in any one of the following ways: 1. Electronically. You may send your comments electronically to https:// www.regulations.gov. Follow the instructions for ‘‘Comment or Submission’’ or ‘‘More Search Options’’ to find the information collection document(s) that are accepting comments. 2. By regular mail. You may mail written comments to the following address: CMS, Office of Strategic Operations and Regulatory Affairs, Division of Regulations Development, Attention: Document Identifier/OMB Control Number lllllll, Room C4–26– SUMMARY: E:\FR\FM\27NON1.SGM 27NON1

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[Federal Register Volume 85, Number 229 (Friday, November 27, 2020)]
[Notices]
[Pages 76077-76078]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-26203]


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ENVIRONMENTAL PROTECTION AGENCY

[EPA-HQ-OPPT-2018-0435; FRL-10017-14]


Di-isodecyl Phthalate (DIDP); Draft Scope of the Risk Evaluation 
to be Conducted Under the Toxic Substances Control Act (TSCA); Notice 
of Availability and Request for Comments

AGENCY: Environmental Protection Agency (EPA).

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Environmental Protection Agency (EPA) is announcing the 
availability of and soliciting public comment on the draft scope 
document for the risk evaluation to be conducted for di-isodecyl 
phthalate (DIDP) (1,2-benzenedicarboxylic acid, 1,2-diisodecyl ester 
and 1,2-benzenedicarboxylic acid, di-C9-11-branched alkyl esters, C10-
rich; Chemical Abstracts Service Registry Number (CASRN) 26761-40-0 and 
CASRN 68515-49-1), a category of chemical substances for which EPA 
received a manufacturer request for risk evaluation. The draft scope 
document for this category of chemical substances includes the 
conditions of use, hazards, exposures, and the potentially exposed or 
susceptible subpopulations EPA plans to consider in conducting the risk 
evaluation for this category of chemical substances. EPA is also asking 
the public to provide additional data or information that could be 
useful to the Agency in finalizing the scope of the risk evaluation.

DATES: Comments must be received on or before January 11, 2021.

ADDRESSES: Submit your comments, identified by docket identification 
(ID) number EPA-HQ-OPPT-2018-0435, 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. To make special 
arrangements for hand delivery or delivery of boxed information, please 
follow the instructions at https://www.epa.gov/dockets/contacts.html.
    Due to the public health concerns related to COVID-19, the EPA 
Docket Center (EPA/DC) and Reading Room is closed to visitors with 
limited exceptions. The staff continues to provide remote customer 
service via email, phone, and webform. For the latest status 
information on EPA/DC services and docket access, visit https://www.epa.gov/dockets.

FOR FURTHER INFORMATION CONTACT: 
    For technical information contact: Collin Beachum, Existing 
Chemical Risk Assessment Division (Mailcode E205-02), Office of 
Pollution Prevention and Toxics, Environmental Protection Agency, 109 
T.W. Alexander Drive, RTP, NC 27711; telephone number: (919) 541-7554; 
email address: [email protected].
    For general information contact: The TSCA-Hotline, ABVI-Goodwill, 
422 South Clinton Ave., Rochester, NY 14620; telephone number: (202) 
554-1404; email address: [email protected].

SUPPLEMENTARY INFORMATION:

I. General Information

A. Does this action apply to me?

    This action is directed to the public in general and may be of 
interest to entities that manufacture (including import) a chemical 
substance regulated under TSCA (e.g., entities identified under North 
American Industrial Classification System (NAICS) codes 325 and 
324110). The action may also be of interest to chemical processors, 
distributors in commerce, and users; non-governmental organizations in 
the environmental and public health sectors; state and local government 
agencies; and members of the public. Since other entities may also be 
interested, the Agency has not attempted to describe all the specific 
entities and corresponding NAICS codes for entities that may be 
interested in or affected by this action.

B. What is the Agency's authority for taking this action?

    The draft scope document is issued pursuant to TSCA section 6(b) 
and EPA's implementing regulations at 40 CFR 702.41(c)(7).

C. What action is the Agency taking?

    EPA is publishing the draft scope of the risk evaluation for DIDP 
under TSCA. Through the risk evaluation process, EPA will determine 
whether the category of chemical substances presents an unreasonable 
risk of injury to health or the environment under the conditions of 
use, as determined by the Administrator, in accordance with TSCA 
section 6(b)(4).

II. Background

    TSCA allows chemical manufacturers to request an EPA-conducted risk 
evaluation of a chemical under 40 CFR 702.37. On May 24, 2019, EPA 
received a manufacturer request for a risk

[[Page 76078]]

evaluation of DIDP. On December 20, 2019, the Agency granted the 
request, and subsequently initiated the scoping process for a risk 
evaluation for this category of chemical substances. The purpose of a 
risk evaluation is to determine whether a chemical substance, or group 
of chemical substances, presents an unreasonable risk to health or the 
environment, under the conditions of use, including an unreasonable 
risk to a relevant potentially exposed or susceptible subpopulation (15 
U.S.C. 2605(b)(4)(A)). As part of this process, EPA must evaluate both 
hazards and exposures for the conditions of use; describe whether 
aggregate or sentinel exposures were considered and the basis for 
consideration; not consider costs or other nonrisk factors; take into 
account where relevant, likely duration, intensity, frequency, and 
number of exposures and describe the weight of the scientific evidence 
for hazards and exposures (15 U.S.C. 2605(b)(4)(F)). This process will 
culminate in a determination of whether or not the category of chemical 
substances presents an unreasonable risk of injury to health or the 
environment under the conditions of use (15 U.S.C. 2605(b)(4)(A); 40 
CFR 702.47).

III. Draft Scope of the Risk Evaluation for Di-isodecyl phthalate 
(DIDP)

    The category of chemical substances for which EPA is publishing the 
draft scope of the risk evaluation includes the following chemical 
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). The draft scope of the risk 
evaluation for this category of chemical substances includes the 
conditions of use, hazards, exposures, and the potentially exposed or 
susceptible subpopulations EPA plans to consider in the risk evaluation 
(15 U.S.C. 2605(b)(4)(D)).
    Development of the scope is the first step of a risk evaluation. 
The draft scope of the risk evaluation will include the following 
components (40 CFR 702.41(c)):
     The conditions of use, as determined by the Administrator, 
that EPA plans to consider in the risk evaluation.
     The potentially exposed populations that EPA plans to 
evaluate; the ecological receptors that EPA plans to evaluate; and the 
hazards to health and the environment that EPA plans to evaluate.
     A description of the reasonably available information and 
the science approaches that the Agency plans to use.
     A conceptual model that will describe the actual or 
predicted relationships between the chemical substance, the conditions 
of use within the scope of the evaluation and the receptors, either 
human or environmental, with consideration of the life cycle of the 
chemical substance--from manufacturing, processing, distribution in 
commerce, use, to release or disposal--and identification of human and 
ecological health hazards EPA plans to evaluate for the exposure 
scenarios EPA plans to evaluate.
     An analysis plan, which will identify the approaches and 
methods EPA plans to use to assess exposure, hazards, and risk, 
including associated uncertainty and variability, as well as a strategy 
for using reasonably available information and best available science 
approaches.
     A plan for peer review.
    EPA encourages commenters to provide information they believe might 
be missing or may further inform the risk evaluation. EPA will publish 
a notice in the Federal Register announcing the availability of the 
final scope within three months of publishing the draft scope.

IV. References

    The following is a listing of the documents that are specifically 
referenced in this Federal Register notice. The docket for this action 
includes these documents and other information considered by EPA, 
including documents that are referenced within the documents that are 
included in the docket. For assistance in locating these referenced 
documents, please consult the technical person listed under FOR FURTHER 
INFORMATION CONTACT.
    1. EPA. Di-isodecyl Phthalate (DIDP) (1,2-Benzene-dicarboxylic 
acid, 1,2- diisodecyl ester); Manufacturer Request for Risk Evaluation 
Under the Toxic Substances Control Act (TSCA); Notice of Availability 
and Request for Comments. Federal Register. (84 FR 42914, August 30, 
2019) (FRL-9998-26).

(Authority: 15 U.S.C. 2601 et seq.)

Andrew Wheeler,
Administrator.
[FR Doc. 2020-26203 Filed 11-25-20; 8:45 am]
BILLING CODE 6560-50-P


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