1-Bromopropane (1-BP); Revision to Toxic Substances Control Act (TSCA) Risk Determination; Notice of Availability, 77603-77609 [2022-27439]

Download as PDF tkelley on DSK125TN23PROD with NOTICE Federal Register / Vol. 87, No. 242 / Monday, December 19, 2022 / Notices Agency may not conduct or sponsor and a person is not required to respond to a collection of information unless it displays a currently valid OMB control number. DATES: Comments must be submitted on or before February 17, 2023. ADDRESSES: Submit your comments, referencing Docket ID No. EPA–HQ– ORD–2018–0774, online using www.regulations.gov (our preferred method), by email to ord.docket@ epa.gov, or by mail to: EPA Docket Center, Environmental Protection Agency, Mail Code 28221T, 1200 Pennsylvania Ave. NW, Washington, DC 20460. EPA’s policy is that all comments received will be included in the public docket without change including any personal information provided, unless the comment includes profanity, threats, information claimed to be Confidential Business Information (CBI) or other information whose disclosure is restricted by statute. FOR FURTHER INFORMATION CONTACT: Alyssa Gurkas, U.S. Environmental Protection Agency, Office of Research and Development, Office of Resource Management, Improvement and Accountability Division, Mail Code 41182, Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington, DC 20460; telephone number: 202–564–4863; email address: Gurkas.alyssa@epa.gov. SUPPLEMENTARY INFORMATION: Supporting documents which explain in detail the information that the EPA will be collecting are available in the public docket for this ICR. The docket can be viewed online at www.regulations.gov or in person at the EPA Docket Center, WJC West, Room 3334, 1301 Constitution Ave. NW, Washington, DC. The telephone number for the Docket Center is 202–566–1744. For additional information about EPA’s public docket, visit https://www.epa.gov/dockets. Pursuant to section 3506(c)(2)(A) of the PRA (44 U.S.C. 3501 et seq.), EPA is soliciting comments and information to enable it to: (i) evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the Agency, including whether the information will have practical utility; (ii) evaluate the accuracy of the Agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (iii) enhance the quality, utility, and clarity of the information to be collected; and (iv) minimize the burden of the collection of information on those who are to respond, including through VerDate Sep<11>2014 19:38 Dec 16, 2022 Jkt 259001 the use of appropriate automated electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses. EPA will consider the comments received and amend the ICR as appropriate. The final ICR package will then be submitted to OMB for review and approval. At that time, EPA will issue another Federal Register notice to announce the submission of the ICR to OMB and the opportunity to submit additional comments to OMB. Abstract: The purpose of this information collection is to survey partners currently using the EPA’s Office of Research and Development’s (ORD) scientific research products to increase transparency and public participation, and to ascertain the quality, usability, and timeliness of the research products. ORD will collect these data to inform the annual end-ofyear performance reporting to the Office of Management and Budget (OMB) that will be published each year in the Annual Performance Report (APR), which is part of the President’s Budget Request and mandated under the Government Performance and Results Act (GPRA). The survey results will be used to estimate the degree to which ORD research products meet partner needs and will enable the improvement of the development and delivery of products. Some of the information reported on the form is confidential, which will be withheld from the public pursuant to Section 107(1) of the Ethics in Government Act of 1978. Participation is voluntary. Form Numbers: None. Respondents/affected entities: Life, physical and social science professionals. Respondent’s obligation to respond: Voluntary. Estimated number of respondents: 225. Frequency of response: Annually. Total estimated burden: .25 hours (per year). Burden is defined at 5 CFR 1320.03(b). Total estimated cost: $3,493 (per year). Changes in Estimates: There is a decrease of .08 hours in the total estimated respondent burden compared with the ICR previously approved by OMB. There is a decrease in the total estimated number of respondents by 25 individuals. This burden reduction is due to the decrease in time for survey completion and the decrease in estimated respondents. The slight PO 00000 Frm 00057 Fmt 4703 Sfmt 4703 77603 decrease from the original ICR is by $1,292 (decrease from $4,785 to $3,493). Henry Frey, Assistant Administrator, Office of Research and Development. [FR Doc. 2022–27388 Filed 12–16–22; 8:45 am] BILLING CODE 6560–50–P ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–OPPT–2016–0741; FRL–9944–02– OCSPP] 1-Bromopropane (1–BP); Revision to Toxic Substances Control Act (TSCA) Risk Determination; Notice of Availability Environmental Protection Agency (EPA). ACTION: Notice. AGENCY: The Environmental Protection Agency (EPA) is announcing the availability of the final revision to the risk determination for the 1bromopropane (1–BP) risk evaluation issued under the Toxic Substances Control Act (TSCA). The revision to the 1–BP risk determination reflects the announced policy changes to ensure the public is protected from unreasonable risks from chemicals in a way that is supported by science and the law. EPA determined that 1–BP, as a whole chemical substance, presents an unreasonable risk of injury to health when evaluated under its conditions of use. In addition, this revised risk determination does not reflect an assumption that workers always appropriately wear personal protective equipment (PPE). EPA understands that there could be adequate occupational safety protections in place at certain workplace locations; however, not assuming use of PPE reflects EPA’s recognition that unreasonable risk may exist for subpopulations of workers that may be highly exposed because they are not covered by Occupational Safety and Health Administration (OSHA) standards, or their employers are out of compliance with OSHA standards, or because many of OSHA’s chemicalspecific permissible exposure limits largely adopted in the 1970’s are described by OSHA as being ‘‘outdated and inadequate for ensuring protection of worker health,’’ or because OSHA has not issued a chemical-specific permissible exposure limit (PEL) (as is the case for 1–BP), or because EPA finds unreasonable risk for purposes of TSCA notwithstanding OSHA requirements. This revision supersedes the condition of use-specific no unreasonable risk SUMMARY: E:\FR\FM\19DEN1.SGM 19DEN1 77604 Federal Register / Vol. 87, No. 242 / Monday, December 19, 2022 / Notices determinations in the August 2020 1–BP Risk Evaluation and withdraws the associated TSCA order included in the August 2020 1–BP Risk Evaluation. ADDRESSES: The docket for this action, identified by docket identification (ID) number EPA–HQ–OPPT–2016–0741, is available online at https:// www.regulations.gov or in-person at the Office of Pollution Prevention and Toxics Docket (OPPT Docket), Environmental Protection Agency Docket Center (EPA/DC), West William Jefferson Clinton Bldg., Rm. 3334, 1301 Constitution Ave. NW, Washington, DC 20460–0001. The Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding legal holidays. The telephone number for the Public Reading Room is (202) 566–1744, and the telephone number for the OPPT Docket is (202) 566–0280. Additional instructions on visiting the docket, along with more information about dockets generally, is available at https:// www.epa.gov/dockets. FOR FURTHER INFORMATION CONTACT: For technical information contact: Amy Shuman Office of Pollution Prevention and Toxics (7404M), Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington, DC 20460–0001; telephone number: (202) 564–2978; email address: shuman.amy@ 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: tkelley on DSK125TN23PROD with NOTICE 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 those involved in the manufacture, processing, distribution, use, disposal, and/or the assessment of risks involving chemical substances and mixtures. You may be potentially affected by this action if you manufacture (defined under TSCA to include import), process (including recycling), distribute in commerce, use or dispose of 1–BP, including 1–BP in products. Since other entities may also be interested in this revision to the risk determination, EPA has not attempted to describe all the specific entities that may be affected by this action. B. What is 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 VerDate Sep<11>2014 19:38 Dec 16, 2022 Jkt 259001 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 (PESS) 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 provide instruction on chemical substances that must undergo evaluation, the minimum components of a TSCA risk evaluation, and the timelines for public comment and completion of the risk evaluation. TSCA also requires that EPA operate in a manner that is consistent with the best available science, make decisions based on the weight of the scientific evidence, and consider reasonably available information. 15 U.S.C. 2625(h), (i), and (k). The statute identifies the minimum components for 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 exposures for the conditions of use of the chemical substance, including information that is relevant to 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 exposures. 15 U.S.C. 2605(b)(4)(F)(i) through (ii) and (iv) through (v). Each risk evaluation must not consider costs or other nonrisk factors. 15 U.S.C. 2605(b)(4)(F)(iii). EPA has inherent authority to reconsider previous decisions and to revise, replace, or repeal a decision to the extent permitted by law and supported by reasoned explanation. FCC v. Fox Television Stations, Inc., 556 U.S. 502, 515 (2009); see also Motor Vehicle Mfrs. Ass’n v. State Farm Mutual Auto. Ins. Co., 463 U.S. 29, 42 (1983). Pursuant to such authority, EPA has PO 00000 Frm 00058 Fmt 4703 Sfmt 4703 reconsidered and is now finalizing a revised risk determination for 1–BP. C. What action is EPA taking? EPA is announcing the availability of the final revision to the risk determination for the 1–BP risk evaluation issued under TSCA that published in August 2020 (Ref. 1). In July 2022, EPA sought public comment on the draft revisions (87 FR 43265, July 20, 2022). EPA appreciates the public comments received on the draft revision to the 1–BP risk determination. After review of these comments and consideration of the specific circumstances of 1–BP, EPA concludes that the Agency’s risk determination for 1–BP is better characterized as a whole chemical risk determination rather than condition-of-use-specific risk determinations. Accordingly, EPA is revising and replacing Section 5 of the August 2020 1–BP Risk Evaluation (Ref. 2) where the findings of unreasonable risk to health were previously made for the individual conditions of use evaluated. EPA is also withdrawing the previously issued TSCA section 6(i)(l) order for nine conditions of use previously determined not to present unreasonable risk which was included in Section 5.4.1 of the August 2020 1– BP Risk Evaluation (Ref. 2). This final revision to the 1–BP risk determination is consistent with EPA’s plans to revise specific aspects of the first ten TSCA chemical risk evaluations to ensure that the risk evaluations better align with TSCA’s objective of protecting health and the environment. As a result of this revision, removing the assumption that workers always and appropriately wear PPE (see Unit II.C.) means that: seven conditions of use in addition to the original 16 conditions of use drive the unreasonable risk for 1– BP; additional risks of cancer from dermal exposures are also identified as driving the unreasonable risk to workers in six conditions of use; additional risks for acute and chronic non-cancer effects from inhalation exposures drive the unreasonable risk to workers in two conditions of use; and additional risks for acute and chronic non-cancer effects and cancer from inhalation and dermal exposures to workers drive the unreasonable risk in one condition of use (where previously this condition of use was identified as presenting unreasonable risk only to ONUs). However, EPA is not making conditionof-use-specific risk determinations for those conditions of use, and for purposes of TSCA section 6(i), EPA is not issuing a final order under TSCA section 6(i)(1) for the conditions of use that do not drive the unreasonable risk, E:\FR\FM\19DEN1.SGM 19DEN1 Federal Register / Vol. 87, No. 242 / Monday, December 19, 2022 / Notices and does not consider the revised risk determination to constitute a final agency action at this point in time. Overall, 23 conditions of use out of 25 EPA evaluated drive the 1–BP whole chemical unreasonable risk determination due to risks identified for human health. The full list of the conditions of use evaluated for the 1–BP TSCA risk evaluation is in Table 4–58 and Table 4–59 of the August 2020 1– BP Risk Evaluation (Ref. 2). tkelley on DSK125TN23PROD with NOTICE II. Background A. Why is EPA re-issuing the risk determination for the 1–BP risk evaluation conducted under TSCA? In accordance with Executive Order 13990 (‘‘Protecting Public Health and the Environment and Restoring Science to Tackle the Climate Crisis’’) and other Administration priorities (Refs. 3, 4, 5, and 6), EPA reviewed the risk evaluations for the first ten chemical substances, including 1–BP, to ensure that they meet the requirements of TSCA, including conducting decisionmaking in a manner that is consistent with the best available science. As a result of this review, EPA announced plans to revise specific aspects of the first ten risk evaluations in order to ensure that the risk evaluations appropriately identify unreasonable risks and thereby help ensure the protection of human health and the environment (Ref. 7). Following a review of specific aspects of the August 2020 1–BP Risk Evaluation (Ref. 2) and after considering comments received on a draft revised risk determination for 1–BP, EPA has determined that making an unreasonable risk determination for 1– BP as a whole chemical substance, rather than making unreasonable risk determinations separately on each individual condition of use evaluated in the risk evaluation, is the most appropriate approach for 1–BP under the statute and implementing regulations. In addition, EPA’s final risk determination is explicit insofar as it does not rely on assumptions regarding the use of PPE in making the unreasonable risk determination under TSCA section 6, even though some facilities might be using PPE as one means to reduce worker exposures; rather, the use of PPE as a means of addressing unreasonable risk will be considered during risk management, as appropriate. Separately, EPA is conducting a screening approach to assess risks from the air and water pathways for several of the first 10 chemicals, including this chemical. For 1–BP, certain exposure VerDate Sep<11>2014 19:38 Dec 16, 2022 Jkt 259001 pathways that were or could be regulated under another EPA administered statute were excluded from the final risk evaluation (see section 1.4.2 of the August 2020 1–BP Risk Evaluation). This resulted in the air exposure pathway for 1–BP not being fully assessed. The goal of the recentlydeveloped screening approach is to remedy this exclusion and to determine if there may be risks that were unaccounted for in the 1–BP risk evaluation. The screening-level approach has gone through public comment and independent external peer review through the Science Advisory Committee on Chemicals (SACC). The Agency received the final peer review report on May 18, 2022, and has reviewed public comments and SACC comments. EPA expects to describe its findings regarding the chemical-specific application of this screening-level approach in the forthcoming proposed rule under TSCA section 6(a) for 1–BP. This action pertains only to the risk determination for 1–BP. While EPA intends to consider and may take additional similar actions on other of the first ten chemicals, EPA is taking a chemical-specific approach to reviewing these risk evaluations and is incorporating new policy direction in a surgical manner, while being mindful of Congressional direction on the need to complete risk evaluations and move toward any associated risk management activities in accordance with statutory deadlines. B. What is a whole chemical view of the unreasonable risk determination for the 1–BP risk evaluation? TSCA section 6 repeatedly refers to determining whether a chemical substance presents unreasonable risk under its conditions of use. Stakeholders have disagreed over whether a chemical substance should receive: A single determination that is comprehensive for the chemical substance after considering the conditions of use, referred to as a wholechemical determination; or multiple determinations, each of which is specific to a condition of use, referred to as condition-of-use-specific determinations. As explained in the Federal Register document announcing the availability of the draft revised risk determination for 1–BP (87 FR 43265, July 20, 2022 (FRL– 9944–01–OCSPP)), the proposed Risk Evaluation Procedural Rule (Ref. 8) was premised on the whole chemical approach to making unreasonable risk determinations. In that proposed rule, EPA acknowledged a lack of specificity in statutory text that might lead to PO 00000 Frm 00059 Fmt 4703 Sfmt 4703 77605 different views about whether the statute compelled EPA’s risk evaluations to address all conditions of use of a chemical substance or whether EPA had discretion to evaluate some subset of conditions of use (i.e., to scope out some manufacturing, processing, distribution in commerce, use, or disposal activities), but also stated that ‘‘EPA believes the word ‘the’ [in TSCA section 6(b)(4)(A)] is best interpreted as calling for evaluation that considers all conditions of use.’’ The proposed rule, however, was unambiguous on the point that unreasonable risk determinations would be for the chemical substance as a whole, even if based on a subset of uses. See Ref. 8 at pages 7565–66 (‘‘TSCA section 6(b)(4)(A) specifies that a risk evaluation must determine whether ‘a chemical substance’ presents an unreasonable risk of injury to health or the environment ‘under the conditions of use.’ The evaluation is on the chemical substance—not individual conditions of use—and it must be based on ‘the conditions of use.’ In this context, EPA believes the word ‘the’ is best interpreted as calling for evaluation that considers all conditions of use.’’). In the proposed regulatory text, EPA proposed to determine whether the chemical substance presents an unreasonable risk of injury to health or the environment under the conditions of use. (Ref. 8 at 7480.) The final Risk Evaluation Procedural Rule stated (82 FR 33726, July 20, 2017 (FRL–9964–38)) (Ref. 9): ‘‘As part of the risk evaluation, EPA will determine whether the chemical substance presents an unreasonable risk of injury to health or the environment under each condition of uses [sic] within the scope of the risk evaluation, either in a single decision document or in multiple decision documents’’ (40 CFR 702.47). For the unreasonable risk determinations in the first ten risk evaluations, EPA applied this provision by making individual risk determinations for each condition of use evaluated as part of each risk evaluation document (i.e., the condition-of-usespecific approach to risk determinations). That approach was based on one particular passage in the preamble to the final Risk Evaluation Rule which stated that EPA will make individual risk determinations for all conditions of use identified in the scope. (Ref. 9 at 33744). In contrast to this portion of the preamble of the final Risk Evaluation Rule, the regulatory text itself and other statements in the preamble reference a risk determination for the chemical substance under its conditions of use, rather than separate risk determinations E:\FR\FM\19DEN1.SGM 19DEN1 tkelley on DSK125TN23PROD with NOTICE 77606 Federal Register / Vol. 87, No. 242 / Monday, December 19, 2022 / Notices for each of the conditions of use of a chemical substance. In the key regulatory provision excerpted previously from 40 CFR 702.47, the text explains that ‘‘[a]s part of the risk evaluation, EPA will determine whether the chemical substance presents an unreasonable risk of injury to health or the environment under each condition of uses [sic] within the scope of the risk evaluation, either in a single decision document or in multiple decision documents’’ (Ref. 9, emphasis added). Other language reiterates this perspective. For example, 40 CFR 702.31(a) states that the purpose of the rule is to establish the EPA process for conducting a risk evaluation to determine whether a chemical substance presents an unreasonable risk of injury to health or the environment as required under TSCA section 6(b)(4)(B). Likewise, there are recurring references to whether the chemical substance presents an unreasonable risk in 40 CFR 702.41(a). See, for example, 40 CFR 702.41(a)(6), which explains that the extent to which EPA will refine its evaluations for one or more condition of use in any risk evaluation will vary as necessary to determine whether a chemical substance presents an unreasonable risk. Notwithstanding the one preambular statement about condition-of-use-specific risk determinations, the preamble to the final rule also contains support for a risk determination on the chemical substance as a whole. In discussing the identification of the conditions of use of a chemical substance, the preamble notes that this task inevitably involves the exercise of discretion on EPA’s part, and ‘‘as EPA interprets the statute, the Agency is to exercise that discretion consistent with the objective of conducting a technically sound, manageable evaluation to determine whether a chemical substance—not just individual uses or activities—presents an unreasonable risk’’ (Ref. 9 at 33729). Therefore, notwithstanding EPA’s choice to issue condition-of-use-specific risk determinations to date, EPA interprets its risk evaluation regulation to also allow the Agency to issue wholechemical risk determinations. Either approach is permissible under the regulation. A panel of the Ninth Circuit Court of Appeals also recognized the ambiguity of the regulation on this point. Safer Chemicals v. EPA, 943 F.3d. 397, 413 (9th Cir. 2019) (holding a challenge about ‘‘use-by-use risk evaluations [was] not justiciable because it is not clear, due to the ambiguous text of the Risk Evaluation Rule, whether the Agency will actually conduct risk VerDate Sep<11>2014 19:38 Dec 16, 2022 Jkt 259001 evaluations in the manner Petitioners fear’’). EPA plans to consider the appropriate approach for each chemical substance risk evaluation on a case-by-case basis, taking into account considerations relevant to the specific chemical substance in light of the Agency’s obligations under TSCA. The Agency expects that this case-by-case approach will provide greater flexibility in the Agency’s ability to evaluate and manage unreasonable risk from individual chemical substances. EPA believes this is a reasonable approach under TSCA and the Agency’s implementing regulations. With regard to the specific circumstances of 1–BP, EPA has determined that a whole chemical approach is appropriate for 1–BP in order to protect health and the environment. The whole chemical approach is appropriate for 1–BP because there are benchmark exceedances for a substantial number of conditions of use (spanning across most aspects of the chemical lifecycle—from manufacturing (including import), processing, industrial and commercial use, consumer use, and disposal) for workers, occupational non-users, consumers, and bystanders and risk of irreversible health effects (specifically developmental toxicity and cancer) associated with 1–BP exposures. Because these chemical-specific properties cut across the conditions of use within the scope of the risk evaluation, a substantial amount of the conditions of use drive the unreasonable risk; therefore, it is appropriate for the Agency to make a determination for 1– BP that the whole chemical presents an unreasonable risk. As explained later in this document, the revisions to the unreasonable risk determination (Section 5 of the August 2020 1–BP Risk Evaluation (Ref. 2)) follow the issuance of a draft revision to the TSCA 1–BP unreasonable risk determination (87 FR 43265, July 20, 2022) and the receipt of public comment. A response to comments document is also being issued with the final revised unreasonable risk determination for 1–BP (Ref. 10). The revisions to the unreasonable risk determination are based on the existing risk characterization section of the August 2020 1–BP Risk Evaluation (Ref. 2) (Section 4) and do not involve additional technical or scientific analysis. The discussion of the issues in this Federal Register document and in the accompanying final revised risk determination for 1–BP supersede any conflicting statements in the August 2020 1–BP Risk Evaluation (Ref. 2) and PO 00000 Frm 00060 Fmt 4703 Sfmt 4703 the earlier response to comments document (Ref. 11). EPA views the peer reviewed hazard and exposure assessments and associated risk characterization as robust and upholding the standards of best available science and weight of the scientific evidence per TSCA sections 26(h) and (i). For purposes of TSCA section 6(i), EPA is making a risk determination on 1–BP as a whole chemical. Under the revised approach, the ‘‘whole chemical’’ risk determination for 1–BP supersedes the no unreasonable risk determinations for 1–BP that were premised on a condition-of-use-specific approach to determining unreasonable risk and also contains an order withdrawing the TSCA section 6(i)(1) order in Section 5.4.1 of the August 2020 1–BP Risk Evaluation (Ref. 2). C. What revision is EPA now making final about the use of PPE for the 1–BP risk evaluation? In the risk evaluations for the first ten chemical substances, as part of the unreasonable risk determination, EPA assumed for several conditions of use that workers were provided and always used PPE in a manner that achieves the stated assigned protection factor (APF) for respiratory protection, or used impervious gloves for dermal protection. In support of this assumption, EPA used reasonably available information such as public comments indicating that some employers, particularly in the industrial setting, provide PPE to their employees and follow established worker protection standards (e.g., OSHA requirements for protection of workers). For the August 2020 1–BP Risk Evaluation (Ref. 2), EPA assumed, based on reasonably available information that workers use PPE—specifically, respirators with an APF of 10 or 50, or gloves with a protection factor (PF) of 5—for 15 of 16 occupational conditions of use. In the August 2020 1–BP Risk Evaluation, EPA determined that there is unreasonable risk for nine of these occupational conditions of use even with this assumed PPE use. EPA is revising the assumption for 1– BP that workers always and properly use PPE. However, this does not mean that EPA questions the veracity of public comments which describe occupational safety practices often followed by industry. EPA believes it is appropriate when conducting risk evaluations under TSCA to evaluate the levels of risk present in baseline scenarios where PPE is not assumed to be used by workers. This approach of not assuming PPE use by workers E:\FR\FM\19DEN1.SGM 19DEN1 tkelley on DSK125TN23PROD with NOTICE Federal Register / Vol. 87, No. 242 / Monday, December 19, 2022 / Notices considers the risk to potentially exposed or susceptible subpopulations of workers who may not be covered by OSHA standards, such as self-employed individuals and public sector workers who are not covered by a State Plan. It should be noted that, in some cases, baseline conditions may reflect certain mitigation measures, such as engineering controls, in instances where exposure estimates are based on monitoring data at facilities that have engineering controls in place. In addition, EPA believes it is appropriate to evaluate the levels of risk present in scenarios considering applicable OSHA requirements (e.g., chemical-specific permissible exposure limits (PELs) and/or chemical-specific PELs with additional substance-specific standards), as well as scenarios considering industry or sector best practices for industrial hygiene that are clearly articulated to the Agency. Consistent with this approach, the August 2020 1–BP Risk Evaluation (Ref. 2) characterized risk to workers both with and without the use of PPE. By characterizing risks using scenarios that reflect different levels of mitigation, EPA risk evaluations can help inform potential risk management actions by providing information that could be used during risk management to tailor risk mitigation appropriately to address any unreasonable risk identified, or to ensure that applicable OSHA requirements or industry or sector best practices that address the unreasonable risk are required for all potentially exposed and susceptible subpopulations (including self-employed individuals and public sector workers who are not covered by an OSHA State Plan). When undertaking unreasonable risk determinations as part of TSCA risk evaluations, however, EPA does not believe it is appropriate to assume as a general matter that an applicable OSHA requirement or industry practice related to PPE use is consistently and always properly applied. Mitigation scenarios included in the EPA risk evaluation (e.g., scenarios considering use of various PPE) likely represent what is happening already in some facilities. However, the Agency cannot assume that all facilities have adopted these practices for the purposes of making the TSCA risk determination (Ref. 12). Therefore, EPA is making a determination of unreasonable risk for 1–BP from a baseline scenario that does not assume compliance with OSHA standards, including any applicable exposure limits or requirements for use of respiratory protection or other PPE. Making unreasonable risk determinations based on the baseline VerDate Sep<11>2014 19:38 Dec 16, 2022 Jkt 259001 scenario should not be viewed as an indication that EPA believes there are no occupational safety protections in place at any location, or that there is widespread non-compliance with applicable OSHA standards. Rather, it reflects EPA’s recognition that unreasonable risk may exist for subpopulations of workers that may be highly exposed because they are not covered by OSHA standards, such as self-employed individuals and public sector workers who are not covered by a State Plan, or because their employer is out of compliance with OSHA standards, or because many of OSHA’s chemical-specific permissible exposure limits largely adopted in the 1970’s are described by OSHA as being ‘‘outdated and inadequate for ensuring protection of worker health,’’ (Ref. 13), or because OSHA has not issued a chemicalspecific permissible exposure limit (PEL) (as is the case for 1–BP), or because EPA finds unreasonable risk for purposes of TSCA notwithstanding OSHA requirements. In accordance with this approach, EPA is finalizing the revision to the 1– BP risk determination without relying on assumptions regarding the occupational use of PPE in making the unreasonable risk determination under TSCA section 6; rather, information on the use of PPE as a means of mitigating risk (including public comments received from industry respondents about occupational safety practices in use) will be considered during the risk management phase, as appropriate. This represents a change from the approach taken in the August 2020 1–BP Risk Evaluation (Ref. 2). As a general matter, when undertaking risk management actions, EPA intends to strive for consistency with applicable OSHA requirements and industry best practices, including appropriate application of the hierarchy of controls, to the extent that applying those measures would address the identified unreasonable risk, including unreasonable risk to potentially exposed or susceptible subpopulations. Consistent with TSCA section 9(d), EPA will consult and coordinate TSCA activities with OSHA and other relevant Federal agencies for the purpose of achieving the maximum applicability of TSCA while avoiding the imposition of duplicative requirements. Informed by the mitigation scenarios and information gathered during the risk evaluation and risk management process, the Agency might propose rules that require risk management practices that may be already common practice in many or most facilities. Adopting clear, PO 00000 Frm 00061 Fmt 4703 Sfmt 4703 77607 comprehensive regulatory standards will foster compliance across all facilities (ensuring a level playing field) and assure protections for all affected workers, especially in cases where current OSHA standards may not apply or be sufficient to address the unreasonable risk. Removing the assumption that workers always and appropriately wear PPE in making the whole chemical risk determination for 1–BP means that: seven conditions of use in addition to the original 16 conditions of use drive the unreasonable risk for 1–BP; additional risk of cancer from dermal exposures is also identified as driving the unreasonable risk to workers in six conditions of use; additional risks for acute and chronic non-cancer effects from inhalation exposures drive the unreasonable risk to workers in two conditions of use; and additional risks for acute and chronic non-cancer effects and cancer from inhalation and dermal exposures to workers drive the unreasonable risk in one condition of use (where previously this condition of use was identified as presenting unreasonable risk only to ONUs). The finalized revision to the 1–BP risk determination clarifies that EPA does not rely on the assumed use of PPE when making the risk determination for the whole substance; rather, the use of PPE as a means of addressing unreasonable risk will be considered during risk management, as appropriate. D. What is 1–BP? 1–BP is a colorless liquid with a sweet odor. It is a brominated hydrocarbon that is slightly soluble in water. 1–BP is a volatile organic compound that exhibits high volatility, a low boiling point, low flammability and no explosivity. 1–BP is produced and imported in the United States and has a wide range of uses, including as a solvent in degreasing operations, spray adhesives and dry cleaning; as a reactant in the manufacturing of other chemical substances; and in laboratory uses. There are also a variety of consumer and commercial products that contain 1–BP, such as aerosol degreasers, spot cleaners, stain removers, and insulation for building and construction materials. E. What conclusions is EPA finalizing today in the revised TSCA risk evaluation based on the whole chemical approach and not assuming the use of PPE? EPA determined that 1–BP presents an unreasonable risk to health under the conditions of use. EPA’s unreasonable risk determination for 1–BP as a E:\FR\FM\19DEN1.SGM 19DEN1 tkelley on DSK125TN23PROD with NOTICE 77608 Federal Register / Vol. 87, No. 242 / Monday, December 19, 2022 / Notices chemical substance is driven by risks associated with the following conditions of use, considered singularly or in combination with other exposures: • Manufacture (domestic manufacturing); • Manufacture (import); • Processing as a reactant; • Processing for incorporation into formulation, mixture or reaction product; • Processing for incorporation into articles; • Processing: Repackaging; • Processing: Recycling; • Industrial and commercial use as solvent for cleaning and degreasing in vapor degreaser (batch vapor degreaser—open-top, inline vapor degreaser); • Industrial and commercial use as solvent for cleaning and degreasing in vapor degreaser (batch vapor degreaser—closed-loop); • Industrial and commercial use as solvent for cleaning and degreasing in cold cleaners; • Industrial and commercial use as solvent in aerosol spray degreaser/ cleaner; • Industrial and commercial use in adhesives and sealants; • Industrial and commercial use in dry cleaning solvents, spot cleaners and stain removers; • Industrial and commercial use in liquid cleaners (e.g., coin and scissor cleaner) and liquid spray/aerosol cleaners; • Other industrial and commercial uses: arts, crafts, hobby materials (adhesives accelerant); automotive care products (engine degrease, brake cleaner, refrigerant flush); anti-adhesive agents (mold cleaning and release product); electronic and electronic products and metal products; functional fluids (close/open-systems)— refrigerant/cutting oils; asphalt extraction; laboratory chemicals; and temperature indicator—coatings; • Consumer use as solvent in aerosol spray degreasers/cleaners; • Consumer use in spot cleaners and stain removers; • Consumer use in liquid cleaners (e.g., coin and scissor cleaners); • Consumer use in liquid spray/ aerosol cleaners; • Consumer use in arts, crafts, hobby materials (adhesive accelerant); • Consumer use in automotive care products (refrigerant flush); • Consumer use in anti-adhesives agents (mold cleaning and release product); and • Disposal. The following conditions of use do not drive EPA’s unreasonable risk determination for 1–BP: VerDate Sep<11>2014 19:38 Dec 16, 2022 Jkt 259001 • Distribution in commerce; • Commercial and consumer uses of building/construction materials (insulation). EPA is not making condition of usespecific risk determinations for these conditions of use, is not issuing a final order under TSCA section 6(i)(1) for the conditions of use that do not drive the unreasonable risk and does not consider the revised risk determination for 1–BP to constitute a final agency action at this point in time. Consistent with the statutory requirements of TSCA section 6(a), EPA will propose a risk management regulatory action to the extent necessary so that 1–BP no longer presents an unreasonable risk. EPA expects to focus its risk management action on the conditions of use that drive the unreasonable risk. However, it should be noted that, under TSCA section 6(a), EPA is not limited to regulating the specific activities found to drive unreasonable risk and may select from among a suite of risk management requirements in section 6(a) related to manufacture (including import), processing, distribution in commerce, commercial use, and disposal as part of its regulatory options to address the unreasonable risk. As a general example, EPA may regulate upstream activities (e.g., processing, distribution in commerce) to address downstream activities (e.g., consumer uses) driving unreasonable risk, even if the upstream activities do not drive the unreasonable risk. III. Summary of Public Comments EPA received a total of seven public comments on the July 20, 2022, draft revised risk determination for 1–BP during the comment period that ended August 19, 2022. Commenters included trade organizations, industry stakeholders, a union, and an environmental group. A separate document that summarizes all comments submitted and EPA’s responses to those comments has been prepared and is available in the docket for this notice (Ref. 10). IV. Revision of the August 2020 1–BP Risk Evaluation A. Why is EPA revising the risk determination for the 1–BP risk evaluation? EPA is finalizing the revised risk determination for the 1–BP risk evaluation pursuant to TSCA section 6(b) and consistent with Executive Order 13990, (‘‘Protecting Public Health and the Environment and Restoring Science to Tackle the Climate Crisis’’) PO 00000 Frm 00062 Fmt 4703 Sfmt 4703 and other Administration priorities (Refs. 3, 4, 5, and 6). EPA is revising specific aspects of the first ten TSCA existing chemical risk evaluations in order to ensure that the risk evaluations better align with TSCA’s objective of protecting health and the environment. For the 1–BP risk evaluation, this includes: (1) Making the risk determination in this instance based on the whole chemical substance instead of by individual conditions of use and (2) Emphasizing that EPA does not rely on the assumed use of PPE when making the risk determination. B. What are the revisions? EPA is now finalizing the revised risk determination for the August 2020 1–BP Risk Evaluation (Ref. 2) pursuant to TSCA section 6(b). Under the revised determination (Ref. 1), EPA concludes that 1–BP, as evaluated in the risk evaluation as a whole, presents an unreasonable risk of injury to health when evaluated under its conditions of use. This revision replaces the previous unreasonable risk determinations made for 1–BP by individual conditions of use, supersedes the determinations (and withdraws the associated order) of no unreasonable risk for the conditions of use identified in the TSCA section 6(i)(1) no unreasonable risk order, and clarifies the lack of reliance on assumed use of PPE as part of the risk determination. These revisions do not alter any of the underlying technical or scientific information that informs the risk characterization, and as such the hazard, exposure, and risk characterization sections are not changed, except to statements about PPE assumptions in Section 2.3.1.3 (Consideration of Engineering Controls and PPE) and Section 4.2.2 (Occupational Inhalation Exposure Summary and PPE Use Determinations by OES). The discussion of the issues in this Notice and in the accompanying final revision to the risk determination supersede any conflicting statements in the prior executive summary, and Section 2.3.1.3 and Section 4.2.2 from the August 2020 1–BP Risk Evaluation (Ref. 2) and the response to comments document (Ref. 11). The revised unreasonable risk determination for 1–BP includes additional explanation of how the risk evaluation characterizes the applicable OSHA requirements, or industry or sector best practices, and also clarifies that no additional analysis was done, and the risk determination is based on the risk characterization (Section 4) of the August 2020 1–BP Risk Evaluation (Ref. 2). E:\FR\FM\19DEN1.SGM 19DEN1 Federal Register / Vol. 87, No. 242 / Monday, December 19, 2022 / Notices C. Will the revised risk determination be peer reviewed? The risk determination (Section 5 of the August 2020 1–BP Risk Evaluation (Ref. 2)) was not part of the scope of the Science Advisory Committee on Chemicals (SACC) peer review of the 1– BP risk evaluation. Thus, consistent with that approach, EPA did not conduct peer review of the final revised unreasonable risk determination for the 1–BP risk evaluation because no technical or scientific changes were made to the hazard or exposure assessments or the risk characterization. V. Order Withdrawing Previous Order Regarding Unreasonable Risk Determinations for Certain Conditions of Use EPA is also issuing a new order to withdraw the TSCA Section 6(i)(1) no unreasonable risk order issued in Section 5.4.1 of the August 2020 1–BP Risk Evaluation (Ref. 2). This final revised risk determination supersedes the condition of use-specific no unreasonable risk determinations in the August 2020 1–BP Risk Evaluation (Ref. 2). The order contained in Section 5.5 of the revised risk determination (Ref. 1) withdraws the TSCA section 6(i)(1) order contained in Section 5.4.1 of the August 2020 1–BP Risk Evaluation (Ref. 2). Consistent with the statutory requirements of section 6(a), the Agency will propose risk management action to address the unreasonable risk determined in the 1–BP risk evaluation. tkelley on DSK125TN23PROD with NOTICE VI. References The following is a listing of the documents that are specifically referenced in this document. The docket includes these documents and other information considered by EPA, including documents that are referenced within the documents that are included in the docket, even if the referenced document is not physically located in the docket. For assistance in locating these other documents, please consult the person listed under FOR FURTHER INFORMATION CONTACT. 1. EPA. Unreasonable Risk Determination for 1-Bromopropane (1–BP). December 2022. 2. EPA. Risk Evaluation for 1-Bromopropane (1–BP). August 2020. EPA Document #740–R1–8013. https:// www.regulations.gov/document/EPAHQ-OPPT-2019-0235-0085. 3. Executive Order 13990. Protecting Public Health and the Environment and Restoring Science to Tackle the Climate Crisis. Federal Register. 86 FR 7037, January 25, 2021. 4. Executive Order 13985. Advancing Racial Equity and Support for Underserved Communities Through the Federal Government. Federal Register. 86 FR VerDate Sep<11>2014 19:38 Dec 16, 2022 Jkt 259001 7009, January 25, 2021. 5. Executive Order 14008. Tackling the Climate Crisis at Home and Abroad. Federal Register. 86 FR 7619, February 1, 2021. 6. Presidential Memorandum. Memorandum on Restoring Trust in Government Through Scientific Integrity and Evidence-Based Policymaking. Federal Register. 86 FR 8845, February 10, 2021. 7. EPA. Press Release; EPA Announces Path Forward for TSCA Chemical Risk Evaluations. June 2021. https:// www.epa.gov/newsreleases/epaannounces-path-forward-tsca-chemicalrisk-evaluations. 8. EPA. Proposed Rule; Procedures for Chemical Risk Evaluation Under the Amended Toxic Substances Control Act. Federal Register. 82 FR 7562, January 19, 2017 (FRL–9957–75). 9. EPA. Final Rule; Procedures for Chemical Risk Evaluation Under the Amended Toxic Substances Control Act. Federal Register. 82 FR 33726, July 20, 2017 (FRL–9964–38). 10. EPA. Response to Public Comments to the Revised Unreasonable Risk Determination; 1-Bromopropane (1–BP). December 2022. 11. EPA. Summary of External Peer Review and Public Comments and Disposition for 1-Bromopropane (1–BP). August 2020. Available at: https:// www.regulations.gov/document/EPAHQ-OPPT-2019-0235-0066. 12. Occupational Safety and Health Administration (OSHA). Top 10 Most Frequently Cited Standards for Fiscal Year 2021 (Oct. 1, 2020, to Sept. 30, 2021). Accessed October 13, 2022. https://www.osha.gov/ top10citedstandards. 13. OSHA. Permissible Exposure Limits— Annotated Tables. Accessed June 13, 2022. https://www.osha.gov/annotatedpels. Authority: 15 U.S.C. 2601 et seq. Dated: December 13, 2022. Michal Freedhoff, Assistant Administrator, Office of Chemical Safety and Pollution Prevention. [FR Doc. 2022–27439 Filed 12–16–22; 8:45 am] BILLING CODE 6560–50–P EXPORT–IMPORT BANK Sunshine Act Meetings Notice of an Open Meeting of the Board of Directors of the Export-Import Bank of the United States. TIME AND DATE: Thursday, December 22, 2022, at 10:30 a.m. PLACE: The meeting will be held via teleconference. STATUS: The meeting will be open to public observation. MATTERS TO BE CONSIDERED: Facultative Reinsurance and Facultative Risk Sharing with Private Sector Entities PO 00000 Frm 00063 Fmt 4703 Sfmt 4703 77609 CONTACT PERSON FOR MORE INFORMATION: Joyce B. Stone (202–257–4086). Members of the public who wish to attend the meeting via teleconference must register via using the link below by noon Wednesday December 21, 2022. After completing the registration, individuals will receive a confirmation email containing information about joining the webinar. https://teams.microsoft.com/ registration/PAFTuZHHMk2Zb1 GDkIVFJw,pHLqbjVTrkuy_ 9KepKN6dQ, MFtnLzltSEGI6EQECdI5iQ, ZsdHLLqwokW2I3gz6bgB4Q, 1yfct4LeXUOTa6FIziQ9tA, w50RA7BfZE2vhxnxe30hJA? mode=read&tenantId=b953013c-c7914d32-996f-518390854527 Joyce B. Stone, Assistant Corporate Secretary. [FR Doc. 2022–27494 Filed 12–15–22; 11:15 am] BILLING CODE 6690–01–P FEDERAL COMMUNICATIONS COMMISSION [OMB 3060–0905, OMB 3060–1269; FR ID 118551] Information Collections Being Reviewed by the Federal Communications Commission Under Delegated Authority Federal Communications Commission. ACTION: Notice and request for comments. AGENCY: As part of its continuing effort to reduce paperwork burdens, and as required by the Paperwork Reduction Act (PRA) of 1995, the Federal Communications Commission (FCC or the Commission) invites the general public and other Federal agencies to take this opportunity to comment on the following information collection. Comments are requested concerning: whether the proposed collection of information is necessary for the proper performance of the functions of the Commission, including whether the information shall have practical utility; the accuracy of the Commission’s burden estimate; ways to enhance the quality, utility, and clarity of the information collected; ways to minimize the burden of the collection of information on the respondents, including the use of automated collection techniques or other forms of information technology; and ways to further reduce the information collection burden on small business concerns with fewer than 25 employees. SUMMARY: E:\FR\FM\19DEN1.SGM 19DEN1

Agencies

[Federal Register Volume 87, Number 242 (Monday, December 19, 2022)]
[Notices]
[Pages 77603-77609]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-27439]


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

ENVIRONMENTAL PROTECTION AGENCY

[EPA-HQ-OPPT-2016-0741; FRL-9944-02-OCSPP]


1-Bromopropane (1-BP); Revision to Toxic Substances Control Act 
(TSCA) Risk Determination; Notice of Availability

AGENCY: Environmental Protection Agency (EPA).

ACTION: Notice.

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

SUMMARY: The Environmental Protection Agency (EPA) is announcing the 
availability of the final revision to the risk determination for the 1-
bromopropane (1-BP) risk evaluation issued under the Toxic Substances 
Control Act (TSCA). The revision to the 1-BP risk determination 
reflects the announced policy changes to ensure the public is protected 
from unreasonable risks from chemicals in a way that is supported by 
science and the law. EPA determined that 1-BP, as a whole chemical 
substance, presents an unreasonable risk of injury to health when 
evaluated under its conditions of use. In addition, this revised risk 
determination does not reflect an assumption that workers always 
appropriately wear personal protective equipment (PPE). EPA understands 
that there could be adequate occupational safety protections in place 
at certain workplace locations; however, not assuming use of PPE 
reflects EPA's recognition that unreasonable risk may exist for 
subpopulations of workers that may be highly exposed because they are 
not covered by Occupational Safety and Health Administration (OSHA) 
standards, or their employers are out of compliance with OSHA 
standards, or because many of OSHA's chemical-specific permissible 
exposure limits largely adopted in the 1970's are described by OSHA as 
being ``outdated and inadequate for ensuring protection of worker 
health,'' or because OSHA has not issued a chemical-specific 
permissible exposure limit (PEL) (as is the case for 1-BP), or because 
EPA finds unreasonable risk for purposes of TSCA notwithstanding OSHA 
requirements. This revision supersedes the condition of use-specific no 
unreasonable risk

[[Page 77604]]

determinations in the August 2020 1-BP Risk Evaluation and withdraws 
the associated TSCA order included in the August 2020 1-BP Risk 
Evaluation.

ADDRESSES: The docket for this action, identified by docket 
identification (ID) number EPA-HQ-OPPT-2016-0741, is available online 
at https://www.regulations.gov or in-person at the Office of Pollution 
Prevention and Toxics Docket (OPPT Docket), Environmental Protection 
Agency Docket Center (EPA/DC), West William Jefferson Clinton Bldg., 
Rm. 3334, 1301 Constitution Ave. NW, Washington, DC 20460-0001. The 
Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through 
Friday, excluding legal holidays. The telephone number for the Public 
Reading Room is (202) 566-1744, and the telephone number for the OPPT 
Docket is (202) 566-0280. Additional instructions on visiting the 
docket, along with more information about dockets generally, is 
available at https://www.epa.gov/dockets.

FOR FURTHER INFORMATION CONTACT: 
    For technical information contact: Amy Shuman Office of Pollution 
Prevention and Toxics (7404M), Environmental Protection Agency, 1200 
Pennsylvania Ave. NW, Washington, DC 20460-0001; telephone number: 
(202) 564-2978; 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 those involved in the manufacture, processing, 
distribution, use, disposal, and/or the assessment of risks involving 
chemical substances and mixtures. You may be potentially affected by 
this action if you manufacture (defined under TSCA to include import), 
process (including recycling), distribute in commerce, use or dispose 
of 1-BP, including 1-BP in products. Since other entities may also be 
interested in this revision to the risk determination, EPA has not 
attempted to describe all the specific entities that may be affected by 
this action.

B. What is 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 
(PESS) 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 provide instruction on chemical substances that must undergo 
evaluation, the minimum components of a TSCA risk evaluation, and the 
timelines for public comment and completion of the risk evaluation. 
TSCA also requires that EPA operate in a manner that is consistent with 
the best available science, make decisions based on the weight of the 
scientific evidence, and consider reasonably available information. 15 
U.S.C. 2625(h), (i), and (k).
    The statute identifies the minimum components for 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 exposures for the conditions of 
use of the chemical substance, including information that is relevant 
to 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 
exposures. 15 U.S.C. 2605(b)(4)(F)(i) through (ii) and (iv) through 
(v). Each risk evaluation must not consider costs or other nonrisk 
factors. 15 U.S.C. 2605(b)(4)(F)(iii).
    EPA has inherent authority to reconsider previous decisions and to 
revise, replace, or repeal a decision to the extent permitted by law 
and supported by reasoned explanation. FCC v. Fox Television Stations, 
Inc., 556 U.S. 502, 515 (2009); see also Motor Vehicle Mfrs. Ass'n v. 
State Farm Mutual Auto. Ins. Co., 463 U.S. 29, 42 (1983). Pursuant to 
such authority, EPA has reconsidered and is now finalizing a revised 
risk determination for 1-BP.

C. What action is EPA taking?

    EPA is announcing the availability of the final revision to the 
risk determination for the 1-BP risk evaluation issued under TSCA that 
published in August 2020 (Ref. 1). In July 2022, EPA sought public 
comment on the draft revisions (87 FR 43265, July 20, 2022). EPA 
appreciates the public comments received on the draft revision to the 
1-BP risk determination. After review of these comments and 
consideration of the specific circumstances of 1-BP, EPA concludes that 
the Agency's risk determination for 1-BP is better characterized as a 
whole chemical risk determination rather than condition-of-use-specific 
risk determinations. Accordingly, EPA is revising and replacing Section 
5 of the August 2020 1-BP Risk Evaluation (Ref. 2) where the findings 
of unreasonable risk to health were previously made for the individual 
conditions of use evaluated. EPA is also withdrawing the previously 
issued TSCA section 6(i)(l) order for nine conditions of use previously 
determined not to present unreasonable risk which was included in 
Section 5.4.1 of the August 2020 1-BP Risk Evaluation (Ref. 2).
    This final revision to the 1-BP risk determination is consistent 
with EPA's plans to revise specific aspects of the first ten TSCA 
chemical risk evaluations to ensure that the risk evaluations better 
align with TSCA's objective of protecting health and the environment. 
As a result of this revision, removing the assumption that workers 
always and appropriately wear PPE (see Unit II.C.) means that: seven 
conditions of use in addition to the original 16 conditions of use 
drive the unreasonable risk for 1-BP; additional risks of cancer from 
dermal exposures are also identified as driving the unreasonable risk 
to workers in six conditions of use; additional risks for acute and 
chronic non-cancer effects from inhalation exposures drive the 
unreasonable risk to workers in two conditions of use; and additional 
risks for acute and chronic non-cancer effects and cancer from 
inhalation and dermal exposures to workers drive the unreasonable risk 
in one condition of use (where previously this condition of use was 
identified as presenting unreasonable risk only to ONUs). However, EPA 
is not making condition-of-use-specific risk determinations for those 
conditions of use, and for purposes of TSCA section 6(i), EPA is not 
issuing a final order under TSCA section 6(i)(1) for the conditions of 
use that do not drive the unreasonable risk,

[[Page 77605]]

and does not consider the revised risk determination to constitute a 
final agency action at this point in time. Overall, 23 conditions of 
use out of 25 EPA evaluated drive the 1-BP whole chemical unreasonable 
risk determination due to risks identified for human health. The full 
list of the conditions of use evaluated for the 1-BP TSCA risk 
evaluation is in Table 4-58 and Table 4-59 of the August 2020 1-BP Risk 
Evaluation (Ref. 2).

II. Background

A. Why is EPA re-issuing the risk determination for the 1-BP risk 
evaluation conducted under TSCA?

    In accordance with Executive Order 13990 (``Protecting Public 
Health and the Environment and Restoring Science to Tackle the Climate 
Crisis'') and other Administration priorities (Refs. 3, 4, 5, and 6), 
EPA reviewed the risk evaluations for the first ten chemical 
substances, including 1-BP, to ensure that they meet the requirements 
of TSCA, including conducting decision-making in a manner that is 
consistent with the best available science.
    As a result of this review, EPA announced plans to revise specific 
aspects of the first ten risk evaluations in order to ensure that the 
risk evaluations appropriately identify unreasonable risks and thereby 
help ensure the protection of human health and the environment (Ref. 
7). Following a review of specific aspects of the August 2020 1-BP Risk 
Evaluation (Ref. 2) and after considering comments received on a draft 
revised risk determination for 1-BP, EPA has determined that making an 
unreasonable risk determination for 1-BP as a whole chemical substance, 
rather than making unreasonable risk determinations separately on each 
individual condition of use evaluated in the risk evaluation, is the 
most appropriate approach for 1-BP under the statute and implementing 
regulations. In addition, EPA's final risk determination is explicit 
insofar as it does not rely on assumptions regarding the use of PPE in 
making the unreasonable risk determination under TSCA section 6, even 
though some facilities might be using PPE as one means to reduce worker 
exposures; rather, the use of PPE as a means of addressing unreasonable 
risk will be considered during risk management, as appropriate.
    Separately, EPA is conducting a screening approach to assess risks 
from the air and water pathways for several of the first 10 chemicals, 
including this chemical. For 1-BP, certain exposure pathways that were 
or could be regulated under another EPA administered statute were 
excluded from the final risk evaluation (see section 1.4.2 of the 
August 2020 1-BP Risk Evaluation). This resulted in the air exposure 
pathway for 1-BP not being fully assessed. The goal of the recently-
developed screening approach is to remedy this exclusion and to 
determine if there may be risks that were unaccounted for in the 1-BP 
risk evaluation. The screening-level approach has gone through public 
comment and independent external peer review through the Science 
Advisory Committee on Chemicals (SACC). The Agency received the final 
peer review report on May 18, 2022, and has reviewed public comments 
and SACC comments. EPA expects to describe its findings regarding the 
chemical-specific application of this screening-level approach in the 
forthcoming proposed rule under TSCA section 6(a) for 1-BP.
    This action pertains only to the risk determination for 1-BP. While 
EPA intends to consider and may take additional similar actions on 
other of the first ten chemicals, EPA is taking a chemical-specific 
approach to reviewing these risk evaluations and is incorporating new 
policy direction in a surgical manner, while being mindful of 
Congressional direction on the need to complete risk evaluations and 
move toward any associated risk management activities in accordance 
with statutory deadlines.

B. What is a whole chemical view of the unreasonable risk determination 
for the 1-BP risk evaluation?

    TSCA section 6 repeatedly refers to determining whether a chemical 
substance presents unreasonable risk under its conditions of use. 
Stakeholders have disagreed over whether a chemical substance should 
receive: A single determination that is comprehensive for the chemical 
substance after considering the conditions of use, referred to as a 
whole-chemical determination; or multiple determinations, each of which 
is specific to a condition of use, referred to as condition-of-use-
specific determinations.
    As explained in the Federal Register document announcing the 
availability of the draft revised risk determination for 1-BP (87 FR 
43265, July 20, 2022 (FRL-9944-01-OCSPP)), the proposed Risk Evaluation 
Procedural Rule (Ref. 8) was premised on the whole chemical approach to 
making unreasonable risk determinations. In that proposed rule, EPA 
acknowledged a lack of specificity in statutory text that might lead to 
different views about whether the statute compelled EPA's risk 
evaluations to address all conditions of use of a chemical substance or 
whether EPA had discretion to evaluate some subset of conditions of use 
(i.e., to scope out some manufacturing, processing, distribution in 
commerce, use, or disposal activities), but also stated that ``EPA 
believes the word `the' [in TSCA section 6(b)(4)(A)] is best 
interpreted as calling for evaluation that considers all conditions of 
use.'' The proposed rule, however, was unambiguous on the point that 
unreasonable risk determinations would be for the chemical substance as 
a whole, even if based on a subset of uses. See Ref. 8 at pages 7565-66 
(``TSCA section 6(b)(4)(A) specifies that a risk evaluation must 
determine whether `a chemical substance' presents an unreasonable risk 
of injury to health or the environment `under the conditions of use.' 
The evaluation is on the chemical substance--not individual conditions 
of use--and it must be based on `the conditions of use.' In this 
context, EPA believes the word `the' is best interpreted as calling for 
evaluation that considers all conditions of use.''). In the proposed 
regulatory text, EPA proposed to determine whether the chemical 
substance presents an unreasonable risk of injury to health or the 
environment under the conditions of use. (Ref. 8 at 7480.)
    The final Risk Evaluation Procedural Rule stated (82 FR 33726, July 
20, 2017 (FRL-9964-38)) (Ref. 9): ``As part of the risk evaluation, EPA 
will determine whether the chemical substance presents an unreasonable 
risk of injury to health or the environment under each condition of 
uses [sic] within the scope of the risk evaluation, either in a single 
decision document or in multiple decision documents'' (40 CFR 702.47). 
For the unreasonable risk determinations in the first ten risk 
evaluations, EPA applied this provision by making individual risk 
determinations for each condition of use evaluated as part of each risk 
evaluation document (i.e., the condition-of-use-specific approach to 
risk determinations). That approach was based on one particular passage 
in the preamble to the final Risk Evaluation Rule which stated that EPA 
will make individual risk determinations for all conditions of use 
identified in the scope. (Ref. 9 at 33744).
    In contrast to this portion of the preamble of the final Risk 
Evaluation Rule, the regulatory text itself and other statements in the 
preamble reference a risk determination for the chemical substance 
under its conditions of use, rather than separate risk determinations

[[Page 77606]]

for each of the conditions of use of a chemical substance. In the key 
regulatory provision excerpted previously from 40 CFR 702.47, the text 
explains that ``[a]s part of the risk evaluation, EPA will determine 
whether the chemical substance presents an unreasonable risk of injury 
to health or the environment under each condition of uses [sic] within 
the scope of the risk evaluation, either in a single decision document 
or in multiple decision documents'' (Ref. 9, emphasis added). Other 
language reiterates this perspective. For example, 40 CFR 702.31(a) 
states that the purpose of the rule is to establish the EPA process for 
conducting a risk evaluation to determine whether a chemical substance 
presents an unreasonable risk of injury to health or the environment as 
required under TSCA section 6(b)(4)(B). Likewise, there are recurring 
references to whether the chemical substance presents an unreasonable 
risk in 40 CFR 702.41(a). See, for example, 40 CFR 702.41(a)(6), which 
explains that the extent to which EPA will refine its evaluations for 
one or more condition of use in any risk evaluation will vary as 
necessary to determine whether a chemical substance presents an 
unreasonable risk. Notwithstanding the one preambular statement about 
condition-of-use-specific risk determinations, the preamble to the 
final rule also contains support for a risk determination on the 
chemical substance as a whole. In discussing the identification of the 
conditions of use of a chemical substance, the preamble notes that this 
task inevitably involves the exercise of discretion on EPA's part, and 
``as EPA interprets the statute, the Agency is to exercise that 
discretion consistent with the objective of conducting a technically 
sound, manageable evaluation to determine whether a chemical 
substance--not just individual uses or activities--presents an 
unreasonable risk'' (Ref. 9 at 33729).
    Therefore, notwithstanding EPA's choice to issue condition-of-use-
specific risk determinations to date, EPA interprets its risk 
evaluation regulation to also allow the Agency to issue whole-chemical 
risk determinations. Either approach is permissible under the 
regulation. A panel of the Ninth Circuit Court of Appeals also 
recognized the ambiguity of the regulation on this point. Safer 
Chemicals v. EPA, 943 F.3d. 397, 413 (9th Cir. 2019) (holding a 
challenge about ``use-by-use risk evaluations [was] not justiciable 
because it is not clear, due to the ambiguous text of the Risk 
Evaluation Rule, whether the Agency will actually conduct risk 
evaluations in the manner Petitioners fear'').
    EPA plans to consider the appropriate approach for each chemical 
substance risk evaluation on a case-by-case basis, taking into account 
considerations relevant to the specific chemical substance in light of 
the Agency's obligations under TSCA. The Agency expects that this case-
by-case approach will provide greater flexibility in the Agency's 
ability to evaluate and manage unreasonable risk from individual 
chemical substances. EPA believes this is a reasonable approach under 
TSCA and the Agency's implementing regulations.
    With regard to the specific circumstances of 1-BP, EPA has 
determined that a whole chemical approach is appropriate for 1-BP in 
order to protect health and the environment. The whole chemical 
approach is appropriate for 1-BP because there are benchmark 
exceedances for a substantial number of conditions of use (spanning 
across most aspects of the chemical lifecycle--from manufacturing 
(including import), processing, industrial and commercial use, consumer 
use, and disposal) for workers, occupational non-users, consumers, and 
bystanders and risk of irreversible health effects (specifically 
developmental toxicity and cancer) associated with 1-BP exposures. 
Because these chemical-specific properties cut across the conditions of 
use within the scope of the risk evaluation, a substantial amount of 
the conditions of use drive the unreasonable risk; therefore, it is 
appropriate for the Agency to make a determination for 1-BP that the 
whole chemical presents an unreasonable risk.
    As explained later in this document, the revisions to the 
unreasonable risk determination (Section 5 of the August 2020 1-BP Risk 
Evaluation (Ref. 2)) follow the issuance of a draft revision to the 
TSCA 1-BP unreasonable risk determination (87 FR 43265, July 20, 2022) 
and the receipt of public comment. A response to comments document is 
also being issued with the final revised unreasonable risk 
determination for 1-BP (Ref. 10). The revisions to the unreasonable 
risk determination are based on the existing risk characterization 
section of the August 2020 1-BP Risk Evaluation (Ref. 2) (Section 4) 
and do not involve additional technical or scientific analysis. The 
discussion of the issues in this Federal Register document and in the 
accompanying final revised risk determination for 1-BP supersede any 
conflicting statements in the August 2020 1-BP Risk Evaluation (Ref. 2) 
and the earlier response to comments document (Ref. 11). EPA views the 
peer reviewed hazard and exposure assessments and associated risk 
characterization as robust and upholding the standards of best 
available science and weight of the scientific evidence per TSCA 
sections 26(h) and (i).
    For purposes of TSCA section 6(i), EPA is making a risk 
determination on 1-BP as a whole chemical. Under the revised approach, 
the ``whole chemical'' risk determination for 1-BP supersedes the no 
unreasonable risk determinations for 1-BP that were premised on a 
condition-of-use-specific approach to determining unreasonable risk and 
also contains an order withdrawing the TSCA section 6(i)(1) order in 
Section 5.4.1 of the August 2020 1-BP Risk Evaluation (Ref. 2).

C. What revision is EPA now making final about the use of PPE for the 
1-BP risk evaluation?

    In the risk evaluations for the first ten chemical substances, as 
part of the unreasonable risk determination, EPA assumed for several 
conditions of use that workers were provided and always used PPE in a 
manner that achieves the stated assigned protection factor (APF) for 
respiratory protection, or used impervious gloves for dermal 
protection. In support of this assumption, EPA used reasonably 
available information such as public comments indicating that some 
employers, particularly in the industrial setting, provide PPE to their 
employees and follow established worker protection standards (e.g., 
OSHA requirements for protection of workers).
    For the August 2020 1-BP Risk Evaluation (Ref. 2), EPA assumed, 
based on reasonably available information that workers use PPE--
specifically, respirators with an APF of 10 or 50, or gloves with a 
protection factor (PF) of 5--for 15 of 16 occupational conditions of 
use. In the August 2020 1-BP Risk Evaluation, EPA determined that there 
is unreasonable risk for nine of these occupational conditions of use 
even with this assumed PPE use.
    EPA is revising the assumption for 1-BP that workers always and 
properly use PPE. However, this does not mean that EPA questions the 
veracity of public comments which describe occupational safety 
practices often followed by industry. EPA believes it is appropriate 
when conducting risk evaluations under TSCA to evaluate the levels of 
risk present in baseline scenarios where PPE is not assumed to be used 
by workers. This approach of not assuming PPE use by workers

[[Page 77607]]

considers the risk to potentially exposed or susceptible subpopulations 
of workers who may not be covered by OSHA standards, such as self-
employed individuals and public sector workers who are not covered by a 
State Plan. It should be noted that, in some cases, baseline conditions 
may reflect certain mitigation measures, such as engineering controls, 
in instances where exposure estimates are based on monitoring data at 
facilities that have engineering controls in place.
    In addition, EPA believes it is appropriate to evaluate the levels 
of risk present in scenarios considering applicable OSHA requirements 
(e.g., chemical-specific permissible exposure limits (PELs) and/or 
chemical-specific PELs with additional substance-specific standards), 
as well as scenarios considering industry or sector best practices for 
industrial hygiene that are clearly articulated to the Agency. 
Consistent with this approach, the August 2020 1-BP Risk Evaluation 
(Ref. 2) characterized risk to workers both with and without the use of 
PPE. By characterizing risks using scenarios that reflect different 
levels of mitigation, EPA risk evaluations can help inform potential 
risk management actions by providing information that could be used 
during risk management to tailor risk mitigation appropriately to 
address any unreasonable risk identified, or to ensure that applicable 
OSHA requirements or industry or sector best practices that address the 
unreasonable risk are required for all potentially exposed and 
susceptible subpopulations (including self-employed individuals and 
public sector workers who are not covered by an OSHA State Plan).
    When undertaking unreasonable risk determinations as part of TSCA 
risk evaluations, however, EPA does not believe it is appropriate to 
assume as a general matter that an applicable OSHA requirement or 
industry practice related to PPE use is consistently and always 
properly applied. Mitigation scenarios included in the EPA risk 
evaluation (e.g., scenarios considering use of various PPE) likely 
represent what is happening already in some facilities. However, the 
Agency cannot assume that all facilities have adopted these practices 
for the purposes of making the TSCA risk determination (Ref. 12).
    Therefore, EPA is making a determination of unreasonable risk for 
1-BP from a baseline scenario that does not assume compliance with OSHA 
standards, including any applicable exposure limits or requirements for 
use of respiratory protection or other PPE. Making unreasonable risk 
determinations based on the baseline scenario should not be viewed as 
an indication that EPA believes there are no occupational safety 
protections in place at any location, or that there is widespread non-
compliance with applicable OSHA standards. Rather, it reflects EPA's 
recognition that unreasonable risk may exist for subpopulations of 
workers that may be highly exposed because they are not covered by OSHA 
standards, such as self-employed individuals and public sector workers 
who are not covered by a State Plan, or because their employer is out 
of compliance with OSHA standards, or because many of OSHA's chemical-
specific permissible exposure limits largely adopted in the 1970's are 
described by OSHA as being ``outdated and inadequate for ensuring 
protection of worker health,'' (Ref. 13), or because OSHA has not 
issued a chemical-specific permissible exposure limit (PEL) (as is the 
case for 1-BP), or because EPA finds unreasonable risk for purposes of 
TSCA notwithstanding OSHA requirements.
    In accordance with this approach, EPA is finalizing the revision to 
the 1-BP risk determination without relying on assumptions regarding 
the occupational use of PPE in making the unreasonable risk 
determination under TSCA section 6; rather, information on the use of 
PPE as a means of mitigating risk (including public comments received 
from industry respondents about occupational safety practices in use) 
will be considered during the risk management phase, as appropriate. 
This represents a change from the approach taken in the August 2020 1-
BP Risk Evaluation (Ref. 2). As a general matter, when undertaking risk 
management actions, EPA intends to strive for consistency with 
applicable OSHA requirements and industry best practices, including 
appropriate application of the hierarchy of controls, to the extent 
that applying those measures would address the identified unreasonable 
risk, including unreasonable risk to potentially exposed or susceptible 
subpopulations. Consistent with TSCA section 9(d), EPA will consult and 
coordinate TSCA activities with OSHA and other relevant Federal 
agencies for the purpose of achieving the maximum applicability of TSCA 
while avoiding the imposition of duplicative requirements. Informed by 
the mitigation scenarios and information gathered during the risk 
evaluation and risk management process, the Agency might propose rules 
that require risk management practices that may be already common 
practice in many or most facilities. Adopting clear, comprehensive 
regulatory standards will foster compliance across all facilities 
(ensuring a level playing field) and assure protections for all 
affected workers, especially in cases where current OSHA standards may 
not apply or be sufficient to address the unreasonable risk.
    Removing the assumption that workers always and appropriately wear 
PPE in making the whole chemical risk determination for 1-BP means 
that: seven conditions of use in addition to the original 16 conditions 
of use drive the unreasonable risk for 1-BP; additional risk of cancer 
from dermal exposures is also identified as driving the unreasonable 
risk to workers in six conditions of use; additional risks for acute 
and chronic non-cancer effects from inhalation exposures drive the 
unreasonable risk to workers in two conditions of use; and additional 
risks for acute and chronic non-cancer effects and cancer from 
inhalation and dermal exposures to workers drive the unreasonable risk 
in one condition of use (where previously this condition of use was 
identified as presenting unreasonable risk only to ONUs). The finalized 
revision to the 1-BP risk determination clarifies that EPA does not 
rely on the assumed use of PPE when making the risk determination for 
the whole substance; rather, the use of PPE as a means of addressing 
unreasonable risk will be considered during risk management, as 
appropriate.

D. What is 1-BP?

    1-BP is a colorless liquid with a sweet odor. It is a brominated 
hydrocarbon that is slightly soluble in water. 1-BP is a volatile 
organic compound that exhibits high volatility, a low boiling point, 
low flammability and no explosivity. 1-BP is produced and imported in 
the United States and has a wide range of uses, including as a solvent 
in degreasing operations, spray adhesives and dry cleaning; as a 
reactant in the manufacturing of other chemical substances; and in 
laboratory uses. There are also a variety of consumer and commercial 
products that contain 1-BP, such as aerosol degreasers, spot cleaners, 
stain removers, and insulation for building and construction materials.

E. What conclusions is EPA finalizing today in the revised TSCA risk 
evaluation based on the whole chemical approach and not assuming the 
use of PPE?

    EPA determined that 1-BP presents an unreasonable risk to health 
under the conditions of use. EPA's unreasonable risk determination for 
1-BP as a

[[Page 77608]]

chemical substance is driven by risks associated with the following 
conditions of use, considered singularly or in combination with other 
exposures:
     Manufacture (domestic manufacturing);
     Manufacture (import);
     Processing as a reactant;
     Processing for incorporation into formulation, mixture or 
reaction product;
     Processing for incorporation into articles;
     Processing: Repackaging;
     Processing: Recycling;
     Industrial and commercial use as solvent for cleaning and 
degreasing in vapor degreaser (batch vapor degreaser--open-top, inline 
vapor degreaser);
     Industrial and commercial use as solvent for cleaning and 
degreasing in vapor degreaser (batch vapor degreaser--closed-loop);
     Industrial and commercial use as solvent for cleaning and 
degreasing in cold cleaners;
     Industrial and commercial use as solvent in aerosol spray 
degreaser/cleaner;
     Industrial and commercial use in adhesives and sealants;
     Industrial and commercial use in dry cleaning solvents, 
spot cleaners and stain removers;
     Industrial and commercial use in liquid cleaners (e.g., 
coin and scissor cleaner) and liquid spray/aerosol cleaners;
     Other industrial and commercial uses: arts, crafts, hobby 
materials (adhesives accelerant); automotive care products (engine 
degrease, brake cleaner, refrigerant flush); anti-adhesive agents (mold 
cleaning and release product); electronic and electronic products and 
metal products; functional fluids (close/open-systems)--refrigerant/
cutting oils; asphalt extraction; laboratory chemicals; and temperature 
indicator--coatings;
     Consumer use as solvent in aerosol spray degreasers/
cleaners;
     Consumer use in spot cleaners and stain removers;
     Consumer use in liquid cleaners (e.g., coin and scissor 
cleaners);
     Consumer use in liquid spray/aerosol cleaners;
     Consumer use in arts, crafts, hobby materials (adhesive 
accelerant);
     Consumer use in automotive care products (refrigerant 
flush);
     Consumer use in anti-adhesives agents (mold cleaning and 
release product); and
     Disposal.
    The following conditions of use do not drive EPA's unreasonable 
risk determination for 1-BP:
     Distribution in commerce;
     Commercial and consumer uses of building/construction 
materials (insulation).
    EPA is not making condition of use-specific risk determinations for 
these conditions of use, is not issuing a final order under TSCA 
section 6(i)(1) for the conditions of use that do not drive the 
unreasonable risk and does not consider the revised risk determination 
for 1-BP to constitute a final agency action at this point in time.
    Consistent with the statutory requirements of TSCA section 6(a), 
EPA will propose a risk management regulatory action to the extent 
necessary so that 1-BP no longer presents an unreasonable risk. EPA 
expects to focus its risk management action on the conditions of use 
that drive the unreasonable risk. However, it should be noted that, 
under TSCA section 6(a), EPA is not limited to regulating the specific 
activities found to drive unreasonable risk and may select from among a 
suite of risk management requirements in section 6(a) related to 
manufacture (including import), processing, distribution in commerce, 
commercial use, and disposal as part of its regulatory options to 
address the unreasonable risk. As a general example, EPA may regulate 
upstream activities (e.g., processing, distribution in commerce) to 
address downstream activities (e.g., consumer uses) driving 
unreasonable risk, even if the upstream activities do not drive the 
unreasonable risk.

III. Summary of Public Comments

    EPA received a total of seven public comments on the July 20, 2022, 
draft revised risk determination for 1-BP during the comment period 
that ended August 19, 2022. Commenters included trade organizations, 
industry stakeholders, a union, and an environmental group. A separate 
document that summarizes all comments submitted and EPA's responses to 
those comments has been prepared and is available in the docket for 
this notice (Ref. 10).

IV. Revision of the August 2020 1-BP Risk Evaluation

A. Why is EPA revising the risk determination for the 1-BP risk 
evaluation?

    EPA is finalizing the revised risk determination for the 1-BP risk 
evaluation pursuant to TSCA section 6(b) and consistent with Executive 
Order 13990, (``Protecting Public Health and the Environment and 
Restoring Science to Tackle the Climate Crisis'') and other 
Administration priorities (Refs. 3, 4, 5, and 6). EPA is revising 
specific aspects of the first ten TSCA existing chemical risk 
evaluations in order to ensure that the risk evaluations better align 
with TSCA's objective of protecting health and the environment. For the 
1-BP risk evaluation, this includes: (1) Making the risk determination 
in this instance based on the whole chemical substance instead of by 
individual conditions of use and (2) Emphasizing that EPA does not rely 
on the assumed use of PPE when making the risk determination.

B. What are the revisions?

    EPA is now finalizing the revised risk determination for the August 
2020 1-BP Risk Evaluation (Ref. 2) pursuant to TSCA section 6(b). Under 
the revised determination (Ref. 1), EPA concludes that 1-BP, as 
evaluated in the risk evaluation as a whole, presents an unreasonable 
risk of injury to health when evaluated under its conditions of use. 
This revision replaces the previous unreasonable risk determinations 
made for 1-BP by individual conditions of use, supersedes the 
determinations (and withdraws the associated order) of no unreasonable 
risk for the conditions of use identified in the TSCA section 6(i)(1) 
no unreasonable risk order, and clarifies the lack of reliance on 
assumed use of PPE as part of the risk determination.
    These revisions do not alter any of the underlying technical or 
scientific information that informs the risk characterization, and as 
such the hazard, exposure, and risk characterization sections are not 
changed, except to statements about PPE assumptions in Section 2.3.1.3 
(Consideration of Engineering Controls and PPE) and Section 4.2.2 
(Occupational Inhalation Exposure Summary and PPE Use Determinations by 
OES). The discussion of the issues in this Notice and in the 
accompanying final revision to the risk determination supersede any 
conflicting statements in the prior executive summary, and Section 
2.3.1.3 and Section 4.2.2 from the August 2020 1-BP Risk Evaluation 
(Ref. 2) and the response to comments document (Ref. 11).
    The revised unreasonable risk determination for 1-BP includes 
additional explanation of how the risk evaluation characterizes the 
applicable OSHA requirements, or industry or sector best practices, and 
also clarifies that no additional analysis was done, and the risk 
determination is based on the risk characterization (Section 4) of the 
August 2020 1-BP Risk Evaluation (Ref. 2).

[[Page 77609]]

C. Will the revised risk determination be peer reviewed?

    The risk determination (Section 5 of the August 2020 1-BP Risk 
Evaluation (Ref. 2)) was not part of the scope of the Science Advisory 
Committee on Chemicals (SACC) peer review of the 1-BP risk evaluation. 
Thus, consistent with that approach, EPA did not conduct peer review of 
the final revised unreasonable risk determination for the 1-BP risk 
evaluation because no technical or scientific changes were made to the 
hazard or exposure assessments or the risk characterization.

V. Order Withdrawing Previous Order Regarding Unreasonable Risk 
Determinations for Certain Conditions of Use

    EPA is also issuing a new order to withdraw the TSCA Section 
6(i)(1) no unreasonable risk order issued in Section 5.4.1 of the 
August 2020 1-BP Risk Evaluation (Ref. 2). This final revised risk 
determination supersedes the condition of use-specific no unreasonable 
risk determinations in the August 2020 1-BP Risk Evaluation (Ref. 2). 
The order contained in Section 5.5 of the revised risk determination 
(Ref. 1) withdraws the TSCA section 6(i)(1) order contained in Section 
5.4.1 of the August 2020 1-BP Risk Evaluation (Ref. 2). Consistent with 
the statutory requirements of section 6(a), the Agency will propose 
risk management action to address the unreasonable risk determined in 
the 1-BP risk evaluation.

VI. References

    The following is a listing of the documents that are specifically 
referenced in this document. The docket includes these documents and 
other information considered by EPA, including documents that are 
referenced within the documents that are included in the docket, even 
if the referenced document is not physically located in the docket. For 
assistance in locating these other documents, please consult the person 
listed under FOR FURTHER INFORMATION CONTACT.

1. EPA. Unreasonable Risk Determination for 1-Bromopropane (1-BP). 
December 2022.
2. EPA. Risk Evaluation for 1-Bromopropane (1-BP). August 2020. EPA 
Document #740-R1-8013. https://www.regulations.gov/document/EPA-HQ-OPPT-2019-0235-0085.
3. Executive Order 13990. Protecting Public Health and the 
Environment and Restoring Science to Tackle the Climate Crisis. 
Federal Register. 86 FR 7037, January 25, 2021.
4. Executive Order 13985. Advancing Racial Equity and Support for 
Underserved Communities Through the Federal Government. Federal 
Register. 86 FR 7009, January 25, 2021.
5. Executive Order 14008. Tackling the Climate Crisis at Home and 
Abroad. Federal Register. 86 FR 7619, February 1, 2021.
6. Presidential Memorandum. Memorandum on Restoring Trust in 
Government Through Scientific Integrity and Evidence-Based 
Policymaking. Federal Register. 86 FR 8845, February 10, 2021.
7. EPA. Press Release; EPA Announces Path Forward for TSCA Chemical 
Risk Evaluations. June 2021. https://www.epa.gov/newsreleases/epa-announces-path-forward-tsca-chemical-risk-evaluations.
8. EPA. Proposed Rule; Procedures for Chemical Risk Evaluation Under 
the Amended Toxic Substances Control Act. Federal Register. 82 FR 
7562, January 19, 2017 (FRL-9957-75).
9. EPA. Final Rule; Procedures for Chemical Risk Evaluation Under 
the Amended Toxic Substances Control Act. Federal Register. 82 FR 
33726, July 20, 2017 (FRL-9964-38).
10. EPA. Response to Public Comments to the Revised Unreasonable 
Risk Determination; 1-Bromopropane (1-BP). December 2022.
11. EPA. Summary of External Peer Review and Public Comments and 
Disposition for 1-Bromopropane (1-BP). August 2020. Available at: 
https://www.regulations.gov/document/EPA-HQ-OPPT-2019-0235-0066.
12. Occupational Safety and Health Administration (OSHA). Top 10 
Most Frequently Cited Standards for Fiscal Year 2021 (Oct. 1, 2020, 
to Sept. 30, 2021). Accessed October 13, 2022. https://www.osha.gov/top10citedstandards.
13. OSHA. Permissible Exposure Limits--Annotated Tables. Accessed 
June 13, 2022. https://www.osha.gov/annotated-pels.

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

    Dated: December 13, 2022.
Michal Freedhoff,
Assistant Administrator, Office of Chemical Safety and Pollution 
Prevention.
[FR Doc. 2022-27439 Filed 12-16-22; 8:45 am]
BILLING CODE 6560-50-P


This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.