[Federal Register Volume 87, Number 242 (Monday, December 19, 2022)]
[Notices]
[Pages 77596-77602]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-27438]
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ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2016-0743; FRL-9943-02-OCSPP]
n-Methylpyrrolidone (NMP); Revision to Toxic Substances Control
Act (TSCA) Risk Determination; Notice of Availability
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
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SUMMARY: The Environmental Protection Agency (EPA) is announcing the
availability of the final revision to the risk determination for the n-
methylpyrrolidone (NMP) risk evaluation issued under the Toxic
Substances Control Act (TSCA). The revision to the NMP 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 NMP, 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described by OSHA as being ``outdated and inadequate for ensuring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
NMP), or because EPA finds unreasonable risk for purposes of TSCA
notwithstanding OSHA requirements. This revision supersedes the
condition of use-specific no unreasonable risk determinations in the
December 2020 NMP Risk Evaluation and withdraws the associated TSCA
order included in the December 2020 NMP Risk Evaluation.
ADDRESSES: The docket for this action, identified by docket
identification (ID) number EPA-HQ-OPPT-2016-0743, 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: Clara Hull, Office of Pollution
Prevention and Toxics (7404M), Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC 20460-0001; telephone number:
(202)
[[Page 77597]]
564-3954; 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 NMP, including NMP 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 NMP.
C. What action is EPA taking?
EPA is announcing the availability of the final revision to the
risk determination for the NMP risk evaluation issued under TSCA that
published in December 2020 (Ref. 1). In July 2022, EPA sought public
comment on the draft revisions (87 FR 39511, July 1, 2022). EPA
appreciates the public comments received on the draft revision to the
NMP risk determination. After review of these comments and
consideration of the specific circumstances of NMP, EPA concludes that
the Agency's risk determination for NMP 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 December 2020 NMP 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 11 conditions of use previously
determined not to present unreasonable risk which was included in
section 5.4.1 of the December 2020 NMP Risk Evaluation (Ref. 2).
This final revision to the NMP 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: three
additional conditions of use in addition to the original 26 drive the
unreasonable risk for NMP, and for five conditions of use, acute
effects in addition to chronic effects also drive the unreasonable risk
to workers. 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, and does not consider the revised risk determination to
constitute a final agency action at this point in time. Overall, 29
conditions of use out of 37 EPA evaluated drive the NMP whole chemical
unreasonable risk determination due to risks identified for human
health. The full list of the conditions of use evaluated for the NMP
TSCA risk evaluation is in Table 1-6 of the December 2020 NMP Risk
Evaluation (Ref. 2).
II. Background
A. Why is EPA re-issuing the risk determination for the NMP 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 NMP, 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 December 2020 NMP
Risk Evaluation (Ref. 2) and after considering comments received on a
draft revised risk determination for NMP, EPA has determined that
making an
[[Page 77598]]
unreasonable risk determination for NMP 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 NMP 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 NMP the exposure pathways that were or
could be regulated under another EPA administered statute were not
fully assessed as part of the final risk evaluation (see section 1.4.2
of the December 2020 NMP Risk Evaluation). For NMP, some exposure
pathways received only a screening-level analysis. During problem
formulation, EPA conducted a first-tier screening analysis for the
ambient air pathway to near-field populations downwind from industrial
and commercial facilities releasing NMP which indicated low risk. In
the December 2020 NMP Risk Evaluation EPA conducted a first-tier
analysis to estimate NMP surface water concentrations and did not
identify risks from incidental ingestion or dermal contact during
swimming. This resulted in the ambient air and drinking water pathways
for NMP not being fully assessed in the risk evaluation published in
December 2020. The goal of the recently-developed screening approach is
to provide a more robust assessment of these pathways for NMP and to
determine if there may be risks that were unaccounted for in the NMP
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 NMP.
This action pertains only to the risk determination for NMP. 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 NMP 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 NMP (87 FR
39511, July 1, 2022 (FRL-9943-01-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
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
[[Page 77599]]
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 NMP, EPA has
determined that a whole chemical approach is appropriate for NMP in
order to protect health and the environment. The whole chemical
approach is appropriate for NMP 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 and consumers and risk of irreversible health
effects (specifically developmental post implantation fetal loss and
reduced fertility and fecundity) associated with NMP 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 NMP 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 December 2020 NMP
Risk Evaluation (Ref. 2)) follow the issuance of a draft revision to
the TSCA NMP unreasonable risk determination (87 FR 39511, July 1,
2022) and the receipt of public comment. A response to comments
document is also being issued with the final revised unreasonable risk
determination for NMP (Ref. 10). The revisions to the unreasonable risk
determination are based on the existing risk characterization section
of the December 2020 NMP 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 NMP supersede any conflicting
statements in the December 2020 NMP 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 NMP as a whole chemical. Under the revised approach,
the ``whole chemical'' risk determination for NMP supersedes the no
unreasonable risk determinations for NMP 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 December 2020 NMP Risk Evaluation (Ref. 2).
C. What revision is EPA now making final about the use of PPE for the
NMP 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 chemically-resistant 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 December 2020 NMP Risk Evaluation (Ref. 2), EPA assumed,
based on reasonably available information, including public comment and
safety data sheets for NMP, that workers use PPE--specifically,
respirators with an APF 10 and gloves with a protection factor (PF)
ranging from 5 to 10--for all occupational conditions of use. In the
December 2020 NMP Risk Evaluation, EPA determined that there is
unreasonable risk to these workers for 25 of the 28 occupational COUs
even with this assumed PPE use.
EPA is revising the assumption for NMP 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 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 December 2020 NMP Risk Evaluation
[[Page 77600]]
(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
NMP 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 permissible exposure limit (PEL) (as is the case for NMP), 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 NMP 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 December 2020 NMP
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 NMP means that:
three conditions of use in addition to the original 26 drive the
unreasonable risk for NMP (industrial and commercial use in ink, toner,
and colorant products; industrial and commercial use in other uses
soldering materials; and industrial and commercial use in other uses in
fertilizer and other agricultural chemical manufacturing--processing
aids and solvents). Additionally, for five conditions of use, acute
effects in addition to chronic effects also drive the unreasonable risk
to workers (the five conditions of use are: processing for
incorporation into articles in paint additives and coating additives
not described by other codes in transportation equipment manufacturing;
industrial and commercial use in paints, coatings, and adhesive
removers; industrial and commercial use in paints and coatings in
lacquers, stains, varnishes, primers, and floor finishes, powder
coatings (surface preparation); industrial and commercial use paint
additives and coating additives in multiple manufacturing sectors; and
industrial and commercial use in adhesives and sealants including
binding agents, single component glues and adhesives, including
lubricant additives, two-component glues, and adhesives including some
resins). The finalized revision to the NMP 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 NMP?
NMP is a water-miscible, organic solvent that is often used as a
substitute for halogenated solvents. NMP exhibits a unique set of
physical and chemical properties that have proven useful in a range of
industrial, commercial, and consumer applications. NMP has a wide range
of uses, including in the production of paints and coatings, as a
solvent for cleaning and degreasing, and in the manufacture of
electronics. There are also a variety of consumer and commercial
products that contain NMP, such as adhesives and sealants, as well as
adhesive removers, automotive care products, and paints and coatings.
NMP is both manufactured domestically and imported into the United
States.
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 NMP presents an unreasonable risk to health
under the conditions of use. EPA's unreasonable risk determination for
NMP as a chemical substance is driven by risks associated with the
following conditions of use, considered singularly or in combination
with other exposures:
Manufacturing--Domestic manufacture;
Manufacturing--Import;
Processing as a reactant or intermediate in plastic
material and resin manufacturing and other non-incorporative
processing;
[[Page 77601]]
Processing for incorporation into a formulation, mixture,
or reaction product in multiple sectors;
Processing for incorporation into articles--in lubricants
and lubricant additives in machinery manufacturing;
Processing for incorporation into articles in paint
additives and coating additives not described by other codes in
transportation equipment manufacturing;
Processing for incorporation into articles as a solvent
(which become part of product formulation or mixture), including in
textiles, apparel, and leather manufacturing;
Processing for incorporation into articles in other
sectors, including in plastic product manufacturing;
Processing in recycling;
Processing for repackaging (wholesale and retail trade);
Industrial and commercial use in paints, coatings, and
adhesive removers;
Industrial and commercial use in paints and coatings in
lacquers, stains, varnishes, primers, and floor finishes, powder
coatings (surface preparation);
Industrial and commercial use in paint additives and
coating additives not described by other codes in computer and
electronic product manufacturing in electronic parts manufacturing;
Industrial and commercial use paint additives and coating
additives not described by other codes in computer and electronic
product manufacturing in semiconductor manufacturing;
Industrial and commercial use paint additives and coating
additives in multiple manufacturing sectors;
Industrial and commercial use as a solvent (for cleaning
or degreasing) in electrical equipment, appliance and component
manufacturing;
Industrial and commercial use as a solvent (for cleaning
or degreasing) in electrical equipment appliance and component
manufacturing in semiconductor manufacturing;
Industrial and commercial use in processing aids specific
to petroleum production in petrochemical manufacturing, in other uses
in oil and gas drilling, extraction, and support activities, and in
functional fluids (closed systems);
Industrial and commercial use in adhesives and sealants
including binding agents, single component glues and adhesives,
including lubricant additives, two-component glues, and adhesives
including some resins;
Industrial and commercial use in other uses in anti-freeze
and de-icing products, automotive care products, and lubricants and
greases;
Industrial and commercial use in metal products not
covered elsewhere and lubricant and lubricant additives including
hydrophilic coatings;
Industrial and commercial uses in other uses in laboratory
chemicals;
Industrial and commercial uses in other uses in lithium
ion battery manufacturing;
Industrial and commercial uses in other uses in cleaning
and furniture care products including wood cleaners and gasket
removers;
Industrial and commercial use in ink, toner, and colorant
products (printer ink; inks in writing equipment);
Industrial and commercial use in other uses in soldering
materials;
Industrial and commercial use in other uses in fertilizer
and other agricultural chemical manufacturing in processing aids and
solvents;
Consumer use in adhesives and sealants (glues and
adhesives including lubricant adhesives); and
Disposal.
The following conditions of use do not drive EPA's unreasonable
risk determination for NMP:
Distribution in commerce;
Consumer use in paint and coating removers;
Consumer use in adhesive removers;
Consumer use in paints and coatings in lacquers, stains,
varnishes, primers and floor finishes;
Consumer use in paint additives and coating additives not
described by other codes in paints and arts and crafts paints;
Consumer use in other uses in automotive car products;
Consumer use in other uses in cleaning and furniture care
products, including wood cleaners and gasket removers; and
Consumer use in other uses in lubricant and lubricant
additives, including hydrophilic coatings.
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
unreasonable risk, and does not consider the revised risk determination
for NMP 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 NMP 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 22 public comments on the July 1, 2022,
draft revised risk determination for NMP during the comment period that
ended August 1, 2022, of which 20 were unique and responsive to the
request for comments. Commenters included trade organizations, industry
stakeholders, environmental groups, and non-governmental health
advocacy organizations. 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 December 2020 NMP Risk Evaluation
A. Why is EPA revising the risk determination for the NMP risk
evaluation?
EPA is finalizing the revised risk determination for the NMP 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
NMP 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
December 2020 NMP Risk Evaluation (Ref. 2) pursuant to TSCA section
6(b). Under the revised determination (Ref. 1), EPA concludes that NMP,
as evaluated in the risk
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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 NMP 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 2.4.1.1
(Occupational Exposures Approach and Methodology) and 4.2.2 (Risk
Estimation for Worker Exposures for Occupational Use of NMP). 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 2.4.1.1 and section 4.2.2
from the December 2020 NMP Risk Evaluation (Ref. 2) and the response to
comments document (Ref. 11).
The revised unreasonable risk determination for NMP 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
December 2020 NMP Risk Evaluation (Ref. 2).
C. Will the revised risk determination be peer reviewed?
The risk determination (section 5 of the December 2020 NMP Risk
Evaluation (Ref. 2)) was not part of the scope of the Science Advisory
Committee on Chemicals (SACC) peer review of the NMP risk evaluation.
Thus, consistent with that approach, EPA did not conduct peer review of
the final revised unreasonable risk determination for the NMP 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
December 2020 NMP Risk Evaluation (Ref. 2). This final revised risk
determination supersedes the condition of use-specific no unreasonable
risk determinations in the December 2020 NMP 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 December 2020 NMP 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 NMP 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 n-Methylpyrrolidone
(NMP). December 2022.
2. EPA. Risk Evaluation for n-Methylpyrrolidone (NMP). December
2020. EPA Document #740-R-18-009. https://www.regulations.gov/document/EPA-HQ-OPPT-2019-0236-0081.
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; n-Methylpyrrolidone (NMP). December 2022.
11. EPA. Summary of External Peer Review and Public Comments and
Disposition for n-Methylpyrrolidone (NMP). December 2020. Available
at: https://www.regulations.gov/document/EPA-HQ-OPPT-2019-0236-0082.
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. 2022-27438 Filed 12-16-22; 8:45 am]
BILLING CODE 6560-50-P