[Federal Register Volume 90, Number 77 (Wednesday, April 23, 2025)]
[Notices]
[Pages 17032-17036]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2025-06934]


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DEPARTMENT OF COMMERCE

International Trade Administration

[C-583-880]


Certain Monomers and Oligomers From Taiwan: Initiation of 
Countervailing Duty Investigation

AGENCY: Enforcement and Compliance, International Trade Administration, 
Department of Commerce.

DATES: Applicable April 16, 2025.

FOR FURTHER INFORMATION CONTACT: Suresh Maniam, Office I, AD/CVD 
Operations, Enforcement and Compliance, International Trade 
Administration, U.S. Department of Commerce, 1401 Constitution Avenue 
NW, Washington, DC 20230; telephone: (202) 482-1603.

SUPPLEMENTARY INFORMATION:

The Petition

    On March 27, 2025, the U.S. Department of Commerce (Commerce) 
received a countervailing duty (CVD) petition concerning imports of 
certain monomers and oligomers (monomers and oligomers) from Taiwan, 
filed in proper form on behalf of Arkema, Inc. (the petitioner), a 
domestic producer of monomers and oligomers.\1\ The CVD Petition was 
accompanied by antidumping duty (AD) petitions concerning imports of 
monomers and oligomers from the Republic of Korea and Taiwan.\2\
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    \1\ See Petitioner's Letter, ``Petition for the Imposition of 
Antidumping and Countervailing Duties,'' dated March 27, 2025 
(Petition).
    \2\ Id.
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    Between March 31 and April 8, 2025, Commerce requested supplemental 
information pertaining to certain aspects of the Petition in 
supplemental questionnaires.\3\ Between April 4 and 11, 2025, the 
petitioner filed timely responses to these requests for additional 
information.\4\
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    \3\ See Commerce's Letters, ``Supplemental Questions,'' dated 
March 31, 2025 (First General Issues Questionnaire) and 
``Supplemental Questions,'' dated April 2, 2025; see also 
Memorandum, ``Phone Call with Counsel to the Petitioner,'' dated 
April 8, 2025 (April 8 Memorandum).
    \4\ See Petitioner's Letters, ``Response to General Issues and 
Injury Supplemental Questions,'' dated April 4, 2025 (First General 
Issues Supplement); ``Response to Volume III Supplemental 
Questions,'' dated April 8, 2025; and ``Response to Supplemental 
Questions,'' dated April 11, 2025 (Second General Issues 
Supplement).
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    In accordance with section 702(b)(1) of the Tariff Act of 1930, as 
amended (the Act), the petitioner alleges that the Taiwan Authorities 
(TA) are providing countervailable subsidies, within the meaning of 
sections 701 and 771(5) of the Act, to producers of monomers and 
oligomers in Taiwan, and that such imports are materially injuring, or 
threatening material injury to, the domestic industry producing 
monomers and oligomers in the United States. Consistent with section 
702(b)(1) of the Act and 19 CFR 351.202(b), for those alleged programs 
on which we are initiating a CVD investigation, the Petition was 
accompanied by information reasonably available to the petitioner 
supporting its allegations.
    Commerce finds that the petitioner filed the Petition on behalf of 
the domestic industry, because the petitioner is an interested party, 
as defined in section 771(9)(C) of the Act. Commerce also finds that 
the petitioner demonstrated sufficient industry support with respect to 
the initiation of the requested CVD investigation.\5\
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    \5\ See section on ``Determination of Industry Support for the 
Petition,'' infra.
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Period of Investigation (POI)

    Because the Petition was filed on March 27, 2025, the POI is 
January 1, 2024, through December 31, 2024.\6\
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    \6\ See 19 CFR 351.204(b)(2).
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Scope of the Investigation

    The product covered by this investigation is monomers and oligomers 
from Taiwan. For a full description of the scope of this investigation, 
see the appendix to this notice.

Comments on the Scope of the Investigation

    On March 31 and April 8, 2025, Commerce requested information and 
clarification from the petitioner regarding the proposed scope to 
ensure that the scope language in the Petitions is an accurate 
reflection of the products for which the domestic industry is seeking 
relief.\7\ Between March 31 and April 11, 2025, the petitioner provided 
clarifications and revised the scope.\8\ The description of merchandise 
covered by this investigation, as described in the appendix to this 
notice, reflects these clarifications.
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    \7\ See First General Issues Questionnaire; see also April 8 
Memorandum.
    \8\ See First General Issues Supplement at 9-11 and Exhibits 
Supp-I-2 and Supp-I-3; see also Second General Issues Supplement at 
1-6 and Exhibits Supp2-I-1 through Supp2-I-3. On March 31, 2025, the 
petitioner also filed an amendment containing technical 
modifications to the scope in the Petition. See Petitioner's Letter, 
``Amendment to Petition,'' dated March 31, 2025.
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    As discussed in the Preamble to Commerce's regulations, we are 
setting aside a period for interested parties to raise issues regarding 
product coverage (i.e., scope).\9\ Commerce will consider all scope 
comments received from interested parties and, if necessary, will 
consult with interested parties prior to the issuance of the 
preliminary determination. If scope comments include factual 
information, all such factual information should be limited to public 
information.\10\ To facilitate preparation of its questionnaires, 
Commerce requests that scope comments be submitted by 5:00 p.m. Eastern 
Time (ET) on May 6, 2025, which is 20 calendar days from the signature 
date of this notice. Any rebuttal comments, which may include

[[Page 17033]]

factual information, and should also be limited to public information, 
must be filed by 5:00 p.m. ET on May 16, 2025, which is 10 calendar 
days from the initial comment deadline.
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    \9\ See Antidumping Duties; Countervailing Duties, Final Rule, 
62 FR 27296, 27323 (May 19, 1997) (Preamble); see also 19 CFR 
351.312.
    \10\ See 19 CFR 351.102(b)(21) (defining ``factual 
information'').
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    Commerce requests that any factual information that parties 
consider relevant to the scope of this investigation be submitted 
during that period. However, if a party subsequently finds that 
additional factual information pertaining to the scope of the 
investigation may be relevant, the party must contact Commerce and 
request permission to submit the additional information. All scope 
comments must be filed simultaneously on the records of the concurrent 
AD and CVD investigations.

Filing Requirements

    All submissions to Commerce must be filed electronically via 
Enforcement and Compliance's Antidumping Duty and Countervailing Duty 
Centralized Electronic Service System (ACCESS), unless an exception 
applies.\11\ An electronically filed document must be received 
successfully in its entirety by the time and date it is due.
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    \11\ See Antidumping and Countervailing Duty Proceedings: 
Electronic Filing Procedures; Administrative Protective Order 
Procedures, 76 FR 39263 (July 6, 2011); see also Enforcement and 
Compliance; Change of Electronic Filing System Name, 79 FR 69046 
(November 20, 2014), for details of Commerce's electronic filing 
requirements, effective August 5, 2011. Information on using ACCESS 
can be found at https://access.trade.gov/help.aspx and a handbook 
can be found at https://access.trade.gov/help/Handbook_on_Electronic_Filing_Procedures.pdf.
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Consultations

    Pursuant to sections 702(b)(4)(A)(i) and (ii) of the Act, Commerce 
notified the TA of the receipt of the Petition and provided an 
opportunity for consultations with respect to the Petition.\12\ 
Commerce held consultations with the TA on April 14, 2025.\13\
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    \12\ See Commerce's Letter, ``Invitation for Consultations to 
Discuss the Countervailing Duty Petition,'' dated March 28, 2025.
    \13\ See Memorandum, ``Consultations with the Government of 
Taiwan,'' dated April 14, 2025; see also TA's Letter, ``GOT's 
Submission,'' dated April 14, 2025.
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    Additionally, given the nature of certain subsidy programs alleged 
in the Petition, on March 28, 2025, Commerce issued a letter to the 
Government of the People's Republic of China (GOC), providing the GOC 
with the opportunity to meet with Commerce officials.\14\ The GOC did 
not request to meet with Commerce officials.\15\
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    \14\ See Commerce's Letter, ``Alleged Transnational Subsidy 
Programs,'' dated March 28, 2025.
    \15\ The GOC submitted comments on the CVD petition. See GOC's 
Letter, ``Comments on the Countervailing Duty Petition,'' dated 
April 11, 2025.
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Determination of Industry Support for the Petition

    Section 702(b)(1) of the Act requires that a petition be filed on 
behalf of the domestic industry. Section 702(c)(4)(A) of the Act 
provides that a petition meets this requirement if the domestic 
producers or workers who support the petition account for: (i) at least 
25 percent of the total production of the domestic like product; and 
(ii) more than 50 percent of the production of the domestic like 
product produced by that portion of the industry expressing support 
for, or opposition to, the petition. Moreover, section 702(c)(4)(D) of 
the Act provides that, if the petition does not establish support of 
domestic producers or workers accounting for more than 50 percent of 
the total production of the domestic like product, Commerce shall: (i) 
poll the industry or rely on other information in order to determine if 
there is support for the petition, as required by subparagraph (A); or 
(ii) determine industry support using a statistically valid sampling 
method to poll the ``industry.''
    Section 771(4)(A) of the Act defines the ``industry'' as the 
producers as a whole of a domestic like product. Thus, to determine 
whether a petition has the requisite industry support, the statute 
directs Commerce to look to producers and workers who produce the 
domestic like product. The U.S. International Trade Commission (ITC), 
which is responsible for determining whether ``the domestic industry'' 
has been injured, must also determine what constitutes a domestic like 
product in order to define the industry. While both Commerce and the 
ITC apply the same statutory definition regarding the domestic like 
product,\16\ they do so for different purposes and pursuant to a 
separate and distinct authority. In addition, Commerce's determination 
is subject to limitations of time and information. Although this may 
result in different definitions of the like product, such differences 
do not render the decision of either agency contrary to law.\17\
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    \16\ See section 771(10) of the Act.
    \17\ See USEC, Inc. v. United States, 132 F. Supp. 2d 1, 8 (CIT 
2001) (citing Algoma Steel Corp., Ltd. v. United States, 688 F. 
Supp. 639, 644 (CIT 1988), aff'd Algoma Steel Corp., Ltd. v. United 
States, 865 F.2d 240 (Fed. Cir. 1989)).
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    Section 771(10) of the Act defines the domestic like product as ``a 
product which is like, or in the absence of like, most similar in 
characteristics and uses with, the article subject to an investigation 
under this title.'' Thus, the reference point from which the domestic 
like product analysis begins is ``the article subject to an 
investigation'' (i.e., the class or kind of merchandise to be 
investigated, which normally will be the scope as defined in the 
petition).
    With regard to the domestic like product, the petitioner does not 
offer a definition of the domestic like product distinct from the scope 
of the investigation.\18\ Based on our analysis of the information 
submitted on the record, we have determined that monomers and 
oligomers, as defined in the scope, constitute a single domestic like 
product, and we have analyzed industry support in terms of that 
domestic like product.\19\
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    \18\ See Petition at Volume I (pages I-10 through I-12); see 
also First General Issues Supplement at 12-17 and Exhibit I-Supp-7; 
and Second General Issues Supplement at 6-7.
    \19\ For a discussion of the domestic like product analysis as 
applied to this case and information regarding industry support, see 
Checklist, ``Countervailing Duty Investigation Initiation Checklist: 
Certain Monomers and Oligomers from Taiwan,'' dated concurrently 
with, and hereby adopted by, this notice (Taiwan CVD Initiation 
Checklist), at Attachment II, Analysis of Industry Support for the 
Antidumping and Countervailing Duty Petitions Covering Certain 
Monomers and Oligomers from the Republic of Korea and Taiwan 
(Attachment II). This checklist is on file electronically via 
ACCESS.
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    In determining whether the petitioner has standing under section 
702(c)(4)(A) of the Act, we considered the industry support data 
contained in the Petition with reference to the domestic like product 
as defined in the ``Scope of the Investigation,'' in the appendix to 
this notice. To establish industry support, the petitioner provided its 
own 2024 production of the domestic like product and compared this to 
the estimated total production of the domestic like product in 2024 by 
the entire domestic industry.\20\ We relied on data provided by the 
petitioner for purposes of measuring industry support.\21\
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    \20\ For further discussion, see Attachment II of the Taiwan CVD 
Initiation Checklist.
    \21\ Id.
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    Our review of the data provided in the Petition, the First General 
Issues Supplement, and other information readily available to Commerce 
indicates that the petitioner has established industry support for the 
Petition.\22\ First, the Petition established support from domestic 
producers (or workers) accounting for more than 50 percent of the total 
production of the domestic like product and, as such, Commerce is not 
required to take further action in order to evaluate industry support 
(e.g., polling).\23\ Second, the domestic producers (or workers) have 
met the statutory criteria for industry support

[[Page 17034]]

under section 702(c)(4)(A)(i) of the Act because the domestic producers 
(or workers) who support the Petition account for at least 25 percent 
of the total production of the domestic like product.\24\ Finally, the 
domestic producers (or workers) have met the statutory criteria for 
industry support under section 702(c)(4)(A)(ii) of the Act because the 
domestic producers (or workers) who support the Petition account for 
more than 50 percent of the production of the domestic like product 
produced by that portion of the industry expressing support for, or 
opposition to, the Petition.\25\ Accordingly, Commerce determines that 
the Petition was filed on behalf of the domestic industry within the 
meaning of section 702(b)(1) of the Act.\26\
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    \22\ Id.
    \23\ Id.; see also section 702(c)(4)(D) of the Act.
    \24\ See Attachment II of the Taiwan CVD Initiation Checklist.
    \25\ Id.
    \26\ Id.
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Injury Test

    Because Taiwan is a ``Subsidies Agreement Country'' within the 
meaning of section 701(b) of the Act, section 701(a)(2) of the Act 
applies to this investigation. Accordingly, the ITC must determine 
whether imports of the subject merchandise from Taiwan materially 
injure, or threaten material injury to, a U.S. industry.

Allegations and Evidence of Material Injury and Causation

    The petitioner alleges that imports of the subject merchandise are 
benefiting from countervailable subsidies and that such imports are 
causing, or threaten to cause, material injury to the U.S. industry 
producing the domestic like product. In addition, the petitioner 
alleges that subject imports from Taiwan exceed the negligibility 
threshold provided for under section 771(24)(A) of the Act.\27\
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    \27\ For further information regarding negligibility and the 
injury allegation, see Taiwan CVD Initiation Checklist at Attachment 
III, Analysis of Allegations and Evidence of Material Injury and 
Causation for the Antidumping Duty and Countervailing Duty Petitions 
Covering Certain Monomers and Oligomers from the Republic of Korea 
and Taiwan (Attachment III).
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    The petitioner contends that the industry's injured condition is 
illustrated by a significant volume of subject imports; reduced market 
share; underselling and price depression and/or suppression; declines 
in production, capacity, capacity utilization, and U.S. shipments; 
declines in profitability, operating income, net income, cash flow, 
return on assets, capital expenditures, and research and development 
expenditures; and lost sales and revenues.\28\ We assessed the 
allegations and supporting evidence regarding material injury, threat 
of material injury, causation, as well as negligibility, and we have 
determined that these allegations are properly supported by adequate 
evidence and meet the statutory requirements for initiation.\29\
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    \28\ Id.
    \29\ Id.
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Initiation of CVD Investigation

    Based upon the examination of the Petition and supplemental 
responses, we find that they meet the requirements of section 702 of 
the Act. Therefore, we are initiating a CVD investigation to determine 
whether imports of monomers and oligomers from Taiwan benefit from 
countervailable subsidies conferred by the TA. In accordance with 
section 703(b)(1) of the Act and 19 CFR 351.205(b)(1), unless 
postponed, we will make our preliminary determination no later than 65 
days after the date of this initiation.
    Based on our review of the Petition, we find that there is 
sufficient information to initiate a CVD investigation on 38 of the 43 
programs alleged by the petitioner. For a full discussion of the basis 
for our decision to initiate on each program, see the Taiwan CVD 
Initiation Checklist. A public version of the initiation checklist for 
this investigation is available on ACCESS.

Respondent Selection

    In the Petition, the petitioner identified seven Companies in 
Taiwan as producers/exporters of monomers and oligomers.\30\ Commerce 
intends to follow its standard practice in CVD investigations and 
calculate company-specific subsidy rates in this investigation. In the 
event that Commerce determines that the number of companies is large 
and it cannot individually examine each company based on Commerce's 
resources, Commerce intends to select mandatory respondents based on 
U.S. Customs and Border Protection (CBP) entry data for U.S. imports 
under the appropriate Harmonized Tariff Schedule of the United States 
(HTSUS) subheading(s) listed in the ``Scope of the Investigation'' in 
the appendix.
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    \30\ See Petitions at Volume I (pages I-8 and I-9 and Exhibit I-
7).
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    On April 15, 2025, Commerce released CBP data on imports of 
monomers and oligomers from Taiwan under administrative protective 
order (APO) to all parties with access to information protected by APO 
and indicated that interested parties wishing to comment on CBP data 
and/or respondent selection must do so within three business days of 
the publication date of the notice of initiation of this 
investigation.\31\ Comments must be filed electronically using ACCESS. 
An electronically-filed document must be received successfully in its 
entirety via ACCESS by 5 p.m. ET on the specified deadline. Commerce 
will not accept rebuttal comments regarding the CBP data or respondent 
selection.
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    \31\ See Memorandum, ``Release of U.S. Customs and Border 
Protection Entry Data,'' dated April 15, 2025.
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    Interested parties must submit applications for disclosure under 
APO in accordance with 19 CFR 351.305(b). Instructions for filing such 
applications may be found on Commerce's website at https://www.trade.gov/administrative-protective-orders.

Distribution of a Copy of the Petition

    In accordance with section 702(b)(4)(A) of the Act and 19 CFR 
351.202(f), a copy of the public version of the Petition has been 
provided to the TA via ACCESS. To the extent practicable, we will 
attempt to provide a copy of the public version of the Petition to each 
exporter named in the Petition, as provided under 19 CFR 351.203(c)(2).

ITC Notification

    Commerce will notify the ITC of its initiation, as required by 
section 702(d) of the Act.

Preliminary Determination by the ITC

    The ITC will preliminarily determine, within 45 days after the date 
on which the Petition was filed, whether there is a reasonable 
indication that imports of monomers and oligomers from Taiwan are 
materially injuring, or threatening material injury to, a U.S. 
industry.\32\ A negative ITC determination will result in the 
investigation being terminated.\33\ Otherwise, this CVD investigation 
will proceed according to statutory and regulatory time limits.
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    \32\ See section 703(a)(1) of the Act.
    \33\ Id.
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Submission of Factual Information

    Factual information is defined in 19 CFR 351.102(b)(21) as: (i) 
evidence submitted in response to questionnaires; (ii) evidence 
submitted in support of allegations; (iii) publicly available 
information to value factors of production under 19 CFR 351.408(c) or 
to measure the adequacy of remuneration under 19 CFR 351.511(a)(2); 
(iv) evidence placed on the record by Commerce; and (v)

[[Page 17035]]

evidence other than factual information described in (i)-(iv). Section 
351.301(b) of Commerce's regulations requires any party, when 
submitting factual information, to specify under which subsection of 19 
CFR 351.102(b)(21) the information is being submitted \34\ and, if the 
information is submitted to rebut, clarify, or correct factual 
information already on the record, to provide an explanation 
identifying the information already on the record that the factual 
information seeks to rebut, clarify, or correct.\35\ Time limits for 
the submission of factual information are addressed in 19 CFR 351.301, 
which provides specific time limits based on the type of factual 
information being submitted. Interested parties should review the 
regulations prior to submitting factual information in this 
investigation.
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    \34\ See 19 CFR 351.301(b).
    \35\ See 19 CFR 351.301(b)(2).
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Extensions of Time Limits

    Parties may request an extension of time limits before the 
expiration of a time limit established under 19 CFR 351.301, or as 
otherwise specified by Commerce. In general, an extension request will 
be considered untimely if it is filed after the expiration of the time 
limit established under 19 CFR 351.301, or as otherwise specified by 
Commerce.\36\ For submissions that are due from multiple parties 
simultaneously, an extension request will be considered untimely if it 
is filed after 10 a.m. ET on the due date. Under certain circumstances, 
Commerce may elect to specify a different time limit by which extension 
requests will be considered untimely for submissions which are due from 
multiple parties simultaneously. In such a case, we will inform parties 
in a letter or memorandum of the deadline (including a specified time) 
by which extension requests must be filed to be considered timely. An 
extension request must be made in a separate, standalone submission; 
under limited circumstances we will grant untimely filed requests for 
the extension of time limits, where we determine, based on 19 CFR 
351.302, that extraordinary circumstances exist. Parties should review 
Commerce's regulations concerning the extension of time limits and the 
Time Limits Final Rule prior to submitting factual information in this 
investigation.\37\
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    \36\ See 19 CFR 351.302.
    \37\ See 19 CFR 351.301; see also Extension of Time Limits; 
Final Rule, 78 FR 57790 (September 20, 2013) (Time Limits Final 
Rule), available at https://www.gpo.gov/fdsys/pkg/FR-2013-09-20/html/2013-22853.htm.
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Certification Requirements

    Any party submitting factual information in an AD or CVD proceeding 
must certify to the accuracy and completeness of that information.\38\ 
Parties must use the certification formats provided in 19 CFR 
351.303(g).\39\ Commerce intends to reject factual submissions if the 
submitting party does not comply with the applicable certification 
requirements.
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    \38\ See section 782(b) of the Act.
    \39\ See Certification of Factual Information to Import 
Administration During Antidumping and Countervailing Duty 
Proceedings, 78 FR 42678 (July 17, 2013) (Final Rule); see also 
frequently asked questions regarding the Final Rule, available at 
https://enforcement.trade.gov/tlei/notices/factual_info_final_rule_FAQ_07172013.pdf.
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Notification to Interested Parties

    Interested parties must submit applications for disclosure under 
APO in accordance with 19 CFR 351.305. Parties wishing to participate 
in this investigation should ensure that they meet the requirements of 
19 CFR 351.103(d) (e.g., by filing the required letters of appearance). 
Note that Commerce has amended certain of its requirements pertaining 
to the service of documents in 19 CFR 351.303(f).\40\
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    \40\ See Administrative Protective Order, Service, and Other 
Procedures in Antidumping and Countervailing Duty Proceedings, 88 FR 
67069 (September 29, 2023).
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    This notice is issued and published pursuant to sections 702 and 
777(i) of the Act, and 19 CFR 351.203(c).

    Dated: April 16, 2025.
Christopher Abbott,
Deputy Assistant Secretary for Policy and Negotiations, performing the 
non-exclusive functions and duties of the Assistant Secretary for 
Enforcement and Compliance.

Appendix

Scope of the Investigation

    The products subject to this investigation are certain 
multifunctional acrylate and methacrylate monomers, and acrylated 
bisphenol-A epoxy based oligomers (collectively, certain monomers 
and oligomers or CMOs) that are derived from chemical reactions 
involving the use of acrylic or methacrylic acid. Products within 
the scope are listed below and have the following Chemical Abstracts 
Service (CAS) numbers:

------------------------------------------------------------------------
           CAS No.                 Description        Molecular formula
------------------------------------------------------------------------
109-16-0....................  Triethylene glycol    C14H22O6.
                               dimethacrylate
                               (TEGDMA).
13048-33-4..................  1,6-hexanediol        C12H18O4.
                               diacrylate (HDDA).
42978-66-5..................  Tripropylene glycol   C15H24O6.
                               diacrylate (TPGDA).
3290-92-4...................  Trimethylolpropane    C18H26O6.
                               trimethacrylate
                               (TMPTMA).
15625-89-5..................  Trimethylolpropane    C15H20O6.
                               triacrylate (TMPTA).
28961-43-5..................  Ethoxylated           (C2H4O)n(C2H4O)n(C2H
                               trimethylol-propane   4O)nC15H20O6.
                               triacrylate
                               (EOTMPTA).
57472-68-1..................  Dipropylene glycol    C12H18O5.
                               diacrylate (DPGDA).
55818-57-0..................  Bisphenol-A-          (C15H16O2[middot]C3H
                               epichlorohydrin       5ClO)x[middot]xC3H4
                               copolymer acrylate    O2.
                               (EPOXY ACRYLATE).
------------------------------------------------------------------------

    The monomers are generally known as multifunctional acrylates 
(MFAs) or multifunctional methacrylates (MFMAs) depending on whether 
the functional groups are acrylate or methacrylate. The monomers 
generally contain stabilizers/inhibitors, which include but are not 
limited to Hydroquinone, Methyl Hydroquinone, and Butylated Hydroxy 
Toluene. The monomers are either difunctional or trifunctional 
(having 2 or 3 functional groups/molecule), have viscosities of 9 to 
15 centipoise (cPs) at 25 degrees Celsius (if difunctional) or 44 to 
110 cPs at 25 degrees Celsius (if trifunctional), have (meth) 
acrylate equivalent weights (molecular weight per number of 
functional groups) between 99 and 158 and molecular weights between 
226 and 472 grams per mol.
    The acrylated bisphenol-A epoxy based oligomer is commonly 
referred to as epoxy acrylate or acrylated epoxy. In contrast to 
epoxy resin, the main characteristic of the epoxy acrylate oligomer 
is that it contains acrylate functional groups which make them 
curable by free-radical polymerization. The epoxy acrylate has a 
molecular weight between 508 to 536 grams per mol and a viscosity of 
2400 to 3600 cPs at 65 degrees Celsius. The epoxy acrylate generally 
contains stabilizers/inhibitors, which include but are not limited 
to Hydroquinone, Methyl Hydroquinone, and Butylated Hydroxy Toluene.
    Certain monomers and oligomers are subject to the scope even if 
an in-scope monomer or oligomer is blended or mixed with one or more 
other in-scope monomers or oligomers.
    Certain monomers and oligomers in any blend or mixture are also 
subject to the scope, so long as the blend or mixture

[[Page 17036]]

contains no less than 20 percent by weight of in-scope CMOs.
    The scope includes merchandise matching the above description 
that has been processed in a third country, including by 
commingling, diluting, introducing, or removing ingredients, or 
performing any other processing that would not otherwise remove the 
merchandise from the scope of the investigation if performed in the 
subject country.
    The scope also includes CMOs that are commingled, mixed or 
blended with in-scope product from sources not subject to this 
investigation.
    Only the subject component(s) of such blends, mixtures or 
commingled products described above is covered by the scope of this 
investigation. Subject merchandise contained in a blended, mixed or 
commingled product described above will not have undergone a 
chemical reaction as a result of being blended, mixed or commingled.
    Notwithstanding the above, specifically excluded from the scope 
are downstream products, including but not limited to, inks, 
coatings and overprint varnishes. For purposes of this exclusion, 
the downstream product requires only the application of energy to be 
cured, e.g., inks or varnish applied to packaging, coatings applied 
to wood flooring, etc. The energy source required to cure the 
downstream product to its substrate can be thermal, ultraviolet 
radiation, visible light, electron beam radiation, or infrared 
radiation.
    This merchandise is currently classifiable under Harmonized 
Tariff Schedule of the United States (HTSUS) subheadings 
2916.12.5050, 2916.14.2050, 3824.99.2900, 3907.29.0000 and 
3907.30.0000. Subject merchandise may also be entered under 
subheadings 2916.12.1000 and 3824.99.9397. The HTSUS subheadings and 
CAS registry numbers are provided for convenience and customs 
purposes only; the written description of the scope is dispositive.

[FR Doc. 2025-06934 Filed 4-22-25; 8:45 am]
BILLING CODE 3510-DS-P