What This Bill Does
This bill adds specific fentanyl-related substances to the list of Schedule I controlled substances (drugs with no approved medical use and high abuse potential). It also creates a process for removing or rescheduling these substances if they are found to have no abuse potential, and it streamlines how researchers can register to study controlled substances.
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Who It Affects
- Researchers studying controlled substances
- The Attorney General (who enforces drug laws)
- The Secretary of Health and Human Services
- Anyone possessing the newly listed fentanyl-related substances
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Key Provisions
- Five specific fentanyl-related substances are added to Schedule I controlled substances: isobutyryl fentanyl, para-methoxybutyrylfentanyl, valeryl fentanyl, cyclopentyl fentanyl, and para-chloroisobutyryl fentanyl. (Sec. 2)
- Any substance that is chemically similar to fentanyl through specific modifications to its chemical structure is automatically classified as a Schedule I controlled substance, unless the substance is specifically exempted or listed in another schedule. (Sec. 2)
- The Secretary of Health and Human Services can petition the Attorney General to remove a fentanyl-related substance from Schedule I if it has no abuse potential. The Attorney General must rule within 90 days of receiving the petition. (Sec. 3)
- Researchers already registered to study one controlled substance can conduct research on a newly added Schedule I substance at the same location under a single registration, provided they notify the Attorney General of all research sites on a contiguous campus. (Sec. 4)
- Researchers registered to study controlled substances can conduct certain activities like creating extracts, oils, or solutions without obtaining a separate manufacturing registration, as long as they use small quantities and follow their approved research plan. (Sec. 4)
- The Attorney General does not need to conduct a new inspection when a registered researcher applies to study a second controlled substance that is in the same schedule or a higher numerical schedule. (Sec. 4)
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What Changes
If this bill becomes law, possessing, manufacturing, or distributing the five named fentanyl-related substances and any chemically similar fentanyl-related substances will be illegal under federal law unless specifically exempted. This makes violations subject to the same criminal penalties as other Schedule I drugs.
Researchers will face fewer regulatory barriers. They can work with multiple controlled substances under one registration on the same campus and can perform processing activities without separate manufacturing licenses. The Attorney General will have clear timelines to approve or deny removal requests for fentanyl-related substances.
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Important Definitions
- **Schedule I controlled substances**: Drugs classified by law as having no currently accepted medical use in the United States and a high potential for abuse.
- **Fentanyl-related substances**: Includes five specifically named drugs plus any substance structurally related to fentanyl through specific chemical modifications, such as replacing parts of the molecule or substituting groups of atoms.
- **Isomers**: Different chemical compounds that have the same atoms arranged in different patterns (a chemistry term).
- **Contiguous campus**: A single connected piece of land where a university or research facility operates.
- **Diversion**: Illegal transfer of controlled substances from their intended medical or research use to illegal use.
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Effective Date
Not specified in bill text
I
118TH CONGRESS
1ST SESSION H. R. 1758
To amend the Controlled Substances Act to list fentanyl-related substances
as schedule I controlled substances.
IN THE HOUSE OF REPRESENTATIVES
MARCH 23, 2023
Mr. LUETKEMEYER (for himself, Mrs. HINSON, Mr. BACON, Mr. DESJARLAIS,
and Mr. EZELL) introduced the following bill; which was referred to the
Committee on Energy and Commerce, and in addition to the Committee
on the Judiciary, for a period to be subsequently determined by the
Speaker, in each case for consideration of such provisions as fall within
the jurisdiction of the committee concerned
A BILL
To amend the Controlled Substances Act to list fentanyl-
related substances as schedule I controlled substances.
Be it enacted by the Senate and House of Representa-
1
tives of the United States of America in Congress assembled,
2
SECTION 1. SHORT TITLE.
3
This Act may be cited as the ‘‘Stopping Illicit
4
Fentanyl Trafficking Act of 2023’’ or the ‘‘SIFT Act of
5
2023’’.
6
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SEC. 2. FENTANYL-RELATED SUBSTANCES.
1
Section 202(c) of the Controlled Substances Act (21
2
U.S.C. 812) is amended—
3
(1) by adding at the end of subsection (b) of
4
Schedule I the following:
5
‘‘(23) Isobutyryl fentanyl.
6
‘‘(24) Para-Methoxybutyrylfentanyl.
7
‘‘(25) Valeryl fentanyl.
8
‘‘(26) Cyclopentyl fentanyl.
9
‘‘(27) Para-Chloroisobutyryl fentanyl.’’; and
10
(2) by adding at the end of Schedule I the fol-
11
lowing:
12
‘‘(e)(1) Unless specifically exempted or unless listed
13
in another schedule, any material, compound, mixture, or
14
preparation which contains any quantity of fentanyl-re-
15
lated substances, or which contains their salts, isomers,
16
and salts of isomers whenever the existence of such salts,
17
isomers, and salts of isomers is possible within the specific
18
chemical designation.
19
‘‘(2) In paragraph (1), the term ‘fentanyl-related sub-
20
stances’ includes the following:
21
‘‘(A) Any substance that is structurally related
22
to fentanyl by one or more of the following modifica-
23
tions:
24
‘‘(i) By replacement of the phenyl portion
25
of the phenethyl group by any monocycle,
26
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•HR 1758 IH
whether or not further substituted in or on the
1
monocycle.
2
‘‘(ii) By substitution in or on the phenethyl
3
group with alkyl, alkenyl, alkoxy, hydroxy, halo,
4
haloalkyl, amino or nitro groups.
5
‘‘(iii) By substitution in or on the piper-
6
idine ring with alkyl, alkenyl, alkoxy, ester,
7
ether, hydroxy, halo, haloalkyl, amino or nitro
8
groups.
9
‘‘(iv) By replacement of the aniline ring
10
with any aromatic monocycle whether or not
11
further substituted in or on the aromatic mono-
12
cycle.
13
‘‘(v) By replacement of the N-propionyl
14
group by another acyl group.
15
‘‘(B) 4′-Methyl acetyl fentanyl.
16
‘‘(C) Crotonyl fentanyl.
17
‘‘(D) 2′-Fluoro ortho-fluorofentanyl.
18
‘‘(E) Ortho-Methyl acetylfentanyl.
19
‘‘(F) Thiofuranyl fentanyl.
20
‘‘(G) Ortho-Fluorobutyryl fentanyl.
21
‘‘(H) Ortho-Fluoroacryl fentanyl.
22
‘‘(I) Beta-Methyl fentanyl.
23
‘‘(J) Phenyl fentanyl.
24
‘‘(K) Para-Methylfentanyl.
25
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•HR 1758 IH
‘‘(L) Beta′-Phenyl fentanyl.
1
‘‘(M) Benzodioxole fentanyl.’’.
2
SEC. 3. REMOVAL FROM SCHEDULE I(e) OF FENTANYL-RE-
3
LATED SUBSTANCES.
4
Section 201 of the Controlled Substances Act (21
5
U.S.C. 811) is amended by adding at the end the following
6
new subsection:
7
‘‘(k)(1) If the Secretary finds, based on the factors
8
specified in paragraph (4), that a substance listed in
9
schedule I(e) has no potential for abuse, the Secretary
10
shall—
11
‘‘(A) notify the Attorney General at least 90
12
days prior to submitting an evaluation scientific and
13
medical evaluation of that substance supporting that
14
conclusion; and
15
‘‘(B) submit to the Attorney General such eval-
16
uation and conclusion that—
17
‘‘(i) is in writing; and
18
‘‘(ii) includes the bases for such conclu-
19
sion.
20
‘‘(2) Not later than 90 days after the receipt of such
21
evaluation and conclusion, the Attorney General shall
22
issue an order removing such substance from the schedule.
23
‘‘(3)(A) If the Secretary finds, based on the factors
24
specified in paragraph (4), that a substance listed in
25
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•HR 1758 IH
schedule I(e) does not meet the requirements for inclusion
1
in that schedule, and that the substance has a low poten-
2
tial for abuse, the Secretary shall submit to the Attorney
3
General a scientific and medical evaluation of that sub-
4
stance supporting those conclusions that is in writing and
5
that includes the bases for that conclusion.
6
‘‘(B) Within 180 days of receipt of such evaluation
7
and conclusion, the Attorney General shall—
8
‘‘(i) issue an order removing such substance
9
from scheduling for research purposes only; or
10
‘‘(ii) notify the Secretary in writing that the At-
11
torney General declines to issue such an order.
12
‘‘(4) In making the evaluation and conclusion de-
13
scribed in paragraph (1) or (3), the Secretary—
14
‘‘(A) shall consider the factors specified in
15
paragraphs (1), (2), (3), and (6) of subsection (c)
16
and any information submitted to the Attorney Gen-
17
eral under paragraph (1) of this subsection; and
18
‘‘(B) may also consider factors specified in
19
paragraphs (4), (5), and (7) of subsection (c) if the
20
Secretary finds that reliable evidence exists with re-
21
spect to such factors.
22
‘‘(5) Nothing in this subsection shall preclude the At-
23
torney General from transferring a substance listed in
24
schedule I to another schedule, or removing such sub-
25
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•HR 1758 IH
stance entirely from the schedules, pursuant to other pro-
1
visions of this section or section 202.
2
‘‘(6) A substance removed from schedule I(e) pursu-
3
ant to paragraph (1) or (3) may, at any time, be controlled
4
pursuant to the other provisions of this section or section
5
202 without regard to that removal.’’.
6
SEC. 4. CLARIFICATION OF CERTAIN REGISTRATION RE-
7
QUIREMENTS RELATED TO RESEARCH.
8
(a) EXCEPTION FOR AGENTS OR EMPLOYEES OF
9
REGISTERED RESEARCHERS.—Section 302(c)(1) of the
10
Controlled Substances Act (21 U.S.C. 822(c)(1)) is
11
amended by striking ‘‘or dispenser’’ and inserting ‘‘dis-
12
penser, or researcher’’.
13
(b) CONFORMING AMENDMENT.—Section 102(3) of
14
the Controlled Substances Act (21 U.S.C. 802(3)) is
15
amended by striking ‘‘or dispenser’’ and inserting ‘‘dis-
16
penser, or researcher’’.
17
(c) SINGLE REGISTRATION FOR CONTIGUOUS RE-
18
SEARCH SITES.—Section 302(e) of the Controlled Sub-
19
stances Act (21 U.S.C. 822(e)) is amended by adding at
20
the end the following new paragraph:
21
‘‘(3) Notwithstanding paragraph (1), a person reg-
22
istered to conduct research with a controlled substance
23
under section 303(f) may conduct such research under a
24
single registration if such research occurs exclusively on
25
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•HR 1758 IH
a single, contiguous campus and the registrant notifies the
1
Attorney General in writing of all sites on the campus
2
where the research will be conducted or where the con-
3
trolled substance will be stored or administered. If the reg-
4
istrant seeks to conduct such research at additional sites,
5
the registrant shall submit a new notification before con-
6
ducting such research at any such additional sites.’’.
7
(d) NEW INSPECTION NOT REQUIRED IN CERTAIN
8
SITUATIONS.—Section 303(f) of the Controlled Sub-
9
stances Act (21 U.S.C. 823(f)) is amended—
10
(1) by redesignating paragraphs (1) through
11
(5) as subparagraphs (A) through (E), respectively,
12
and by moving the margins of such subparagraphs
13
(as so redesignated) two ems to the right;
14
(2) by striking ‘‘(f) The’’ and inserting ‘‘(f)(1)
15
The’’; and
16
(3) by adding at the end the following new
17
paragraph:
18
‘‘(2)(A) If a person is registered to conduct research
19
with a controlled substance and applies to be registered,
20
or to modify a registration to conduct research with a sec-
21
ond controlled substance that is in the same schedule or
22
in a schedule with a higher numerical designation, a new
23
inspection by the Attorney General of the registered loca-
24
tion is not required.
25
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•HR 1758 IH
‘‘(B) Nothing in this paragraph shall prohibit the At-
1
torney General from conducting any inspection if the At-
2
torney General determines such an inspection is nec-
3
essary.’’.
4
(e) CONTINUATION OF RESEARCH ON NEWLY ADDED
5
SUBSTANCES; AUTHORITY TO CONDUCT RESEARCH WITH
6
OTHER SUBSTANCES.—Section 302 of the Controlled
7
Substances Act (21 U.S.C. 822), as amended by sub-
8
sections (a) and (c), is further amended by adding at the
9
end the following new subsection:
10
‘‘(h)(1) In the case of a person who is conducting
11
research on a substance at the time the substance is added
12
to schedule I and who is already registered to conduct re-
13
search with another controlled substance in schedule I or
14
II, the person—
15
‘‘(A) within 30 days of the scheduling of such
16
substance, shall submit a completed application for
17
registration or modification of the existing registra-
18
tion of such person, to conduct research on such
19
substance, in accordance with the regulations issued
20
by the Attorney General; and
21
‘‘(B) notwithstanding subsections (a) and (b),
22
may continue to conduct the research on such sub-
23
stance until the date on which—
24
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•HR 1758 IH
‘‘(i) the application referred to in subpara-
1
graph (A) is withdrawn by the applicant; or
2
‘‘(ii) the Attorney General serves on the
3
applicant an order to show cause proposing the
4
denial of the application pursuant to section
5
304(c).
6
‘‘(2) If the Attorney General serves an order to show
7
cause under paragraph (1)(B) and the applicant requests
8
a hearing, such hearing shall be held—
9
‘‘(A) on an expedited basis; and
10
‘‘(B) not later than 45 days after the request
11
is made, or such a later time as requested by the ap-
12
plicant.
13
‘‘(3)(A) A person who is registered to conduct re-
14
search with a controlled substance in schedule I may, not-
15
withstanding subsections (a) and (b), conduct research
16
with another controlled substance in schedule I, if each
17
of following conditions are met:
18
‘‘(i) The person has applied for a modification
19
of the person’s registration to authorize research
20
with such other controlled substance in accordance
21
with the regulations issued by the Attorney General.
22
‘‘(ii) The Attorney General has obtained
23
verification from the Secretary that the research
24
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•HR 1758 IH
protocol submitted with the application is meri-
1
torious.
2
‘‘(iii) The Attorney General has determined
3
under subparagraph (B) that the conduct of such re-
4
search is consistent with United States obligations
5
under the Single Convention on Narcotic Drugs,
6
1961.
7
‘‘(B) Not later than 30 days after receiving an appli-
8
cation under clause (i), the Attorney General shall deter-
9
mine whether the conduct of research that is the subject
10
of the application is consistent with United States obliga-
11
tions under the Single Convention on Narcotic Drugs,
12
1961.
13
‘‘(C) Nothing in this section shall be construed to
14
alter the authority of the Attorney General to initiate pro-
15
ceedings to deny, suspend, or revoke any registration in
16
accordance with sections 303 and 304.’’.
17
(f) TREATMENT OF CERTAIN ACTIVITIES AS COINCI-
18
DENT TO RESEARCH.—Section 302 of the Controlled Sub-
19
stances Act (21 U.S.C. 822), as amended by subsections
20
(a), (c), and (e), is further amended by adding at the end
21
the following new subsection:
22
‘‘(i) A person who is registered to perform research
23
with a controlled substance (other than marihuana) under
24
this title may, without being required to registered to man-
25
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•HR 1758 IH
ufacture such substance, using small quantities of such
1
substance, perform the following activities:
2
‘‘(1) Processing the substance to create ex-
3
tracts, tinctures, oils, solutions, derivatives, or other
4
forms of the substance consistent with the approved
5
research protocol.
6
‘‘(2) Dosage form development for the purpose
7
of satisfying requirements with respect to the sub-
8
mission of an investigational new drug application
9
under section 505(i) of the Federal Food, Drug, and
10
Cosmetic Act.’’.
11
SEC. 5. REVIEW OF RESEARCH REGISTRATION PROCESS.
12
(a) REVIEW.—Not later than one year after the date
13
of the enactment of this section, the Attorney General and
14
the Secretary of Health and Human Services shall jointly
15
conduct a review of the processes used to register or mod-
16
ify a registration to conduct research with controlled sub-
17
stances under the Controlled Substances Act (21 U.S.C.
18
801 et seq.), including—
19
(1) an evaluation of the impacts of the amend-
20
ments made by this Act on the risk of the diversion
21
of controlled substances used in research and related
22
public safety considerations; and
23
(2) an identification of opportunities to reduce
24
any unnecessary burden on persons seeking registra-
25
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•HR 1758 IH
tion, potential redundancies, and inefficiencies in
1
such processes, including—
2
(A) the process for obtaining a registration
3
under section 303 of the
[Text truncated for display. Full text available on Congress.gov.]