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S 1039
South Carolina Senate•In Senate Committee
Summary
S 1039, “Schedule I substances”, was introduced in the Senate on Mar 19, 2026 by Sen. Everett Stubbs (R) with 2 co-sponsors. It was referred to Medical Affairs, and last saw action on Mar 19, 2026: Referred to Committee on Medical Affairs.
Record
Text
S 1039 has 2 co-sponsors.
s1039/introduced.txtSouth Carolina General Assembly126th Session, 2025-2026Bill 1039Indicates Matter StrickenIndicates New Matter(Text matches printed bills. Document has been reformatted to meet World Wide Web specifications.)A billTO AMEND THE SOUTH CAROLINA CODE OF LAWS BY AMENDINGSECTION 44-53-190, RELATING TO SCHEDULE I SUBSTANCES, SO AS TO ADD SUBSTITUTEDTRYPTAMINES TO THE LIST OF SCHEDULE I SUBSTANCES.Be it enacted by theGeneral Assembly of the State of South Carolina:SECTION 1. Section 44-53-190(D) of the S.C. Code is amended toread:(D) Any material, compound, mixture,or preparation which contains any quantity of the following hallucinogenicsubstances, their salts, isomers, and salts of isomers, unless specificallyexcepted, whenever the existence of such salts, isomers, and salts of isomersis possible within the specific chemical designation:1. 3,4-methylenedioxyamphetamine2. 5-methoxy-3,4-methylenedioxyamphetamine3. 3,4-methylenedioxymethamphetamine(MDMA)4. 3,4,5-trimethoxyamphetamine5. Bufotenine6. Diethyltryptamine(DET)7. Dimethyltryptamine(DMT)8.5. 4-methyl-2,5-dimethoxyamphetamine(STP)9.6. Ibogaine10.7. Lysergic aciddiethylamide (LSD)11.8. Marijuana12.9. Mescaline13.10. Peyote14.11. N-ethyl-3-piperidylbenzilate15.12. N-methyl-3-piperidylbenzilate16.13. Psilocybin17.14. Psilocyn18.15. Tetrahydrocannabinol(THC)19.16. 2,5-dimethoxyamphetamine20.17. 4-bromo-2,5-dimethoxyamphetamine21.18. 4-Methoxyamphetamine22.19. Thiophene analog ofphencyclidine23.20. Parahexyl24.21. Syntheticcannabinoids.-Any material, compound, mixture, or preparation that is notlisted as a controlled substance in Schedule I through V, is not anFDA-approved drug, and contains any quantity of the following substances, theirsalts, isomers (whether optical, positional, or geometric), homologues, andsalts of isomers and homologues, unless specifically excepted, whenever theexistence of these salts, isomers, homologues, and salts of isomers andhomologues is possible within the specific chemical designation:a. Naphthoylindoles.Any compound containing a 3-(1-naphthoyl)indole structure with substitution atthe nitrogen atom of the indole ring by an alkyl, haloalkyl, alkenyl,cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl, or2-(4-morpholinyl)ethyl group, whether or not further substituted in the indolering to any extent and whether or not substituted in the naphthyl ring to anyextent. Including, but not limited to, JWH-015, JWH-018, JWH-019, JWH-073,JWH-081, JWH-122, JWH-200, JWH-210, JWH-398, AM-2201, WIN 55-212, AM-2201 (C1analog), AM-1220.b. Naphthylmethylindoles.Any compound containing a 1H-indol-3-yl-(1-naphthyl)methane structure withsubstitution at the nitrogen atom of the indole ring by an alkyl, haloalkyl,alkenyl, cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl,or 2-(4-morpholinyl)ethyl group, whether or not further substituted in theindole ring to any extent and whether or not substituted in the naphthyl ringto any extent.c. Naphthoylpyrroles.Any compound containing a 3-(1-naphthoyl)pyrrole structure with substitution atthe nitrogen atom of the pyrrole ring by an alkyl, haloalkyl, alkenyl,cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl, or2-(4-morpholinyl)ethyl group, whether or not further substituted in the pyrrolering to any extent and whether or not substituted in the naphthyl ring to anyextent. Including, but not limited to, JWH-307, JWH-370, JWH-176.d. Naphthylmethylindenes.Any compound containing a naphthylideneindene structure with substitution atthe 3-position of the indene ring by an alkyl, haloalkyl, alkenyl,cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl, or2-(4-morpholinyl)ethyl group, whether or not further substituted in the indenering to any extent and whether or not substituted in the naphthyl ring to anyextent.e. Phenylacetylindoles.Any compound containing a 3-phenylacetylindole structure with substitution atthe nitrogen atom of the indole ring by an alkyl, haloalkyl, alkenyl,cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl, or2-(4-morpholinyl)ethyl group, whether or not further substituted in the indolering to any extent and whether or not substituted in the phenyl ring to anyextent. Including, but not limited to, SR-18, RCS-8, JWH-203, JWH-250, JWH-251.f. Cyclohexylphenols.Any compound containing a 2-(3-hydroxycyclohexyl)phenol structure withsubstitution at the 5-position of the phenolic ring by an alkyl, haloalkyl,alkenyl, cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl,or 2-(4-morpholinyl)ethyl group, whether or not substituted in the cyclohexylring to any extent. Including, but not limited to, CP 47,497 (and homologues),cannabicyclohexanol, CP-55, 940.g. Benzoylindoles.Any compound containing a 3-(benzoyl)indole structure with substitution at thenitrogen atom of the indole ring by an alkyl, haloalkyl, alkenyl,cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl, or2-(4-morpholinyl)ethyl group, whether or not further substituted in the indolering to any extent and whether or not substituted in the phenyl ring to anyextent. Including, but not limited to, AM-694, Pravadoline (WIN 48,098), RCS-4,AM-630, AM-1241, AM-2233.h. 2,3-Dihydro-5-methyl-3-(4-morpholinylmethyl)pyrrolo[1,2,3-de]-1, 4-benzoxazin-6-yl]-1-napthalenylmethanone (WIN 55,212-2).i. 9-(hydroxymethyl)-6,6-dimethyl-3-(2-methyloctan-2-yl)-6a,7,10,10a-tetrahydrobenzo[c]chromen-1-ol 7370(HU-210, HU-211).j. Adamantoylindoles.Any compound containing a 3-(1-adamantoyl)indole structure with substitution atthe nitrogen atom of the indole ring by a alkyl, haloalkyl, alkenyl,cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl or2-(4-morpholinyl)ethyl group, whether or not further substituted in the indolering to any extent and whether or not substituted in the adamantyl ring systemto any extent.22.Substituted Tryptamines. Any material, compound, mixture, or preparationcontaining a 2-(1H-indol-3-yl)ethanamine, for example tryptamine, structurewith or without mono- or di-substitution of the amine nitrogen with alkyl oralkenyl groups, or by inclusion of the amino nitrogen atom in a cyclicstructure, whether or not substituted at the alpha position with an alkylgroup, whether or not substituted on the indole ring to any extent with anyalkyl, alkoxy, halo, hydroxyl, or acetoxy groups, including, but not limitedto:a. Bufotenine,b. DET (Diethyltryptamine),c. DMT (Dimethyltryptamine),d. Methyltryptamine,e. 5-MeO-DMT (5-Methoxy-N,N,Dimethyltryptamine),f. 5-MeO-DiPT (5-Methoxy-N,N-Diisopropyltryptamine),g. MET (N-Methyl-N-ethyltryptamine),h. DALT (N,N-Diallyltryptamine),i. EiPT (N-Ethyl-N-isopropyltryptamine),j. MiPT (N-Methyl-N-isopropyltryptamine),k. 5-Hydroxy-AMT (5-Hydroxy-alpha-methyltryptamine),l. 5-Hydroxy-N-methyltryptamine,m. 5-MeO-MiPT(5-Methoxy-N-methyl-N-isopropyltryptamine),n. 5-MeO-AMT (5-Methoxy-alpha-methyltryptamine),o. 5-Me-DMT (5-Methyl-N,N-dimethyltryptamine),p. DiPT (N,N-Diisopropyltryptamine),q. DPT (N,N-Dipropyltryptamine),r. 4-Hydroxy-DiPT(4-Hydroxy-N,N-diisopropyltryptamine),s. 5-MeO-DALT (5-Methoxy-N,N-Diallyltryptamine),t. 4-AcO-DMT (4-Acetoxy-N,N-dimethyltryptamine),u. 4-AcO-DiPT (4-Acetoxy-N,N-diisopropyltryptamine),v. 4-Hydroxy-DET (4-Hydroxy-N,N-diethyltryptamine),x. 4-Hydroxy-MET(4-Hydroxy-N-methyl-N-ethyltryptamine),y. 4-Hydroxy-MiPT(4-Hydroxy-N-methyl-N-isopropyltryptamine),z. Methyl-alpha-ethyltryptamine,aa. Bromo-DALT (Bromo-N,N-diallyltryptamine),bb. 6-MeO-DMT (6-methoxy-N,N-dimethyltryptamine),cc. 5-OH-DMT (5-hydroxy-N,N-dimethyltryptamine),dd. 4-AcO-DET (4-Acetoxy-N,N-diethyltryptamine).SECTION 2. This act takes effect upon approvalby the Governor.----XX----This web page was last updated on March 19, 2026 at 11:38 AM
Amend The South Carolina Code Of Laws By Amending Section 44-53-190, Relating To Schedule I Substances, So As To Add Substituted Tryptamines To The List Of Schedule I Substances.
Sponsors
Sen. Everett Stubbs (R) sponsors S 1039, and 2 members have co-sponsored it.
Committees
S 1039 went before 1 committee: Medical Affairs.
History
S 1039 has taken 2 actions since Mar 19, 2026.
| Chamber | Action | |||
|---|---|---|---|---|
Mar 19, 2026 | Senate | Introduced and read first time | ||
Mar 19, 2026 | Senate | Referred to Committee on Medical Affairs |
Votes
S 1039 has not gone to a roll call.
Source: scstatehouse.gov · legiscan.com