D.C. Act 22-550
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ENROLLED ORIGINAL AN ACT D.C. ACT 22-550 IN TFIE COUNCIL OF"IIIE DISTRICT OF COLUMBIA DEGEMBER 26,2018 To amcnd, on an emergency basis, due to congressional review, the District of Columbia ljniform Controlled Substances Act of 198 I to add certain classes and substances to the list of Schedule I controlled substances. BE IT ENACTED BY THE COTJNCIL OF THE DISTRICT OF COLUMBIA, That this act may be cited as the "Revised Synthetics Abatement and F-ull Enforcement Drug Control Congressional Review Emergency Amendment Act of 20 I 8". Sec. 2. The District of Columbia Uniform Controlled Substances Act of 1981, effective August 5, 1981 (D.C. Law 4-29: D.C. Official Code $ 48-901.01 et seq.), is amended as follows: (a) Section 102(27) (D.C. Official Code $ 48-901.02(27) is amended as fo[[ows: ( I ) Strike the phrase "as used in section 204(l) and section 206( IXD)" and insert the phrase "as used in section 204(3), (5), and (6) and section 206( I )(D)" in its place. (2) Strike the phrase "As used in section 204(3)" and insert the phrase "As used in section 204(3). (5), and (6)" in its place. (b) Section 204 (D.C. Official Code $ 48-902.04) is amended as follows: (1) Paragraph (3) is amended as lollows: (A) The lead-in language is amended by striking the phrase "(for purposes of this paragraph only. the term "isomer" includes the optical, position, and geometric isomers):" and insening a colon in its place. (B) New subparagraphs (G-i) through (G-xii) are added to read as follows: "(G-i) 251-NBOMe (also known as 4-iodo-2,5-dimethoxy-N-[(2- methoxyphenyl)methyl]-benzeneethanamine); "(G-ii) 258-NBOMe (also known as 4-bromo-2.5-dimethoxy-N-[(2- methoxyphenyl)methyll-benzeneethanamine); "(C-iiD 25C-NBOMe (also known as 2-(4-chloro-2,5-dimethoxyphenyl)- N-(2-mcthoxybenzyl)ethanamine); "(G-iv) 5-APB (also known as a-methyl-5-benzofuranethanamine); ENROLLED OR]GINAL "(G-v) 5-APDB (also known as 2,3-dihydro-o-methyl-5- benzof uranethanamine) ; "(G-vi) 6-APB (also known as o-methyl-6-benzofuranethanamine); "(G-vii) 6-APDB (also known as 2,3-dihydro-o-methyl-6- benzofuranethanamine) ; "(G-viii) 3-methoxy-PCE (also known as N-ethyt-1 -(3-methoxyphenyl)- cyclohexanamine); "(G-ix) 3-methoxy-PCP (also knor.vn as 1 -[ -(3- methoxyphenyl)cyclohexyll -piperidine) ; "(G-x) 4-methoxy-PCP (also known as l-[1-(4- methoxyphenyl)cyclohexyll -piperidine); "(G-xi) 5-methoxy-DALT , also known as: "(i) 5-MeO-DALT; or "(ii) 5-methoxy-N,N-di-2-propen-l -yl- I H-indole-3-ethanamine; "(G-xii) 4-acetoxy DMT, also known as: "(i) 4-AcO-DMT; or "(ii) 3-[2-(dimethylamino)ethyl]- I H-indol-4-ol-4-acetate; (C) A new subparagraph (M-i) is added to read as follows: "(M-i) Methoxetamine (also known as 2-(ethylamino)-2-(3- methoxyphenyl)cyclohexanone);". (D) Subparagraph (JJ) is amended by striking the phrase "; and" and inserting a semicolon in its place. (E) Subparagraph (KK) is amended by striking the semicolon and inserting the phrase "; and" in its place. (F) A new subparagraph (LL) is added to read as follows: "(LL) Cathinone;". (2) Paragraph (5) is amended to read as follows: "(5) As used in this paragraph, the term "synthetic cathinones" includes any material, compound, mixture, or preparation that is not otherwise listed as a controlled substance in this schedule or in Schedules II through V, is not approved by the Food and Drug Administration as a drug, and is structurally derived from or contains any quantity of the following substances, their salts, isomers, homologues, analogues, and salts of isomers, homologues, and analogues, unless specifrcally excepted, whenever the existence ofthese salts, isomers, homologues, analogues, and salts of isomers, homologues, and analogues is possible within the specific chemical designation: "(A) Classified Synthetic Cathinones: "(i) Cathinones. Any compound, other than methylnenedioxy cathinones and pyrrolidine cathinones, containing a 2-amino- 1-propanone structure with substitution at the l-position with a monocyclic ring system, with or without alkyl, alkoxyl, or 2 ENROI,I,E,D ORIGINAL halo substitutions, and a substitution at the nitrogen atom by an alkyl group, cycloalkyl group, or incorporation into a heterocyclic structure. Examples of this structural class include: "(I) Mephedrone, also known as: "(aa) 2-(methylamino)-1-(4-methylphenyl)-1- propanone; "(bb) 4-MeMC: "(cc) 4-Methylmethcathinone ; "(dd) 4-Methylephedrone; or "(ee) 4-MMC; "(ll) Dimethylcathinone, also known as: "(aa) 2-(dimethylamino)- 1 -phenyl-1 -propanone; or "(bb) N,N-Dimethylcathinone; "(III) Ethcathinone, also knou,n as: "(aa) 2-(ethylamino)-1-phenyl-1-propanone; "(bb) Ethylcathinone; "(cc) N-Ethylcathinone; or "(dd) 2-Ethylaminobuphedro; "(IV) Buphedrone, also known as; "(aa) 2-(methylamino)-1-phenylbutan-l-one; or "(bb) MABP; "(V) 3,4-DMMC, also known as: "(aa) I-(3,4-dimethylphenyl)-2-(methylamino)-1- propanone; or "(bb) 3,4-Dimethylmethcathinone; "(VI) EMC, also known as: "(aa) l-(4-ethylphenyl)-2-(methylamino)propan-1- one; "(bb) 4-EMC; or "(cc) 4-Ethylmethcathinone; "(VII) Fluoromethcathinone (also krown as 1-(4- fl uorophenyl)-2-(methylamino) propan- 1 -one) ; "(VIII) 3-FMC, also known as: "(aa) 3-fluoro-N-methylcathinone); or "(bb) 1 -(3-fluorophenyl)-2-(methylamino)propan- l - one; '(lX) 4-FMC, also known as: "(aa) 1-(4-fluorophenyl)-2-(methylamino)propan-1- one; "(bb) 4-fluoro-N-methylcathinone; or J ENROLLED ORIGINAL "(cc) Flephedrone; "(X) 4-MeBP, also known as: "(aa) 2-(methylamino)- 1 -(4-methylphenyl)- I - butanone; "(bb) 4-Methylbuphedrone; "(cc) 4-methyl BP; or "(dd) 4-MeMABP; "(XI) 3-MEC, also known as: "(aa) 2-(ethylamino )-1-(m+olyl)propan-l-one; or "(bb) 3-Methyl-N-ethylcathinone; "(XII) 4-MEC, also known as: "(aa) 2-(ethylamino)-l -(4-methylphenyl)-l- propanone; or "(bb) 4-Methyl-N-ethylcathinone; "(XIID 3-MMC, also known as: "(aa) 2-(methylamino)- 1 -(3-methylphenyl)- I - propanone; "(bb) 3-methyl MS; or "(cc) 3-Methylmethcathinone; "(XIV) Methedrone (also known as l-(4-methoxyphenyl)- 2-(methylamino)- 1 -propanone); and "(XV) Pentedrone (also known as 2-(methylamino)- 1 - phenylpentan- I -one); "(ii) Methylenedioxy Cathinones. Any compound containing a 2- amino- l-propanone structure with substitution at the l-position with a monocyclic or fused polycyclic ring system and a substitution at any position ofthe ring system with an alkyl, haloalkyl, halogen, alkylenedioxy, or alkoxy group, whether or not further substituted at anv position on the ring system to any extent. Examples of this structural class include: "(l) 3-fl uoromethylone; "(ll) Methylone, also known as "(aa) l -(1,3 -benzodioxol-5-yl)-2-(methylamino)- 1 - propanone; or "(bb) 3,4-Methylenedioxy-N-methylcathinone); "flII) N-ethyl Pentylone, also known as: "(aa) Ephylone; or "(bb) 1 -( 1,3-benzodioxol-5-yl)-2-(ethylamino)- 1 - pentanone; *(IV) bk-MDDMA, also known as 4 ENROLLED ORIGINAL "(aa) I -( I ,3-benzodioxol-5-yl)-2- (dimethylamino)propan- I -one; "(bb) Dimethylone; "(cc) N,N-dimethyl-3',4' -methylenedioxycathinone; "(dd) N,N-dimethyl-3,4-methylenedioxycathinone ; or "(ee) N,N-Dimethyl MDCATH; "(V) Butylone, also known as 1-( 1,3-benzodioxol-5-yl)-2- (methylamino)butan- I -one); and "(VI) Ethylone, also known as: "(aa) 3,4-Methylenedioxy-N-ethylcathinone; or "(bb) MDEC; "(iii) Pynolidine Cathinones. Any compound containing a 2- amino- 1-propanone structure with substitution at the 1-position with an alkyl, cyclic, or fused polycyclic ring system and a substitution at the 3-position carbon with an alkyl, haloalkyl, halogen, alkoxy or alkylenedioxy group, and a substitution at the nitrogen atom incorporation into a heterocyclic structure, with or without further halogen substitutions. Examples include: "(l) o-PVP (also known as o-pyrrolidinopentiophenone); "(ll) o-pynolidinopropiophenone, also knor.m as: "(aa) l-phenyt-2-(1-pynolidinyl)-l-propanone; or "(bb) u-PPP; "(III) a-PBP, also known as: "(aa) 1 -phenyl-2-(1 -pyrrolidinyl)-1 -butanone; or " (bb) u-pyrrolidinobutiophenone; "(IV) MDPBP, also known as: "(aa) l-(1,3-benzodioxol-5-yl)-2-(1-pyrrolidinyl)-1- butanone; "(bb) 3,4-Methylenedioxy-o- Pynolidinobutiophenone; or "(cc) 3,4-MDPBP; '(V) MDPPP, also known as: "(aa) 1 -(1,3-benzodioxol-5-yl)-2-( 1 -pynolidinyl)- I - propanone; or "(bb) 3,4-Methylenedioxy-o- Pynolidinopropiophenone; "(VI) MDPV, also known as: "(aa) I -(1,3-benzodioxol-5-yl)-2-(1 -pyrrotidinyl)-1 - pentanone; or "(bb) 3,4-Methylenedioxy Pyrovalerone; 5 ENROLLED ORIGINAL "(VII) 4-MePPP, also known as "(aa) 4'-methyl-o-Pyrrolidinopropiophenone; "(bb) 4'-methyl PPP; or "(cc) 2-(pynolidin-l-yl)- 1 -(p-tolyl)propan-l-one; "(VIII) 4'-methyl PHP, also known as: '' (aa) 4'-methyl-o-pyrrolidinohexanophenone; "(bb) MPHP; "(cc) 4'-methyl-o-PHP; or ''(dd) Pva; "(IX) Naphyrone, also known as: " (aa) (RS )- 1 -naphthalen-2-yl-2-pyrrolidin-l- ylpentan- 1-one; or "(bb) Naphpyrovalerone; and '(X) C-PVP, also known as: "(aa) 4-Chloro-u-PVP; or "(bb) l-(4-chlorophenyl)-2-(pyrrolidin-1-yl)pentan- 1-one; or "(iv) Piperazine Stimulants. Any compound containing or structurally derived from a piperazine, or diethylenediamine, structure with or without substitution at one of the nitrogen atoms ofthe piperazine ring to any extent, including alkyl, cycloalkyl, or fused ring systems, with or without further halogen substitutions. Examples include: "(l) BZP, also known as: "(aa) 1 -(phenylmethyl)-piperazine; "(bb) I -Benzylpiperazine; or "(cc) N-Benzylpiperazine; and "(II) TMFPP, also known as: "(aa) 1 - [3-(trifl uoromethyl)pheny[] -piperazine ; "(bb) I -(m-Trifluoromethylphenyl) piperazine; or "(cc) 3 -Tri fl uoromethylphenylpiperazine.