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Pursuant to § 1301.33(a), Title 21 of the Code of Federal Regulations (CFR), this is notice that on May 16, 2011, Cayman Chemical Company, 1180 East Ellsworth Road, Ann Arbor, Michigan 48108, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the following basic classes of controlled substances:
Drug Schedule Cathinone (1235) I Methcathinone (1237) I N-Ethylamphetamine (1475) I N-N-Dimethylamphetamine (1480) I Aminorex (1585) I 4-Methylaminorex (cis isomer) (1590) I 1-Pentyl-3-(1-naphthoyl)indole (7118) I 1-Butyl-3-(1-naphthoyl)indole (7173) I 1-[2-(4-Morpholinyl)ethyl]-3-(1-naphthoyl) Indole (7200) I Alpha-ethyltryptamine (7249) I 5-(1,1-Dimethulheptyl)-2-[(1R,3S)-3-hydroxycyclohexyl]-phenol (7297) I 5-(1,1-Dimethyloctyl)-2-[(1R,3S)-3-hydroxycyclohexyl]-phenol (7298) I Lysergic acid diethylamide (7315) I 2,5-Dimethoxy-4-(n)-propylthiophenethylamine (7348) I Marihuana (7360) I Tetrahydrocannabinols (7370) I 3,4,5-Trimethoxyamphetamine (7390) I 4-Bromo-2,5-dimethoxyamphetamine (7391) I 4-Bromo-2,5-dimethoxyphenethylamine (7392) I 4-Methyl-2,5-dimethoxyamphetamine (7395) I 2,5-Dimethoxyamphetamine (7396) I 2,5-Dimethoxy-4-ethylamphetamine (7399) I 3,4-Methylenedioxyamphetamine (7400) I 5-Methoxy-3,4-methylenedioxyamphetamine (7401) I N-Hydroxy-3,4-methylenedioxyamphetamine (7402) I 3,4-Methylenedioxy-N-ethylamphetamine (7404) I 3,4-Methylenedioxymethamphetamine (7405) I 4-Methoxyamphetamine (7411) I 5-Methoxy-N-N-dimethyltryptamine (7431) I Alpha-methyltryptamine (7432) I Diethyltryptamine (7434) I Dimethyltryptamine (7435) I 5-Methoxy-N,N-diisopropyltryptamine (7439) I Amphetamine (1100) II Methamphetamine (1105) II Lisdexamfetamine (1205) II The company plans to manufacture small quantities of marihuana derivatives for research purposes. In reference to drug code 7360 (Marihuana), the company plans to bulk manufacture cannabidol. In reference to drug code 7370 (Tetrahydrocannabinols), the company will manufacture a synthetic THC. No other activity for this drug code is authorized for this registration.
Any other such applicant, and any person who is presently registered with DEA to manufacture such substances, may file comments or objections to the issuance of the proposed registration pursuant to 21 CFR 1301.33(a).
Any such written comments or objections should be addressed, in quintuplicate, to the Drug Enforcement Administration, Office of Diversion Control, Federal Register Representative (ODL), 8701 Morrissette Drive, Springfield, Virginia 22152; and must be filed no later than September 6, 2011.
Start SignatureDated: June 23, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.
[FR Doc. 2011-16791 Filed 7-1-11; 8:45 am]
BILLING CODE 4410-09-P
Document Information
- Published:
- 07/05/2011
- Department:
- Drug Enforcement Administration
- Entry Type:
- Notice
- Document Number:
- 2011-16791
- Pages:
- 39127-39127 (1 pages)
- PDF File:
- 2011-16791.pdf