Class i narcotics

Added: Graeme Yarber - Date: 04.10.2021 23:51 - Views: 16242 - Clicks: 2139

These drugs are known in the UK as controlled drugsbecause this is the term by which the act itself refers to them. In more general terms, however, many of these drugs are also controlled by the Medicines Actthere are many other drugs which are controlled by the Medicines Act but not by the Misuse of Drugs Act, and other substances which may be considered drugs alcoholfor example are controlled by other laws. Class A drugs represent those deemed most dangerous, and so carry the harshest punishments.

Class C represents those thought to have the least capacity for harm, and so the Act demands more lenient punishment. In reality the potential harm has little bearing on the class, [1] which has led to dissatisfaction with drug laws. Being found in possession of a drug on this list is dealt with less seriously than would be if it were deemed that there is intent to supply even without payment the drug to others.

Possession with intent to supply carries a maximum penalty of life imprisonment. With regard to lawful possession and supply, a different set Class i narcotics apply which are set out in the Misuse of Drugs Regulations as amended. This sets out five schedules each with their own restrictions. Schedule 1 contains substances considered by the government to have no medicinal value, such as hallucinogensand their use is limited primarily to research, whereas schedules 2—5 contain the other regulated drugs.

For example, morphine is a Class A drug under the Misuse of Drugs Actbut when lawfully supplied falls under the category of a Schedule 2 controlled drug. Substances may be removed and added to different parts of the schedule by statutory instrumentprovided a report of the Advisory Council on the Misuse of Drugs has been commissioned and has reached a conclusion, although the Secretary of State is not bound by the council's findings.

This list has in practice been modified a great of times, sometimes removing substances, but more commonly adding some; for example, many benzodiazepines became Class C drugs inand many cathinones became Class B drugs in The following substances, namely:— [3].

Any stereoisomeric form of a substance for the time being specified in paragraph 1 above not being dextromethorphan or dextrorphan. Any ester or ether of a substance for the time being specified in paragraph 1 or 2 above [not being a substance for the time being specified in Part II of this Schedule]. Any preparation or other product containing a substance or product for the time being specified in any of paragraphs 1 to 4 above.

Any preparation deed for administration by injection which includes a substance or product for the time being specified in any of paragraphs 1 to 3 of Part II of this Schedule. WIN 55, Any compound structurally derived from 3— 1—naphthoyl indole or 1H—indol—3—yl— 1—naphthyl methane by substitution at the nitrogen atom of the indole ring by alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2— 4—morpholinyl ethyl, whether or not further substituted in the indole ring to any extent and whether or not substituted in the naphthyl ring to any extent. Any compound structurally derived from 3— 1—naphthoyl pyrrole by substitution at the nitrogen atom of the pyrrole ring by alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2— 4—morpholinyl ethyl, whether or not further substituted in the pyrrole ring to any extent and whether or not substituted in the naphthyl ring to any extent.

Any compound structurally derived from 1— 1—naphthylmethyl indene by substitution at the 3—position of the indene ring by alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2— 4—morpholinyl ethyl, whether or not further substituted in the indene ring to any extent and whether or not substituted in the naphthyl ring to any extent. Any compound structurally derived from 3—phenylacetylindole by substitution at the nitrogen atom of the indole ring with alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2— 4—morpholinyl ethyl, whether or not further substituted in the indole ring to any extent and whether or not substituted in the phenyl Class i narcotics to any extent.

Any compound structurally derived from 2— 3—hydroxycyclohexyl phenol by substitution at the 5—position of the phenolic ring by alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2— 4—morpholinyl ethyl, whether or not further substituted in the cyclohexyl ring to any extent. Any compound structurally derived from 3-benzoylindole by substitution at the nitrogen atom of the indole ring by alkyl, haloalkyl, alkenyl, cyanoalkyl, hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl, N-methylpiperidinyl methyl or 2— 4—morpholinyl ethyl, whether or not further substituted in the indole ring to any extent and whether or not substituted in the phenyl ring to any extent.

Any compound structurally derived from 3- 1-adamantoyl indole or 3- 2-adamantoyl indole by substitution at the nitrogen atom of the indole ring by alkyl, haloalkyl, alkenyl, cyanoalkyl, hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl, N-methylpiperidinyl methyl or 2— 4—morpholinyl ethyl, whether or not further substituted in the indole ring to any extent and whether or not substituted in the adamantyl ring to any extent.

Any compound structurally derived from Class i narcotics 2,2,3,3-tetramethylcyclopropylcarbonyl indole by substitution at the nitrogen atom of the indole ring by alkyl, haloalkyl, alkenyl, cyanoalkyl, hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl, N-methylpiperidinyl methyl or 2— 4—morpholinyl ethyl, whether or not further substituted in the indole ring to any extent.

Any stereoisomeric form of a substance for the time being specified in paragraph 1 of this Part of this Schedule. Any salt of a substance for the time being specified Class i narcotics paragraph 1 or 2 of this Part of this Schedule. Any preparation or other product containing a substance or product for the time being specified in any of paragraphs 1 to 3 of this Part of this Schedule, not being a preparation falling within paragraph 6 of Part I of this Schedule. Class C drugssupposedly the least harmful drugs, include the following substances:— [3].

Any stereoisomeric form of a substance for the time being specified in paragraph 1 of this Part of this Class i narcotics [not being phenylpropanolamine. Any preparation or other product containing a substance for the time being specified in any of paragraphs 1 to 3 of this Part of this Schedule. The act contains several references to "derivatives" of compounds but the extent of this term is not fully clarified. Where unspecified it is thought to indicate derivatives which can be made from the specified compound in a single synthetic step, although such a definition would indicate that alkyllysergamide analogues would be uncontrolled.

Where the derivatives are specified to be "structural derivatives" there is precedent that the statute applies whenever the structure could be converted to the specified derivatives in any of synthetic steps. This article incorporates text published under the British Open Government Licence v3. The Lancet. CiteSeerX PMID S2CID Retrieved 8 February Alcohol, heroin and crack were found to be most harmful, while LSD, Buprenorphine and psilocybin mushrooms were found to be least harmful.

The Guardian. We will give the public the kind of high-quality evidence on drug harms our current crop of politicians apparently do not feel they need before making far reaching decisions around drugs classification. Office of Public Sector Information. Retrieved 15 June UK Home Office. Retrieved 11 March Cambridge: RSC Publishing.

Isomer De. Retrieved 12 March Amendment Order ". UK Government. Retrieved 25 September This article contains quotations from this source, which is available under the Open Government Licence v3. Drugs in Society: European Perspectives. Oxford: Radcliffe Publishing. ISBN King Recreational drug use. Calea zacatechichi Silene capensis. Coffee break Coffeehouse Latte art Teahouse. Abuse Addiction Date rape drug Dependence Opioid replacement therapy Prevention Rehabilitation Responsible use Driving impaired Drug checking Reagent testing Drug harmfulness Effects of cannabis Drug-related crime Fetal alcohol spectrum disorder Long-term effects of cannabis Neurotoxicity Overdose Passive smoking of tobacco or other substances.

Arguments for and against drug prohibition Capital punishment for drug trafficking Cognitive liberty Deer drug Drug court Drug possession Drug test Narc Politics of drug abuse War on drugs Mexican drug war Plan Colombia Philippine drug war Zero tolerance. Alcohol legality Alcohol consumption Anabolic steroid legality Cannabis legality Annual use Lifetime use Tobacco consumption Cocaine legality Cocaine use Methamphetamine legality Opiates use Psilocybin mushrooms legality Salvia legality.

Namespaces Article Talk. Views Read Edit View history. Help Learn to edit Community portal Recent changes file. Download as PDF Printable version. Simple English Edit links. Strongest known opioid; 10, times more potent than morphine, times more potent than fentanyl.

Used as a tranquiliser for large game elephants etc. Semi-synthetic opioid; derivative of etorphine [4]. Lysergic acid diethylamide. Methadyl acetate. Morphine methobromide. Psilocybe mushrooms. Very similar to phencyclidine PCPbut considerably more potent. Dual action as a norepinephrine reuptake inhibitor. Commonly used in the production of Pethidine, although it has little opioid activity in its own right. Allyl a-methyl-3,4-methylenedioxyphenethyl amine 2-Amino 2,5-dimethoxymethylphenyl ethanol 2-Amino 3,4-dimethoxyphenyl ethanol Benzyl a-methyl-3,4-methylenedioxyphenethyl amine 4-Bromo-b,2,5-trimethoxyphenethylamine N- 4-sec-Butylthio-2,5-dimethoxyphenethyl hydroxylamine Cyclopropylmethyl a-methyl-3,4-methylenedioxyphenethyl amine 2- 4,7-Dimethoxy-2,3-dihydro-1H-indanyl ethylamine 2- 4,7-Dimethoxy-2,3-dihydro-1H-indanyl methylethylamine 2- 2,5-Dimethoxymethylphenyl cyclopropylamine 2- 1,4-Dimethoxynaphthyl ethylamine 2- 1,4-Dimethoxynaphthyl methylethylamine N- 2,5-Dimethoxypropylthiophenethyl hydroxylamine 2- 1,4-Dimethoxy-5,6,7,8-tetrahydronaphthyl ethylamine 2- 1,4-Dimethoxy-5,6,7,8-tetrahydronaphthyl methylethylamine a,a-Dimethyl-3,4-methylenedioxyphenethylamine a,a-Dimethyl-3,4-methylenedioxyphenethyl methyl amine.

Dimethyl a-methyl-3,4-methylenedioxyphenethyl amine N- 4-Ethylthio-2,5-dimethoxyphenethyl hydroxylamine 4-Iodo-2,5-dimethoxy-a-methylphenethyl dimethyl amine 2- 1,4-Methano-5,8-dimethoxy-1,2,3,4-tetrahydronaphthyl ethylamine 2- 1,4-Methano-5,8-dimethoxy-1,2,3,4-tetrahydronaphthyl methylethylamine 2- 5-Methoxy-2,2-dimethyl-2,3-dihydrobenzo[b]furanyl methylethylamine 2-Methoxyethyl a-methyl-3,4-methylenedioxyphenethyl amine 2- 5-Methoxymethyl-2,3-dihydrobenzo[b]furanyl methylethylamine b-Methoxy-3,4-methylenedioxyphenethylamine 1- 3,4-Methylenedioxybenzyl butyl ethyl amine 1- 3,4-Methylenedioxybenzyl butyl methyl amine 2- a-Methyl-3,4-methylenedioxyphenethylamino ethanol a-Methyl-3,4-methylenedioxyphenethyl propynyl amine N-Methyl-N- a-methyl-3,4-methylenedioxyphenethyl hydroxylamine O-Methyl-N- a-methyl-3,4-methylenedioxyphenethyl hydroxylamine a-Methyl methylthio phenethylamine b,3,4,5-Tetramethoxyphenethylamine b,2,5-Trimethoxymethylphenethylamine.

UK Codeine law. All cannabis varieties, including those grown as hempare controlled under the act, not just drug varieties Downgraded from class B to class C in [14] and upgraded to class B in [15]. Used by Doctors on Air Ambulance duties to provide pain relief for serious or life-threatening injuries in extreme circumstances, when casualty sedation is required prior to a potential RSI. Khat Catha edulisthe plant in which Cathine originates, is now also illegal in the UK [24] [25].

Khat Catha Class i narcoticsthe plant in which Cathinone originates, is now also illegal in the UK [24] [25]. Metabolised to GHB in the body. Classified in December [26].

Class i narcotics

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Drugs controlled by the UK Misuse of Drugs Act