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desomorphine

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desomorphine

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Also known as dihydrodesoxymorphine, krokodil, 4,5-epoxy-3-hydroxy-n-methylmorphinan, 6-deoxy-7,8-dihydromorphine, deoxydihydromorphine D, dihydrodeoxymorphine, dihydrodesoxymorphine D, krok

Desomorphine (or in some formulations known as Krokodil) is a semi-synthetic opioid commercialized by Roche, with powerful, fast-acting effects, such as sedation and analgesia. It was first discovered and patented in Germany by a German team working for Knoll in 1920 but was not generally recognized. It was later synthesized in 1932 by American chemist Lyndon Frederick Small. Small also successfully patented it in 1934 in the United States. Desomorphine was used in Germany, Austria, and Switzerland under the brand name Permonid and was described as having a fast onset and a short duration of a

Chemical data

Formula
C17H21NO2
Molecular weight
271.35 g/mol
IUPAC name
(4R,4aR,7aS,12bS)-3-methyl-2,4,4a,5,6,7,7a,13-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinolin-9-ol
SMILES
CN1CC[C@]23[C@@H]4[C@H]1CC5=C2C(=C(C=C5)O)O[C@H]3CCC4
InChIKey
LNNWVNGFPYWNQE-GMIGKAJZSA-N
XLogP
2.8
Polar surface area
32.7 Ų
H-bond donors
1
H-bond acceptors
3
Formal charge
0

via PubChem

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Encyclopedic overview

17 sections
Contents
  • Uses
  • Medical
  • Recreational
  • Adverse effects
  • Toxicity
  • Toxicity of desomorphine
  • Toxicity of krokodil
  • Reinforcement disorders
  • Chemistry
  • History
  • Society and culture
  • Legal status
  • North American media
  • See also
  • Notes
  • References
  • External links

Desomorphine (or in some formulations known as Krokodil) is a semi-synthetic opioid commercialized by Roche, with powerful, fast-acting effects, such as sedation and analgesia. It was first discovered and patented in Germany by a German team working for Knoll in 1920 but was not generally recognized. It was later synthesized in 1932 by American chemist Lyndon Frederick Small. Small also successfully patented it in 1934 in the United States. Desomorphine was used in Germany, Austria, and Switzerland under the brand name Permonid and was described as having a fast onset and a short duration of action, with relatively little nausea compared to equivalent doses of morphine. Dose for dose it is roughly ten times more potent than morphine, with 1 mg desomorphine being equivalent 10 mg morphine, via the intravenous (IV) or intramuscular (IM) routes.

Desomorphine is a morphine analogue where the 6-hydroxyl group and the 7,8 double bond have been reduced. The traditional synthesis of desomorphine starts from α-chlorocodide, which is itself obtained by treating codeine with thionyl chloride. By catalytic reduction, α-chlorocodide gives dihydrodesoxycodeine, which yields desomorphine on demethylation.

Excerpted from Wikipedia’s “desomorphine” article, available under the CC BY-SA 4.0 licence.

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