| Weight | 271.36 g/mol |
|---|---|
| Formula | C17H21NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
Desomorphine (427-00-9)
krokodil
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- Sigma-Aldrich - Desomorphine107.00 USD
- Fisher Scientific - Search for Desomorphine
- TCI - Search for Desomorphine
- STUDIES OF CERTAIN ADDICTION CHARACTERISTICS OF (a) DIHYDROMORPHINE ("PARAMORPHAN"), (b) DIHYDRODESOXYMORPHINE-D ("DESOMORPHINE"), (c) DIHYDRODESOXYCODEINE-D ("DESOCODEINE"), AND (d) METHYLDIHYDROMORPHINONE ("METOPON") (Journal of Pharmacology and Experimental Therapeutics, 1939)
- Breaking worse: The emergence of krokodil and excessive injuries among people who inject drugs in Eurasia (International Journal of Drug Policy, 2013)
- Desomorphine Goes Crocodile (Journal of Addictive Diseases, 2012)
- Agonists-antagonists derived from desomorphine and metopon (Journal of Medicinal Chemistry, 1970)
- "Krokodil":revival of an old drug with new problems. (Substance Use & Misuse, 2012)
- The harmful chemistry behind krokodil (desomorphine) synthesis and mechanisms of toxicity (Forensic Science International, 2015)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - krokodil
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SMILESCN1CCC23C4C1CC5=C2C(=C(C=C5)O)OC3CCC4
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InChIKeyLNNWVNGFPYWNQE-UHFFFAOYSA-N
- Pubchem - Desomorphine
- Wikipedia - desomorphine
Desomorphine is a synthetic opioid developed by Roche. With powerful, fast-acting effects, such as sedation and analgesia. First synthesized in 1932 and patented in 1934 in the United States, desomorphine was used in 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.
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