Norpipanone
 | |
| Clinical data | |
|---|---|
| ATC code | None |
| Legal status | |
| Legal status |
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| Identifiers | |
| |
| Synonyms | Herchst 10495, NIH-7557 |
| CAS Number | 561-48-8 |
| PubChem (CID) | 22391 |
| ChemSpider | 21015 |
| UNII |
127X8DJ74M  |
| ECHA InfoCard | 100.008.383 |
| Chemical and physical data | |
| Formula | C23H29NO |
| Molar mass | 335.483 g/mol |
| 3D model (Jmol) | Interactive image |
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Norpipanone (INN, BAN; Hexalgon) is an opioid analgesic related to methadone which was developed in Germany and distributed in Hungary, Argentina, and other countries.[1][2] It had originally not been under international control but upon observation of case reports of addiction it was reviewed and shortly thereafter became a controlled substance.[1][2] In the United States, it is a Schedule I controlled substance (ACSCN 9636, zero annual manufacturing quota as of 2014). The salts in use are the hydrobromide (free base conversion ratio 0.806) and hydrochloride (0.902).
Synthesis
See also
- Dipipanone
- Normethadone
- Valeronitrile
References
- 1 2 John B Buckingham (December 1995). Dictionary of Organic Compounds. CRC Press. p. 2883. ISBN 978-0-412-54090-5. Retrieved 11 May 2012.
- 1 2 David S. Patterson (12 March 2002). Foreign Relations of the United States, 1961-1963, Volume XXV: Organization of Foreign Policy; Information Policy; United Nations; Scientific Matters. Government Printing Office. pp. 766–767. ISBN 978-0-16-050885-1. Retrieved 11 May 2012.
- ↑ Duprè, D. J.; Elks, J.; Hems, B. A.; Speyer, K. N.; Evans, R. M. (1949). "113. Analgesics. Part I. Esters and ketones derived from α-amino-ω-cyano-ωωdiarylalkanes". Journal of the Chemical Society (Resumed). Chemical Society: 500. doi:10.1039/JR9490000500.
- ↑ Bockmühl, M.; Ehrhart, G. (1949). "Über eine neue Klasse von spasmolytisch und analgetisch wirkenden Verbindungen, I". Justus Liebigs Annalen der Chemie. 561: 52. doi:10.1002/jlac.19495610107.
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