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Name |
Oxymorphinone hydrochloride |
EINECS | N/A |
CAS No. | 357-07-3 | Density | 1.5g/cm3 |
PSA | 70.00000 | LogP | 1.48510 |
Solubility | N/A | Melting Point |
N/A |
Formula | C17H19 N O4 . Cl H | Boiling Point | 518.6°Cat760mmHg |
Molecular Weight | 337.803 | Flash Point | 267.5°C |
Transport Information | N/A | Appearance | N/A |
Safety | Poison by ingestion, intravenous, intraperitoneal, and subcutaneous routes. An experimental teratogen. When heated to decomposition it emits toxic fumes of NOx and HCl. | Risk Codes | N/A |
Molecular Structure | Hazard Symbols | N/A | |
Synonyms |
Morphinan-6-one,4,5-epoxy-3,14-dihydroxy-17-methyl-, hydrochloride, (5a)- (9CI); Morphinan-6-one, 4,5a-epoxy-3,14-dihydroxy-17-methyl-,hydrochloride (8CI); Morphinone, dihydro-14-hydroxy-, hydrochloride (7CI);14-Hydroxydihydromorphinone hydrochloride; Numorphan; Numorphan hydrochloride;Opana; Opana ER; Oxymorphinone hydrochloride; Oxymorphone hydrochloride;Oxymorphone hydrochloride ER |
Article Data | 8 |
Product Name: Oxymorphone HCL narcotic analgesic
Synonyms: (1S,5R,13R,17S)-10,17-Dihydroxy-4-méthyl-12-oxa-4-azapentacyclo[9.6.1.0~1,13~.0~5,17~.0~7,18~]octadéca-7(18),8,10-trién-14-one chlorhydrate ; (1S,5R,13R,17S)-10,17-Dihydroxy-4-methyl-12-oxa-4-azapentacyclo[9.6.1.0~1,13~.0~5,17~.0~7,18~]octadeca-7(18),8,10-trien-14-one hydrochloride ; (1S,5R,13R,17S)-10,17-Dihydroxy-4-methyl-12-oxa-4-azapentacyclo[9.6.1.0~1,13~.0~5,17~.0~7,18~]octadeca-7(18),8,10-trien-14-onhydrochlorid ;(5alpha)-3,14-Dihydroxy-17-methyl-4,5-epoxymorphinan-6-one hydrochloride
CAS NO:357-07-3
Molecular Formula of Oxymorphinone hydrochloride (CAS NO.357-07-3) :C17H20ClNO4
Molecular Weight of Oxymorphinone hydrochloride (CAS NO.357-07-3) :337.798
Molecular Structure of Oxymorphinone hydrochloride (CAS NO.357-07-3) :
Flash Point: 267.5 °C
Enthalpy of Vaporization: 83.3 kJ/mol
Boiling Point: 518.6 °C at 760 mmHg
Vapour Pressure: 1.39E-11 mmHg at 25°C
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intraperitoneal | 301mg/kg (301mg/kg) | BEHAVIORAL: ANALGESIA | Therapie. Vol. 15, Pg. 1208, 1960. |
mouse | LD50 | intravenous | 185mg/kg (185mg/kg) | BEHAVIORAL: ANALGESIA | Therapie. Vol. 15, Pg. 1208, 1960. |
mouse | LD50 | oral | 402mg/kg (402mg/kg) | BEHAVIORAL: ANALGESIA | Therapie. Vol. 15, Pg. 1208, 1960. |
mouse | LD50 | subcutaneous | 285mg/kg (285mg/kg) | BEHAVIORAL: ANALGESIA | Therapie. Vol. 15, Pg. 1208, 1960. |
Poison by ingestion, intravenous, intraperitoneal, and subcutaneous routes. An experimental teratogen. When heated to decomposition it emits toxic fumes of NOx and HCl.
RIDADR 3249
HazardClass 6.1(b)
PackingGroup III