MORPHINE SULFATE NARCOTIC ANALGESIC
- CAS No.
- 64-31-3
- Chemical Name:
- MORPHINE SULFATE NARCOTIC ANALGESIC
- Synonyms
- Capros;Avinza;Skenan;Kadian;Kapanol;NIH 0001;Oblioser;Oramorph;Relipain;Morphelan
- CBNumber:
- CB1497069
- Molecular Formula:
- C18H25NO8S
- Molecular Weight:
- 415.458
- MDL Number:
- MFCD00069309
- MOL File:
- 64-31-3.mol
| Melting point | 250 °C |
|---|---|
| Flash point | 11℃ |
| storage temp. | −20°C |
| CAS DataBase Reference | 64-31-3 |
| FDA UNII | DY70C97N30 |
| NCI Drug Dictionary | Avinza |
| EPA Substance Registry System | Morphinan-3,6-diol, 7,8-didehydro-4,5-epoxy-17-methyl-(5.alpha.,6.alpha.)-, sulfate (2:1) (64-31-3) |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |    GHS02,GHS06,GHS08 |
|---|---|
| Signal word | Danger |
| Hazard statements | H225-H301-H311-H331-H370 |
| Precautionary statements | P210-P260-P280-P301+P310-P311 |
| Hazard Codes | F,T |
| Risk Statements | 11-23/24/25-39/23/24/25 |
| Safety Statements | 7-16-36/37-45 |
| RIDADR | UN 1230 3/PG 2 |
| WGK Germany | 1 |
MORPHINE SULFATE NARCOTIC ANALGESIC Chemical Properties,Uses,Production
Originator
Avinza,Aetna Inc.
Uses
Analgesic (narcotic).
Definition
ChEBI: Morphine sulfate is an alkaloid sulfate salt. It contains a morphine.
Manufacturing Process
Morphin was extracted from the plant vegetable (the poppy) by the mixture of
water and methanol or the aqueous solution of potassium pyrosulfate. The
precipitation of the morphin was carried out by addition to the extract the
aqueous solution of sodium carbonate.
Morphin can be obtained from the extract by using the cation exchanger.
Free base of morphin was transformated to the sulfate salt.
brand name
Astramorph (AstraZeneca); Avinza (Ligand); Depodur (Skyepharma); Duramorph (Baxter Healthcare); Infumorph (Baxter Healthcare); Kadian (Alpharma); Ms Contin (Purdue Frederick); Oramorph (Xanodyne).
Therapeutic Function
Narcotic analgesic, Sedative
Safety Profile
Poison by subcutaneous, intravenous, intraperitoneal, and intramuscular routes. Moderately toxic by ingestion and parenteral routes. An experimental teratogen. Experimental reproductive effects. Mutation data reported. Used as a narcotic. Abuse leads to habituation or addiction. When heated to decomposition it emits very toxic fumes of NOx and SOx.