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| Name |
PROTIRELIN TARTRATE |
EINECS | N/A |
| CAS No. | 53935-32-3 | Density | N/A |
| PSA | 273.31000 | LogP | -1.72690 |
| Solubility | N/A | Melting Point |
N/A |
| Formula | C16H22N6O4•C4H6O4 | Boiling Point | 978.4°C at 760 mmHg |
| Molecular Weight | 480.54 | Flash Point | 545.5°C |
| Transport Information | N/A | Appearance | N/A |
| Safety | Moderately toxic by intravenous and intramuscular routes. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx. | Risk Codes | N/A |
| Molecular Structure |
|
Hazard Symbols | N/A |
| Synonyms |
L-Prolinamide,5-oxo-L-prolyl-L-histidyl-,tartrate;TRH-T;Protirelin tartrate;L-Pyroglutamyl-L-histidyl-L-prolineamide-L-tartrate; |
PROTIRELIN TARTRATE Toxicity Data With Reference
| 1. | orl-rat LD50:18 g/kg | TAKHAA Takeda Kenkyusho Ho. Journal of the Takeda Research Laboratories. 36 (1977),22A. | ||
| 2. | ipr-rat LD50:2700 mg/kg | TAKHAA Takeda Kenkyusho Ho. Journal of the Takeda Research Laboratories. 36 (1977),22A. | ||
| 3. | scu-rat LD50:6600 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982” Edited by Japan Pharmaceutical Information Center. 6 (1982),727. | ||
| 4. | ivn-rat TDLo:580 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982” Edited by Japan Pharmaceutical Information Center. 6 (1982),727. | ||
| 5. | ims-rat TDLo:2900 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982” Edited by Japan Pharmaceutical Information Center. 6 (1982),727. | ||
| 6. | orl-mus LD50:16 g/kg | TAKHAA Takeda Kenkyusho Ho. Journal of the Takeda Research Laboratories. 36 (1977),22A. | ||
| 7. | scu-mus LD50:5400 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982” Edited by Japan Pharmaceutical Information Center. 6 (1982),727. | ||
| 8. | ivn-mus LD50:520 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982” Edited by Japan Pharmaceutical Information Center. 6 (1982),727. | ||
| 9. | ims-mus LD50:3300 mg/kg | NIPROTIRELIN TARTRATE Safety ProfileModerately toxic by intravenous and intramuscular routes. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx.
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5-oxoprolylhistidylprolinamide 2,3-dihydroxybutanedioate (1:1)
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