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Basic Information
| CAS No.: | 964-52-3 |
|---|---|
| Name: | MOXISYLYTE HYDROCHLORIDE |
| Molecular Structure: | |
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| Formula: | C16H25 N O3 . Cl H |
| Molecular Weight: | 315.84 |
| Synonyms: | Carvacrol,5-[2-(dimethylamino)ethoxy]-, acetate (ester), hydrochloride (8CI); Carvacrol,5-[2-(dimethylamino)ethoxy]-, acetate, hydrochloride (6CI,7CI); Phenol,4-[2-(dimethylamino)ethoxy]-2-methyl-5-(1-methylethyl)-, acetate (ester),hydrochloride (9CI); 4-(2-Dimethylaminoethoxy)-5-isopropyl-2-methylphenyl acetatehydrochloride; Arlitine; Carlytene; M 101; M 101 (vasodilator); Moxisylytehydrochloride; Moxyl; Opilon; Opilon hydrochloride; Thymoxamine hydrochloride;Uroalpha; Vasoklin |
| Density: | 1.018g/cm3 |
| Melting Point: | 208-210° |
| Boiling Point: | 371°Cat760mmHg |
| Flash Point: | 178.2°C |
| Hazard Symbols: |
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| Risk Codes: | 20/21/22 |
| Safety: | Poison by ingestion, subcutaneous, intravenous and intraperitoneal routes. Experimental reproductive effects. Used as an adrenergic blocker. When heated to decomposition it emits toxic fumes of NOx and HCl. |
| PSA: | 38.77000 |
| LogP: | 3.78610 |
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MOXISYLYTE HYDROCHLORIDE
Chemistry
The molecular formula of THYMOXAMINE HYDROCHLORIDE (964-52-3) is C16H26ClNO3 and its formula weight is 315.84 g/mol.Its EINECS is 213-519-4. The density of THYMOXAMINE HYDROCHLORIDE (964-52-3) is 1.018g/cm3 and it has a melting point of 208–210°C.The boiling point is 371°C at 760mmHg.Polarizability is 10-24cm3.Enthalpy of vaporization is 61.8 kJ/mol.Its flash point is 178.2°C and the vapor pressure is 1.06E-05 mmHg at 25°C .The chemical synonyms of THYMOXAMINE HYDROCHLORIDE (964-52-3) are (2-(4-acetoxy-2-isopropyl-5-methylphenoxy)ethyl)dimethylaminehydrochloride;5-(2-(n,n-dimethylamino)ethoxy)carvacrolacetatehydrochloride;arlitene;carlytene;carvacrol,5-(2-(n,n-dimethylamino)ethoxy)-,acetate,hydrochloride;chlorhydratedeacetoxy-thymoxy-ethyl-dimethylamine;m-101 and opilonhydrochloride .The molecular structure of THYMOXAMINE HYDROCHLORIDE (964-52-3) is 
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.Toxicity Data With Reference
| 1. | orl-rat LD50:740 mg/kg | THERAP Therapie. 26 (1971),775. | ||
| 2. | ipr-rat LD50:96 mg/kg | KSRNAM Kiso to Rinsho. Clinical Report. 16 (1982),1147. | ||
| 3. | scu-rat LD50:190 mg/kg | THERAP Therapie. 26 (1971),775. | ||
| 4. | ivn-rat LD50:32 mg/kg | KSRNAM Kiso to Rinsho. Clinical Report. 16 (1982),1147. | ||
| 5. | orl-mus LD50:255 mg/kg | JPPMAB Journal of Pharmacy and Pharmacology. 32 (1980),209. | ||
| 6. | ipr-mus LD50:81 mg/kg | KSRNAM Kiso to Rinsho. Clinical Report. 16 (1982),1147. | ||
| 7. | scu-mus LD50:152 mg/kg | KSRNAM Kiso to Rinsho. Clinical Report. 16 (1982),1147. | ||
| 8. | ivn-mus LD50:28 mg/kg | KSRNAM Kiso to Rinsho. Clinical Report. 16 (1982),1147. | ||
| 9. | orl-dog LDLo:700 mg/kg | KSRNAM Kiso to Rinsho. Clinical Report. 16 (1982),1147. | ||
| 10. | ivn-dog LD50:54,500 µg/kg | KSRNAM Kiso to Rinsho. Clinical Report. 16 (1982),1147. | ||
| 11. | orl-mky LDLo:1500 mg/kg |
Safety Profile
Poison by ingestion, subcutaneous, intravenous and intraperitoneal routes. Experimental reproductive effects. Used as an adrenergic blocker. When heated to decomposition it emits toxic fumes of NOx and HCl. Hazard symbols is Xn.
Risk statements is 20/21/22.
Safety statements is 36.
Risk statements is 20/21/22.
Safety statements is 36.
Specification
Its extinguishing agent is foam, carbon dioxide , sand and dry powder.