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| Name |
Fencamine hydrochloride |
EINECS | N/A |
| CAS No. | 63918-50-3 | Density | 1.23g/cm3 |
| PSA | 77.09000 | LogP | 1.82060 |
| Solubility | N/A | Melting Point |
N/A |
| Formula | C20H28 N6 O2 . Cl H | Boiling Point | 564°C at 760 mmHg |
| Molecular Weight | 421.00 | Flash Point | 294.9°C |
| Transport Information | N/A | Appearance | N/A |
| Safety | Poison by intraperitoneal route. Moderately toxic by ingestion. A central nervous system stimulant. When heated to decomposition it emits very toxic fumes of Cl− and NOx. | Risk Codes | N/A |
| Molecular Structure |
|
Hazard Symbols | N/A |
| Synonyms |
1H-Purine-2,6-dione,3,7-dihydro-1,3,7-trimethyl-8-[[2-[methyl(1-methyl-2-phenylethyl)amino]ethyl]amino]-,monohydrochloride (9CI) |
Fencamine hydrochloride Chemical Properties
IUPAC Name: 1,3,7-Trimethyl-8-[2-[methyl(1-phenylpropan-2-yl)amino]ethylamino]purine-2,6-dione hydrochloride
Synonyms of Fencamine hydrochloride (CAS NO.63918-50-3) : Altimina ; Fencamine HCl ; Fencamine hydrochloride ; Sicoclor ; Ethylenediamine, 1-(1,3,7-trimethyl-2,6-dioxopurin-8-yl)-4-(2-phenyl-1-methyl)ethyl-4-methyl-, hydrochloride
InChI:InChI=1/C20H28N6O2.ClH/c1-14(13-15-9-7-6-8-10-15)23(2)12-11-21-19-22-17-16(24(19)3)18(27)26(5)20(28)25(17)4;/h6-10,14H,11-13H2,1-5H3,(H,21,22);1H
CAS NO:63918-50-3
Molecular Formula:C20H29ClN6O2
Molecular Weight :420.9363
Molecular Structure :.png)
Flash Point: 294.9 °C
Enthalpy of Vaporization: 84.75 kJ/mol
Boiling Point: 564 °C at 760 mmHg
Vapour Pressure: 9.6E-13 mmHg at 25°C
Fencamine hydrochloride Toxicity Data With Reference
| Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source | |
|---|---|---|---|---|---|
| mouse | LD50 | intraperitoneal | 82mg/kg (82mg/kg) | "Psychotropic Drugs and Related Compounds," 2nd ed., Usdin, E., and D.H. Efron, Washington, DC, 1972Vol. -, Pg. 229, 1972. | |
| mouse | LD50 | oral | 418mg/kg (418mg/kg) | "Psychotropic Drugs and Related Compounds," 2nd ed., Usdin, E., and D.H. Efron, Washington, DC, 1972Vol. -, Pg. 229, 1972. | |
| rat | LD50 | intraperitoneal | 93mg/kg (93mg/kg) | "Psychotropic Drugs and Related Compounds," 2nd ed., Usdin, E., and D.H. Efron, Washington, DC, 1972Vol. -, Pg. 229, 1972. | |
| rat | LD50 | oral | 508mg/kg (508mg/kg) | "Psychotropic Drugs and Related Compounds," 2nd ed., Usdin, E., and D.H. Efron, Washington, DC, 1972Vol. -, Pg. 229, 1972. |
Fencamine hydrochloride Safety Profile
Poison by intraperitoneal route. Moderately toxic by ingestion. A central nervous system stimulant. When Fencamine hydrochloride (CAS NO.63918-50-3) is heated to decomposition ,it emits very toxic fumes of Cl− and NOx.
RIDADR :3249
HazardClass: 6.1(b)
PackingGroup :III
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