Molecular Formula | C22H26N2O2 |
Molar Mass | 350.46 |
Density | 1.1260 (rough estimate) |
Melting Point | 147-153 °C dec. |
Boling Point | 484.44°C (rough estimate) |
Specific Rotation(α) | D20 +114° (c = 1 in pyridine) |
Flash Point | 207.506°C |
Solubility | Soluble in chloroform or 96% ethanol, almost insoluble in water. |
Vapor Presure | 0mmHg at 25°C |
Appearance | White fine powder |
Color | white |
Maximum wavelength(λmax) | ['315nm(EtOH)(lit.)'] |
Merck | 14,9991 |
pKa | 7.87±0.60(Predicted) |
Storage Condition | Sealed in dry,2-8°C |
Stability | Photosensitive |
Sensitive | Sensitive to light |
Refractive Index | 1.6500 (estimate) |
MDL | MFCD00211233 |
Physical and Chemical Properties | White crystalline powder, odorless and tasteless. Soluble in chloroform or 96% ethanol, a few insoluble in water. Melting point 147-153 °c (decomposition). [Α] D20 +114 °(C = 1, pyridine). UV maximum absorption (96% ethanol):229,275,315nm (h28200, 12000,7100). Acute toxicity LD50 mice, rats (mg/kg):534,503 oral; 240,133.8 intraperitoneal injection; 58.7,42.6 intravenous injection. |
Use | Cerebrovascular medication |
Hazard Symbols | Xn - Harmful |
Risk Codes | 22 - Harmful if swallowed |
Safety Description | 36 - Wear suitable protective clothing. |
WGK Germany | 3 |
RTECS | JW4792000 |
HS Code | 29399990 |
Toxicity | LD50 in mice, rats (mg/kg): 534, 503 orally; 240, 133.8 i.p.; 58.7, 42.6 i.v. (Pálosi, Szporny), also reported as 161.2 mg/kg i.p. in mice (Cholnoky, Dmk) |