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| CAS No.: | 60607-34-3 |
|---|---|
| Name: | Oxatomide |
| Article Data: | 2 |
| Molecular Structure: | |
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|
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| Formula: | C27H30N4O |
| Molecular Weight: | 426.561 |
| Synonyms: | Celtect;Cobiona;Dasten;KW 4354;NSC 309710;Oxatomide;R 35443;Tinset; |
| EINECS: | 262-320-9 |
| Density: | 1.175 g/cm3 |
| Melting Point: | 153.60C |
| Boiling Point: | 621.1 °C at 760 mmHg |
| Flash Point: | 329.4 °C |
| Solubility: | DMSO: soluble |
| Appearance: | White powder |
| Hazard Symbols: |
 Xi;  Xn
|
| Risk Codes: | 22-36/37/38 |
| Safety: | 26-36 |
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Chemistry
Molecular Formula: C27H30N4O
Molecular Weight: 426.55
EINECS: 262-320-9
Density: 1.175 g/cm3
Flash Point: 329.4 °C
Melting Point: 153.6 °C
Appearance: White powder.
Enthalpy of Vaporization: 95.4 kJ/mol
Boiling Point: 621.1 °C at 760 mmHg
Vapour Pressure: 5.1E-16 mmHg at 25°C
Solubility: DMSO: soluble Insoluble in water
Stability of Oxatomide (60607-34-3): Stable at normal temperatures and pressures.
Synonyms: Oxatomide ; 1-(3-(4-(Diphenylmethyl)-1-piperazinyl)propyl)-1,3-dihydro-2h-benzimidazol-2 ; 1-(3-(4-(Diphenylmethyl)-1-piperazinyl)propyl)-2-benzimidazolinone ; 1,3-Dihydro-1-(3-(4-(diphenylmethyl)-1-piperazinyl)propyl)-2h-benzimidazol-2-on ; 2H-benzimidazol-2-one,1,3-Dihydro-1-(3-(4-(diphenylmethyl)-1-piperazinyl)propy ; KW-4354 ; Oxatimide
Product Categories: Intermediates & Fine Chemicals ; Pharmaceuticals
Following is the molecular structure of Oxatomide (60607-34-3):
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Uses
Usage of Oxatomide (60607-34-3): Orally active anti-allergic agent; related structurally to cinnarizine and having a novel biphasic mode of action
Safety Information of Oxatomide (60607-34-3):
Hazard Codes: Xn,Xi
Xi: Irritant.gif){kind=small}
Xn: Harmful.gif){kind=small}
Risk Statements: 22-36/37/38
22: Harmful if swallowed
36/37/38: Irritating to eyes, respiratory system and skin
Safety Statements: 26-36
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice 36: Wear suitable protective clothing
WGK Germany: 3
RTECS: DE2276000
Toxicity Data With Reference
| 1. | orl-rat LD50:1410 mg/kg | YACHDS Yakuri to Chiryo. Pharmacology and Therapeutics. 12 (1984),2769. | ||
| 2. | ipr-rat LD50:63 mg/kg | YACHDS Yakuri to Chiryo. Pharmacology and Therapeutics. 12 (1984),2769. | ||
| 3. | ivn-rat LD50:29 mg/kg | YACHDS Yakuri to Chiryo. Pharmacology and Therapeutics. 12 (1984),2769. | ||
| 4. | orl-mus LD50:9596 mg/kg | YACHDS Yakuri to Chiryo. Pharmacology and Therapeutics. 12 (1984),2769. | ||
| 5. | ipr-mus LD50:7926 mg/kg | YACHDS Yakuri to Chiryo. Pharmacology and Therapeutics. 12 (1984),2769. | ||
| 6. | ivn-mus LD50:25 mg/kg | YACHDS Yakuri to Chiryo. Pharmacology and Therapeutics. 12 (1984),2769. | ||
| 7. | orl-gpg LD50:320 mg/kg | DRFUD4 Drugs of the Future. 3 (1978),465. | ||
| 8. | ivn-gpg LD50:23 mg/kg | DRFUD4 Drugs of the Future. 3 (1978),465. |
Safety Profile
Poison by ingestion, intraperitoneal, and intravenous routes. An experimental teratogen. Experimental reproductive effects. Used to treat allergies and asthma. When heated to decomposition it emits toxic fumes of NOx.