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OXAZEPAM

OXAZEPAM

CAS:
604-75-1
MF:
C15H11ClN2O2
MW:
286.71

Properties

Melting point:
205-206°
Boiling point:
506.5±50.0 °C(Predicted)
Density 
1.3052 (rough estimate)
refractive index 
1.5200 (estimate)
Flash point:
11 °C
storage temp. 
−20°C
solubility 
Practically insoluble in water, slightly soluble in ethanol (96 per cent).
pka
pKa 1.6/11.6(5% MeOH in H2O,t =20,I=0.15) (Uncertain)
Water Solubility 
20mg/L(22 ºC)

Safety Information

Symbol(GHS) 

GHS07,GHS08
Signal word 
Warning
Hazard statements 
H336-H351
Precautionary statements 
P202-P261-P271-P280-P304+P340+P312-P308+P313
Hazard Codes 
Xn,T,F
Risk Statements 
40-39/23/24/25-23/24/25-11
Safety Statements 
7-16-36/37-45
RIDADR 
UN 1230 3/PG 2
WGK Germany 
3
RTECS 
DF1400000
HazardClass 
6.1(b)
PackingGroup 
III
HS Code 
2933910000
Toxicity
LD50 in mice, rats (mg/kg): >5010, >5010 orally (Goldenthal)

Use

Oxazepam, 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzodiazpin-2-one (Serax), isan active metabolite of both chlordiazepoxide and diazepamand can be considered a prototype for the 3-hydroxy benzo-diazepines. It is much more polar than diazepam. Oxazepam is rapidlyinactivated to glucuronidated metabolites that are excretedin the urine. Thus, the half-life of oxazepam is about 4 to 8hours, and it is marketed as a short-acting anxiolytic. As aresult, its cumulative effects with chronic therapy are muchless than with long-acting benzodiazepine such as chlordiazepoxideand diazepam.

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OXAZEPAMDoxefazepamLorazepamTEMAZEPAMCinolazepam
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