| Identification | Back Directory | [Name]
ALLOBARBITAL | [CAS]
52-43-7 | [Synonyms]
Dial
Dorm
Malil
Alnox
go1058
Dialog
Curral
Diadol
Malilum
Novallyl
NSC-9324
Barbidal
Barballyl
Diallymal
Dormallyl
Alobarbital
Allbarbital
ALLOBARBITAL
Allobarbitone
Allybarbitural
Allylbarbitural
Diallylbarbital
Allobarbital,99%
dial(barbiturate)
Allobarbital 13C4
Dial (barbiturate)
component of Dialog
diallylbarbituricacid
Diallylbarbituric acid
ALLOBARBITAL USP/EP/BP
5,5-diallyl-barbituricaci
5,5-DIALLYLBARBITURIC ACID
Barbituric acid, 5,5-diallyl-
ALLOBARBITAL (5,5-DIALLYLBARBITURIC ACID)
5,5-Diallyl-2,4,6(1H,3H,5H)-pyrimidinetrione
5-5-DIALLYLBARBITURIC ACID*METHANOL SOLU TION
5,5-di(prop-2-enyl)-1,3-diazinane-2,4,6-trione
5,5-bis(prop-2-enyl)-1,3-diazinane-2,4,6-trione
6(1h,3h,5h)-pyrimidinetrione,5,5-di-2-propenyl-4
5,5-diallylbarbituric acid free*acid--dea schedul
5,5-Di-2-propenyl-2,4,6(1H,3H,5H)-pyrimidinetrione
5,5-DIALLYLBARBITURIC ACID FREE*ACID--DE A SCHEDULE
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-di-2-propenyl-
5,5-Di-2-propen-1-yl-2,4,6(1H,3H,5H)-pyriMidinetrione
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-di-2-propen-1-yl- | [EINECS(EC#)]
200-140-4 | [Molecular Formula]
C10H12N2O3 | [MDL Number]
MFCD00056090 | [MOL File]
52-43-7.mol | [Molecular Weight]
208.21 |
| Safety Data | Back Directory | [Hazard Codes ]
T | [Risk Statements ]
25 | [Safety Statements ]
45 | [RIDADR ]
UN 2811 6.1/PG 3
| [WGK Germany ]
3
| [RTECS ]
CQ3325000
| [HazardClass ]
6.1(b) | [PackingGroup ]
III | [Toxicity]
LD50 i.p. in rats: 127.3 mg/kg (Sandberg) |
| Hazard Information | Back Directory | [Originator]
Allobarbital, Fluorochem Ltd. | [Uses]
Allobarbital is a barbiturate derivative that is primarily used as an anticonvulsant. Allobarbital also shows hypnotic activity and is used to boost the activity of analgesic drugs. Studies show that Allobarbital is an effective promoters of hepatocarcinogenesis.
Allobarbital is a Controlled Substance. | [Definition]
ChEBI: Allobarbital is a member of barbiturates. | [Manufacturing Process]
To a mixture of 43 parts barbituric acid, 200 parts of water and 5 parts of
cuprous sulfate in 10 parts of water is added 82 parts of allylbromide. Then at
room temperature is added 27 parts of sodium hydroxide (10% aqueous
solution). 5,5-Diallylbarbituric acid is isolated by filtration. After
recrystallization from water 5,5-diallylbarbituric acid has melting polint 169-
170°C. | [Therapeutic Function]
Sedative, Hypnotic |
|