| Identification | Back Directory | [Name]
emylcamate | [CAS]
78-28-4 | [Synonyms]
JD 91
MK-250
Statran
Nuncital
KABI-925
Striatran
emylcamate
3-methylpentan-3-yl carbamate
3-Pentanol, 3-Methyl-, 3-carbaMate
carbamic acid (1-ethyl-1-methyl-propyl) ester | [EINECS(EC#)]
201-101-4 | [Molecular Formula]
C7H15NO2 | [MDL Number]
MFCD00868182 | [MOL File]
78-28-4.mol | [Molecular Weight]
145.2 |
| Hazard Information | Back Directory | [Originator]
Striatin,MSD,US,1960 | [Uses]
Emylcamate is used in combination with compounds that influence brain function and or psychological state to treat herpes virus infection and outbreaks. | [Definition]
ChEBI: Emylcamate is a carbamate ester. | [Manufacturing Process]
30.5 g of 3-methyl-3-pentanol, 8.1 g of potassium cyanate and 16.3 g of
trichloroacetic acid are heated while stirring at 45°C to 50°C for 24 hours,
neutralized by successive addition of anhydrous sodium carbonate. The
precipitate is removed from the reaction mixture. Unreacted 3-methyl-3-
pentanol is distilled off and the residue is added to a small volume of distilled
water. After precipitation and filtration the resulting 3-methyl-3-pentanol
carbamate is dried and recrystallized from petroleum ether. MP 54°C to 55°C. | [Therapeutic Function]
Tranquilizer | [Purification Methods]
Crystallise the carbamate from 30% aqueous EtOH. [Beilstein 1 IV 1773.] |
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