| Identification | Back Directory | [Name]
carbutamide | [CAS]
339-43-5 | [Synonyms]
Emedan
Oranil
U-6987
Bucrol
Burcol
Alentin
Invenol
Nadisan
Bucarban
Bukarban
Diaboral
Glucidoral
CarbutaMid
Butisulfina
carbutamide
AMinophenurobutane
carbutamide USP/EP/BP
1-Butyl-3-sulfanilylurea
UREA,1-BUTYL-3-SULFANILYL-
UREA,1-BUTYL-3-SULPHANILYL
N1-(ButylcarbaMoyl)
sulfanilaMide
1-(4-aminophenyl)sulfonyl-3-butyl-urea
1-(4-azanylphenyl)sulfonyl-3-butyl-urea
4-Amino-N-(butylcarbamoyl)benzenesulfonamide
Benzenesulfonamide, 4-amino-N-[(butylamino)carbonyl]- | [EINECS(EC#)]
206-424-4 | [Molecular Formula]
C11H17N3O3S | [MDL Number]
MFCD00025344 | [MOL File]
339-43-5.mol | [Molecular Weight]
271.34 |
| Hazard Information | Back Directory | [Chemical Properties]
Off-White to Pale Peach Solid | [Uses]
Antidiabetic. | [Originator]
Carbutamide,Servier | [Definition]
ChEBI: Carbutamide is a sulfonamide and a member of benzenes. | [Manufacturing Process]
223 g of the sodium salt of acetylsulfaniamide are stirred with 223 ml of
triethylene glycol. 118 g of n-butyl isothiocyanate are added to the resulting
homogeneous mixture. The resulting syrup is heated to 85°C for 4 hours. The
mixture is then stirred with 1000 ml of chloroform and 1000 ml of water. The
chloroform layer is twice shaken with water, each time with 250 ml. The
aqueous extracts are combined and rendered weakly alkaline to
phenolphthalein by addition of hydrochloric acid. Unreacted acetyl
sulfanilamide precipitates and filtered off. The filtrate is acidified to a pH of
6.5 by the addition of HCl. An oily precipitate settles from the reaction
solution and is separated therefrom. N-Butyl acetyl sulfanilylthiourea is
precipitated from mother liquors obtained thereby by addition of HCl until
Congo paper changes its color to blue. 210 g N-butyl acetyl sulfanilylthiourea
are dissolved in 1400 ml of acetone while heating. The solution is mixed with
500 ml of water. A solution of 63 g of sodium nitrite in 120 ml of water is
added thereto within about 45 minutes while stirring and cooling to 15°-20°C.
A suspension of crystals is obtained. 240 ml of 25% glacial acid are added
thereto within 30 minutes. Stirring of the mixture is continued for 6 hours. N-Butyl acetyl sulfanilylurea mixed with sulfur is precipitated and filtered off. The
crude reaction product is suspended in 1000 ml of water and is rendered
weakly alkaline to phenolphthalein. Undissolved sulfur is filtered off. The
filtrate is acidified by the addition of HCl. 250 g of N-butyl acetyl
sulfanilylthiourea having a melting point of 186°-189°C are obtained. It is
heated with 500 ml of 5 N potassium hydroxide solution to a temperature of
92°C for 2 hours while stirring. The solid reaction product is dissolved by
heating with 750 ml of water and is purified by means of activated charcoal.
The resulting solution is heated to 60°C and acidified by addition of HCl. 187 g
of N-butyl acetyl sulfanilylthiourea melting at 139°-141°C obtained thereby. | [Therapeutic Function]
Oral hypoglycemic |
| Safety Data | Back Directory | [Safety Profile]
A poison by
intraperitoneal route. Moderately toxic by
ingestion and subcutaneous routes. An
experimental teratogen. Other experimental
reproductive effects. When heated to
decomposition it emits very toxic fumes of
NO, and SOx. | [Hazardous Substances Data]
339-43-5(Hazardous Substances Data) | [Toxicity]
LD50 s.c. in mice: 3 g/kg (Haack, Hagedorn) |
|
| Company Name: |
LGM Pharma
|
| Tel: |
1-(800)-881-8210 |
| Website: |
www.lgmpharma.com |
|