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butalamine

CAS No.
22131-35-7
Chemical Name:
butalamine
Synonyms
butalamine;Butalamina;3-Phenyl-5-(dibutylaMinoethylaMino)-1,2,4-oxadiazole;5-[2-(Dibutylamino)ethylamino]-3-phenyl-1,2,4-oxadiazole;N1,N1-Dibutyl-N2-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,2-ethanediaMi;N,N-Dibutyl-N'-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,2-ethanediaMine;1,2-Ethanediamine, N1,N1-dibutyl-N2-(3-phenyl-1,2,4-oxadiazol-5-yl)-
CBNumber:
CB8933148
Molecular Formula:
C18H28N4O
Molecular Weight:
316.44
MDL Number:
MFCD00868274
MOL File:
22131-35-7.mol
Last updated:2023-05-04 17:34:35

butalamine Properties

storage temp. Refrigerator
solubility Chloroform )Slightly), Ethyl Acetate (Slightly)
form Oil
color Dark Brown
FDA UNII 140T9JTG43
ATC code C04AX23

butalamine price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC B689930 Butalamine 22131-35-7 250mg $1190 2021-12-16 Buy
American Custom Chemicals Corporation API0010890 BUTALAMINE 95.00% 22131-35-7 250MG $1963.5 2021-12-16 Buy
Biosynth Carbosynth FB19369 Butalamine 22131-35-7 1mg $70 2021-12-16 Buy
Biosynth Carbosynth FB19369 Butalamine 22131-35-7 2mg $110 2021-12-16 Buy
Biosynth Carbosynth FB19369 Butalamine 22131-35-7 5mg $190 2021-12-16 Buy
Product number Packaging Price Buy
B689930 250mg $1190 Buy
API0010890 250MG $1963.5 Buy
FB19369 1mg $70 Buy
FB19369 2mg $110 Buy
FB19369 5mg $190 Buy

butalamine Chemical Properties,Uses,Production

Originator

Surheme,Aron,France,1969

Uses

Butalamine is a vasodilator (peripheral) with local anesthetic effects. Butalamine has been shown to inhibit state 3 respiration and decrease ADP/O in rat liver.

Definition

ChEBI: Butalamine is an oxadiazole and a ring assembly.

Manufacturing Process

Benzaldehyde and hydroxylamine may be reacted, the product chlorinated and then reacted with cyanamide to give 5-amino-3-phenyl-1,2,4-oxadiazole.
32 grams of 3-phenyl-5-amino-1,2,4-oxadiazole dissolved in about 150 ml of anhydrous benzene, 7.8 grams of sodium amide are added and the reaction mixture heated at the boiling point with stirring for 2 hours. A solution of 38.3 grams of dibutylaminoethyl chloride in benzene is then added and the mixture heated to boiling under reflux for four hours. The sodium chloride is separated as previously described, the benzene removed by vacuum distillation and 56 grams of 3-phenyl-5-(dibutylaminoethylamino)-1,2,4-oxadiazole is obtained in the form of an oil which is then converted directly to the crystalline hydrochloride. This is accomplished by dissolving the oil in ethanol and adding the stoichiometric equivalent of anhydrous ethyl ether saturated with gaseous hydrogen chloride. The recrystallized salt is found to have a melting point of 145°C.

Therapeutic Function

Vasodilator

butalamine Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 26)Suppliers
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TargetMol Chemicals Inc.
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J & K SCIENTIFIC LTD. 010-82848833 400-666-7788 jkinfo@jkchemical.com China 96815 76
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TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 24017 58
Shaanxi Dideu Newmaterial Co., Ltd. 029-63373950 15353716720 1052@dideu.com China 10011 58
Carbosynth -- sales@carbosynth.com United Kingdom 6018 58
butalamine 5-[2-(Dibutylamino)ethylamino]-3-phenyl-1,2,4-oxadiazole 3-Phenyl-5-(dibutylaMinoethylaMino)-1,2,4-oxadiazole N,N-Dibutyl-N'-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,2-ethanediaMine N1,N1-Dibutyl-N2-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,2-ethanediaMi 1,2-Ethanediamine, N1,N1-dibutyl-N2-(3-phenyl-1,2,4-oxadiazol-5-yl)- Butalamina 22131-35-7 C18H28N4O