Basic information Safety Supplier Related

Buflomedil

Basic information Safety Supplier Related

Buflomedil Basic information

Product Name:
Buflomedil
Synonyms:
  • 1-Butanone, 4-(1-pyrrolidinyl)-1-(2,4,6-trimethoxyphenyl)-
  • 2',4',6'-Trimethoxy-4-(1-pyrrolidinyl)butyrophenone
  • 4-(1-pyrrolidinyl)-1-(2,4,6-trimethoxyphenyl)-1-butanon
  • AURORA KA-850
  • BUFLOMEDIL
  • BufluomedilHcl
  • Buflomedil Hcl 35543-24-9 / Base
  • Buflomedil (base and/or unspecified salts)
CAS:
55837-25-7
MF:
C17H25NO4
MW:
307.38
EINECS:
259-851-3
Product Categories:
  • API
  • Adrenoceptor
  • Pharmaceutical
  • Active Pharmaceutical Ingredients
Mol File:
55837-25-7.mol
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Buflomedil Chemical Properties

Boiling point:
454.5±45.0 °C(Predicted)
Density 
1.090±0.06 g/cm3(Predicted)
pka
10.15±0.20(Predicted)
LogP
3.131 (est)
CAS DataBase Reference
55837-25-7(CAS DataBase Reference)
NIST Chemistry Reference
Buflomedil(55837-25-7)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
EL9885000
HS Code 
29339990
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Buflomedil Usage And Synthesis

Originator

Fonzylane,Lafon,France,1976

Uses

BAN; DCF; MI.

Definition

ChEBI: 4-(1-pyrrolidinyl)-1-(2,4,6-trimethoxyphenyl)-1-butanone is an aromatic ketone.

Manufacturing Process

Introduce 33.6 g (0.2 mol) of 1,3,5-trimethoxybenzene and 100 ml of chlorobenzene into a 500 ml three-neck flask with stirrer, hydrochloric acid bubbler and condenser. Stir to dissolve and add 27.7 g of 4- pyrrolidinobutyronitrile (from 4-chlorobutyronitrile and pyrrolidine). Cool to about 15°-20°C and bubble hydrochloric acid gas in for 4 hours. Cool to about 5°C and add 200 cm3 of water. Stir. Decant the aqueous layer, wash again with 150 cm3 of water. Combine the aqueous layers, drive off the traces of chlorobenzene by distilling 150 cm3 of water, and heat under reflux for one hour. Cool and render alkaline by means of 60 ml of sodium hydroxide solution of 36° Baume. Extract twice with 100 ml of ether. Wash the ether with 100 ml of water. Dry the ether over sodium sulfate and slowly run in 50 ml of 5N hydrogen chloride solution in ether, at the boil. Cool in ice. Filter, wash with ether and dry in a vacuum oven. 33.6 g of crude product are obtained. Recrystallize from 200 ml of isopropanol in the presence of 3 SA carbon black. Filter. Wash and dry in a vacuum oven.
26.9 g of a white, crystalline water-soluble powder are obtained. Yield: 39.2%. Instantaneous melting point: 192°-193°C.

Therapeutic Function

Vasodilator

BuflomedilSupplier

LGM Pharma
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1-(800)-881-8210
Email
inquiries@lgmpharma.com
China Langchem Inc.
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0086-21-58956006
Hangzhou Yuhao Chemical Technology Co., Ltd
Tel
0571-82693216
Email
info@yuhaochemical.com
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611
Eastbang Pharmaceuticals Technology Co., Ltd.
Tel
+86 (20) 28996708,29078958,28139708,29076128,28133708,28139728,28139738,28133718,021-31663278,021-31663578,021-60538387