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BAMIPINE

BAMIPINE Structure
CAS No.
4945-47-5
Chemical Name:
BAMIPINE
Synonyms
Soventol;BAMIPINE;Taumidrin;Piperamine;BAMIPINE USP/EP/BP;4-(N-Benzylanilino)-1-methylpiperidine;N-benzyl-N-(1-methyl-4-piperidyl)aniline;N-Benzyl-1-methyl-N-phenyl-4-piperidinamine;4-(N-Benzyl-N-phenylamino)-1-methylpiperidine;4-(n-benzyl-n-phenylamino)-1-methyl-piperidin
CBNumber:
CB3372285
Molecular Formula:
C19H24N2
Molecular Weight:
280.41
MOL File:
4945-47-5.mol
MSDS File:
SDS
Modify Date:
2023/5/4 17:34:39

BAMIPINE Properties

Melting point 115°
Boiling point 413.12°C (rough estimate)
Density 0.9608 (rough estimate)
refractive index 1.8676 (estimate)
pka pKa 3.34±0.04 (H2O t unde?ned I=0.30(NaCl)) (Uncertain);8.04±0.11(H2O t unde?ned I=0.30(NaCl)) (Uncertain)

BAMIPINE Chemical Properties,Uses,Production

Originator

Bamipine,Pharm Chemical

Manufacturing Process

80 g of 1-methyl-piperidone-4 and 70 g of aniline are boiled, using a water separator in 350 ml of toluene to which several drops of glacial acetic acid have been added, until the theoretical quantity of water (12.7 ml) has separated out. The toluene is then distilled off and the remains are fractionated at reduced pressure. At a boiling point of 156°C/13 mm of Hg pressure, 118 g of a weakly yellow colored oil of the anil of 1-methyl-1- piperidone-4 are obtained.
100 g of the above described anil of 1-methyl-1-piperidone-4 are boiled for 8 hours, using a reflux condenser, with 30 g of activated borings of aluminum in 300 ml of methanol diluted with 60 ml of water. The liquid phase is then separated from the solid phase, the solvent is evaporated and the residuum is fractionated at reduced pressure, 95 g of a colorless oil being obtained boiling at 163-165°C at 15 mm of Hg pressure. The oil solidifies at once to a mass of crystals of 4-N-phenylaimno-1-methylpiperidine. After having been recrystallized from dibutyl ether the base melts at 87°C, its dihydrochloride has the melting point of 246°C.
95 g of 4-N-phenylamino-1-methylpiperidine are boiled together with 22 g of pulverized sodium amide in 300 ml of benzene, using a reflux condenser, while nitrogen is passed through the reaction mixture, until the evolution of ammonia has ceased. 64 g of benzyl chloride are then gradually added drop by drop to the boiling reaction product and boiling is continued for several hours. After having been cooled the solution is shaken with water and subsequently dried with potassium carbonate. The solvent having been evaporated the remaining base of 4-(N-phenyl-N-benzyl)-amino-1- methylpiperidine solidifies with the formation of crystals, the yield amounting to 123 g. The base is recrystallized from dibutyl ether and has a melting point of 115°C; its dihydrochloride melts at 189°C.

Therapeutic Function

Antihistaminic, Antiallergic

BAMIPINE Preparation Products And Raw materials

Raw materials

Preparation Products

BAMIPINE Suppliers

Global( 14)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
Shaanxi Didu New Materials Co. Ltd +86-89586680 +86-13289823923 China 8673 58 Inquiry
Hubei Nordina Biotechnology Co., Ltd. 19371278702 China 972 58 Inquiry
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd 17691182729 18161915376 China 10011 58 Inquiry
ChemPacific Corporation 410 633 5771 United States 6902 51 Inquiry
BOSCHE SCIENTIFIC, LLC 732 565 9988 United States 6486 55 Inquiry
APAC Pharmaceutical, LLC +1(410) 997 5552 United States 6332 38 Inquiry
Waterstone Technology, LLC 317 644 0862 United States 6801 30 Inquiry
AlliChem, LLC 301-317-5072 United States 6527 60 Inquiry
Lanospharma Laboratories Co.,Ltd 13440048448 China 6343 56 Inquiry

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Taumidrin BAMIPINE 4-(N-Benzylanilino)-1-methylpiperidine 4-(n-benzyl-n-phenylamino)-1-methyl-piperidin 4-(N-Benzyl-N-phenylamino)-1-methylpiperidine 4-Piperidinamine, 1-methyl-N-phenyl-N-(phenylmethyl)- N-Benzyl-1-methyl-N-phenyl-4-piperidinamine N-Phenyl-N-benzyl-4-amino-1-methyl-piperidine Piperamine Piperidine, 4-(N-benzyl-N-phenylamino)-1-methyl- Soventol N-benzyl-N-(1-methyl-4-piperidyl)aniline BAMIPINE USP/EP/BP 4945-47-5