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Benzetimide

Benzetimide Suppliers list
Company Name: LGM Pharma  
Tel: 1-(800)-881-8210
Email: inquiries@lgmpharma.com
Company Name: Credit Asia Chemical Co., Ltd.  
Tel: +86 (21) 61124340
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Company Name: Beijing Solarbio Science & Tecnology Co., Ltd.  
Tel: 17801761073 18101056239
Email: 3193328036@qq.com
Company Name: Nanjing crow LuNing pharmaceutical technology co., LTD  
Tel: 13382066392
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Company Name: Fan De(Beijing) Biotechnology Co., Ltd.  
Tel: 15911056312
Email: liming@bio-fount.com

Benzetimide manufacturers

  • Dexetimide
  • Dexetimide pictures
  • $57.00
  • 2026-05-11
  • CAS:21888-98-2
  • Purity:
  • Supply Ability: 10g
Benzetimide Basic information
Product Name:Benzetimide
Synonyms:[3,4'-Bipiperidine]-2,6-dione, 3-phenyl-1'-(phenylmethyl)-, (S)-;Dexbenzetimide;Dextrobenzetimide;DEXETIMIDE HCL;(+)-DEXETIMIDE HYDROCHLORIDE;3-PHENYL-1'-(PHENYLMETHYL)-[3,4'-BIPIPERIDINE]-2,6-DIONE HYDROCHLORIDE;R 16470;(S)-(+)-3-PHENYL-1'-(PHENYLMETHYL)-[3,4'-BIPIPERIDINE]-2,6-DIONE, HCL
CAS:21888-98-2
MF:C23H26N2O2
MW:362.46
EINECS:244-633-2
Product Categories:
Mol File:21888-98-2.mol
Benzetimide Structure
Benzetimide Chemical Properties
Melting point 181-183°
alpha D20 +125° (chloroform)
Boiling point 543.9±50.0 °C(Predicted)
density 1.178±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO: ≥ 100 mg/mL (275.89 mM)
pka11.20±0.40(Predicted)
form Solid
color White to off-white
Safety Information
RIDADR 3249
HazardClass 6.1(b)
PackingGroup III
MSDS Information
Benzetimide Usage And Synthesis
OriginatorTremblex,Brocades,Italy,1981
UsesAnticholinergic.
DefinitionChEBI: Dexetimide is a member of piperidines.
Manufacturing Process400 parts glacial acetic acid are cooled to 10°C to 20°C. Then there are added first dropwise 300 parts concentrated sulfuric acid followed by portionwise addition of 50 parts dl-1-benzyl-4-(1,3-dicyano-1-phenylpropyl)-piperidine hydrochloride at the same temperature. After the addition is complete, the whole is heated to 125°C in the course of 15 to 20 minutes. This temperature is then maintained for 10 minutes. After cooling, the reaction mixture is poured into ice, alkalized with NH4OH at a temperature < 20°C and extracted with chloroform. The chloroform layer is first washed twice with a K2CO3 5% solution, and then washed twice with water, dried over MgSO4, filtered and evaporated. The residue is dissolved in a mixture of 320 parts acetone and 600 parts diisopropylether, filtered and HCl gas is introduced into the filtrate. The solid hydrochloride is filtered off and dried, to yield 43 parts less pure lbenzyl-4-(2.6-dioxo-3-phenyl-3-piperidyl)-piperidine hydrochloride, melting point 283°C to 294°C.
A sample of 4 parts is recrystallized from a boiling mixture of 80 parts isopropanol, 40 parts methanol and 500 parts water. The whole is filtered and after cooling the filtrate overnight at -20°C, 1-benzyl-4-(2,6-dioxo-3phenyl-3- piperidyl)-piperidine hydrochloride is obtained, melting point 299°C to 301.5°C, as a white amorphous powder.
The dextro-isomer may be separated via the dextro-camphorsulfonate of the base.
Therapeutic FunctionAnticholinergic (ophthalmic)
Benzetimide Preparation Products And Raw materials
Raw materialsHydrochloric acid
Tag:Benzetimide(21888-98-2) Related Product Information
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