Basic information Safety Supplier Related

PIPERIDOLATE HYDROCHLORIDE

Basic information Safety Supplier Related

PIPERIDOLATE HYDROCHLORIDE Basic information

Product Name:
PIPERIDOLATE HYDROCHLORIDE
Synonyms:
  • aceticacid,diphenyl-,1-ethyl-3-piperidylester,hydrochloride
  • benzeneaceticacid,alpha-phenyl-,1-ethyl-3-piperidinylester,hydrochloride
  • benzeneaceticacid,alpha-phenyl-,1-ethyl-3-piperidylester,hydrochloride
  • dactilhydrochloride
  • diphenylaceticacid,1-ethyl-3-piperidylesterhydrochloride
  • n-ethyl-3-piperidyldiphenylacetatehydrochloride
  • PIPERIDOLATE HYDROCHLORIDE
  • 3,3-Diethyl-2,4-piperidinedione
CAS:
129-77-1
MF:
C21H26ClNO2
MW:
359.89
EINECS:
204-964-5
Mol File:
129-77-1.mol
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PIPERIDOLATE HYDROCHLORIDE Chemical Properties

Melting point:
195-196°
storage temp. 
Store at -20°C
solubility 
DMSO (Slightly, Heated), Methanol (Slightly), Water (Slightly, Sonicated)
form 
Solid
color 
White to Off-White
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PIPERIDOLATE HYDROCHLORIDE Usage And Synthesis

Originator

Dactil, Merrell National ,US ,1954

Uses

Piperidolate Hydrochloride acts as an anticholinergic agent. Also a potential inhibitor of human glutathione transferase P1-1.

Definition

ChEBI: Piperidolate hydrochloride is a diarylmethane.

Manufacturing Process

To obtain the free base, 34 g (0.256 mol) of N-ethyl-3-piperidinol and 20 g (0.22 mol) of diphenylacetyl chloride were mixed in 80 cc of isopropanol and the solution was refluxed for 2 hours. The isopropanol was evaporated in vacuo at 30 mm pressure, the residue was dissolved in 150 cc of water and the aqueous solution was extracted several times with ether. The aqueous solution was then neutralized with potassium carbonate and extracted withether. The ethereal solution was dried over anhydrous potassium carbonate and the ether removed by distillation. The product was then distilled at its boiling point 180° to 181°C at 0.13 mm of mercury whereby 14 g of a clear yellow, viscous liquid was obtained. The nitrogen content for C21H25NO2 was calculated as 4.33% and the nitrogen content found was 4.21%.
The starting material was produced by the reaction of furfural with ethylamine followed by hydrogenation to give N-ethyl-N-(2-tetrahydrofurfuryl)amine. Treatment of that material with hydrogen bromide in acetic acid gives N-ethyl3-piperidinol.

brand name

Dactil (Marion Merrell Dow).

Therapeutic Function

Spasmolytic

PIPERIDOLATE HYDROCHLORIDESupplier

Sinopharm Chemical Reagent Co,Ltd.
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86-21-63210123
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sj_scrc@sinopharm.com
MedChemexpress LLC
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021-58955995
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HangZhou YuHao Chemical Technology Co., Ltd.
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Hangzhou ChangCun Biotechnology Co., Ltd.
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0571-; 13567100326
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MQ (shanghai) Pharmaceuticals Co., Ltd.
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13761635123
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1014988033@qq.com