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PROCYCLIDINE HYDROCHLORIDE

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PROCYCLIDINE HYDROCHLORIDE Basic information

Product Name:
PROCYCLIDINE HYDROCHLORIDE
Synonyms:
  • a-Cyclohexyl-a-phenyl-1-pyrrolidinepropanol hydrochloride
  • alpha-cyclohexyl-alpha-phenyl-1-pyrrolidinepropanomonohydrochloride
  • kemadrin
  • kemadrinhydrochloride
  • PROCYCLIDINE HCL
  • PROCYCLIDINE HYDROCHLORIDE
  • ALPHA-CYCLOHEXYL-ALPHA-PHENYL-1-PYRROLIDINEPROPANOL HYDROCHLORIDE
  • α-Cyclohexyl-α-phenyl-1-pyrrolidinepropanol
CAS:
1508-76-5
MF:
C19H30ClNO
MW:
323.9
EINECS:
216-141-8
Product Categories:
  • KEMADRIN
  • Aromatics
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Neurochemicals
  • Pharmaceuticals
Mol File:
1508-76-5.mol
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PROCYCLIDINE HYDROCHLORIDE Chemical Properties

Melting point:
159-164 °C
storage temp. 
2-8°C
solubility 
Chloroform (Slightly), Methanol (Slightly), Water (Slightly)
form 
Solid
color 
White to Off-White
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22
Safety Statements 
36
WGK Germany 
3
RTECS 
UY1926000
HS Code 
2933997500
Toxicity
mouse,LD50,intravenous,14mg/kg (14mg/kg),BEHAVIORAL: TREMORLUNGS, THORAX, OR RESPIRATION: DYSPNEABEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD,British Journal of Pharmacology and Chemotherapy. Vol. 10, Pg. 383, 1955.

MSDS

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PROCYCLIDINE HYDROCHLORIDE Usage And Synthesis

Uses

An anticholinergic drug used in the treatment parkinson’s disease. It is also used to treat patients suffering from drug-induced parkinsonism, akathisia and acute dystonia.

brand name

Kemadrin (Monarch).

General Description

Procyclidine hydrochloride,α-cyclohexyl-α-phenyl-1-pyrrolidinepropanolhydrochloride (Kemadrin), was introduced in 1956. Althoughit is an effective peripheral anticholinergic and, indeed, hasbeen used for peripheral effects similar to its methochloride(i.e., tricyclamol chloride), its clinical usefulness lies inits ability to relieve voluntary muscle spasticity by its centralaction. Therefore, it has been used with success in thetreatment of Parkinson syndrome. It is said to be as effectiveas trihexyphenidyl and is used to reduce muscle rigidityin postencephalitic, arteriosclerotic, and idiopathic types ofthe disease. Its effect on tremor is not predictable and probablyshould be supplemented by combination with othersimilar drugs.
The toxicity of the drug is low, but when the dosageof the drug is high, side effects are noticeable. At therapeuticdosage levels, dry mouth is the most common sideeffect. The same care should be exercised with this drugas with all other anticholinergics when it is administeredto patients with glaucoma, tachycardia, or prostatichypertrophy.

Biochem/physiol Actions

Procyclidine is a synthetic anti-cholinergic agent and atropine-like antispasmodic. It exhibits therapeutic effects against Parkinson′s disease and schizophrenia. Procyclidine acts as a muscarinic receptor antagonist. It also affects N-methyl-D-aspartate (NMDA) glutamine and nicotinic acetylcholine receptors to a lower extent.

Clinical Use


Control of extrapyramidal symptoms
Acute dystonias

Metabolism

When given orally about one fifth of the dose is known to be metabolised in the liver, principally by cytochrome P450 and then conjugated with glucuronic acid. Metabolites have been found in the urine.

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