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OXYPHENCYCLIMINE

CAS No.
125-52-0
Chemical Name:
OXYPHENCYCLIMINE
Synonyms
oximin;setrol;daricon;daricol;dominil;enterex;s1-1236;syklifen;Spazamin;vio-thene
CBNumber:
CB6180823
Molecular Formula:
C20H28N2O3.ClH
Molecular Weight:
380.91
MDL Number:
MFCD00079209
MOL File:
125-52-0.mol
MSDS File:
SDS
Last updated:2023-09-04 16:42:00

OXYPHENCYCLIMINE Properties

Melting point 231-232 °C (decomp)
FDA UNII GWO1432WOU
ATC code A03AA01

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H312-H302-H332
Precautionary statements  P280-P302+P352-P312-P322-P363-P501-P261-P271-P304+P340-P312-P264-P270-P301+P312-P330-P501
Hazard Codes  Xn
Risk Statements  20/21/22
Safety Statements  36
WGK Germany  3
RTECS  GV3030000
Toxicity LD50 oral in rat: 1370mg/kg

OXYPHENCYCLIMINE price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0002218 OXYPHENCYCLIMINE HYDROCHLORIDE 95.00% 125-52-0 5G $836.01 2021-12-16 Buy
Crysdot CD31004084 Oxyphencycliminehydrochloride 98+% 125-52-0 100mg $49 2021-12-16 Buy
Product number Packaging Price Buy
API0002218 5G $836.01 Buy
CD31004084 100mg $49 Buy

OXYPHENCYCLIMINE Chemical Properties,Uses,Production

Originator

Vio-Thene ,Rowell,US,1959

Uses

Oxyphencyclimine is widely used for the same indications as dicyclomine and oxybutynin.

Definition

ChEBI: Oxyphencyclimine hydrochloride is a member of pyrimidines.

Manufacturing Process

To a stirred solution of 8.8 grams (0.1 mol) of 1,3-diaminobutane in 150 ml of ethanol maintained at 0° to 5°C, there was added 25.8 grams (0.1 mol) of ethyl chlorimidoacetate hydrochloride during a period of 20 minutes. After the mixture had been stirred at 0° to 5°C for two hours, it was acidified at this temperature by the addition of ethanolic hydrogen chloride. The mixture was warmed to room temperature and filtered to remove 4.3 grams of solid ammonium chloride. The filtrate was concentrated to approximately 40 ml, filtered and refrigerated. The solid which separated was isolated, washed with acetone and dried. There was obtained 7.4 grams (40% of the theoretical yield) of 2-chloromethyl-4-methyl-1,4,5,6-tetrahydropyrimidine hydrochloride melting at 158° to 160°C.
In a second step, cyclohexyl bromide was reacted with magnesium, then with benzoyl formic acid to give cyclohexylphenyl glycolic acid. A solution of 1.8 grams (0.01 mol) of 2-chloromethyl-1-methyl-1,4,5,6-tetrahydropyrimidine hydrochloride in 5 ml of water was made alkaline with 5 ml of 50% NaOH and extracted with ether. The ether solution, which contained the basic chloride, was dried over calcium sulfate and added to a solution of 2.3 grams (0.01 mol) of α-cyclohexylphenylglycolic acid in 75 ml of isopropanol. The solution was distilled to remove the ether, and 0.1 gram of powdered potassium iodide added to the residual isopropanol solution which was then refluxed for 6 hours. The solid which had separated was redissolved by the addition of 20 ml of ethanol and the solution charcoaled, concentrated, and cooled. The solid which separated, 1-methyl-1,4,5,6-tetrahydro-2-pyrimidylmethyl αcyclohexylphenyl-glycolate hydrochloride, weighed 1.4 grams and melted at 228° to 229°C with decomposition after recrystallization from ethanol.

brand name

Daricon (Pfizer).

Therapeutic Function

Spasmolytic

General Description

Oxyphencycliminehydrochloride, 1,4,5,6-tetrahydro-1-methyl-2-pyrimidinyl)methyl -phenylcyclohexaneglycolate monohydrochloride(Daricon, Vistrax), was introduced in 1958 and promoted asa peripheral anticholinergic–antisecretory agent, with little orno curare-like activity and little or no ganglionic blocking activity.These activities are probably absent because of the tertiarycharacter of the molecule. This activity is in contrastwith that of compounds that couple antimuscarinic actionwith ganglionic blocking action. The tertiary character of thenitrogen promotes intestinal absorption of the molecule.Perhaps the most significant activity of this compound is itsmarked ability to reduce both the volume and the acid contentof the gastric juices, a desirable action in view of the more recenthypotheses pertaining to peptic ulcer therapy. Anotherimportant feature of this compound is its low toxicity in comparisonwith many of the other available anticholinergics.Oxyphencyclimine hydrochloride is hydrolyzed in the presenceof excessive moisture and heat. It is absorbed from theGI tract and has a duration of action of up to 12 hours.

Clinical Use

Oxyphencyclimine hydrochloride is suggested for usein peptic ulcer, pylorospasm, and functional bowel syndrome.It is contraindicated, as are other anticholinergics,in patients with prostatic hypertrophy and glaucoma.

Synthesis

Oxyphencylimine, the 1,4,5,6-tetrahydro-1-methyl-2-pyrimidinylmethanolic ester of |á-phenylcyclohexaneglycolic acid (14.1.37), is synthesized by the esterification of |á-phenyl-|á-cyclohexaneglycolic acid with 2-chloromethyl-1-methyl- 1,4,5,6-tetrahydropyrimidine (14.1.36) in the presence of potassium iodide. The initial 2-chloromethyl-1-methyl-1,4,5,6-tetrahydropyrimidine (14.1.36), is synthesized in turn by reacting methyl ester of iminochloracetic acid with 3-methylaminopropylamine [27¨C29].

Synthesis_125-52-0

OXYPHENCYCLIMINE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 63)Suppliers
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career henan chemical co
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Alfa Chemistry
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ZHEJIANG JIUZHOU CHEM CO., LTD
+86-0576225566889 +86-13454675544 admin@jiuzhou-chem.com;jamie@jiuzhou-chem.com;alice@jiuzhou-chem.com China 20000 58
Shanghai Hanhong Scientific Co.,Ltd. 021-54306202 13764082696; info@hanhongsci.com China 42982 64

View Lastest Price from OXYPHENCYCLIMINE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
OXYPHENCYCLIMINE pictures 2019-07-06 OXYPHENCYCLIMINE
125-52-0
US $1.00 / KG 1G 98% 100KG Career Henan Chemical Co

OXYPHENCYCLIMINE Spectrum

1-methyl-1,4,5,6-tetrahydro-2-pyrimidylmethyl-alpha-cyclohexyl-phenylglycola cyclohexaneglycolicacid,alpha-phenyl-,(1,4,5,6-tetrahydro-1-methyl-2-pyrimid daricol daricon tehydrochloride ulcociclinina vio-thene OXYPHENCYCLIMINE OXYPHENCYCLIMINE HYDROCHLORIDE OXYPHENCYCLIMINE HYDROCHLORIDE 98% oxyphencyclimineHCl Hydrobenzole Hydrochloridum Benzeneacetic acid, .alpha.-cyclohexyl-.alpha.-hydroxy-, (1,4,5,6-tetrahydro-1-methyl-2-pyrimidinyl)methyl ester, monohydrochloride dominil enterex inyl)methylester,monohydrochloride oximin s1-1236 setrol syklifen Hydrobenzole Hydrochlordum Spazamin 125-52-0 C20H28N2O3 Analytical Standards Analytical Chromatography Product Catalog Alphabetic API