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Ethopropazine Hydrochloride

CAS No.
1094-08-2
Chemical Name:
Ethopropazine Hydrochloride
Synonyms
parfezin;NSC 64074;NSC 169467;PROFENAMIN HCL;ProphenamineHCl;Profenamine HCl;ethopropazine hcl;Ethopropazine hydroc;lysivanehydrochloride;parsidolhydrochloride
CBNumber:
CB3149595
Molecular Formula:
C19H25ClN2S
Molecular Weight:
348.93
MDL Number:
MFCD00012653
MOL File:
1094-08-2.mol
MSDS File:
SDS
Last updated:2023-06-08 09:02:11

Ethopropazine Hydrochloride Properties

Melting point 223-225° (some decompn)
storage temp. 2-8°C
solubility DMSO: >5mg/mL at ~60°C, clear
form powder
color white
Merck 13,3783
Stability Hygroscopic
FDA UNII O00T1I1VRN

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P330-P501
Hazard Codes  Xn
Risk Statements  22
WGK Germany  3
RTECS  SO5002000
Toxicity LD50 s.c. in mice: 670 mg/kg (Farquharson, Johnston)
NFPA 704
0
1 0

Ethopropazine Hydrochloride price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich E5406 Ethopropazine hydrochloride ≥98% (HPLC), powder 1094-08-2 50mg $208 2024-03-01 Buy
Sigma-Aldrich E5406 Ethopropazine hydrochloride ≥98% (HPLC), powder 1094-08-2 250mg $922 2024-03-01 Buy
Cayman Chemical 28493 Ethopropazine (hydrochloride) 1094-08-2 10mg $56 2024-03-01 Buy
Cayman Chemical 28493 Ethopropazine (hydrochloride) 1094-08-2 25mg $111 2024-03-01 Buy
Cayman Chemical 28493 Ethopropazine (hydrochloride) 1094-08-2 50mg $194 2024-03-01 Buy
Product number Packaging Price Buy
E5406 50mg $208 Buy
E5406 250mg $922 Buy
28493 10mg $56 Buy
28493 25mg $111 Buy
28493 50mg $194 Buy

Ethopropazine Hydrochloride Chemical Properties,Uses,Production

Originator

Parsidol,Warner Lambert,US,1954

Uses

Antiparkinsonian;Anticholinergic

Uses

Ethopropazine hydrochloride is a drug that shifts energy metabolism from mitochondrial respiration to glycolysis.

Definition

ChEBI: The monohydrochloride salt of profenamine. An antimuscarinic, it is used for the symptomatic treatment of Parkinson's disease.

Manufacturing Process

6.2 grams of phenthiazine in 100 cc of warm dry benzene was added during 1 hour with stirring, and in an atmosphere of hydrogen, to the Grignard reagent prepared from 1 gram of magnesium, 6.2 grams of methyl iodide, and 20 cc of dry ether. After boiling for 30 minutes, a solution of 6.6 grams of 2-chloro- 1-diethylamino propane in 10 cc of dry benzene was added during 1 hour to the boiling solution, and heating was maintained for a further 1.5 hours.
The reaction mixture was then cooled and treated with aqueous ammonium chloride and chloroform added to dissolve an oil at the interface of the benzene and aqueous layers. The chloroform-benzene extract was extracted with 2 N hydrochloric acid and the acid extract was basified at 5° to 10°C with 50% aqueous sodium hydroxide.
There was obtained a mixture of N-(2'-diethylamino-2'- methylethyl)phenthiazine and N-(2'-diethylamino-1'-methylethyl)phenthiazine in the form of a viscous yellow oil, BP 202° to 205°C/2 mm. This oil was treated in ethereal solution with ethereal hydrogen chloride and gave a white solid which was fractionally crystallized from ethylene dichloride. The less soluble fraction, N-(2'-diethylamino-2'-methylethyl)phenthiazine hydrochloride formed colorless rhombs, MP 223° to 225°C. The more soluble N-(2'- diethylamino-1'-methylethyl)phenthiazine hydrochloride was obtained as colorless prismatic needles, MP 166° to 168°C.

Therapeutic Function

Antiparkinsonian

General Description

Ethopropazinehydrochloride, 10-[2-(diethylamino)propyl]phenothiazinemonohydrochloride (Parsidol), introduced to therapy in1954, has antimuscarinic activity and is especially useful inthe symptomatic treatment of parkinsonism. In this capacity,it has value in controlling rigidity, and it also has a favorableeffect on tremor, sialorrhea, and oculogyric crises.

Biochem/physiol Actions

Ethoproprazine hydrochloride is an inhibitor of butyrylcholinesterase; antiparkinsonian. It reduces extrapyramidal motor effects, characteristic of Parkinson′s disease; also alleviates thermal hyperalgesia in rats.

Clinical Use

Ethopropazine Hydrochloride is oftenused in conjunction with other antiparkinsonian drugs forcomplementary activity.Side effects are common with this drug but are usuallynot severe. Drowsiness and dizziness are the most commonside effects at ordinary dosage levels, and as the dose increases,xerostomia, mydriasis, and others become evident.It is contraindicated in conditions such as glaucoma becauseof its mydriatic effect.

Ethopropazine Hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

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lysivanehydrochloride n,n-diethyl-alpha-methyl-10h-phenothiazine-10-ethanaminmonohydrochloride n,n-diethyl-alpha-methyl-10-phenothiazineethylaminhydrochloride profenaminemonohydrochloride ethopropazine hcl 10H-Phenothiazine-10-ethanamine, N,N-diethyl-.alpha.-methyl-, monohydrochloride 10H-Phenothiazine-10-ethanamine, N,N-diethyl-a-methyl-, monohydrochloride (9CI) NSC 169467 NSC 64074 Phenothiazine, 10-[2-(diethylamino)propyl]-, hydrochloride (7CI) Phenothiazine, 10-[2-(diethylamino)propyl]-, monohydrochloride (8CI) 10-(2-Diethylaminopropyl)phenothiazine, 10-[2-(Diethylamino)propyl]phenothiazine hydrochloride, Dibutil hydrochloride, Parkin N,N-diethyl-alpha-methyl-10H-phenothiazine-10-ethylamine monohydrochloride ProphenamineHCl 10-[2-(Diethylamino)propyl]phenothiazine hydrochloride N-(2-diethylaMinopropyl)-phenothiazine hydrochloride N,N-diethyl-1-(10H-phenothiazin-10-yl)propan-2-amine hydrochloride parfezin parsidolhydrochloride parsidolmonohydrochloride profenaminehydrochloride 10-[2-DIETHYLAMINOPROPYL]PHENOTHIAZINE LABOTEST-BB LT00452011 ETHOPROPAZINE HYDROCHLORIDE SALOR-INT L308765-1EA 10-(2-(diethylamino)propyl)-phenothiazinmonohydrochloride isothazinehydrochloride l-10-(2-diethylaminopropyl)phenothiazinehydrochloride Profenamine HCl Ethopropazine hydroc PROFENAMIN HCL Ethopropazine hydrochloride >=98% (HPLC), powder 1094-08-2 C19H24N2SHCl C19H25ClN2S