Ethopropazine Hydrochloride

Ethopropazine Hydrochloride Suppliers list
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Products Intro: Product Name:N,N-diethyl-1-(10H-phenothiazin-10-yl)propan-2-amine hydrochloride
CAS:1094-08-2
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:ethopropazine hydrochloride
CAS:1094-08-2
Purity:0.99 Package:1kg
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Products Intro: Product Name:Ethopropazine Hydrochloride;Lysivane;Pardisol;Parphezein;Parfezin;Dibutil;Profenamine HCl
CAS:1094-08-2
Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
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Products Intro: Product Name:profenamine hydrochloride
CAS:1094-08-2
Purity:95%-99% crystal Liu Package:1KG;0.01USD
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Products Intro: Product Name:ethopropazine hydrochloride
CAS:1094-08-2
Ethopropazine Hydrochloride Basic information
Product Name:Ethopropazine Hydrochloride
Synonyms: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
CAS:1094-08-2
MF:C19H25ClN2S
MW:348.93
EINECS:214-134-4
Product Categories:
Mol File:1094-08-2.mol
Ethopropazine Hydrochloride Structure
Ethopropazine Hydrochloride Chemical 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
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
RTECS SO5002000
ToxicityLD50 s.c. in mice: 670 mg/kg (Farquharson, Johnston)
MSDS Information
Ethopropazine Hydrochloride Usage And Synthesis
OriginatorParsidol,Warner Lambert,US,1954
UsesAntiparkinsonian;Anticholinergic
UsesEthopropazine hydrochloride is a drug that shifts energy metabolism from mitochondrial respiration to glycolysis.
DefinitionChEBI: The monohydrochloride salt of profenamine. An antimuscarinic, it is used for the symptomatic treatment of Parkinson's disease.
Manufacturing Process6.2 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 FunctionAntiparkinsonian
General DescriptionEthopropazinehydrochloride, 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 ActionsEthoproprazine hydrochloride is an inhibitor of butyrylcholinesterase; antiparkinsonian. It reduces extrapyramidal motor effects, characteristic of Parkinson′s disease; also alleviates thermal hyperalgesia in rats.
Clinical UseEthopropazine 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 materialsIodomethane-->Magnesium-->Hydrochloric acid-->Phenothiazine
Tag:Ethopropazine Hydrochloride(1094-08-2) Related Product Information
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