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Home > Encyclopedia > Chlorprothixene hydrochloride

Chlorprothixene hydrochloride

pharmaceutical raw materials
Chlorprothixene hydrochloride structure

Chlorprothixene hydrochloride 

structure
  • CAS No:

    6469-93-8

  • Formula:

    C18H18ClNS.ClH

  • Chemical Name:

    Chlorprothixene hydrochloride

  • Synonyms:

    1-Propanamine,3-(2-chloro-9H-thioxanthen-9-ylidene)-N,N-dimethyl-,hydrochloride (1:1),(3Z)-;Thioxanthene-Δ9,γ-propylamine,2-chloro-N,N-dimethyl-,hydrochloride,(Z)-;1-Propanamine,3-(2-chloro-9H-thioxanthen-9-ylidene)-N,N-dimethyl-,hydrochloride,(Z)-;1-Propanamine,3-(2-chloro-9H-thioxanthen-9-ylidene)-N,N-dimethyl-,hydrochloride,(3Z)-;9H-Thioxanthene,1-propanamine deriv.;Truxal hydrochloride;cis-Chlorprothixene hydrochloride;Chlorprothixene hydrochloride;NSC 169899

  • Categories:

    Active Pharmaceutical Ingredients  >  Nervous System Drugs

Description

Pale Yellow Solid

Chlorprothixene hydrochloride Basic Attributes

352.32

351.06200

229-289-3

Characteristics

28.54000

5.99000

White powder

207.5-208 °C

461.8ºC at 760 mmHg

233.1ºC

soluble in water and in alcohol, slightly soluble in methylene chloride.

2-8°C

Safety Information

III

6.1(b)

UN 2811 6.1/PG 3

3

20/21/22

36

XO0610000

Xn

Missing Phrase - N15.00950417

H301

|Danger|H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]|P264, P270, P301+P310, P321, P330, P405, and P501|Aggregated GHS information provided by 40 companies from 2 notifications to the ECHA C&L Inventory.

Chlorprothixene hydrochloride Use and Manufacturing

Neuroleptic;D2 dopamine receptor antagonist

Computed Properties

Molecular Weight:352.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:351.0615262
Monoisotopic Mass:351.0615262
Topological Polar Surface Area:28.5
Heavy Atom Count:22
Complexity:381
Undefined Bond Stereocenter Count:1
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

Drug Function and Efficacy

It can improve mental disorders by blocking postsynaptic dopamine receptors in the brain, inhibit the ascending activation system of the brainstem reticular formation, cause sedation, and inhibit the medulla chemoreceptor area to exert an antiemetic effect. This product has weak anti-adrenergic and anti-cholinergic effects, and has anti-depressant and anti-anxiety effects.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

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