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Amodiaquine hydrochloride

pharmaceutical raw materials
Amodiaquine hydrochloride structure

Amodiaquine hydrochloride 

structure
  • CAS No:

    69-44-3

  • Formula:

    C20H22ClN3O.2ClH

  • Chemical Name:

    Amodiaquine hydrochloride

  • Synonyms:

    Phenol,4-[(7-chloro-4-quinolinyl)amino]-2-[(diethylamino)methyl]-,hydrochloride (1:2);o-Cresol,4-[(7-chloro-4-quinolyl)amino]-α-(diethylamino)-,dihydrochloride;Phenol,4-[(7-chloro-4-quinolinyl)amino]-2-[(diethylamino)methyl]-,dihydrochloride;Amodiaquine dihydrochloride;Camoquin hydrochloride;7-Chloro-4-(3′-diethylaminomethyl-4′-hydroxyanilino)quinoline dihydrochloride;4-(7-Chloro-4-quinolylamino)-α-(diethylamino)-o-cresol dihydrochloride;Amodiaquine hydrochloride;Amodiaquin dihydrochloride;Basoquine

  • Categories:

    Pharmaceutical Intermediates  >  Oled Material Intermediate

Description

Yellow crystalline solid; odorless; bitter. Soluble in water; sparingly soluble in alcohol; very slightly soluble in benzene, chloroform, and ether.


A 4-aminoquinoline compound with anti-inflammatory properties.

Amodiaquine hydrochloride Basic Attributes

428.78

391.121826

200-706-0

DTXSID20219036

2933499090

Characteristics

48.4

6.05420

478ºC at 760 mmHg

Safety Information

3

P264, P270, P301+P312, P330, P501

H302

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|Aggregated GHS information provided by 18 companies from 1 notifications to the ECHA C&L Inventory.

Drug Information

Agents used in the treatment of malaria. They are usually classified on the basis of their action against plasmodia at different stages in their life cycle in the human. (From AMA, Drug Evaluations Annual, 1992, p1585) (See all compounds classified as Antimalarials.)

Amodiachin

Amodiaquine hydrochloride Use and Manufacturing

Methods of Manufacturing

In the three-neck bottle 16.0g diethylamine, 40.0g deionized water, 30.0g acetaminophen and 6.6g paraformaldehyde, heating to 80 °C, thermal insulation reaction 30 minutes, cooling to 40 °C the following, by adding 48g37percent after the hydrochloric acid, is heated to 104 °C, thermal insulation reaction 2 hours, after the reaction, lowering the temperature to 38 °C -42 °C, dropwise NaOH solution, adjusted to pH 3.0, adding 4, 7-chloroquinoline 36.2g, heating to 100 °C, thermal insulation reaction 1 hour, after the reaction, cooling to 3 °C -7 °C, stirring crystallization 2 hours to 3 hours, filtered, to control the temperature to 60 °C -70 °C, vacuum ≥ - 0.080 MPa, drying 8 hours to obtain Amodiaquine hydrochloride 85.69g, yield 92.89percent, purity of 99.96percent.

Uses

Medicine (antimalarial).

Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients

Computed Properties

Molecular Weight:392.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:391.1218178
Monoisotopic Mass:391.1218178
Topological Polar Surface Area:48.4
Heavy Atom Count:26
Complexity:406
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

Drug Function and Efficacy

Unspecified

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)

Related Drugs

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