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Amodiaquine

CAS No.
86-42-0
Chemical Name:
Amodiaquine
Synonyms
CAM-AQI;CAM-AQ1;Miaquin;Camoquin;Camochin;Camoquine;SN 10,751;NSC 13453;Camoquinal;Flavoquine
CBNumber:
CB8344720
Molecular Formula:
C20H22ClN3O
Molecular Weight:
355.86
MDL Number:
MFCD00552927
MOL File:
86-42-0.mol
Last updated:2023-06-08 09:01:57

Amodiaquine Properties

Melting point 208°C
Boiling point 478.0±45.0 °C(Predicted)
Density 1.258
storage temp. -20°C Freezer
solubility DMSO (Slightly, Sonicated), Methanol (Slightly)
form Solid
pka 9.43±0.50(Predicted)
color Pale Yellow to Light Yellow
CAS DataBase Reference 86-42-0(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 220236ED28
NIST Chemistry Reference Amodiaquine(86-42-0)
ATC code P01BA06

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
Toxicity LD50 oral in mouse: 550mg/kg
NFPA 704
0
1 0

Amodiaquine price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 15954 Amodiaquine ≥95% 86-42-0 1mg $37 2024-03-01 Buy
Cayman Chemical 15954 Amodiaquine ≥95% 86-42-0 5mg $134 2024-03-01 Buy
Cayman Chemical 15954 Amodiaquine ≥95% 86-42-0 10mg $236 2024-03-01 Buy
Cayman Chemical 15954 Amodiaquine ≥95% 86-42-0 50mg $723 2024-03-01 Buy
TRC A634200 Amodiaquine 86-42-0 100mg $520 2021-12-16 Buy
Product number Packaging Price Buy
15954 1mg $37 Buy
15954 5mg $134 Buy
15954 10mg $236 Buy
15954 50mg $723 Buy
A634200 100mg $520 Buy

Amodiaquine Chemical Properties,Uses,Production

Description

Amodiaquine is a prodrug form of the antimalarial compound N-desethyl amodiaquine . It is active against several strains of P. falciparum in vitro (EC50s = 0.23-0.52 nM) and exhibits a synergistic effect when used in combination with N-desethyl amodiaquine. Amodiaquine dose-dependently inhibits development of parasitemia in a mouse model of P. berghei infection.

Chemical Properties

Cyrstalline Solid

Originator

Camoquin HCl,Parke Davis,US,1950

Uses

An antimalarial

Definition

ChEBI: A quinoline having a chloro group at the 7-position and an aryl amino group at the 4-position.

Indications

Amodiaquine (Camoquin) is another 4-aminoquinoline derivative whose antimalarial spectrum and adverse reactions are similar to those of chloroquine, although chloroquine-resistant parasites may not be amodiaquine- resistant to the same degree. Prolonged treatment with amodiaquine may result in pigmentation of the palate, nail beds, and skin. There is a 1:2000 risk of agranulocytosis and hepatocellular dysfunction when the drug is used prophylactically.

Manufacturing Process

72.8 g (0.5 mol) of p-aminophenol hydrochloride is dissolved in 500 cc of water and added to 99 g (0.5 mol) of 4,7-dichloroquinoline. After a few minutes of warming in a steam bath, 4-(4'-hydroxyanilino)-7-chloroquinoline hydrochloride, of sufficient purity for use in further experiments, precipitates as a yellow crystalline solid. Recrystallized from methanol, the MP is over 300°C.
A mixture consisting of 13.5 g of 4-(4'-hydroxyanilino)-7-chloroquinoline hydrochloride dissolved in absolute ethanol is treated with a solution of 4.38 g of diethylamine and 1.8 g of paraformaldehyde in 20 cc of absolute ethanol. The reaction mixture is heated under reflux for 16 hours, evaporated to onehalf volume and the warm solution treated with an excess of hydrogen chloride dissolved in absolute ethanol. Acetone is added to the warm solution until it becomes turbid and then the solution is cooled. The crude dihydrochloride which separates is collected and purified by recrystallization from methanol; MP 240-242°C.
By using an equivalent amount of 4-(4'-hydroxyanilino)-7-bromoquinoline in the above procedure, 4-(3'-diethylaminomethyl-4'-hydroxyanilino)-7- bromoquinoline dihydrochloride is obtained; MP (base) 206-208°C dec.

brand name

Camoquin (Parke-Davis);Amodoquin tablets;Basoquin;Caniquin.

Therapeutic Function

Antimalarial

World Health Organization (WHO)

Amodiaquine, an antimalarial agent related to chloroquine, was introduced over 40 years ago for the treatment and prophylaxis of malaria. The drug was voluntarily withdrawn in the United Kingdom in 1975 for commercial reasons but was subsequently reintroduced in 1985 to meet the medical demand for an antimalarial drug to deal with the rapid spread of chloroquine-resistant falciparum malaria in Asia and Africa. By 1986 a significant number of cases of agranulocytosis associated with prophylactic use, some of which were fatal, had been reported there and it has been estimated that the frequency of this risk is of the order of 1:2,000. Although most cases occurred when amodiaquine had been used in combination with other antimalarials, the major manufacturer decided to withdraw the prophylactic indication worldwide following discussions with experts. Preparations remain available for the treatment of acute attacks of malaria which involves only a short period of exposure to the drug. (Reference: (WHODI) WHO Drug Information, 1, 5, 1987)

Pharmaceutical Applications

A mono-Mannich-base 4-aminoquinoline, formulated as the dihydrochloride dihydrate or free base for oral administration. It is active against P. falciparum and P. vivax and is more active than chloroquine for the treatment of uncomplicated P. falciparum malaria. Chloroquine-resistant strains may remain susceptible, but resistance to amodiaquine is also spreading in some regions of Africa. The pharmacological properties are similar to those of chloroquine. The terminal elimination halflife is 1–3 weeks. It is rapidly and extensively metabolized to the desethyl derivative which has reduced antiplasmodial activity. Prophylactic use has been abandoned because of agranulocytosis and hepatotoxicity due to formation of a quinoneimine metabolite. A fixed dose combination with artesunate and derivatives (for example, isoquine) with altered metabolism and reduced toxicity is in development.

Clinical Use

Mechanistically, it is very similar to chloroquine and does nothave any advantages over the other 4-aminoquinoline drugs.When used for prophylaxis of malaria, it had a higher incidenceof hepatitis and agranulocytosis than that was chloroquine.There is evidence that the hydroquinone (phenol)amine system readily oxidizes to a quinone imine either autoxidatively and/or metabolically, and this productmay contribute to amodiaquine’s toxicity.

Clinical Use

Treatment of falciparum malaria

Synthesis

Amodiaquin, 4-[(7-chloro-4-quinilyl)amino]-|á-diethylmaino-o-cresol (37.1.1.21), is made by reacting 4,7-dichloroquineoline (37.1.1.1) with 4-aminophenol to make 7-chloro-4-(4-hydroxyphenylamino)-quiniline (37.1.1.20), which then undergoes an aminomethylation reaction using formaldehyde and diethylamine, giving amodiaquin.

Synthesis_86-42-0

Purification Methods

Amodiaquin crystallises from 2-ethoxyethanol or EtOH. [Burckhalter et al. J Am Chem Soc 70 1363 1948, Beilstein 22 III/IV 4647.]

86-98-6
123-30-8
109-89-7
86-42-0
Synthesis of Amodiaquine from 4,7-Dichloroquinoline and 4-Aminophenol and Diethylamine

Amodiaquine Preparation Products And Raw materials

Global( 124)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21691 55
Xiamen AmoyChem Co., Ltd
+86-592-6051114 +8618959220845 sales@amoychem.com China 6387 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
zhangjiagang vinsce bio-pharm. limited.
86-512-58389969 sales1@swellxin.com CHINA 111 58
SIMAGCHEM CORP
+86-13806087780 sale@simagchem.com China 17367 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671 sales@tnjchem.com China 34572 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29271 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com CHINA 52867 58
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923 1026@dideu.com China 9116 58

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View Lastest Price from Amodiaquine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Amodiaquine USP/EP/BP pictures 2021-06-18 Amodiaquine USP/EP/BP
86-42-0
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited
Amodiaquine pictures 2020-02-06 Amodiaquine
86-42-0
US $1.00 / KG 1KG Min98% HPLC g/kg/ton Career Henan Chemical Co
  • Amodiaquine pictures
  • Amodiaquine
    86-42-0
  • US $1.00 / KG
  • Min98% HPLC
  • Career Henan Chemical Co
4-((7-chloro-4-quinolyl)amino)-alpha-(diethylamino)-o-creso 4-((7-Chloro-4-quinolyl)amino)-alpha-(diethylamino)-o-cresol 4-[(7-Chloro-4-quinolinyl)amino]-alpha-(diethylamino)-o-cresol 7-Chloro-4-(3-diethylaminomethyl-4-hydroxyphenylamino)quinoline Amodiaquine, ring-closed CAM-AQ1 CAM-AQI Camochin Camoquin Camoquinal Camoquine Flavoquine Miaquin o-Cresol, 4-((7-chloro-4-quinolyl)amino)-alpha-(diethylamino)- Phenol, 4-[(7-chloro-4-quinolinyl)amino]-2-[(diethylamino)methyl]- Quinoline, 7-chloro-4-((3-((diethylamino)methyl)-4-hydroxyphenyl)amino)- S. N. 10751 SN 10,751 7-chloro-4-(3-diethylaminomethyl-4-hydroxyanilino)quinoline AMODIAQUIN AMODIAQUINE 4-[(7-chloro-4-quinolinyl)amino]-2-[(diethylamino)methyl]-phenol Amodiaquine USP24 4-[3'-Dimethyl-aminomethyl-4'-hydroxyanilino]-7-chloroquinoline 4-[7-Chloro-4-quinolylamino]-α-diethylamino-o-cresol 4-[(7-Chloro-4-quinolinyl)amino]-2-[(diethylamino)methyl]phenol, SN-10751 Amodiaquine (base and/or unspecified salts) 4-[(7-Chloro-4-quinolynyl)amino]-2-[(diethylamino)methyl]phenol 4-[(7-Chloroquinolin-4-yl)amino]-2-[(diethylamino)methyl]phenol 4-[(7-chloro-4-quinolyl)amino]-2-(diethylaminomethyl)phenol DRUGS: AMODIAQUINE USP NSC 13453 Amodiaquine USP/EP/BP AmodiaquineQ: What is Amodiaquine Q: What is the CAS Number of Amodiaquine Q: What is the storage condition of Amodiaquine Q: What are the applications of Amodiaquine Amodiaquine 150-200 mg Tablet AMODIQUINE BASE 86-42-0 C20H12ClN3OD10 C20H22ClN3O Amines Aromatics Heterocycles Intermediates & Fine Chemicals Pharmaceuticals