raw Materials powder Amprolium Hydrochloride

CAS:137-88-2

MF:C14H20Cl2N4

MW:315.24

EINECS:205-307-5

Specification: 99% min Amprolium Hydrochloride powder

Sample:Amprolium Hydrochloride powder

Packaging:1kg/bag, 25kg/drum

Brand:Henrikang

Appearance:white

Storage: Cool Dry Place

Shelf Life: 2 Years

Test Method: HPLC

Amprolium Hydrochloride powder Usage and Synthesis.

Aminoproline hydrochloride is used in chickens, rabbits, calves and lambs, and is effective against Eimeria tender and pile of chicken and against coccidia lamb and calves. It can be used in combination with other drugs to make water dispersing agent or premix agent. It is the main anticocciditic drug for laying hens. The product has low toxicity, large safety range, less residue and no need to stop the drug period. It was prepared with ethoxamide phenylmethyl ester and sulfaquinoxaline compound to enlarge the anti-coccidian spectrum and enhance the anti-coccidian effect. The combination with sulfaquinoxaline also has a good inhibitory effect on concurrent bacterial infection, and is a widely used anticoccidial drug at present. 

Uses of Amprolium Hydrochloride.

Anti-coccidiosis drug, good effect, less residual, can prevent and treat chicken coccidiosis, and can promote growth. For chicken feed, the dosage is 62.5-125g/t. It can also be mixed with ethoxyamide phenymethyl ester at 125:8 to form two mixtures, the dosage is (62.5+4-125+8)g/t, the drug withdrawal period is 7 days, and the egg production period is prohibited. It was mixed with ethoxamide phenylmethyl ester and sulfaquinoxaline at 100:5:60 to form three mixtures, the highest dosage was (100+5+60) g/t, the egg production period was prohibited, and the drug withdrawal period was 7 days. It is used as an anticoccidial drug and is effective against Eimeria chicken, Eimeria tender and pile, lamb and calf.

Pharmacological action of Amprolium Hydrochloride.

Product Methods of Amprolium Hydrochloride.

Taking the intermediate of vitamin B1 as raw material, the amino group is converted to hydroxyl group by cyclization, water unwinding, and then diazotization, and finally by condensation.