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Anti-insect and anti-bacterial Sulfaquinoxaline raw Powder
Product Overview:
Sulfaquinoxaline, also known as sulfaquinoxaline, is a highly effective anti-insect agent and antibacterial drug, which is absorbed quickly after oral administration, has a good effect on poultry diseases, and is widely used, but has certain toxicity, and is easy to remain in the edible tissues of animals. Due to the good efficacy of sulfaquinoxaline, the farms added sulfaquinoxaline into the feed or drinking water of animals during the feeding process, and did not fully comply with the provisions of the National Veterinary Pharmacopoeia on the dosage, administration period and withdrawal period, resulting in a large amount of sulfaquinoxaline residues in animal food.
Anti-insect and anti-bacterial Sulfaquinoxaline raw Powder Attributes
CAS:59-40-5
MF:C14H12N4O2S
MW:300.34
EINECS:200-423-2
Specification: 99% min Sulfaquinoxaline Powder
Sample:Sulfaquinoxaline Powder
Packaging:1kg/bag, 25kg/drum
Brand: Henrikang
Appearance:yellow
Storage: Cool Dry Place
Shelf Life: 2 Years
Test Method: HPLC
Anti-insect and anti-bacterial Sulfaquinoxaline raw Powder Details
Sulfaquinoxaline powder Usage and Synthesis.
Sulfaquinoxaline is a sulfanilamide antibacterial drug used for coccidiosis in livestock and poultry. Sulfaquinoxaline can affect the synthesis of bacterial nucleoprotein, thus inhibiting the growth and reproduction of bacteria and coccidia. This product can be used with trimethoprim, the effect is stronger. This product is toxic to chicks and should not be used for a long time.
Uses of Sulfaquinoxaline.
Sulfaquinoxaline is an effective drug for treating coccidiosis of poultry and rabbit. As a broad spectrum antimicrobial agent for animals, it is more toxic to mammals and is only used for various coccidiosis in chickens. Not allowed for laying hens.
Pharmacological action of Bulk Sulfaquinoxaline powder.
Product Methods of Sulfaquinoxaline.
N-cyanomethyl-o-phenylenediamine was synthesized by reaction with sodium cyanide, formaldehyde and acid medium. It is then cycled with potassium hydroxide to form 2-amino-3, 4-dihydroazole. Using ferrous chloride as catalyst, 2-aminoquinoxaline was obtained by oxidative dehydrogenation of hydrogen peroxide. Finally, sulfonaminoquinoyl chloride was synthesized by condensation and hydrolysis.
