Antimicrobials CAS 91296-87-6 Sarafloxacin HCl Raw Material Sarafloxacin Hydrochloride Veterinary Sarafloxacin Hydrochloride

• Customization: Available
• Varieties: Sarafloxacin Hydrochlorid
• Component: Sarafloxacin Hydrochlorid
• Model NO.: D-Sung Sarafloxacin hydrochloride
• Type: Sarafloxacin Hydrochlorid
• Pharmacodynamic Influential Factors: Animal Species
• Storage Method: Prevent High or LowTemperature
• Product Name: Sarafloxacin Hydrochlorid
• Name: Sarafloxacin Hydrochlorid Powder
• Appearance: White Power
• Color: White
• Grade: Pharmaceutical Grade Veterinary Grade
• Assay: HPLC 99%
• Application: Anthelmintics
• Specific: COA
• Test Method: HPLC
• Shelf Life: 2 Years
• CAS No.: 91296-87-6
• Molecular Formu: C20h18clf2n3o3
• Melting Point: 275c
• Boiling Point: 621.4 C at 760 Mmhg
• Storage Tempera: 0~6c
• Transport Package: Negotiable
• Specification: 99%
• Trademark: D-Sung
• Origin: Xi′an Shaanxi
• Production Capacity: 1000kg/Month

Product Description

Antimicrobials CAS 91296-87-6 Sarafloxacin HCL Raw Material Sarafloxacin Hydrochloride Veterinary Sarafloxacin Hydrochloride

Product Details

Product Name	Sarafloxacin Hydrochloride
CAS No	91296-87-6
Appearance	White to light yellow Powder
Purity	99%

Salafloxacin is a new animal drug after Enoxacin. The antibacterial activity of salafloxacin is stronger than that of difloxacin and the antibacterial activity of salafloxacin against anaerobic bacteria is comparable.

Application&Function

Function  of Sarafloxacin Hydrochloride

(1) blocking the replication of DNA and acting directly on the nucleus of bacteria.
(2) interfere with the synthesis of DNA, thus completely kill bacteria, no recurrence after withdrawal.
(3) widely distributed, through the blood-brain barrier, which is good for the treatment of two kinds of diseases which are difficult to cure, such as respiratory diseases and brain colibacillosis.

Application of Sarafloxacin Hydrochloride

(1) it can be absorbed quickly in the body, and the serum concentration can reach the peak value after 1.5 hours oral administration.(2) good distribution in all tissues of the body.
(3) because of the rapid absorption of excretion, continuous medication for five days, 6 hours of withdrawal, residues are much lower than the required amount.
(4) do not need to consider the stopping time of this product, and do not need to stop the drug before the slaughter.
(5)there is no cross resistance to other drugs, and it is still very sensitive to strains that are resistant to antibiotics, sulfonamides, and furans.
(6) good stability, low toxicity, safe medication, cheap price, low treatment cost and low cost.

Specification