High Purity Fleroxacin Powder CAS 79660-72-3 Fleroxacin

• Customization: Available
• Powder: Yes
• Customized: Customized
• Model NO.: Fleroxacin
• Certification: GMP, ISO 9001, USP, BP
• Suitable for: Elderly, Children, Adult
• State: White Powder
• Purity: >99%
• CAS: 79660-72-3
• Mf: C17h18f3n3o3
• MW: 369.338
• Test Method: HPLC
• Shelf Life: 24 Months
• Storage: Cool Dry Place
• Transport Package: 1LG/Bag, 25kg/Drum
• Specification: Fleroxacin
• Trademark: HNB
• Origin: China
• Production Capacity: 2000kg/Month

Product Description

Common Name	Fleroxacin	CAS Number	79660-72-3
Density	1.4±0.1 g/cm3	Assay	99%
Molecular Weight	369.338	Boiling Point	535.3±50.0 °C at 760 mmHg
Molecular Formula	C17H18F3N3O3	Melting Point	264-266°C
Flash Point	277.6±30.1 °C	Storage condition	Airtight, cool, dry place

 

Fleroxacin can be used to cause infectious bronchitis in susceptible bacteria, respiratory tract infections such as acute
exacerbation of chronic bronchitis and pneumonia, cystitis, pyelonephritis, prostatitis, epididymitis, Neisseria gonorrhoeae
urethritis and other genitourinary system Infection, Salmonella typhi infection, bacterial dysentery and other digestive system infections, skin and soft tissue infections, bone infections, abdominal infections and pelvic infections.

Fleroxacin is a third-generation quinolone drug that has a good killing effect against gram-negative bacteria (such as Pseudomonas aeruginosa) and gram-positive bacteria (such as Staphylococcus aureus). Its mechanism of action is through inhibition of bacterial DNA. Rotazyme to achieve bactericidal effect, with a wide spectrum of antibacterial activity, strong antibacterial activity, high bioavailability, strong tissue penetration, elimination of long half-life (10 ~ 20 h), can be used once a day and so on.

Item	Standard
Structural data confirmation	1. H-NMR: The data of structure are identical with reference standard
	2. HPLC-MS: Ensure the molecular weight of main peak and fragment peak are identical with reference standard
	3. IR:The data of IR are identical with that of reference standard
Purity(HPLC)	≥99.0%
Related impurities	Specific single impurity	Meets EP/USP/BP standards
	Non-specific single impurity	≤0.10%
	Total Impurities	≤0.50%
Crystal form	Meets EP/USP/BP standards
Loss on drying	≤1.0%
Water	≤1.0%
Inorganic salt	≤0.1%
Heavy metals	≤10 ppm
Assay	99.0%~101.0%(According to EP/USP/BP standards)
Microbiological Analysis
Total plate count	≤1000cfu/g
Yeast and Moulds	≤100cfu/g
E. Coli.	Absent
Salmonella	Absent
S.aureus	Absent