GMP USP Quality Pharmaceutical Ciprofloxacin Base CAS: 86393-32-0

• Powder: Yes
• Certification: GMP, USP, BP
• Suitable for: Ciprofloxacin Intermediate
• State: Solid
• Purity: >99%
• Shelf Time: 3 Years
• Model NO.: BP/USP/EP
• Transport Package: 25kg/Drum
• Specification: USP/BP
• Trademark: SINOAH
• Origin: China
• HS Code: 3003101100
• Production Capacity: 100mt/Month

Product Description

ciprofloxacin intermediate Ciprofloxacin Q-acid CAS:86393-33-1
 

Chemical name:Ciprofloxacin Q-acid

CAS No:86393-33-1

Molecular formula: C₁₃H₉ClFNO₃

Molecular weight: 281.67

Melting range: 239-244ºC

Appearance: White or light yellow crystalline powder

Intermediate of Ciprofloxacin Hcl

Ceftriaxone sodium sterile Specifications
Ceftriaxone Sodium sterile
CAS No.: 74578-69-1
Standard: EP/BP/USP
Assay: 99%
White or almost white crystalline powder
Ceftriaxone Sodium sterile

Name	Ceftriaxone Sodium sterile
Assay:	99%
CAS No	74578-69-1
Standard:	EP/BP/USP
Appearance	White or almost white crystalline powder
Uses	The drug as a semi-synthetic third-generation cephalosporins, for most Gram-positive bacteria and-negative bacteria have strong antibacterial activity, antibacterial spectrum, including Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, Haemophilus influenzae, bacterial intestinal gas production, Proteus, and Staphylococcus aureus meningitis is so. The drug on β-lactamase stability.  The main clinical infection for susceptible strains of meningitis, pneumonia, skin and soft tissue infections, peritonitis, urinary tract infections, gonorrhea, liver and gallbladder infection, surgical trauma, sepsis, and genital infections. As a treatment for gonorrhea has been first-line drugs.