99% High Purity Pharmaceutical Raw Material CAS 79350-37-1 Cefixime

• Varieties: Other
• Component: Chemical Synthetic Drugs
• Type: Other
• Pharmacodynamic Influential Factors: Other
• Storage Method: Prevent Exceeding Quality Guarantee Period
• Veterinary Reg. No.: Other
• Model NO.: Cefixime
• CAS No: 79350-37-1
• Mf: C16h15n5o7s2
• Purity: ≥ 99.0%
• Appearance: White Powder
• Grade Standard: Medicine Grade
• Shelf Life: 2 Years
• Transport Package: Bag, Carton, Drum
• Specification: 25kg/drum
• Trademark: Arshine
• Origin: China
• HS Code: 2941905990
• Production Capacity: 200 Tons/Year

Product Description

 99% High Purity Pharmaceutical Raw Material CAS 79350-37-1 Cefixime

Cefiximeis a broad spectrum antibiotic which means it is active against a wide variety of bacteria. It treats infections by killing or stopping the growth of the bacteria that cause them.Cefixime is an oral third generation cephalosporin antibiotic.
Cefixime is an oral third generation cephalosporin antibiotic. Cefixime is a cephalosporin antibiotic used to treat infections caused by bacteria. These include infections of the: Ear (otitis media caused by Haemophilus influenzae, Moraxella catarrhalis,and S. pyogenes.) Nose, sinuses (sinusitis), Throat (tonsillitis, pharyngitis caused by S. pyogenes ), Chest and lungs (bronchitis, pneumonia caused by Streptococcus pneumoniae and Haemophilus influenzae) and Urinary system and Uncomplicated gonorrhea caused by Neisseria gonorrhoeae.

Function & Application

Cefixime is a cephalosporin antibiotic used to treat infections caused by bacteria. These include infections of the:
1. Ear (otitis media caused by Haemophilus influenzae, Moraxella catarrhalis,and S. pyogenes.)
2. Nose, sinuses (sinusitis), Throat (tonsillitis, pharyngitis caused by S. pyogenes )
3. Chest and lungs (bronchitis, pneumonia caused by Streptococcus pneumoniae and Haemophilus influenzae)
4. and Urinary system and Uncomplicated gonorrhea caused by Neisseria gonorrhoeae.
Suitable for bronchitis, pneumonia, pyelonephritis, cystitis, urethritis, cholecystitis, cholangitis, scarlet fever, otitis media, sinusitis

Items		Specification	Analysis Result
Appearance		White to light yellow crystalline powder	Conform
Identification		1. The retention times of the major peaks in the chromatogram of the assay preparation correspond to those of the Standard preparation obtained in the assay	Conform
		2. The IR absorption spectrum of the substance to be examined corresponds to that of the reference standard.	Conform
soluble		55.11 mg/L	Conform
Crystallinity		Meets the USP test requirements	Conform
PH		2.6~4.1	3.6
Water Content		9.0%~12.0%	10.4
Residue of ignition		Not more than 0.1%	Conform
Heavy Metals		Not more than 20ppm	Conform
Chromatographic purity		Meets the USP test requirements	Conform
Assay (anhydrous)		98.0%~103.0%	99%
Related Impurities	Individual impurities	Not more than1.00%	0.30%
	Total impurities	Not more than2.00%	0.80%