Supply Antibiotic Powder CAS 104376-79-6 Ceftriaxone Sodium

• Customization: Available
• Powder: Yes
• Customized: Customized
• Model NO.: TGY2021110901
• Certification: GMP, HSE, ISO 9001, USP, BP
• Suitable for: Elderly, Children, Adult
• State: Solid
• Purity: >99%
• Product Name: Ceftriaxone Sodium
• Appearance: White Powder
• Assay: 99%
• Test Methods: HPLC
• MOQ: 1kg
• Sample: Availabel
• CAS No.: 74578-69-1
• Shelf Life: 2 Years
• Transport Package: Foil Bag, Box, Drum
• Specification: 99%min
• Trademark: TGY
• Origin: China
• HS Code: 29242930
• Production Capacity: 2500kg/Month

Product Description

Product Name	Ceftriaxone Sodium Powder CAS 104376-79-6 Ceftriaxone Sodium
Appearance	white powder
Assay	99%min, 98.0% --101.0%
Test	HPLC
Certificate	ISO9001
CAS	104376-79-6
Storage	Cool Dry Place
Shelf Life	2 years

Ceftriaxone sodium is the semi-synthetic drugs as third-generation cephalosporins,for most Gram-positive and Gram-negative bacteria have strongantibacterial activity,antimicrobial spectrum,including Pseudomonas aeruginosa,Escherichia coli,Klebsiella pneumoniae,Haemophilus influenzae,intestinal gas production bacteria, Proteus,Staphylococcus aureus and other metals and meningitis.The drugson the β-lactamase stability. Ceftriaxone sodium;ceftriaxone sodium powder.

 

 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.

Ceftriaxone Sodium is an antibiotic useful for the treatment of a number of bacterial infections. Ceftriaxone Sodium is a third-generation cephalosporin.

Specification:

Item			Specification	Results
Characters			Appearance:almost white or yellowish, slightly hygroscopic, crystalline powder Solubility:freely soluble in water, sparingly soluble in meth, very slightly soluble in anhydrous ethanol.	Almost white, slightly hygroscopic, crystalline powder; Solubility: Conform
Identification			1. A. Infrared absorption spectrophotometry, comparison; 2. B. It gives reaction (a) of sodium	Positive
PH			6.0-8.0	7.3
Specific optical rotation			-155°~-170°	-160°
Appearance of solution			It is Clear and not more intensely colored than reference solution Y5 or BY5	Clear,5
Related substances	Any impurity		≤1.0%	0.1%
	Total impurities		≤4.0%	0.4%
Water			≤8.0-11.0%	8.8%
N,N-Dimethylanlline			≤0.0020%	Not detected
2-Ethylhexanoic			≤0.8%	0.002%
Bacterial endotoxins			<0.08IU/mg	<0.08IU/mg
Sterility			Sterile	Sterile
Sub-visible particles		≥10μm	Not more than 2250 particles/g	608 particles/g
		≥25μm	Not more than 225 particles/g	26 particles/g
Assay(based on anhydrous substance)			96.0%-102.0% of C18H16N8Na2O7S3	99.2%
Conclusion			The above results meet the EP8.0th Edition