Ceftriaxone API
Price 100 INR/ Kilograms
Ceftriaxone API Specification
- HS Code
- 2941.90
- Storage
- Store in a cool, dry place, protected from light
- Melting Point
- >200C (decomposes)
- Boiling point
- Not applicable (decomposes)
- Smell
- Odorless
- Solubility
- Soluble in water, slightly soluble in methanol, practically insoluble in chloroform and in ether
- Loss on Drying
- 0.5%
- EINECS No
- 620-320-1
- Molecular Formula
- C18H18N8O7S3
- Poisonous
- No (when handled as per safety norms)
- Heavy Metal (%)
- 0.001%
- Structural Formula
- Refer to image or structure drawn as per chemical name
- Shelf Life
- 3 years
- Molecular Weight
- 554.58 g/mol
- Particle Size
- 90% <10 micron
- Ph Level
- 5.0 7.5 (solution)
- Taste
- Bitter
- Color
- White to yellowish
- Medicine Name
- Ceftriaxone API
- Chemical Name
- (6R,7R)-7-[[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(2-methyl-6-oxido-5-oxo-2,5-dihydro-1,2,4-triazin-3-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
- CAS No
- 104376-79-6
- Type
- Other
- Grade
- Other
- Usage
- Pharmaceutical Intermediates, Antibiotic
- Purity(%)
- 98% min
- Appearance
- White to yellowish crystalline powder
- Physical Form
- Solid
- Stability
- Stable under recommended storage conditions
- Specific Optical Rotation
- Between -160 and -180 (in water)
- Assay
- 98.5% - 101.0% (on anhydrous basis)
- pH of solution (1% w/v)
- 5.0 - 7.0
- Residual Acetone
- 5000 ppm
- Related Substances
- Total impurities 1.0%, individual impurity 0.5%
- Packaging
- HDPE drums with double polythene bags / as per customer requirement
- Water Content (KF)
- 0.5%
- Therapeutic Category
- Cephalosporin Antibiotic
- Residual Solvents
- Complies with ICH guidelines
- Toxicity
- LD50 (oral, rat) >2000 mg/kg
- Endotoxins
- <0.20 IU/mg
Ceftriaxone API Trade Information
- Minimum Order Quantity
- 1 Kilograms
- Supply Ability
- 2000 Kilograms Per Day
- Delivery Time
- 1 Days
- Main Domestic Market
- All India
About Ceftriaxone API
Application Excellence: Where can Ceftriaxone API be used?
Ceftriaxone API is designed for use as a pharmaceutical intermediate and antibiotic. Its application surface includes sterile dosage forms, notably injectable solutions. Common application places are pharmaceutical manufacturing sites, formulation laboratories, and research facilities. The main site of application is within the healthcare sector, notably hospitals and clinics, where its potent antibacterial action supports the fight against bacterial infections. With high solubility in water, it integrates seamlessly into injectables and other medical formulations.
Dominant Export Destinations & Market Reach
We offer Ceftriaxone API at a competitive list price, catering to both main export marketsincluding the USA, Europe, Middle East, Africa, and Asia Pacificand the thriving Indian domestic market. Goods transport is managed with utmost care, ensuring products arrive promptly and safely. Our supply ability meets bulk demands, positioning us as a reliable distributor, exporter, manufacturer, and supplier within global and national pharmaceutical sectors.
FAQs of Ceftriaxone API:
Q: How is Ceftriaxone API typically used in pharmaceutical manufacturing?
A: Ceftriaxone API is mainly used as an active ingredient in the production of sterile injectable antibiotics, supporting the formulation of medicines that treat diverse bacterial infections.Q: What are the benefits of choosing Ceftriaxone API from this supplier?
A: Choosing our Ceftriaxone API ensures high purity (98.5101.0% assay), strict impurity limits, compliance with international safety guidelines, and dependable supply chains, all at a competitive price point.Q: Where are the main export markets for Ceftriaxone API?
A: The main export markets include the USA, Europe, Middle East, Africa, and Asia Pacific, alongside significant distribution within Indias domestic sector.Q: What storage conditions are required for Ceftriaxone API?
A: This API should be stored in a cool, dry place, protected from light, to maintain stability and effectiveness throughout its three-year shelf life.Q: How does the manufacturer ensure quality and compliance with regulatory guidelines?
A: Quality is ensured by strict adherence to assay specifications, impurity limits, residual solvent compliance per ICH, and endotoxin control, guaranteeing each batch meets pharmaceutical standards.Q: When can customers expect delivery for bulk or custom packaging orders?
A: Customers can expect prompt shipment for both standard HDPE drum packaging and custom requirements, with goods transport arranged for reliable and timely delivery levels.
Price:
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