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Cefixime API Powder
Cefixime API Powder

Cefixime API Powder

MOQ : 50 Kilograms

Cefixime API Powder Specification

  • Solubility
  • Slightly soluble in water, freely soluble in dimethylformamide and in methanol
  • Molecular Weight
  • 453.45 g/mol
  • Smell
  • Odorless
  • Color
  • White to cream
  • Heavy Metal (%)
  • Not more than 0.001%
  • Storage
  • Dry Place
  • Particle Size
  • D90 <10 microns
  • Ph Level
  • 4.5 6.5
  • Molecular Formula
  • C16H15N5O7S2
  • HS Code
  • 29414000
  • Structural Formula
  • Available on request
  • EINECS No
  • 620-761-7
  • Loss on Drying
  • Not more than 0.5%
  • Poisonous
  • NO
  • Shelf Life
  • 36 Months
  • Melting Point
  • 210-220C (decomposes)
  • Boiling point
  • Not applicable (decomposes before boiling)
  • Taste
  • Bitter
  • Medicine Name
  • Cefixime API Powder
  • Chemical Name
  • Cefixime
  • CAS No
  • 79350-37-1
  • Type
  • Pharmaceutical Intermediates
  • Grade
  • Medicine Grade
  • Usage
  • Used in the formulation of antibacterial drugs
  • Purity(%)
  • 99.0% min
  • Appearance
  • White to off-white powder
  • Physical Form
  • Powder
  • Identification
  • IR and UV-spectrophotometric methods confirm identity
  • Residue on Ignition
  • Not more than 0.1%
  • Related Substances
  • Not more than 1.0%
  • Assay (HPLC)
  • Not less than 98.0%
  • Microbial Limits
  • Meets pharmacopeial standards
  • Certificate of Analysis (COA)
  • Available with every batch
  • Packing
  • Packed in HDPE drums with double polyethylene bag liner
  • Polymorphic Form
  • Polymorph I (as per pharmacopeial guideline)
 

Cefixime API Powder Trade Information

  • Minimum Order Quantity
  • 50 Kilograms
  • Payment Terms
  • Cash Advance (CA)
  • Supply Ability
  • 1000 Kilograms Per Month
  • Delivery Time
  • 5 Week
  • Main Domestic Market
  • All India
 

About Cefixime API Powder



Discover the freshness of our Cefixime API Powder, crafted with the finest standards for pharmaceutical applications. Experience an unparalleled level of purity (minimum 99%) and reliability with trending quality controls such as HPLC assay (NMT 98.0%), confirming identity by IR and UV-spectrometry. Valorous in compliance, it meets pharmacopeial guidelines for microbial limits and related substances. Benefit from a price cut on this high-grade, medicine-grade pharmaceutical intermediate, packed securely in HDPE drums with double liners. Each batch is supplied with a Certificate of Analysis, assuring uncompromising quality at a competitive outlay.

Key Features and Usage: The Finest Cefixime API Powder

Our Cefixime API Powder boasts a D90 particle size of less than 10 microns, ensuring high dispersibility in formulations. With premium characteristics such as assay (NLT 98.0%), potent antimicrobial efficacy, and compliance with stringent pharmacopeial requirements, it stands as a core intermediate for antibacterial drug manufacturing. Further, its polymorphic purity (Form I) guarantees optimal performance, catering exclusively to the pharmaceutical industry for the valorous development of medicinal products.


Sample, Packaging & Delivery: Unparalleled Value For Export Markets

We offer Cefixime API Powder samples to qualified buyers, letting you experience superior quality before outlaying for bulk orders. Our product comes securely packed in HDPE drums lined with double polyethylene bags, preserving its integrity during transport. With competitive asking prices and rapid delivery times, we cater efficiently to the export market. Each batch is accompanied by a thorough Certificate of Analysis, granting full confidence in your sourcing process.


FAQ's of Cefixime API Powder:


Q: How is the identity of Cefixime API Powder confirmed?

A: The identity of Cefixime API Powder is verified using IR and UV-spectrophotometric methods, ensuring its authenticity and compliance with pharmacopeial standards.

Q: What is the purity level of this Cefixime API Powder?

A: Our Cefixime API Powder guarantees a minimum purity of 99.0%, with an assay (HPLC) not less than 98.0%, supporting its use in high-quality pharmaceutical formulations.

Q: When is the Certificate of Analysis provided for each batch?

A: A Certificate of Analysis (COA) is provided with every batch, detailing assay, physical characteristics, and compliance parameters for complete quality assurance.

Q: Where is this product commonly exported from?

A: This Cefixime API Powder is exported from India and supplied to the global pharmaceutical industry as an essential intermediate in antibacterial drug manufacturing.

Q: What are the primary usage benefits of Cefixime API Powder?

A: The main benefit of using this API powder is its role in the formulation of effective antibacterial drugs, supported by its superior purity and consistent medicinal grade quality.

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