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Ceftiofur Sodium Sterile API

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MOQ : 25 Kilograms

Ceftiofur Sodium Sterile API Specification

Poisonous
No (use as directed for veterinary purpose)

Boiling point
Not applicable (decomposes before boiling)

Taste
Bitter

Solubility
Soluble in water, insoluble in organic solvents

Melting Point
Not less than 145C

Shelf Life
24 months

Molecular Formula
C19H16N5NaO7S3

Structural Formula
Available on request

Molecular Weight
558.54 g/mol

Heavy Metal (%)
0.001%

Ph Level
4.5 - 6.5 (1% solution)

Loss on Drying
1.0%

HS Code
29419090

Color
White to pale yellow

Particle Size
D90 10 microns

Smell
Odorless

Storage
Store in tightly sealed container at 2-8C, protect from light and moisture

Medicine Name
Ceftiofur Sodium Sterile API

Chemical Name
(6R,7R)-7-[[(2-Amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-[[(furan-2-ylcarbonyl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate sodium

CAS No
104010-37-9

Type
Antibacterial API

Grade
Sterile/Pharmaceutical Grade

Usage
Veterinary; Used to manufacture injectable, intramammary, and other formulations

Purity(%)
>=98.0%

Appearance
White to off-white powder

Physical Form
Solid

Identification
By IR and HPLC, complies with reference standard

Bacterial Endotoxins Test
Meets requirements

Assay (on anhydrous basis)
>=98.0%

Endotoxin
<0.5 IU/mg

Standard
USP/BP/EP (as per requirement)

Related Substances
Total impurities 1.0%

Residual Solvents
Complies with pharmacopoeial limits

Certificate of Analysis
Available with each batch

Microbial Limit
Meets specification

Sterility
Complies

Packing
Packed in sterile, double PE bags placed in aluminum foil bags

Ceftiofur Sodium Sterile API Trade Information

Minimum Order Quantity
25 Kilograms

Payment Terms
Cash in Advance (CID), Cash Against Delivery (CAD), Cash on Delivery (COD)

Supply Ability
500 Kilograms Per Month

Delivery Time
5-7 Days

Main Export Market(s)
Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa

Main Domestic Market
All India

Ceftiofur Sodium Sterile API About

Utilise this stellar offer on Ceftiofur Sodium Sterile API, a scarce and highly polished antibacterial active pharmaceutical ingredient designed for veterinary use. Customizable to USP, BP, or EP standards, this enviable product boasts purity 98% and total identifiable impurities 1.0%. Each batch is meticulously tested-identification via IR and HPLC, sterility, low endotoxin levels (<0.5 IU/mg), and precise microbial limits-ensuring absolute quality. Packed securely in sterile, double PE bags within aluminum foil for maximum protection, it is ideal for manufacturing injectable and intramammary veterinary formulations. Certificate of Analysis supplied with each shipment.

Diverse Application Potential

Ceftiofur Sodium Sterile API excels not only in injectable and intramammary veterinary solutions but also in other pharmaceutical formulations, thanks to its adaptable physical form and superior purity. Suitable for use in aqueous media, it meets rigorous standards for competitive sterile APIs and ensures exceptional efficacy in veterinary therapeutic protocols. With its enviable reputation among exporters and traders in India, this API suits various scaled manufacturing operations seeking reliability and flexibility.

Sample Program, Shipping, and Supply Capability

Sample quantities of Ceftiofur Sodium Sterile API are available upon proposal amount and client request, allowing manufacturers to assess quality prior to bulk purchase. Logistics are efficiently managed through the designated FOB port in India, offering global reach at competitive rates. Reliable supply ability ensures prompt fulfillment of orders both large and small, reflecting our commitment to consistent product availability and client satisfaction across diverse veterinary pharmaceutical markets.

FAQ's of Ceftiofur Sodium Sterile API:

Q: How can Ceftiofur Sodium Sterile API be used in veterinary medicine?

A: Ceftiofur Sodium Sterile API is primarily formulated into injectable, intramammary, and other veterinary dosage forms. Its broad-spectrum activity makes it well-suited for treating various bacterial infections in animals.

Q: What processes are followed to ensure the sterility and safety of each batch?

A: Every batch undergoes rigorous testing, including bacterial endotoxins and total impurities evaluation, IR and HPLC identification, as well as comprehensive compliance with pharmacopoeial limits for solvents, heavy metals, and sterility.

Q: Where is the product shipped from and what are the logistics details?

A: The product is exported from India, with orders shipped via an FOB port. Logistics are handled efficiently to ensure timely delivery, and all packaging adheres to international quality standards for sterile APIs.

Q: When is a Certificate of Analysis provided?

A: A detailed Certificate of Analysis is issued with every batch, outlining compliance with all specifications, including purity, sterility, residual solvents, and assay parameters.

Q: What are the benefits of the double-layer sterile packaging used for this API?

A: The sterile, double PE bag packaging, sealed within aluminum foil bags, ensures maximum protection from moisture and contaminants, preserving the product's integrity and shelf life for up to 24 months.

Q: How can a sample of the API be requested, and what is the proposal amount?

A: Interested parties can request a sample through our sales channel by specifying requirements and agreeing on a proposal amount that covers logistics and sample processing, ensuring a seamless evaluation process.

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