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Cefotaxime sodium

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MOQ : 1 Kilograms

Cefotaxime sodium Specification

EINECS No
264-915-9

Structural Formula
Available on request

Physical Form
Powder

Properties
Broad-spectrum cephalosporin antibiotic, stable under standard conditions, light sensitive

Shelf Life
3 years

Molecular Formula
C16H16N5NaO7S2

Taste
Bitter

Purity
98%

Poisonous
Non-poisonous as sold

Ingredients
Cefotaxime sodium

Smell
Odourless

Appearance
White to off-white crystalline powder

Ph Level
4.5-6.5 (in solution)

Storage
Store in a cool, dry place; protect from light

Application
Antibiotic for bacterial infections treatment

CAS No
64485-93-4

Melting Point
178-187C (dec.)

HS Code
29419060

Grade
Pharmaceutical Grade

Molecular Weight
477.45 g/mol

Usage
Used in intravenous or intramuscular administration

Shape
Crystalline powder

Solubility
Freely soluble in water

Product Type
Active Pharmaceutical Ingredient

Cefotaxime sodium Trade Information

Minimum Order Quantity
1 Kilograms

Payment Terms
Cash Against Delivery (CAD)

Supply Ability
Kilograms

Delivery Time
3-4

Sample Available
Yes

Sample Policy
Sample costs shipping and taxes has to be paid by the buyer

Main Export Market(s)
Asia

Main Domestic Market
All India

About Cefotaxime sodium

Cefotaxime sodium

Synonym: Cefotaxim sodium salt, Cefotaxime sodium salt

CAS Number 64485-93-4
Empirical Formula (Hill Notation) C₁₆H₁₆N₅NaO₇S₂
Molecular Weight 477.45
form
neat

format neat

Effective Broad-Spectrum Antibiotic

Cefotaxime sodium is renowned for its efficacy across a wide range of bacterial strains, targeting both Gram-positive and Gram-negative organisms. Its high bioavailability ensures rapid onset of action when administered via intravenous or intramuscular injection. This makes it a trusted choice in hospital and clinical settings for the treatment of serious infections.

Quality and Stability Assured

Manufactured under stringent USP/BP/EP standards, cefotaxime sodium maintains its pharmaceutical-grade purity (98%) and controlled impurity levels (1.0%). Its stability within a pH range of 4.56.5 ensures consistent clinical performance. Sensitive to environmental factors, it is securely packaged and clearly labeled to maintain its integrity during storage and transport.

FAQs of Cefotaxime sodium:

Q: How should cefotaxime sodium be administered for therapeutic effectiveness?

A: Cefotaxime sodium is administered parenterally through intravenous (IV) or intramuscular (IM) injection. This route ensures high bioavailability and rapid clinical action for treating bacterial infections.

Q: What precautions are necessary for storing cefotaxime sodium?

A: Store cefotaxime sodium in a cool, dry place and protect it from light and moisture. Proper storage preserves its potency and extends its shelf life up to three years.

Q: When is cefotaxime sodium indicated for use?

A: It is prescribed to treat severe bacterial infections where a broad-spectrum cephalosporin antibiotic is recommended, particularly in hospital or clinical environments.

Q: Where is cefotaxime sodium typically packaged for distribution?

A: Cefotaxime sodium is packaged in pharmaceutical vials, ampoules, or sealed containers to preserve stability and prevent exposure to moisture and light.

Q: What is the process for ensuring quality and purity in cefotaxime sodium?

A: Manufacturing adheres to USP, BP, or EP standards. Each batch is tested for impurity level (1.0%), residual solvents, and appearance, guaranteeing a minimum purity of 98% before release.

Q: What are the benefits of using cefotaxime sodium for infection treatment?

A: This antibiotic exhibits a broad spectrum of activity, high efficacy, and rapid absorption when administered parenterally, making it valuable for combating difficult or severe infections.

Q: Is cefotaxime sodium affected by prolonged exposure to air or light?

A: Yes. Prolonged exposure to air may cause a slight yellowish color change, while light and moisture can degrade the powder, so storage in sealed, light-protected containers is essential.

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