Amlexanox API
Amlexanox API

Amlexanox API

Price 23.0 USD ($)/ Kilograms

MOQ : 1 Kilograms

Amlexanox API Specification

  • Particle Size
  • 30-50 microns
  • Molecular Formula
  • C16H14N2O4
  • Storage
  • Keep away from moisture
  • Loss on Drying
  • Not more than 0.5%
  • Molecular Weight
  • 298.298 g mol Grams (g)
  • Structural Formula
  • Cloxacillin contains a penicillin core structure with a chlorinated isoxazolyl side chain.
  • Melting Point
  • 195-202 C
  • HS Code
  • 29411010
  • Smell
  • Other
  • EINECS No
  • 200-506-1
  • Shelf Life
  • 5 Years
  • Solubility
  • Slightly soluble in water freely soluble in methanol
  • Heavy Metal (%)
  • Not more than 0.002%
  • Taste
  • Bitter
  • Ph Level
  • 5-7 (1% solution in water)
  • Medicine Name
  • Cloxacillin
  • Chemical Name
  • Cloxacillin Sodium
  • CAS No
  • 68302-57-8
  • Type
  • Other
  • Usage
  • Treatment of bacterial infections
  • Purity(%)
  • 99.0%min
  • Appearance
  • White Crystaline Powder
  • Physical Form
  • Powder
 

Amlexanox API Trade Information

  • Minimum Order Quantity
  • 1 Kilograms
  • FOB Port
  • ALL INDIA
  • Payment Terms
  • Telegraphic Transfer (T/T), Western Union, Paypal, Cash Advance (CA), Cash in Advance (CID)
  • Delivery Time
  • 2-3 Week
  • Sample Policy
  • Sample costs shipping and taxes has to be paid by the buyer
  • Packaging Details
  • 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • All India
  • Certifications
  • WHO,GMP,COA,MSDS As Per Client requirement
 

About Amlexanox API

Amlexanox Ip / Bp / Usp

Amlexanox (trade name Aphthasol) is an anti-inflammatory antiallergic immunomodulator used to treat recurrent aphthous ulcers (canker sores), and (in Japan) several inflammatory conditions.

Items for Detecting The Standard Result
Appearance : Off white crystalline powder
Purity : 99.0%min
Loss on drying(w/w,%) 0.5%max
Acidity(w/w,%): 0.5%max


Packaging details:

Packaging details: 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.
Storage: Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat
Shelf Life: 5 years if sealed and store away from direct sun light.


High-Quality Pharmaceutical API

Our Cloxacillin Sodium (Amlexanox API) is manufactured and distributed to meet stringent industry quality requirements. The powder's white crystalline appearance and controlled particle size guarantee reliable performance in pharmaceutical formulations. Each batch is rigorously tested for heavy metals, pH balance, and purity to support drug safety and efficacy.


Safe Handling and Storage Guidelines

To maintain its effectiveness and long shelf life of up to five years, the Amlexanox API should be stored in a dry environment, protected from moisture. Properly handled and stored, this API retains its chemical integrity, providing consistent results for pharmaceutical manufacturers and healthcare providers.

FAQ's of Amlexanox API:


Q: How should Amlexanox API (Cloxacillin Sodium) powder be stored?

A: Amlexanox API should be kept in a cool, dry place away from moisture. Proper storage in airtight containers ensures maximum stability and maintains its five-year shelf life.

Q: What is the main use of Cloxacillin Sodium in pharmaceuticals?

A: Cloxacillin Sodium is primarily used to formulate medications aimed at treating bacterial infections, leveraging its potent antibacterial properties.

Q: When can I expect the best results using this API in pharmaceutical manufacturing?

A: You will achieve the best results when the API is handled in a moisture-free environment, dissolved as suited (slightly soluble in water, freely soluble in methanol), and used within its shelf life.

Q: Where is this API produced and supplied from?

A: This Cloxacillin Sodium API is produced and supplied by manufacturers, exporters, and distributors based in India, ensuring global standards in quality and delivery.

Q: What is the process for verifying the purity of this API?

A: Purity is established through rigorous laboratory analysis, confirming a minimum of 99.0% purity, with heavy metal content not exceeding 0.002% and minimal loss on drying.

Q: How does the particle size impact its pharmaceutical application?

A: A controlled particle size range of 30-50 microns ensures uniform distribution in formulations, optimizing dissolution rates and consistent medication performance.

Q: What benefits does using this API offer to pharmaceutical manufacturers?

A: Manufacturers benefit from a high-purity, stable, and reliable active pharmaceutical ingredient, supporting efficient production of safe and effective antibacterial medicines.

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