Chlorzoxazone USP

Chlorzoxazone USP Specification

Molecular Formula
C7H4ClNO2

HS Code
2924 29 90

Place of Origin
India

Loss on Drying
0.5% max

EINECS No
202-411-2

Assay
99.0% to 101.0%

Heavy Metal (%)
<0.001%

Residue on Ignition
0.1% max

Melting Point
189C to 193C

Moisture (%)
0.5% max

Particle Size
Passed through 60 mesh

Molecular Weight
169.57 g/mol

Storage
Store in a cool, dry place, protected from light

Other Names
Chlorzoxazone, 5-Chloro-2-benzoxazolinone

CAS No
95-25-0

Type
Pharmaceutical Raw Material

Grade
USP

Usage
Muscle Relaxant

Purity
99% min

Appearance
White to off-white crystalline powder

Application
Active Pharmaceutical Ingredient

Raw Material
Yes

Smell
Odorless

Color
White

Form
Powder

Total impurities
0.3%

Packaging
Packed in HDPE drums, double polyethylene bags inside

Shelf Life
36 months from date of manufacture

Certificate of Analysis
Available upon request

Microbial Limit
Meets USP microbial requirements

Solubility
Slightly soluble in water, freely soluble in alcohol and in chloroform

Identification
Meets USP requirements (IR, TLC) for Chlorzoxazone

Maximum single impurity
0.1%

Chlorzoxazone USP Trade Information

Minimum Order Quantity
500 Kilograms, ,

Supply Ability
10000 Kilograms, , Per Month

Delivery Time
15 Days

Main Domestic Market
All India

About Chlorzoxazone USP

Chlorzoxazone Chemicals are used in the treatment of spasm and to provide relief from pain. It works by depressing reflexes by acting on the spinal cord. It is formulated from high-grade inputs sourced from a reliable vendor base in compliance with the defined industry standards. Moreover, our clients can avail from us Chlorzoxazone Chemicals at fair business norms and timely delivery of consignments.

Exceptional Quality and Compliance

Chlorzoxazone USP is manufactured under stringent quality controls, adhering to all USP standards, including limits for impurities and microbial content. Each shipment is thoroughly tested for identity by IR and TLC, ensuring only pure and potent material reaches you.

Optimal Packaging for Extended Shelf Life

To ensure utmost protection, Chlorzoxazone USP is sealed in HDPE drums lined with double polyethylene bags. This packaging helps maintain product quality during transport and storage, providing a shelf life of up to 36 months from manufacturing date.

Versatile Solubility and Application

Slightly soluble in water but freely soluble in alcohol and chloroform, Chlorzoxazone USP is highly adaptable for various pharmaceutical formulations. Its use as an active pharmaceutical ingredient in muscle relaxant medications highlights its importance in medical manufacturing.

FAQ's of Chlorzoxazone USP:

Q: How should Chlorzoxazone USP be stored to maintain quality?

A: Chlorzoxazone USP should be stored in a cool, dry place, protected from light, and kept in its original packaging to maintain its purity and efficacy throughout its 36-month shelf life.

Q: What is the primary usage of Chlorzoxazone USP?

A: Chlorzoxazone USP is primarily used as an active pharmaceutical ingredient in muscle relaxant medications, helping to relieve muscle spasms and discomfort.

Q: When is a Certificate of Analysis provided for this product?

A: A Certificate of Analysis is available upon request with each batch, ensuring transparency and verifying compliance with all USP and quality parameters.

Q: Where is Chlorzoxazone USP manufactured and exported from?

A: This product is manufactured and supplied from India, with availability for export, trading, and wholesale supply to pharmaceutical companies worldwide.

Q: What processes ensure the purity and safety of Chlorzoxazone USP?

A: Each batch undergoes comprehensive analysis, including IR and TLC identification, impurity testing, and microbial limit assessments as per USP standards, ensuring high purity and safety.

Q: What are the main benefits of using Chlorzoxazone USP in pharmaceutical applications?

A: Chlorzoxazone USP offers high purity, excellent solubility in common solvents, and reliable compliance with international pharmacopoeia requirements, making it ideal for consistent pharmaceutical formulations.

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