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Etoricoxib API Powder

Price 9500.0 INR/ Kilograms

Get a Price/Quote

MOQ : 50 Kilograms

Etoricoxib API Powder Specification

Shelf Life
3 years

Smell
Odorless

Color
White to off-white

HS Code
29420090

Molecular Weight
358.84 g/mol

Molecular Formula
C18H15ClN2O2S

Particle Size
Micronized

Melting Point
137-143C

Heavy Metal (%)
0.001%

Structural Formula
C18H15ClN2O2S (See image for structure)

Loss on Drying
0.5%

Storage
Store in a cool, dry place in tightly closed container

Poisonous
Non-poisonous under prescribed use

Solubility
Slightly soluble in water, freely soluble in methanol, ethanol, and acetone

Medicine Name
Etoricoxib API Powder

Chemical Name
Etoricoxib

CAS No
202409-33-4

Type
Active Pharmaceutical Ingredient (API)

Grade
Pharmaceutical Grade

Usage
Anti-inflammatory, Analgesic

Purity(%)
>99%

Appearance
White to off-white powder

Physical Form
Powder

USP/EP/BP Compliance
Complies

Packing
Packed in HDPE drums with double polythene bags

Related Substances
0.1% by HPLC

Hazard Class
Non-hazardous

Stability
Stable under recommended storage conditions

Identification
IR, HPLC, and UV Spectroscopy conforming to standard

Dosage Form
Intended for formulation use only

Microbial Limits
Total aerobic microbial count <100cfu/g, total yeast and mold count <10cfu/g

Residue on Ignition
0.1%

Bacterial Endotoxins
<0.25 IU/mg

Etoricoxib API Powder Trade Information

Minimum Order Quantity
50 Kilograms

Supply Ability
100 Kilograms Per Day

Delivery Time
7 Days

Sample Available
No

Sample Policy
Contact us for information regarding our sample policy

About Etoricoxib API Powder

Grade Standard	Analytical Grade
Packaging Size	10kg
Packaging Type	Drum
CAS Number	202409-33-4
Purity	98%
Usage/Application	Etoricoxib is used for pain relief. It relieves pain and inflammation in conditions like rheumatoid
Minimum Order Quantity	10

ETORICOXIB

Etoricoxib is used for pain relief. It relieves pain and inflammation in conditions like rheumatoid arthritis, ankylosing spondylitis, and osteoarthritis.

Etoricoxib is a non-steroidal anti-inflammatory drug (NSAID) called COX-2 inhibitors. It works by blocking the release of certain chemical messengers that are responsible for pain and inflammation (redness and swelling).

MOLECULAR STRUCTURE:

Molecular formula:iC18H15CIN2O2S
Molecular weight:i358.84 g/mol
CAS Number:i202409-33-4
Application:iRheumatoid Arthritis

IUPAC Name:
5-Chloro-6'-methyl-3-[4-(methylsulfonyl)phenyl]-2,3'-bipyridine

Chemical Name:
5-chloro-2-(6-methylpyridin-3-yl)-3-(4-methylsulfonylphenyl)pyridine

Pharmaceutical Grade Purity

Etoricoxib API Powder offers exceptional purity levels of over 99%, ensuring consistent and reliable results for pharmaceutical formulations. Rigorous testing through IR, HPLC, and UV spectroscopy validates its quality, while compliance with USP/EP/BP standards supports its use in regulated markets. Its stability and safety profile make it a preferred choice for anti-inflammatory and analgesic medicine production.

Safe and Compliant Manufacturing

Manufactured under strict quality controls, Etoricoxib API Powder meets stringent microbial and endotoxin limits: less than 100 cfu/g for total aerobic microbes and under 0.25 IU/mg for endotoxins. The product is categorized as non-hazardous and non-poisonous under prescribed uses, making it safe for formulation and manufacturing environments.

Flexible Packaging and Long Shelf Life

To protect its integrity and maintain stability, Etoricoxib API Powder is packed in HDPE drums lined with double polythene bags. This ensures effective moisture control and prevents contamination during storage or transport. The powder remains stable for up to three years when stored under recommended conditions, supporting efficient inventory management for suppliers and manufacturers.

FAQ's of Etoricoxib API Powder:

Q: How is the quality of Etoricoxib API Powder verified?

A: The quality of Etoricoxib API Powder is verified through IR, HPLC, and UV spectroscopy. These techniques conform to the standard specifications, ensuring identity, purity (>99%), and compliance with limits for related substances, residue on ignition, and heavy metals. The product also meets USP/EP/BP pharmaceutical quality standards.

Q: What is the recommended process for using Etoricoxib API Powder in formulations?

A: Etoricoxib API Powder is intended solely for pharmaceutical formulation use. It should be handled in a controlled, GMP-compliant environment, accurately weighed according to formulation requirements, and incorporated using standard blending or mixing procedures. Always refer to regulatory guidelines and consult formulary experts during product development.

Q: Where should Etoricoxib API Powder be stored for optimal stability?

A: To maintain its stability and quality, Etoricoxib API Powder should be stored in a cool, dry place inside tightly closed HDPE containers with double polythene bags. Following the recommended storage conditions helps ensure the powder remains effective for up to three years.

Q: What are the key benefits of using Etoricoxib API Powder in pharmaceutical manufacturing?

A: Etoricoxib API Powder provides high purity, excellent stability, and strict microbial and heavy metal limits, contributing to safe, effective, and reliable medicinal products. Its pharmaceutical grade and compliance with international standards make it ideal for the production of anti-inflammatory and analgesic formulations.

Q: When does Etoricoxib API Powder expire, and how is its shelf life determined?

A: The powder has a shelf life of three years from the date of manufacture, as determined by stability studies conducted under recommended storage conditions. Expiry dates should always be observed to ensure product efficacy and safety.

Q: How can exporters, importers, or manufacturers obtain Etoricoxib API Powder from India?

A: Etoricoxib API Powder can be sourced directly from certified exporters, importers, manufacturers, and suppliers in India. Ensure the supplier provides product documentation including certificates of analysis, regulatory compliance statements, and quality assurance details.

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