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Celecoxib Api Powder
Celecoxib Api Powder

Celecoxib Api Powder

Price 3500.0 INR/ Kilograms

MOQ : 20 Kilograms

Celecoxib Api Powder Specification

  • Color
  • White to off-white
  • Molecular Weight
  • 381.37 g/mol
  • Melting Point
  • 159-162C
  • Shelf Life
  • 36 months
  • Heavy Metal (%)
  • 0.001%
  • Loss on Drying
  • 0.5%
  • Molecular Formula
  • C17H14F3N3O2S
  • Ph Level
  • 5.07.0 (1% aqueous suspension)
  • HS Code
  • 29420090
  • Poisonous
  • Non-poisonous under recommended use
  • Storage
  • Store in a cool, dry, and well-ventilated place; protect from light
  • Taste
  • Tasteless
  • Structural Formula
  • C17H14F3N3O2S (see image for structure)
  • EINECS No
  • 686-140-8
  • Boiling point
  • Not applicable (decomposes)
  • Particle Size
  • D90 10 m (micronized grade available)
  • Smell
  • Odorless
  • Solubility
  • Practically insoluble in water; slightly soluble in ethanol and methanol
  • Medicine Name
  • Celecoxib API Powder
  • Chemical Name
  • 4-[5-(4-methylphenyl)-3-(trifluoromethyl)pyrazol-1-yl]benzenesulfonamide
  • CAS No
  • 169590-42-5
  • Type
  • Active Pharmaceutical Ingredient (API)
  • Grade
  • Pharmaceutical Grade
  • Usage
  • Anti-inflammatory, Analgesic (COX-2 inhibitor for relief of pain and inflammation)
  • Purity(%)
  • 99%
  • Appearance
  • White to off-white powder
  • Physical Form
  • Powder
  • Stability
  • Stable under recommended storage conditions
  • Related Substances
  • Total impurities 0.2%
  • Identification
  • Complies to USP/Ph.Eur. standard by IR and HPLC
  • Microbial Limit
  • Total aerobic microbial count 100 CFU/g
  • Residual Solvents
  • Meets ICH Q3C guidelines
  • Specific Rotation
  • Not applicable (non-chiral molecule)
  • Packaging
  • HDPE drum with double-layer polyethylene bags, 1 kg/5 kg/10 kg/25 kg
  • Bacterial Endotoxins
  • < 0.25 EU/mg
 

Celecoxib Api Powder Trade Information

  • Minimum Order Quantity
  • 20 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 Celecoxib Api Powder

Grade
Pharma Grade
Packaging
25Kg Bag
Purity
99%
Packaging Details
1 kg to 25 kg
Celecoxib use
to treat the pain and inflammation in osteoarthritis,acute pain in adults,rheuma
Minimum Order Quantity
50 Box
Packaging Size 1 kg
Manufacturer chemland ind.
Prescription/Non prescription Non prescription
Brand freudence pharma
Form Powder
Shelf life 5 years
Country of Origin Made in India
Product DescriptionCelecoxib API is a raw material.
Celecoxib is used to treat the pain and inflammation in osteoarthritis, acute pain in adults, rheumatoid arthritis, ankylosing spondylitis, painful menstruation, and juvenile rheumatoid arthritis.
Grade - BP


High Purity and Regulatory Compliance

Celecoxib API Powder is produced to meet rigorous pharmaceutical standards, ensuring a purity of at least 99% and compliance with both USP and Ph.Eur. specifications. Each batch undergoes identification via IR and HPLC, and is carefully monitored for related substances, residual solvents, and microbial content. These stringent quality measures deliver a reliable and consistent API suitable for regulated pharmaceutical applications.


Exceptional Stability and Packaging

Packaged in HDPE drums with double-layer polyethylene bags, Celecoxib API Powder retains stability for 36 months when stored in a cool, dry, and well-ventilated space, protected from light. Multiple packaging options (1 kg, 5 kg, 10 kg, 25 kg) cater to a wide range of operational needs, from research to large-scale production, while maintaining protection from contamination and environmental factors.


Efficient Therapeutic Application

Celecoxib API Powder functions as a COX-2 inhibitor, making it essential in medications for pain and inflammation relief. Its high level of purity and stringent impurity thresholds ensure its efficacy and safety for end-users. This API is nearly tasteless, non-poisonous within recommended guidelines, and used globally by pharmaceutical manufacturers creating advanced pain management solutions.

FAQ's of Celecoxib Api Powder:


Q: How is the identification of Celecoxib API Powder confirmed?

A: Identification of Celecoxib API Powder is verified according to USP/Ph.Eur. standards using Infrared Spectroscopy (IR) and High-Performance Liquid Chromatography (HPLC) to ensure authenticity and quality.

Q: What are the packaging options and how does it ensure product stability?

A: Celecoxib API Powder is packaged in HDPE drums with double-layer polyethylene bags, available in 1 kg, 5 kg, 10 kg, and 25 kg sizes. This packaging preserves quality by protecting the powder from moisture, light, and contamination, contributing to its 36-month stability.

Q: When should Celecoxib API Powder be used in pharmaceutical manufacturing?

A: This API is ideal for use in the production of anti-inflammatory and analgesic medications, specifically those requiring a selective COX-2 inhibitor to manage pain and inflammation.

Q: What quality and safety standards does Celecoxib API Powder meet?

A: The product complies with USP/Ph.Eur. standards, meeting total impurity limits ( 0.2%), ICH Q3C guidelines for residual solvents, strict microbial counts ( 100 CFU/g), and low bacterial endotoxin levels (< 0.25 EU/mg) for pharmaceutical safety.

Q: Where should Celecoxib API Powder be stored to maintain its quality?

A: Store Celecoxib API Powder in a cool, dry, well-ventilated area protected from light to maintain its integrity and stability for up to 36 months.

Q: What is the process to source Celecoxib API Powder from India?

A: Manufacturers, exporters, and suppliers in India provide Celecoxib API Powder. Orders can be placed directly with certified producers who adhere to international pharmaceutical quality requirements.

Q: What are the therapeutic benefits of using Celecoxib API Powder in medicines?

A: Celecoxib API Powder offers effective pain and inflammation relief as a selective COX-2 inhibitor, with a high safety profile due to its pharmaceutical-grade purity and stringent impurity controls.

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