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Paracetamol IP BP USP DC 90%
Paracetamol IP BP USP DC 90%

Paracetamol IP BP USP DC 90%

MOQ : 100 Kilograms

Paracetamol IP BP USP DC 90% Specification

  • Poisonous
  • Non Poisonous as per prescribed dose
  • Taste
  • Slightly bitter
  • Structural Formula
  • C8H9NO2
  • Storage
  • Store in a cool, dry, and well-ventilated place
  • Boiling point
  • 387C (decomposes)
  • Loss on Drying
  • 0.5%
  • HS Code
  • 2924.29
  • Molecular Formula
  • C8H9NO2
  • EINECS No
  • 203-157-5
  • Solubility
  • Slightly soluble in water, freely soluble in alcohol
  • Particle Size
  • 90% pass through 100 mesh
  • Melting Point
  • 168-172C
  • Color
  • White
  • Shelf Life
  • 5 years
  • Ph Level
  • 5.5-7.0 (1% solution)
  • Molecular Weight
  • 151.16 g/mol
  • Smell
  • Odorless
  • Heavy Metal (%)
  • 0.001%
  • Medicine Name
  • Paracetamol IP BP USP DC 90%
  • Chemical Name
  • 4-Acetamidophenol / Acetaminophen
  • CAS No
  • 103-90-2
  • Type
  • Directly Compressible Grade
  • Grade
  • IP/BP/USP
  • Usage
  • Pharmaceutical tablets, antipyretic and analgesic preparations
  • Purity(%)
  • 90%
  • Appearance
  • White crystalline powder
  • Physical Form
  • Powder
  • Sulphate
  • 0.02%
  • Flowability
  • Excellent, suitable for direct compression
  • Packing
  • 25 kg HDPE drums or as required
  • Chloride
  • 0.014%
  • Bulk Density
  • 0.55-0.70 g/ml
  • Microbial Limit
  • Conforms to pharmacopeial standards
  • Identification (IR/UV)
  • Complies
  • Residual Solvents
  • Complies with regulatory limits
  • Disintegration Time
  • < 15 minutes (in tablet formulation)
  • Compressibility Index
  • 10%
  • Granule Size
  • Uniform, optimized for direct compression
 

Paracetamol IP BP USP DC 90% Trade Information

  • Minimum Order Quantity
  • 100 Kilograms
  • Supply Ability
  • 1000 Kilograms Per Month
  • Delivery Time
  • 10 Days
 

About Paracetamol IP BP USP DC 90%



Featured as a supreme solution for pharmaceutical manufacturers, Paracetamol IP BP USP DC 90% offers highlighted performance in direct compression. This lavish grade is engineered with bulk density of 0.55-0.70 g/ml and a remarkable compressibility index of 10% ensuring prime flowability and uniform tablet formation. Its personalised 25 kg HDPE drum packaging preserves a white, crystalline powder that complies with IP/BP/USP standards. With optimised granule size and a shelf life of five years, this non-poisonous, slightly bitter formulation elevates your pharmaceutical creations with safety, efficacy, and superior quality.

Versatile Application for Diverse Pharmaceutical Needs

Paracetamol IP BP USP DC 90% is highlighted for its broad surface of application in pharma manufacturing. Commonly used in antipyretic and analgesic tablets, this product is suitable for direct compression processes-saving time and ensuring uniformity. To personalise your formulations, simply blend with excipients and compress. Its supreme flowability and quick disintegration time make it ideal for large-scale tablet production, enhancing operational efficiency for manufacturers and suppliers alike.


Certified Quality with Robust Export and Supply Services

Backed by prime certifications and compliance with pharmacopoeial standards, Paracetamol IP BP USP DC 90% meets demanding export market requirements. Our optimised transport services ensure bulk delivery-25 kg HDPE drums or custom options-minimising expenditure for distributors and traders. With maximum supply ability across international FOB ports, our streamlined processes support seamless shipments for importers, exporters, and wholesalers, ensuring continuous availability and regulatory compliance for clients globally.


FAQ's of Paracetamol IP BP USP DC 90%:


Q: How can Paracetamol IP BP USP DC 90% be used in pharmaceutical formulations?

A: This product is specifically tailored for direct compression in tablet manufacturing, offering excellent flowability and compressibility, which streamlines the tablet-making process.

Q: What benefits does DC 90% grade offer over regular paracetamol powders?

A: DC 90% grade ensures uniform particle size, improved blendability with excipients, faster disintegration, and higher efficiency during direct compression, reducing overall production time.

Q: When should Paracetamol IP BP USP DC 90% be preferred for pharmaceutical applications?

A: Opt for this grade when you require fast, consistent tablet production, superior product safety, and full compliance with IP, BP, and USP pharmacopeial standards.

Q: Where is Paracetamol IP BP USP DC 90% sourced and supplied from?

A: This product is distributed, exported, and supplied by manufacturers, traders, and wholesalers based in India, with robust global export capabilities.

Q: What process ensures the quality and safety of Paracetamol IP BP USP DC 90%?

A: The powder undergoes rigorous quality checks, including tests for flowability, compressibility, heavy metals, residual solvents, microbial limits, and compliance with regulatory pharmacopeial standards.

Q: How should Paracetamol IP BP USP DC 90% be stored for optimal shelf life?

A: Store in a cool, dry, and well-ventilated environment within its original packaging to maintain stability and prolong usability for up to five years.

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