Paracetamol IP BP USP DC 90%

Get a Price/Quote

Product Details:

Color White
Poisonous Non Poisonous as per prescribed dose
Heavy Metal (%) 0.001%
Molecular Formula C8H9NO2
Boiling point 387C (decomposes)
Taste Slightly bitter
Particle Size 90% pass through 100 mesh
Click to view more
Share Your Product:

Request To Call Back Send Inquiry

Paracetamol IP BP USP DC 90% Price And Quantity

Minimum Order Quantity 100 Kilograms

Packing 25 kg HDPE drums or as required
Identification (IR/UV) Complies
Granule Size Uniform, optimized for direct compression
Chloride 0.014%
Microbial Limit Conforms to pharmacopeial standards
Sulphate 0.02%
Bulk Density 0.55-0.70 g/ml
Compressibility Index 10%
Residual Solvents Complies with regulatory limits
Flowability Excellent, suitable for direct compression
Disintegration Time < 15 minutes (in tablet formulation)

Paracetamol IP BP USP DC 90% Product Specifications

Grade IP/BP/USP
Purity(%) 90%
HS Code 2924.29
EINECS No 203-157-5
Storage Store in a cool, dry, and well-ventilated place
Shelf Life 5 years
Appearance White crystalline powder
Solubility Slightly soluble in water, freely soluble in alcohol
Melting Point 168-172C
CAS No 103-90-2
Type Directly Compressible Grade
Molecular Weight 151.16 g/mol
Poisonous Non Poisonous as per prescribed dose
Heavy Metal (%) 0.001%
Boiling point 387C (decomposes)
Molecular Formula C8H9NO2
Usage Pharmaceutical tablets, antipyretic and analgesic preparations
Color White
Loss on Drying 0.5%
Smell Odorless
Structural Formula C8H9NO2
Ph Level 5.5-7.0 (1% solution)
Taste Slightly bitter
Particle Size 90% pass through 100 mesh
Medicine Name Paracetamol IP BP USP DC 90%
Physical Form Powder
Chemical Name 4-Acetamidophenol / Acetaminophen

Packing 25 kg HDPE drums or as required
Identification (IR/UV) Complies
Granule Size Uniform, optimized for direct compression
Chloride 0.014%
Microbial Limit Conforms to pharmacopeial standards
Sulphate 0.02%
Bulk Density 0.55-0.70 g/ml
Compressibility Index 10%
Residual Solvents Complies with regulatory limits
Flowability Excellent, suitable for direct compression
Disintegration Time < 15 minutes (in tablet formulation)

Paracetamol IP BP USP DC 90% Trade Information

Supply Ability 1000 Kilograms Per Month
Delivery Time 10 Days

Product Description

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.