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Paracetamol IP BP USP DC 90% pharmaceutical raw material
Paracetamol IP BP USP DC 90% pharmaceutical raw material

Paracetamol IP BP USP DC 90% pharmaceutical raw material

MOQ : 100 Kilograms

Paracetamol IP BP USP DC 90% pharmaceutical raw material Specification

  • Melting Point
  • 168-172C (pure Paracetamol)
  • HS Code
  • 29242920
  • Ph Level
  • 5.5 - 7.0 (1% solution)
  • Molecular Weight
  • 151.16 g/mol
  • Shelf Life
  • 36 months from date of manufacture if stored properly
  • Taste
  • Slightly bitter
  • Poisonous
  • Non-poisonous at recommended doses
  • Smell
  • Odorless
  • Solubility
  • Freely soluble in alcohol and acetone; slightly soluble in water; very slightly soluble in ether
  • EINECS No
  • 203-157-5
  • Structural Formula
  • C8H9NO2
  • Particle Size
  • 90% passing through 100 mesh (as per typical DC grade standards)
  • Loss on Drying
  • 0.5%
  • Heavy Metal (%)
  • Not more than 0.001%
  • Storage
  • Store in tightly closed container in a cool, dry place, protected from light
  • Molecular Formula
  • C8H9NO2
  • Color
  • White
  • Boiling point
  • Not applicable (decomposes)
  • Medicine Name
  • Paracetamol IP BP USP DC 90%
  • Chemical Name
  • 4-acetamidophenol, N-(4-Hydroxyphenyl)acetamide
  • CAS No
  • 103-90-2
  • Type
  • Pharmaceutical Raw Material, Direct Compressible Grade
  • Grade
  • IP/BP/USP/Direct Compression Grade (DC 90%)
  • Usage
  • Used as an analgesic and antipyretic in tablet formulations
  • Purity(%)
  • 90% (w/w active ingredient by Direct Compression)
  • Appearance
  • White or almost white, crystalline powder
  • Physical Form
  • Powder
  • Bulk Density
  • 0.45 - 0.65 g/ml
  • Packing
  • 25 kg fiber drum with inner liner or as required
  • Binder Content
  • Contains pharmacopoeial excipients to facilitate direct compression
  • Flowability
  • Excellent, suitable for direct tableting
  • Residual Solvents
  • Complies with ICH guidelines
  • Related Substances
  • Total impurities 0.25%
  • Identification (IR/UV)
  • Complies with standard reference
  • Tapped Density
  • 0.65 - 0.85 g/ml
  • Microbial Purity
  • Total Bacterial Count NMT 1000 CFU/g, Yeast & Molds NMT 100 CFU/g
  • Assay (on dried basis)
  • 90-92% (Direct Compressible Paracetamol)
  • Compressibility
  • High, suitable for direct compression process
  • Moisture Content
  • 0.5%
 

Paracetamol IP BP USP DC 90% pharmaceutical raw material Trade Information

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

Paracetamol IP BP USP DC 90% pharmaceutical raw material About



Experience the praiseworthy quality and spectacular performance of Paracetamol IP BP USP DC 90%. This pharmaceutical raw material is trending in the market for its affordable pricing and superb direct compressibility, making it terrific for tablet formulations. With a purity of 90-92%, excellent flowability, and high compressibility, this bulk-grade paracetamol is ideal for direct compression applications. The material complies with stringent standards, ensuring safety and reliability for distributors, exporters, and manufacturers. Reserve your stock today and benefit from a trusted, versatile analgesic and antipyretic solution.

Versatile Usage and Praiseworthy Applications

Paracetamol IP BP USP DC 90% is extensively used in the production of analgesic and antipyretic tablets, thanks to its direct compressible grade. Its high-flowability and compressibility offer seamless plant application in large-scale pharma manufacturing. Commercially, it is the preferred choice for domestic and international suppliers, traders, and distributors who require a dependable, consistent raw material for tablets across the global market.


Sample Availability and Market Policies

A sample of Paracetamol IP BP USP DC 90% is available to facilitate product evaluation or trial batches before bulk orders. Our sample policy accommodates both new and existing clients and allows for easy drop-off services. List price and special offers for domestic market buyers are available upon inquiry. The designated FOB port ensures efficient international shipping to meet your scheduling needs and streamline procurement.


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


Q: How is Paracetamol IP BP USP DC 90% commonly utilized in pharmaceutical production?

A: Paracetamol IP BP USP DC 90% is predominantly used for formulating analgesic and antipyretic tablets, leveraging its exceptional direct compressible properties for efficient, high-speed tableting in modern pharmaceutical manufacturing.

Q: What makes this paracetamol grade terrifically suited for direct compression?

A: This grade exhibits excellent flowability and high compressibility due to its optimized bulk and tapped density. It contains pharmacopoeial excipients, making it perfect for the direct compression process, thus streamlining tablet production without the need for granulation.

Q: Where can the product samples be obtained and what is the sample policy?

A: Samples are readily available for evaluation. Our sample policy covers both new and long-standing clients, and shipments can be arranged for convenient drop-off at your facility or through designated domestic markets.

Q: When should Paracetamol IP BP USP DC 90% be reserved for procurement?

A: It is advisable to reserve or place orders as soon as your production requirements are forecasted, ensuring timely availability and steady supply, given the high demand and trending status of this pharmaceutical raw material.

Q: What are the commercial benefits of using this Paracetamol raw material?

A: Commercial users benefit from its praiseworthy consistency in purity, compliance with global pharmacopeial standards, and reduced processing time, which collectively contribute to cost savings and reliable tablet manufacturing outcomes.

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