Send Inquiry

Request To Call Back

Paracetamol IP BP USP DC 90% WHO GMP

Get a Price/Quote

MOQ : 100 Kilograms

Paracetamol IP BP USP DC 90% WHO GMP Specification

Poisonous
Non-Poisonous as per recommended dose

Loss on Drying
NMT 0.5%

EINECS No
203-157-5

Particle Size
90% through 60 mesh

Boiling point
Not Applicable (Decomposes)

Storage
Store in a cool, dry place, protected from light and moisture

Structural Formula
C8H9NO2

Taste
Slightly Bitter

Solubility
Sparingly soluble in water, freely soluble in alcohol, very slightly soluble in ether

Shelf Life
5 Years

Color
White

Molecular Formula
C8H9NO2

Molecular Weight
151.16 g/mol

Ph Level
5.5 - 7.0 (in 5% solution)

HS Code
29242920

Smell
Odorless

Heavy Metal (%)
NMT 0.001%

Melting Point
168 - 172 C

Medicine Name
Paracetamol IP BP USP DC 90%

Chemical Name
4-hydroxyacetanilide

CAS No
103-90-2

Type
Directly Compressible Grade

Grade
Pharmaceutical Grade

Usage
Analgesic, Antipyretic

Purity(%)
>=90%

Appearance
White or Almost White Crystalline Powder

Physical Form
Powder

Identification
Conforms to IP/BP/USP tests

Assay
90.0% to 101.0% (on dried basis)

Bulk Density
0.5 - 0.6 g/cm3

Microbial Limits
Total aerobic microbial count <1000 cfu/g, Total yeast and molds <100 cfu/g

Tapped Density
0.7 - 0.8 g/cm3

Residual Solvents
Complies with ICH Guidelines

Paracetamol IP BP USP DC 90% WHO GMP Trade Information

Minimum Order Quantity
100 Kilograms

Supply Ability
1000 Kilograms Per Month

Delivery Time
7 Days

About Paracetamol IP BP USP DC 90% WHO GMP

Take advantage of our latest Promotion and Get It Now - Paracetamol IP BP USP DC 90% WHO GMP is the crowning choice for pharmaceutical excellence. With a polished, white crystalline appearance, this directly compressible grade meets prestigious IP/BP/USP standards. Boasting a bulk density of 0.5-0.6 g/cm3 and tapped density of 0.7-0.8 g/cm3, its purity level is guaranteed at 90%. Enjoy robust safety with residual solvents in compliance with ICH guidelines and exceptional microbial limits. Buy Online now from a trusted supplier-your gorgeous solution for analgesic and antipyretic needs.

Comprehensive Applications of Paracetamol IP BP USP DC 90%

Paracetamol IP BP USP DC 90% WHO GMP is ideally suited for oral pharmaceutical preparations, especially in tablet and caplet manufacturing due to its directly compressible form. Frequently applied on solid dose pharmaceutical processes, it ensures uniformity in blending and tablet formation. Other applications extend to its use as an analgesic and antipyretic in medical formulations, making it an indispensable choice for hospitals, clinics, and pharmaceutical companies seeking precise and effective results.

Payment Terms, Logistics, and Export Market Excellence

For your convenience, we offer flexible payment terms to match your business needs, ensuring a seamless transaction experience. Every premium shipment is expertly packed and shipped using reliable logistics partners, guaranteeing safe and timely delivery. With prompt service, your order is typically dispatched within a few working days. Our main export markets include Asia, the Middle East, Africa, and Europe, making us a global supplier committed to excellence and consistent product availability.

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

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

A: Store Paracetamol IP BP USP DC 90% in a cool, dry place, protected from light and moisture. Proper storage under these conditions helps maintain its quality and extends its shelf life to up to 5 years.

Q: What are the primary uses and benefits of this directly compressible paracetamol?

A: The primary uses include pharmaceutical tablet and caplet manufacturing due to its excellent flow properties and direct compressibility. Its benefits are precise dosing, rapid formulation, and proven analgesic and antipyretic effects.

Q: When can I expect delivery after placing an order online?

A: Once your order is confirmed and payment is processed, the product is typically shipped within a few working days, depending on logistics and destination.

Q: Where is your main export market for Paracetamol IP BP USP DC 90%?

A: Our principal export markets are Asia, the Middle East, Africa, and Europe, serving premium pharmaceutical manufacturers and distributors globally.

Q: What process ensures the safety and quality of this product?

A: Paracetamol IP BP USP DC 90% conforms to IP/BP/USP standards, complies with WHO GMP guidelines, and meets ICH standards for residual solvents and strict microbial limits, guaranteeing high safety and consistent quality.

Q: How is Paracetamol IP BP USP DC 90% applied in pharmaceutical preparations?

A: It is predominantly used in the direct compression process for solid oral dosage forms, offering uniform particle size and blending capability critical for reliable tablet production.

Tell us about your requirement