Paracetamol IP BP USP DC 90% pharma grade powder

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Paracetamol IP BP USP DC 90% pharma grade powder

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MOQ : 100 Kilograms

Paracetamol IP BP USP DC 90% pharma grade powder Specification

Heavy Metal (%)
0.001%

Structural Formula
C8H9NO2

Shelf Life
5 years from the date of manufacture

Particle Size
90% below 150 microns (Direct Compressible)

Taste
Slightly bitter

Solubility
Slightly soluble in water, freely soluble in alcohol and acetone

Molecular Weight
151.16 g/mol

Molecular Formula
C8H9NO2

Poisonous
Non-poisonous at prescribed dosage

Boiling point
Not applicable (decomposes)

Color
White

HS Code
29242920

Loss on Drying
0.5%

Ph Level
5.5 - 7.0 (1% solution)

Storage
Store in a cool, dry, and well-ventilated area; keep container tightly closed

EINECS No
203-157-5

Smell
Odorless

Melting Point
168C - 172C

Medicine Name
Paracetamol IP BP USP DC 90%

Chemical Name
4-acetamidophenol / acetaminophen

CAS No
103-90-2

Type
Pharmaceutical Active Ingredient

Grade
Pharma Grade (Direct Compressible 90%)

Usage
Analgesic, Antipyretic, For tablet and pharmaceutical formulations

Purity(%)
99.0% min (as per pharmacopeial standards)

Appearance
White crystalline powder

Physical Form
Powder

Bulk Density
0.40 - 0.60 g/mL

Trace Impurities
Complies with IP/BP/USP limits

Tapped Density
0.60 - 0.80 g/mL

Identification
Positive (by IR & chemical test as per pharmacopeia)

Disintegration Time
15 minutes (in direct compression tablets)

Flowability
Excellent, suitable for direct compression

Microbial Load
Less than 100 cfu/g (Total plate count)

Chloride Content
0.014%

Sulfate Content
0.02%

Packaging
25 kg fiber drum/HDPE drum double polyethylene bag liner

Paracetamol IP BP USP DC 90% pharma grade powder Trade Information

Minimum Order Quantity
100 Kilograms

Supply Ability
1000 Kilograms Per Month

Delivery Time
7 Days

Sample Available
Yes

Sample Policy
If order is confirmed we will reimburse the sample cost

Main Export Market(s)
Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa

Main Domestic Market
All India, South India, Central India, West India, North India, East India, Gujarat, Karnataka, Kerala, Lakshadweep, Mizoram, Meghalaya, Manipur, Andhra Pradesh, Bihar, Chandigarh, Daman and Diu, Goa, Jharkhand, Odisha, Punjab, Assam, Delhi, Dadra and Nagar Haveli, Andaman and Nicobar Islands, Arunachal Pradesh, Chhattisgarh, Haryana, Himachal Pradesh, Jammu and Kashmir, Madhya Pradesh, Maharashtra, Nagaland, Rajasthan, Sikkim, Tamil Nadu, Telangana, Tripura, Pondicherry

Paracetamol IP BP USP DC 90% pharma grade powder About

Order Today and take advantage of a stellar promotion on our Paracetamol IP BP USP DC 90% pharma grade powder. Featuring a spectacular purity of 99.0% min and impressive bulk and tapped density, this imposing white crystalline powder is ideal for direct compression in tablet formulation. Its excellent flowability, rapid disintegration time, and strict compliance with IP/BP/USP standards ensure consistent analytical performance. With secure, double-lined 25 kg drums, advance purchase secures prompt delivery for distributors, manufacturers, and suppliers seeking a trusted analgesic and antipyretic API.

Spectacular Applications and Essential Features

Paracetamol IP BP USP DC 90% is formulated for pharmaceutical direct compression applications, delivering stellar material features such as excellent flowability and rapid tablet disintegration. Widely utilized in commercial plant environments for both tablet production and other pharmaceutical formulations, this powder's compliant trace impurity levels and minimal microbial load ensure imposing efficacy. Its purity and direct compressibility make it the prime active ingredient for high-volume production runs and reliable, high-performance medicine manufacturing.

Sample Policy, Main Markets & Stellar Certification

Samples are handed over promptly upon request, adhering to clear proposal amounts and secure shipping standards. We proudly export to Asia, Africa, the Middle East, and Europe, ensuring timely, reliable deliveries to our global partners. Every shipment is backed by documentation certifying compliance with IP, BP, and USP pharmacopeial standards, reinforcing confidence in our impeccable quality control. Choose us for certified pharma-grade excellence in each securely packaged consignment.

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

Q: How is Paracetamol IP BP USP DC 90% primarily used in pharmaceutical manufacturing?

A: Paracetamol IP BP USP DC 90% is primarily used as an analgesic and antipyretic active ingredient in tablet and pharmaceutical formulations, suitable for direct compression thanks to its excellent flowability and purity.

Q: What are the benefits of using DC 90% (Direct Compressible) grade Paracetamol over standard grades?

A: The DC 90% grade offers imposing advantages including improved compressibility, uniform particle size, and spectacular flow characteristics, resulting in efficient tablet production and rapid disintegration.

Q: When will my bulk order be shipped after placing an advance purchase?

A: Bulk orders are typically processed and shipped swiftly after receiving your proposal amount and completing an advance purchase, ensuring timely and secure shipping to your location.

Q: Where does your Paracetamol IP BP USP DC 90% comply in terms of quality standards?

A: Our product fully complies with IP, BP, and USP pharmacopeial standards for purity, trace impurities, and microbial limits, and comes with relevant certification for each batch.

Q: What is the process for requesting a sample and what does the sample policy include?

A: To request a sample, simply contact us with your requirements. Samples are handed over based on a nominal charge and shipped securely, accompanied by quality and compliance documentation.

Q: How should Paracetamol IP BP USP DC 90% be stored to preserve its quality?

A: Store the powder in a tightly closed container in a cool, dry, and well-ventilated area to maintain its quality and extend shelf life up to 5 years from the date of manufacture.

Technical Details