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Paracetamol IP BP USP DC 90% third party API
Paracetamol IP BP USP DC 90% third party API

Paracetamol IP BP USP DC 90% third party API

Price 200 INR/ Kilograms

MOQ : 50 Kilograms

Paracetamol IP BP USP DC 90% third party API Specification

  • Boiling point
  • Not applicable/decomposes
  • Poisonous
  • No (within prescribed dose)
  • Taste
  • Slightly bitter
  • Shelf Life
  • 36 months
  • Structural Formula
  • C6H4(OH)NHCOCH3
  • Molecular Weight
  • 151.16 g/mol
  • EINECS No
  • 203-157-5
  • HS Code
  • 29242920
  • Particle Size
  • DC Grade, typically 90% passing through 100 mesh
  • Solubility
  • Sparingly soluble in water, freely soluble in alcohol, very slightly soluble in ether
  • Loss on Drying
  • Not more than 0.5%
  • Color
  • White
  • Molecular Formula
  • C8H9NO2
  • Smell
  • Odorless
  • Heavy Metal (%)
  • Not more than 20 ppm
  • Melting Point
  • 168C to 172C
  • Storage
  • Room Temperature
  • Ph Level
  • 5.5 - 7.0 (1% w/v solution)
  • Medicine Name
  • Paracetamol IP BP USP DC 90% Third Party API
  • Chemical Name
  • 4-acetamidophenol, Para-hydroxyacetanilide
  • CAS No
  • 103-90-2
  • Type
  • API (Active Pharmaceutical Ingredient)
  • Grade
  • Medicine Grade
  • Usage
  • Pharmaceuticals, Analgesic & Antipyretic
  • Purity(%)
  • 99%
  • Appearance
  • White or almost white, crystalline powder
  • Physical Form
  • Powder
  • Chloride Content
  • Not more than 0.014%
  • Identification
  • Complies with standard IP, BP, USP methods
  • Residual Solvents
  • Complies with ICH Q3C
  • Sulphate Content
  • Not more than 0.02%
  • Bulk Density
  • 0.50 to 0.70 g/cm3
  • Flowability
  • Good, suitable for direct compression
  • Microbial Limit
  • Total aerobic microbial count not more than 1000 cfu/g, total yeast and moulds not more than 100 cfu/g, absence of E. coli and Salmonella
  • Tapped Density
  • 0.70 to 0.90 g/cm3
 

Paracetamol IP BP USP DC 90% third party API Trade Information

  • Minimum Order Quantity
  • 50 Kilograms
  • FOB Port
  • ALL india and export
  • Payment Terms
  • Cash Advance (CA), Cash in Advance (CID)
  • Delivery Time
  • 7 Days
  • Sample Available
  • Yes
  • Sample Policy
  • Contact us for information regarding our sample policy
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • All India
 

About Paracetamol IP BP USP DC 90% third party API

Paracetamol IP/BP Indian Pharmacopoeia/British Pharmacopoeia is a widely used analgesic (pain reliever) and antipyretic (fever reducer) that acts by inhibiting prostaglandin synthesis in the central nervous system. It is highly effective for treating mild to moderate pain, including headaches, toothaches, muscle pain, and cold

Superior Direct Compression Performance

Specially formulated for direct compression, Paracetamol IP BP USP DC 90% API features excellent flowability and consistent particle size, with 90% passing through 100 mesh. This enhances tablet uniformity and manufacturing efficiency, making it a preferred choice for large scale pharmaceutical production.


Strict Quality Compliance

Adhering to notable pharmacopoeial standards (IP, BP, USP) and ICH Q3C guidelines, our API guarantees minimal residual solvents and low microbial contamination. Purity exceeds 99%, with heavy metal content not exceeding 20 ppm, ensuring a safe and effective product for pharmaceuticals.


Optimal for Analgesic and Antipyretic Applications

With robust analgesic and antipyretic properties, this API is widely used in the pharmaceutical industry for manufacturing pain relievers and fever-reducing medications. Its high potency and stability make it a cornerstone ingredient for reliable therapeutic outcomes.

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


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

A: Paracetamol IP BP USP DC 90% API is primarily utilized as an active ingredient in the production of analgesic and antipyretic tablets, especially through direct compression methods due to its excellent flowability and particle size distribution.

Q: What are the benefits of using the direct compression (DC) grade Paracetamol API?

A: Using DC grade Paracetamol offers manufacturing efficiency, consistent tablet quality, and reduced processing steps, helping ensure uniform dosage forms and streamlined production in pharmaceutical settings.

Q: When should Paracetamol IP BP USP DC 90% be stored and handled with care?

A: It should always be stored at room temperature, away from direct sunlight and moisture, and handled according to GMP guidelines to maintain stability, potency, and ensure safety throughout its 36-month shelf life.

Q: Where can Paracetamol IP BP USP DC 90% API be sourced in India?

A: This API is readily available through numerous distributors, exporters, importers, manufacturers, service providers, suppliers, traders, and wholesalers across India, catering to domestic and international pharmaceutical companies.

Q: What is the process for ensuring compliance with standard quality parameters for this API?

A: Paracetamol IP BP USP DC 90% undergoes rigorous testing to comply with IP, BP, USP standards, including checks for purity, heavy metals, chloride, sulfate, residual solvents, and microbial limits as per established specifications.

Q: How does the API benefit pharmaceutical formulations?

A: It delivers consistent therapeutic effects due to its high purity and stability, reduces production issues related to flow and compression, and ensures compliance with global pharmacopoeial standards, making it valuable in quality drug development.

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