PARACETAMOL DC 96%

Paracetamol DC 96% is a direct compressible, high-purity acetaminophen used as a widely trusted analgesic and antipyretic agent. Its DC 96% grade is optimized for direct compression tableting, providing excellent flowability, uniformity, and compressibility, which ensures consistent tablet quality without additional granulation.

At Bluepill Express, we manufacture and export pharmaceutical-grade Paracetamol DC 96% API that meets IP, BP, USP, and EP pharmacopeial standards. Produced under WHO-GMP, ISO, and cGMP-certified facilities, our API ensures high purity, stable crystalline form, and consistent particle size, suitable for tablets, caplets, and combination formulations.

Each batch undergoes stringent quality testing, including HPLC, IR spectroscopy, and microbial analysis, ensuring reliable performance for global pharmaceutical manufacturers.

Pharmacological Information:

• Therapeutic Class: Analgesic / Antipyretic
• Pharmacological Category: Non-Opioid Analgesic
• CAS Number: 103-90-2
• Molecular Formula: C8H9NO2
• Molecular Weight: 151.16 g/mol
• Appearance: White crystalline powder
• Solubility: Slightly soluble in water, freely soluble in alcohol
• Melting Point: 169°C – 171°C
• Storage: Store in a cool, dry place below 25°C, protected from light

Mode of Action:

Paracetamol DC 96% inhibits central prostaglandin synthesis, reducing pain and fever. Unlike NSAIDs, it has minimal anti-inflammatory activity and is gentle on the gastrointestinal tract, making it safe for routine pain and fever management.

Applications and Uses:

• Pain Relief (Analgesic) – Headache, muscle pain, toothache, arthritis
• Fever Reduction (Antipyretic) – Effective for adults and children
• Combination Formulations – Often combined with caffeine, codeine, or NSAIDs
• Direct Compression Tablets – DC 96% ensures superior flow and compressibility
• Pharmaceutical Formulations – Tablets, caplets, and fixed-dose combinations

Technical Specifications:

• Assay (Purity): ≥ 96% (Direct Compressible Grade)
• Identification: IR spectrum matches reference standard
• Loss on Drying: ≤ 0.5%
• Residue on Ignition: ≤ 0.1%
• Heavy Metals: ≤ 10 ppm
• Particle Size: Optimized for direct compression tableting
• Related Substances: ≤ 0.2% (individual impurity)
• Microbial Limits: Complies with pharmacopeial standards

Manufacturing & Quality Assurance – Bluepill Express:

• Produced under WHO-GMP, ISO 9001:2015, and cGMP-certified facilities
• Direct compressible high-purity API for tablet production
• COA, MSDS, and TDS provided with each batch
• HPLC-tested for purity, stability, and particle consistency
• Pharmacopeial compliance: IP / BP / USP / EP

Packaging & Export Details:

• Available Packs: 1 kg, 5 kg, 10 kg, 25 kg HDPE drums with inner liner
• Shelf Life: 36 months from manufacturing date
• Labeling: Export-compliant with batch number and origin
• Export Markets: Africa, Asia, Europe, Middle East, Latin America
• Documentation Provided:
  • Certificate of Analysis (COA)
  • Material Safety Data Sheet (MSDS)
  • Technical Data Sheet (TDS)
  • Stability Data (on request)
  • Non-GMO & Allergen-Free Declarations