Description

Efferalgan is a high-purity active pharmaceutical ingredient (API) primarily known as paracetamol (acetaminophen). This compound is a cornerstone in the global pharmaceutical industry, valued for its effective analgesic and antipyretic properties. It is essential for manufacturers producing a wide range of over-the-counter and prescription medications, including tablets, capsules, and effervescent formulations. Our supply of Efferalgan CAS NO 77097-85-9 is characterized by stringent quality control to meet the exacting standards of pharmaceutical production.

Application

• Pharmaceutical API: Primary ingredient in analgesic and antipyretic drug formulations.
• Tablet & Capsule Manufacturing: Used in compressed tablets, caplets, and hard/soft gelatin capsules.
• Effervescent Preparations: Key component in fast-dissolving effervescent tablets and powders.
• Pediatric Formulations: Incorporated into syrups, suspensions, and oral solutions.
• Combination Drugs: Used in fixed-dose combinations with other APIs like caffeine or opioids.
• Contract Manufacturing: Supplied to pharmaceutical companies for generic and branded drug production.

Basic Information

Product Name	Efferalgan
CAS No.	77097-85-9
Molecular Formula	C8H9NO2
Molecular Weight	151.16 g/mol
Synonyms	Paracetamol; Acetaminophen; APAP; 4'-Hydroxyacetanilide; N-Acetyl-p-aminophenol; p-Acetamidophenol; N-(4-Hydroxyphenyl)acetamide; PCM
EINECS	200-002-2

Quality Control

Our Efferalgan is manufactured and tested to meet or exceed major pharmacopoeial standards, including USP, EP, and BP. Every batch undergoes rigorous analytical testing for identity, purity, and impurity profiles. A comprehensive Certificate of Analysis (COA) is provided with each shipment, detailing results for assay, related substances, residual solvents, and heavy metals to ensure full traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Keep away from heat, moisture, and incompatible materials.

Specification

Item	Specification
Appearance	White or almost white, crystalline powder
Identification (IR)	Conforms to standard
Identification (HPLC)	Retention time corresponds to reference
Assay (HPLC)	98.0% - 102.0% (on dried basis)
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Individual impurity ≤ 0.1%; Total impurities ≤ 0.5%
Heavy Metals	≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.