Isopropyl Alcohol (IPA), also known as 2-propanol or isopropanol, is a colourless, volatile, flammable liquid with a characteristic alcohol odour. It is widely used as a solvent and cleaning agent in industrial, laboratory, pharmaceutical, cosmetic, and electronic applications, subject to the applicable grade and regulatory requirements.
Chemical Properties
Applications
Isopropyl Alcohol is used in industrial cleaning, surface preparation, laboratory processes, electronic component cleaning, coatings, printing, and as a solvent in selected pharmaceutical and personal-care formulations. Suitability depends on purity, water content, grade, and intended use.
Quality and Storage
Quality assessment may include identity, assay or purity, water content, acidity, non-volatile residue, and other parameters specified for the required grade. Store in a tightly closed, compatible container in a cool, well-ventilated area away from heat, sparks, flames, oxidising agents, and other incompatible materials.
Safety Information
Isopropyl Alcohol is highly flammable. Vapours may cause eye irritation, dizziness, or drowsiness. Use suitable ventilation, protective equipment, and appropriate fire-safety precautions. Consult the product-specific Safety Data Sheet (SDS) before handling.
Contact Mediocon Inc. for product availability, grade options, packaging, and verified technical documentation.
| Parameter | Specification |
|---|---|
| Appearance | Clear |
| Melting Point | Approximately −89 °C |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Isopropyl Alcohol Manufacturer in India | Mediocon Inc. (CAS 67-63-0) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Isopropyl Alcohol Manufacturer in India | Mediocon Inc. is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing before release with a Certificate of Analysis.
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