Mazindol API Manufacturer & Supplier in India
Mazindol is a pharmaceutical active ingredient belonging to the imidazoisoindole class. It is a centrally acting sympathomimetic compound that has historically been used as an anorectic agent. Mazindol has also been investigated in pharmaceutical research for its effects on monoamine neurotransmitter transporters.
Mazindol is chemically identified by the CAS number 22232-71-9, with the molecular formula C16H13ClN2O and molecular weight of approximately 284.74 g/mol.
Mazindol is described as a chemical substance used in pharmaceutical and research applications. MEDIOCON INC can provide Mazindol subject to applicable regulatory requirements, product availability, customer specifications and documentation.
CAS Number: 22232-71-9
Molecular Formula: C16H13ClN2O
Molecular Weight: 284.74 g/mol
Chemical Class: Imidazoisoindole derivative
Store in a tightly closed container under appropriate controlled conditions and protect from unsuitable environmental exposure. Follow the approved product specification and applicable storage requirements.
Mazindol is subject to controlled-substance regulations in certain jurisdictions. PubChem identifies Mazindol as a DEA Schedule IV controlled substance in the United States. Availability, sale, import, export and handling must therefore comply with the laws applicable to the destination and intended use.
| Parameter | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Mazindol API Manufacturer & Supplier in India | MEDIOCON INC (CAS 22232-71-9) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Mazindol API Manufacturer & Supplier 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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