Active Pharmaceutical Ingredient

Salmeterol Xinafoate

Also known as: Salmeterol Xinafoate Salt; Serevent Diskus

CAS: 80214-83-1 Bronchodilator / Long-acting Beta-2 Agonist Salt IP / BP / EP / USP GMP Certified Aurangabad, Maharashtra, India
Salmeterol Xinafoate API — Mediocon Inc, Aurangabad Maharashtra India
Salmeterol Xinafoate — Pharmaceutical Grade API | Mediocon Inc, Aurangabad, Maharashtra, India

Product Overview

CAS No: 80214-83-1  |  MF: C₃₆H₄₅NO₇  |  MW: 603.74 g/mol

Salmeterol Xinafoate is the xinafoate salt form of Salmeterol, exhibiting improved stability and physicochemical properties suitable for dry powder inhaler formulations. Mediocon Inc supplies pharmaceutical-grade Salmeterol Xinafoate conforming to IP / BP / EP / USP specifications from our GMP-certified facility in Aurangabad, Maharashtra, India.

The xinafoate salt provides enhanced powder flow properties essential for DPI manufacturing. It is the commercially dominant salt form found in widely used respiratory products.

Key Features

  • High-purity pharmaceutical grade API
  • IP / BP / EP / USP compliant
  • Full CoA and MSDS documentation
  • GMP certified manufacturing facility

Applications

  • Dry powder inhaler formulations
  • COPD long-term treatment
  • Combination LABA/ICS products
  • Asthma maintenance therapy

Why Choose Mediocon

  • ISO 9001:2015 & GMP certified manufacturing
  • Consistent batch-to-batch quality with full CoA
  • Export-ready documentation: COO, MSDS, DMF
  • Flexible MOQ for both R&D and commercial scale
  • Dedicated QA support for regulatory filings

Product Specifications

Product NameSalmeterol Xinafoate
Also Known AsSalmeterol Xinafoate Salt; Serevent Diskus
CAS Number80214-83-1
Molecular FormulaC₃₆H₄₅NO₇
Molecular Weight603.74 g/mol
CategoryBronchodilator / Long-acting Beta-2 Agonist Salt
AppearanceWhite to off-white crystalline powder
SolubilitySlightly soluble in water; soluble in ethanol
GradeIP / BP / EP / USP

Analytical Specifications

ParameterSpecification
AssayNLT 98.0%
Loss on DryingNMT 0.5%
Heavy MetalsNMT 20 ppm
Residue on IgnitionNMT 0.1%
Microbial LimitsComplies with pharmacopoeia
IdentificationIR, HPLC Compliant
Mfg DateMAR 2025
Exp DateFEB 2030
Packing25 kg HDPE drums / as per requirement
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