Active Pharmaceutical Ingredient

Saxagliptin Hydrochloride

Also known as: Saxagliptin HCl; BMS-477118 HCl

CAS: 89365-50-4 Antidiabetic / DPP-4 Inhibitor Salt IP / BP / EP / USP GMP Certified Aurangabad, Maharashtra, India
Saxagliptin Hydrochloride API — Mediocon Inc, Aurangabad Maharashtra India
Saxagliptin Hydrochloride — Pharmaceutical Grade API | Mediocon Inc, Aurangabad, Maharashtra, India

Product Overview

CAS No: 89365-50-4  |  MF: C₁₈H₂₆ClN₃O₂  |  MW: 351.87 g/mol

Saxagliptin Hydrochloride is the hydrochloride salt of Saxagliptin offering enhanced aqueous solubility for pharmaceutical formulation. Mediocon Inc supplies pharmaceutical-grade Saxagliptin Hydrochloride conforming to IP / BP / EP / USP specifications from our GMP-certified facility in Aurangabad, Maharashtra, India.

The HCl salt form provides superior dissolution characteristics essential for immediate-release oral solid dosage forms. It retains the potent DPP-4 inhibitory activity of the parent compound saxagliptin.

Key Features

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

Applications

  • Type 2 diabetes oral tablets
  • Water-soluble DPP-4 inhibitor formulations
  • Glycaemic management products
  • Fixed-dose combination antidiabetics

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 NameSaxagliptin Hydrochloride
Also Known AsSaxagliptin HCl; BMS-477118 HCl
CAS Number89365-50-4
Molecular FormulaC₁₈H₂₆ClN₃O₂
Molecular Weight351.87 g/mol
CategoryAntidiabetic / DPP-4 Inhibitor Salt
AppearanceWhite crystalline powder
SolubilityFreely soluble in water
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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