Active Pharmaceutical Ingredient

Satraplatin

Also known as: JM-216; Bis-acetatoamminedichlorocyclohexylamine platinum

CAS: 18559-94-9 Antineoplastic / Platinum Complex IP / BP / EP / USP GMP Certified Aurangabad, Maharashtra, India
Satraplatin API — Mediocon Inc, Aurangabad Maharashtra India
Satraplatin — Pharmaceutical Grade API | Mediocon Inc, Aurangabad, Maharashtra, India

Product Overview

CAS No: 18559-94-9  |  MF: C₈H₁₇Cl₂N₂O₄Pt  |  MW: 500.27 g/mol

Satraplatin is an orally bioavailable platinum(IV) complex and the first oral platinum-based anticancer agent to advance to Phase III clinical trials. Mediocon Inc supplies pharmaceutical-grade Satraplatin conforming to IP / BP / EP / USP specifications from our GMP-certified facility in Aurangabad, Maharashtra, India.

Satraplatin forms platinum-DNA adducts that inhibit DNA replication and transcription in rapidly dividing cancer cells. Its oral bioavailability offers significant practical advantages over intravenous platinum agents.

Key Features

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

Applications

  • Prostate cancer chemotherapy
  • Oral platinum-based oncology
  • Cisplatin-resistant cancer treatment
  • Urological oncology R&D

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 NameSatraplatin
Also Known AsJM-216; Bis-acetatoamminedichlorocyclohexylamine platinum
CAS Number18559-94-9
Molecular FormulaC₈H₁₇Cl₂N₂O₄Pt
Molecular Weight500.27 g/mol
CategoryAntineoplastic / Platinum Complex
AppearanceYellow crystalline powder
SolubilitySparingly soluble in water; soluble in DMSO
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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