Active Pharmaceutical Ingredient

Epothilone A API Manufacturer & Supplier in India

High-purity Epothilone A API — GMP Certified

CAS: 152044-53-6 IP / BP / EP / USP GMP Certified Aurangabad, Maharashtra, India
Epothilone A API Manufacturer In India — Mediocon Inc
Epothilone A API Manufacturer In India — Pharmaceutical Grade API

Product Overview

CAS No: 152044-53-6  |  MF: C26H39NO6S  |  MW: 493.66

Epothilone A is a natural macrolide compound with potent antineoplastic activity, acting as a microtubule-stabilising agent similar to taxanes. Mediocon Inc manufactures Epothilone A API to IP/BP/EP/USP standards in its GMP-certified facility in Aurangabad, Maharashtra, India.

Our Epothilone A API is supplied to oncology pharmaceutical manufacturers and research institutions with comprehensive quality documentation, supporting cancer drug development worldwide.

Key Features

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

Applications

  • Anticancer drug research
  • Microtubule-stabilising agent formulations
  • Oncology pharmaceutical development
  • Cancer cell biology research

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 NameEpothilone A
CAS Number152044-53-6
Molecular FormulaC26H39NO6S
Molecular Weight493.66
CategoryActive Pharmaceutical Ingredient
AppearanceWhite to off-white crystalline powder
GradeIP / BP / EP / USP
Batch NoPEMD/24032026
Mfg DateMAR 2026
Exp DateFEB 2031
Quantity25.00 Kg
Gross Weight26.00 Kg

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
Packing25 kg HDPE drums / as per requirement

Sourcing, Regulatory & Export Information

Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Epothilone A (CAS 152044-53-6) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Epothilone A 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 — identity (IR/HPLC), assay, related substances, residual solvents (ICH Q3C), heavy metals, and microbial limits — before release with a Certificate of Analysis.

Export Markets

  • USA — FDA-registered facility; DMF support available for ANDA/NDA filings
  • Europe — EMA-compliant documentation; CEP/EDMF support on request
  • Africa & Middle East — WHO-GMP certified; competitive pricing for emerging markets
  • Southeast Asia — established logistics network; temperature-controlled shipments
  • India domestic — schedule H/X compliance; all state licensing documentation provided

Quality & Compliance

  • ISO 9001:2015 certified quality management system
  • GMP-certified manufacturing facility, Aurangabad, Maharashtra
  • Full batch traceability from raw material to finished API
  • Stability data available (ICH Q1A guidelines) for regulatory submissions
  • Dedicated QA team for customer audits and regulatory queries

Frequently Asked Questions — Epothilone A API

What is the minimum order quantity for Epothilone A API?
Mediocon Inc supplies Epothilone A with a minimum order quantity of 1 kg (sample packs available for R&D). We accommodate both small R&D quantities and large commercial-scale orders. Contact our sales team at akshay@mediocon.com or +91 9309999757 for a tailored quote.
What pharmacopoeial grades of Epothilone A does Mediocon supply?
We supply Epothilone A conforming to IP / BP / EP / USP pharmacopoeial standards. Each batch is tested against full pharmacopoeial specifications and released with a Certificate of Analysis. Custom specifications can be accommodated for regulated markets.
What documentation is provided with Epothilone A API?
Every shipment of Epothilone A comes with: Certificate of Analysis (CoA), MSDS/SDS, Certificate of Origin (COO), and Drug Master File (DMF) support on request. We also provide GMP certification, ISO 9001:2015 compliance documentation, and full regulatory support for filings in USA (FDA), Europe (EMA), and other markets.
What is the lead time and shipping for Epothilone A bulk orders?
Standard lead time for Epothilone A is 2–4 weeks for standard orders; expedited shipments possible for urgent requirements. We ship to 40+ countries worldwide using approved pharmaceutical-grade packaging (25 kg HDPE drums / aluminium foil bags). All shipments include temperature-controlled logistics options where required by the product's storage conditions.
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