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Ravtansine (DM4) API Suppliers & Bulk Manufacturers

Available Forms: API (drug substance)

Available Strengths: Supplied to an in-house or pharmacopoeial specification

Reference Brands: Elahere

Category: Active Pharmaceutical Ingredient

Ravtansine (DM4) is a maytansinoid cytotoxic used as the payload in antibody-drug conjugates. It is sourced by ADC developers, conjugation CDMOs and oncology R&D teams.

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Product Description:

Ravtansine, widely known as DM4, is a thiol-bearing maytansinoid that binds to tubulin and stops cancer cells dividing; it is too toxic to give on its own, so it is linked to antibodies that carry it to tumour cells. The approved conjugate that uses the DM4 payload, attached through a sulfo-SPDB disulfide linker (named soravtansine in that product), is indicated for folate receptor alpha-positive, platinum-resistant epithelial ovarian, fallopian tube or primary peritoneal cancer after one to three prior systemic treatments (reference brand: Elahere).

Specification at a glance

Traded formFree thiol maytansinoid, N2'-deacetyl-N2'-(4-mercapto-4-methyl-1-oxopentyl)maytansine, made semi-synthetically from fermentation-derived ansamitocin P-3; sold as the payload or as a linker-payload
CAS number796073-69-3
Molecular formulaC38H54ClN3O10S
Molecular weight780.4 g/mol
PharmacopoeiaNo pharmacopoeia monograph found; supplied to an in-house specification.

Regulatory files and timing

The FDA list of Drug Master Files (third quarter 2026) shows 0 active Type II API DMFs for this molecule. Few filings usually means few qualified sources, so early contact with suppliers pays off. For Europe, ask whether the supplier holds a CEP or an EU ASMF and, for imports into the EU, a written confirmation.

Generic or biosimilar entry. United States: No confirmed date. European Union: No confirmed date.

Handling and quality points

DM4 is extremely potent and must be handled in isolators with occupational exposure limits in the nanogram per cubic metre range, dedicated equipment and validated deactivation. The free thiol oxidises readily to the disulfide dimer, so it is typically stored cold, under inert gas and protected from light. Watch the epimer at the N-methyl-L-alanine side chain and other maytansinoid-related impurities, as they carry through into the conjugate.

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Brand names are trademarks of their respective owners and identify the reference medicine only. Information is general and was checked in October 2026; confirm specifications and filings with the supplier before purchase.

Ravtansine (DM4) API — third party manufacturing & bulk supply

Ravtansine (DM4) API is available through PharmaTradz for wholesale and bulk supply as well as on a third party (contract) manufacturing basis. Buyers sourcing this product generally take one of three routes:

Wholesale / bulk supply Stock or scheduled supply from an existing manufacturer. The fastest route where the product is already registered in your market.
Third party manufacturing Manufactured to your specification and packed under your own brand and label — suits distributors and brand owners building a portfolio in their market.
Dossier licensing Where a CTD, EU-CTD or ACTD dossier exists it can often be licensed for filing in your name, compressing market entry from years to months.

Indicative minimum order quantity

Ravtansine (DM4) API is supplied as API (drug substance) — a dosage form priced by order value, so the indicative MOQ is a minimum order value of USD 5,000 per product. Actual MOQ is confirmed by the allocated manufacturer against your pack presentation and destination market. See full supply terms for dossier formats, market availability and shelf life.

Manufacturers of Ravtansine (DM4) API listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding.

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Frequently Asked Questions

ADC developers usually ask for a GMP certificate or GMP statement for the payload step, a US DMF letter of access where one exists, a CoA with chiral and related-substance data, and stability data under the proposed storage. Because the starting material comes from fermentation, a TSE/BSE and origin statement is often requested. Containment and exposure data are needed before transfer to a conjugation site.

The cytotoxic is the same DM4 maytansinoid, but the approved product attaches it through a sulfonated SPDB linker, which is why its name ends in soravtansine. Many ravtansine conjugates in development used the non-sulfonated SPDB linker instead. Be clear whether you need free DM4 thiol or a preformed linker-payload, as the documents and specifications differ.

Yes. We help ADC developers, conjugation CDMOs and R&D teams reach GMP-compliant DM4 makers with proven high-containment capability. PharmaTradz reviews the documents first, and your project details stay confidential until both sides agree to share them.

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