Thiotepa
Overview
Thiotepa is a small molecule active pharmaceutical ingredient (ChEMBL CHEMBL671).
API suppliers (13)
Suppliers of Thiotepa evidenced by a US FDA Type II Drug Master File or an EU Certificate of Suitability (CEP). Sources: FDA DMF list, EDQM certification database.
Country recorded for 9 of 13 suppliers.
6 of 13 hold a GMP certificate on record in the EU or UK registers
- Natco PharmaIndia1 active DMF GMP on record
- Emcure Pharmaceuticals LimitedIndia1 active DMF GMP on record
- HERAEUS PRECIOUS METALS GMBH AND CO KGGermany1 active DMF
- IDT AUSTRALIA LTDAustralia1 active DMF
- INDENA SPAItaly1 active DMF GMP on record
- MSN Laboratories Private LimitedIndia1 active DMF GMP on record
- SEACROSS PHARMA USA INCChina1 active DMF
- Teva Pharmaceutical Industries Ltd.Israel GMP on record
- SUMIKA FINE CHEMICALS CO LTD
- SOGO PHARMACEUTICAL CO LTD
- ICI COLOURS AND FINE CHEMS
- Jiangsu Hengrui Medicine Co., Ltd.China
- MYLAN LABORATORIES LTD GMP on record
Patent & exclusivity (US)
Per the FDA Orange Book (18 approved US products), the latest listed US patent on Thiotepa expires 16 Aug 2041. Generic API sourcing typically opens up once these lapse.
Chemical identity
- IUPAC name
- tris(aziridin-1-yl)-sulfanylidene-lambda5-phosphane
- Canonical SMILES
- C1CN1P(=S)(N2CC2)N3CC3
- InChIKey
- FOCVUCIESVLUNU-UHFFFAOYSA-N
Do you supply Thiotepa? Get in front of buyers actively sourcing it.
We route real sourcing requests from pharma buyers to vetted, verified partners — qualified leads, not just a listing. Tell us what you make and we'll be in touch about becoming a Verified Supplier Partner.
Ready to Accelerate Your
Discovery Workflow?
Find, vet, and source drug-manufacturing partners faster — with FDA compliance screening built in. Start free for 7 days.