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VerifiedPharmaceutical Manufacturing· Founded 2006

Chemtos

We custom-synthesize and provide Certified Analytical Reference Standards for bio-assays in Clinical Trials, Diagnostics, Toxicology, Drug screenings, etc. Reference Standards for pharmaceutical active ingredients (API), their stable isotope labeled (SIL) versions, metabolites, and impurities can be custom-synthesized or provided from stock. We are also licensed for US DEA C-I through C-V manufacturing of reference standards (not for human consumption). Solutions of DEA scheduled compounds as DEA Exempt products are available from existing stock.

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HeadquartersRound Rock, United StatesEmployees4(1 to 10)Annual revenue$1M to <$10MFounded year2006Websitechemtos.comLinkedIn profileLinkedIn

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  • 2analytical chemist

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