"CHEMXTREE STANDARDS" is a Research-Based Organization synthesizing Certified Reference Materials, and Impurities Standards at much affordable prices that will meet all the Qualitative and Quantitative standards of R&D and Analytical requirements of the Pharmaceutical Industry & are even easily accessible at your doorstep. We are catering to the various needs of pharmaceutical and biotech companies.

Chemxtree is specialized in developing & manufacturing a wide range of API/Impurities Standards, Certified Reference Materials, Pharmacopeial Reference Standards, Metabolites, Stable Isotope Labelled Compounds, etc. including various complex projects on Custom Synthesis as per USP, BP, EP, IP monographs in accordance with ICH Guidelines.

Each & every Impurity standard will be supplied with detailed COA including the complete structure elucidation and interpretation of supporting data i.e. – IR, MASS, HPLC & NMR Chromatograms. The majority of our Impurities are above 98% pure. However, any additional data like 13C-NMR, CHNS, Q-NMR, Sulphated Ash, LOD, Potency & TGA can be provided on further request. Impurities and standards which are not visible on the website can be Custom Synthesized as per your requirement.

In addition, we also provide various Analytical Testing Services (Pharmaceuticals, Cosmeceuticals, Nutraceuticals) that include Analytical Method Development, Method Validation, Isolation, and Characterization of Unknown Impurities, Stability Studies, BA/BE Studies, Dissolution Testing, Assay for various formulations for drug products. Our state-of-art government-approved analytical laboratory is ISO 9001:2015, ISO/IEC 17025:2017 certified.

We have developed our business model tactically to ensure Product Quality and Regulatory Compliance in a very cost-effective manner, ultimately allowing us to provide our products/services at competitive rates. Our team works closely with clients to provide tailored solutions to their different requirements.