Excipients Standards
The excipients may be used in solid dosage forms to act as binders, diluents, lubricants, disintegrating agents, plasticizers, among others. Excipients are also used in liquid dosage forms as solvents, cosolvents, buffers, antimicrobial agents, emulsifying agents, sweetening agents, flavors, etc. Excipients used in the production of pharmaceutical finished dosage forms must fulfill GMP quality aspects. Quality specifications can be found in compendial monographs, or are set by the excipient manufacturers themselves. Reference materials for excipients are essential tools to determine identity, purity and assay figures according in order to check if the incoming excipients are fulfilling specifications and can be released into the production process.
Our portfolio of Excipients standards comes with a detailed certificate of analysis with Identity, Purity and Assay data. They are also suitable for use with non-compendial analytical methods.
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select productsSpecifically developed to support early-stage development, drug discovery, R&D, and academia, these standards are ideal for qualitative applications. Every product is tested through a consistent set of analytical techniques to ensure identity and purity, with verified chemical structure and a guaranteed HPLC purity above 90%.
Research Chemicals / Analytical Standards
With Klivon Dynamic range you can count on carefully determined ASSAY values. Best cost-benefit ratio for varied non-compendial applications in compliance with ICH, FDA and WHO guidelines. A final remark (conclusion) bellow of each spectra is added.
Characterized Reference Standards
Our premium range of High Purity Reference Standards designed to meet the most demanding pharmaceutical laboratories and highly critical research, Klivon Beyond is accompanied by a comprehensive certificate of analysis (CoA), also comes with a complete spectrum elucidation report. A final remark (conclusion) or Spectra Interpretation bellow of each spectra is added.
Full Characterized Reference Standards
Our Impurity Characterized Standards portfolio comprises more than 5,000 compounds accompanied by a comprehensive CoA which can be found in 3 product categories that include a set of different analytical techniques for determining Identity and Purity.
We have designed a range of primary API standards manufactured according to international regulations that come with the most extensive Certificate of Analysis which includes Identity checks by several techniques.
Excipients standards comes with a detailed Certificate of Analysis with Identity, Purity and Assay data. They are also suitable for use with non-compendial analytical methods.
We offer tailor-made synthesis services of up to gram-quantities of materials for a wide range of pharmaceutical customers. The customer can order a specific molecule that is only synthesized on your request on the scale, with the purity and with the specification or methods you require.
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