Ezetimibe Impurities

Ezetimibe Impurities EP & USP Related Compounds

Synthink Research Chemicals is a manufacturer and supplier of Ezetimibe Impurities which are required for pharmaceutical companies to study quality, stability and biological safety of pharmaceutical products as well as HPLC method validation.

All Ezetimibe impurities / related compounds are provided with certificate of analysis (CoA) along with the comprehensive characterization data like 1H-NMR, IR, MASS, HPLC Purity etc. On request, we also provide additional data like 13C-NMR, 13C-DEPT, CHN, TGA, Potency etc (with extra charge/fees). SynThink provides various Ezetimibe pharmacopeial and non-pharmacopeial Impurities including – Degradation Impurities, Process Impurities, Potential Impurities, KSM impurities, API impurities etc.

Ezetimibe is a drug that lowers plasma cholesterol levels (decreases cholesterol absorption in the small intestine). Ezetimibe can be used alone (as Zetia or Ezetrol), when other cholesterol-lowering medications are not tolerated, or together with statins (e.g., ezetimibe/simvastatin, marketed as Vytorin or Inegy) when statins alone do not control cholesterol.

Please find list of Ezetimibe Impurities offered by SynThink :


Custom Synthesis of Ezetimibe Impurities

In cases when required Ezetimibe impurities are not available anywhere, needs to be custom synthesised. In such cases clients need to send the details of the required product to SynThink.

While doing impurity profiling or any analytical study of a API, factors like potency, retention time (RT), relative retention time (RRT), response factor (RF), relative response factor (RRF) are very important. So, during synthesis / manufacturing process we keep these important factors in mind and produce and supply the highest possible quality material accordingly.

Isolation and purification service are also provided as per clients’ request.

Price and quality of Ezetimibe Impurities

Quality of the material is highest priority at Synthink. So, we synthesise / manufacture and supply as pure as possible material to our clients. We always try to provide highest possible quality material to our clients. About price. we always try to give Ezetimibe impurities at reasonable price. We can also offer discounts, it depends on particular enquiry and size of order. Please feel free to request discount from us.

Availability, stock and delivery/lead time of the impurities

We are completely aware that impurities in pharma product is always a matter of worry within different departments of a pharmaceutical company. At SynThink we are committed to synthesize and characterize required Pharmacopial and non-pharmacopial Reference Standards, API Impurities as well as other working standards in a timely manner. Please feel free to request a quote from us.

Characterisation and data integrity

At SynThink, we are aware that Characterisation and data integrity of the impurities is highly important factors to our clients / FDA. We have placed strict internal standard operating procedures. So, our quality control (QA) and quality assurance department check / analyse all data of every impurity batch very carefully as per strict internal standard operating procedures. By doing critical analysis at every stage Synthink is able to provide accurate characterisation and data of every impurity batch. We can also share the electronic copy of CoA and data by email before delivering the material to the client to get confirmation from end user so client won’t get any surprise.

Moreover, on request we can provide characterization or structural elucidation reports of along with impurities

Support: If you need any support or information please contact us or check our support page (https://synthinkchemicals.com/support/)

Literature / References / Methods / Citations:

 

Keywords Ezetimibe Impurity, Ezetimibe Related Compound, Ezetimibe Reference Standard, Ezetimibe EP Impurity, Ezetimibe USP Impurity, Ezetimibe Pharmaceutical Standard, Analytical standard of Ezetimibe, Ezetimibe Degradation Impurity, Ezetimibe Process Impurity, Ezetimibe Potential Impurity, Ezetimibe Unknown Impurity, Spiking study, Ezetimibe API Impurities, HPLC method validation of Ezetimibe, Analytical method development of Ezetimibe, impurity profiling of Ezetimibe, potency of Ezetimibe impurity, retention time (RT) of Ezetimibe impurity, relative retention time (RRT), response factor (RF), relative response factor (RRF) of Ezetimibe impurity, price of Ezetimibe impurity, manufacturer of Ezetimibe impurity, supplier of Ezetimibe impurity, cost of Ezetimibe impurity