Emtricitabine is used in combination with other HIV medications to help control HIV infection. Emtricitabine helps to decrease the amount of HIV in your body so your immune system can work better. Emtricitabine lowers your chance of getting HIV complications (such as new infections, cancer) and improves your quality of life.
EMTRICITABINE Degradation Impurities, EMTRICITABINE Process Impurities, EMTRICITABINE Potential Impurities, EMTRICITABINE USP Related Compound, EMTRICITABINE N-Nitroso impurities, EMTRICITABINE nitrosamine impurities etc. are listed below
EMTRICITABINE impurities are required at the time to product development, ANDA filing or during production to study quality, stability, and biological safety of EMTRICITABINE related products.
Availability, stock, and delivery/lead time of the EMTRICITABINE impurities
We are completely aware that impurities in pharma product is always a matter of worry within different departments of pharmaceutical companies. So, at SynThink we are committed to synthesize and characterize required EMTRICITABINE Pharmacopeial and non-pharmacopeial Reference Standards, API Impurities as well as other EMTRICITABINE working standards in a timely manner.
We keep stock of some products. For various reasons, we can’t keep stock of all products. If the product is in our stock, we can ship / dispatch the product within 48 hrs after successful quality control check. Please feel free to request a quote / stock availability from us.
Characterisation and data integrity
Carrying critical analysis at every stage Synthink can 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 additional data and characterization or structural elucidation reports of along with impurities (extra charges might be applicable.)
Custom Synthesis / manufacturing of EMTRICITABINE Impurities
In cases when required EMTRICITABINE impurities are not available anywhere, they need to be custom synthesised. In such cases clients need to send the details of the required product to SynThink.
At Synthink, we produce / manufacture / synthesise these impurities using reliable scientific processes / techniques like organic synthesis techniques, degradation and isolation process, enrichment, and isolation by chromatography techniques etc.
While doing EMTRICITABINE impurity profiling or any analytical study of EMTRICITABINE, factors like potency, retention time (RT), relative retention time (RRT), response factor (RF), relative response factor (RRF) are very important. So, during EMTRICITABINE impurity synthesis / manufacturing process we keep these important factors in mind and produce and supply the highest possible quality material accordingly.
EMTRICITABINE impurity Isolation and purification service is also provided as per clients’ request.
Generally custom synthesis EMTRICITABINE impurity products would be shipped in the in 3-6 weeks (as per difficulty level of the product and time mentioned in quote).
Send us a custom synthesis enquiry or email us – enquiry@synthinkchemicals.com
If you need any support or information, please contact us, or check our support page (https://synthinkchemicals.com/support/)
Address
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