Abacavir Impurities & USP Related Compounds
SynThink Research Chemicals is a manufacturer and supplier of Abacavir Impurities which are required for pharmaceutical companies to study quality, stability and biological safety of pharmaceutical products as well as HPLC method validation.
All Abacavir impurities / related compounds are provided with certificate of analysis (CoA) along with the complete 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 Abacavir pharmacopeial and non-pharmacopeial Impurities including – Degradation Impurities, Process Impurities, Potential Impurities, KSM impurities, API impurities etc.
Abacavir (Antiretroviral drug) is a medication used to prevent and treat HIV/AIDS, similar to other Nucleoside Reverse Transcriptase Inhibitor (NRTIs). Abacavir is used together with other HIV medication. Abacavir was patented in 1988 and approved for use in the United States in 1998.
Please find list of Abacavir impurities offered by SynThink:
- Abacavir Impurities, Impurities
CAS No. : 136470-91-2 Mol F. : C7H6Cl2N4O2 Mol W. : 249.05 Cat No. : SA18111
- Abacavir Impurities, Impurities
CAS No. : 1246819-78-2 Mol F. : C11H10ClN5O2 Mol W. : 279.68 Cat No. : SA18115
Custom Synthesis / manufacturing of Abacavir Impurities
In cases when required Abacavir impurities are not available anywhere, they needs 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 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 is also provided as per clients’ request.
Generally custom synthesis 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 – firstname.lastname@example.org
Price and quality of Abacavir 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 Abacavir 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. So, 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.
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 in 48 hrs after successful quality control check. Please feel free to request a quote / stock availability 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:
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