Therapeutic Uses
Anti-Cancer / Oncology
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Dihydrochloride,(3S,4S)-1-benzyl-N,4-dimethylpiperidin-3-amine
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Tofacitinib Impurity G is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
We are committed to offering products of the highest quality in order to meet the needs of our customers, and have elaborate systems in
place to ensure that material specifications, their certification and all handling and storage conditions are communicated at the time of
material handover.
We have invested in the highest quality packaging materials and use international logistics partners to service our customers. While all
possible precautions have been taken to deliver the required product(s), there may be some rare situations when our product does not
meet your requirements. Should that arise, please contact us with your concerns and we will endeavour to address them on a priority
basis. If there is no other option, we will either replace your product(s) or issue a refund or account credit, whichever you prefer.
If there is an issue with one or more of our products, our policy is that it must be reported to us within 45 days of your receiving shipment.
While we will always address product issues after the 45 day return window has passed, we cannot issue a refund or account credit. As
always, we appreciate your support.
Tofacitinib Impurity G usage and description
Tofacitinib impurity G is a chemical compound used in the pharmaceutical industry as an impurity in the production of Tofacitinib, a medication used to treat rheumatoid arthritis and other autoimmune diseases. Tofacitinib impurity G is important because it can affect the purity, stability, and efficacy of the Tofacitinib product.
Chemically, Tofacitinib impurity G is a small, organic molecule with a molecular weight of 285.3 g/mol. Its chemical formula is C13H14N2O2, and it has a melting point of 136-138 °C.
The usage of Tofacitinib impurity G is strictly regulated in the pharmaceutical industry, and its concentration in the final Tofacitinib product must be limited to ensure the safety and efficacy of the medication. The impurity is typically removed during the manufacturing process through various purification techniques, such as chromatography and crystallization.
In conclusion, Tofacitinib impurity G is a crucial component in the production of Tofacitinib, and its careful regulation is important to ensure the purity and effectiveness of the medication.
