Smiles
NC1=CC=CC=C1NC2=C(C#N)C=C(C)S2
Storage Condition
Store at refrigerator (2-8°C) for long term storage
IUPAC Name
2-(2-Aminoanilino)-5-methylthiophene-3-carbonitrile
References
"Rao, R, et al,: J, Sep, Sci,, 31, 107 (2008); Leyva-Perez, A, et al,: Tetrahedron, 66, 8203 (2010); "
Synonyms
2-(1,2-Phenylenediamino)-5-methylthiphene-3-carbonitrile
Application Notes
An impurity of Olanzapine; Impurity in commercial preparations of Olanzapine
Purity by HPLC
Not less than 90%
Hazard Compound
Refer MSDS for accurate information
Olanzapine Impurity is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
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Olanzapine Impurity usage and description
Olanzapine is an atypical antipsychotic drug that is used to treat schizophrenia and bipolar disorder. It works by blocking certain neurotransmitters in the brain, such as dopamine and serotonin, which are known to be involved in the development of these conditions. Olanzapine impurity, on the other hand, is a byproduct of the synthesis of olanzapine, which can be found during the manufacturing process or as a degradation product during storage.
The usage of olanzapine impurity is not intended for any medical purpose. Instead, it is used as a reference standard by analytical laboratories to test the purity of olanzapine in drug formulations. Olanzapine impurity is also used by researchers to investigate the degradation pathways of olanzapine and to develop new analytical methods for detecting and quantifying impurities in pharmaceutical products.
Chemically, olanzapine impurity is a derivative of olanzapine that has a different structure due to a chemical modification during the synthesis process. The exact chemical structure and properties of olanzapine impurity depend on the specific manufacturing process used. However, it is generally considered to be a minor impurity that does not significantly affect the pharmacological activity of olanzapine. Nonetheless, it is important to monitor the levels of impurities in pharmaceutical products to ensure their safety and efficacy.
