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Gefitinib Impurity 24

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For Research Use Only | Not For Clinical Use
CATAPB194423171
CAS194423-17-1
Molecular Weight188.23
Molecular FormulaC10H12N4

What is the product name of CAS 194423-17-1?

The product name is Gefitinib Impurity 24.

What is the molecular weight of Gefitinib Impurity 24?

The molecular weight of Gefitinib Impurity 24 is 188.23.

What is the molecular formula of Gefitinib Impurity 24?

The molecular formula of Gefitinib Impurity 24 is C10H12N4.

What is the structure of Gefitinib Impurity 24 based on its molecular formula?

The structure of Gefitinib Impurity 24 contains 10 carbon atoms, 12 hydrogen atoms, and 4 nitrogen atoms.

Why is it important to identify impurities in gefitinib products?

It is important to identify impurities in gefitinib products to ensure that the drug is safe and effective for use in patients.

How can Gefitinib Impurity 24 be detected in gefitinib samples?

Gefitinib Impurity 24 can be detected in gefitinib samples using analytical techniques such as HPLC or GC-MS.

What are the potential sources of Gefitinib Impurity 24 in Gefitinib products?

Potential sources of Gefitinib Impurity 24 in Gefitinib products include synthetic intermediates or degradation products during manufacturing.

How can the presence of Gefitinib Impurity 24 affect the quality of gefitinib products?

The presence of Gefitinib Impurity 24 can affect the purity and efficacy of gefitinib products, leading to potential health risks for patients.

What measures can be taken to control the levels of Gefitinib Impurity 24 in gefitinib products?

Manufacturers can implement strict quality control measures, such as ensuring proper storage conditions and monitoring the production process, to control the levels of Gefitinib Impurity 24 in gefitinib products.

How can the identification and quantification of impurities like Gefitinib Impurity 24 benef- It the pharmaceutical industry?

The identification and quantification of impurities like Gefitinib Impurity 24 can help ensure the safety and efficacy of pharmaceutical products, improve quality control processes, and maintain regulatory compliance in the industry.

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