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Nintedanib Impurity 6

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For Research Use Only | Not For Clinical Use
CATAPB1038972165
CAS1038972-16-5
Molecular Weight278.31
Molecular FormulaC13H18N4O3

What is the product name of the compound with CAS number 1038972-16-5?

The product name is Nintedanib Impurity 6.

What is the molecular weight of Nintedanib Impurity 6?

The molecular weight is 278.31.

What is the molecular formula of Nintedanib Impurity 6?

The molecular formula is C13H18N4O3.

What is the chemical structure of Nintedanib Impurity 6 based on its molecular formula?

The chemical structure is composed of 13 carbon atoms, 18 hydrogen atoms, 4 nitrogen atoms, and 3 oxygen atoms.

How is Nintedanib Impurity 6 classified based on its molecular composition?

Nintedanib Impurity 6 is classified as an organic compound based on its molecular composition.

What is the significance of identifying impurities such as Nintedanib Impurity 6 in pharmaceutical products?

Identifying impurities such as Nintedanib Impurity 6 in pharmaceutical products is crucial for ensuring the purity, quality, and safety of the final drug formulation.

How can Nintedanib Impurity 6 be detected and quantified in pharmaceutical samples?

Nintedanib Impurity 6 can be detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry.

How does the presence of Nintedanib Impurity 6 impact the overall efficacy and safety of the pharmaceutical product?

The presence of Nintedanib Impurity 6 may impact the efficacy and safety of the pharmaceutical product by potentially altering its pharmacological properties or causing potential adverse effects.

Are there regulatory guidelines in place regarding the acceptable levels of impurities such as Nintedanib Impurity 6 in pharmaceutical products?

Yes, regulatory agencies such as the FDA and EMA have established guidelines on the acceptable levels of impurities, including Nintedanib Impurity 6, in pharmaceutical products.

What steps can be taken to minimize the presence of impurities like Nintedanib Impurity 6 during the manufacturing process of pharmaceutical products?

Steps to minimize the presence of impurities like Nintedanib Impurity 6 may include employing stringent quality control measures, implementing good manufacturing practices, and conducting thorough analytical testing throughout the production process.

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