Nintedanib Impurity 19

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For Research Use Only | Not For Clinical Use

CAT	APB1160293253
CAS	1160293-25-3
Molecular Weight	267.67
Molecular Formula	C12H10ClNO4

What is the product name of the compound with CAS number 1160293-25-3?

The product name is Nintedanib Impurity 19.

What is the molecular weight of Nintedanib Impurity 19?

The molecular weight is 267.67.

What is the molecular formula of Nintedanib Impurity 19?

The molecular formula is C12H10ClNO4.

What is the chemical structure of Nintedanib Impurity 19 based on its molecular formula?

The chemical structure includes 12 carbon atoms, 10 hydrogen atoms, 1 chlorine atom, 1 nitrogen atom, and 4 oxygen atoms.

How does Nintedanib Impurity 19 compare to the main compound Nintedanib in terms of molecular structure?

Nintedanib Impurity 19 is a structural analog or impurity of Nintedanib, containing a different substituent or modification.

What is the significance of identifying impurities like Nintedanib Impurity 19 in pharmaceutical products?

Identifying impurities is important for quality control and safety in pharmaceutical products, as impurities can affect efficacy and potentially cause harm.

Are there specific methods for detecting and quantifying Nintedanib Impurity 19 in pharmaceutical formulations?

Yes, there are analytical methods such as HPLC or mass spectrometry that can be used to detect and quantify impurities like Nintedanib Impurity 19.

How might the presence of Nintedanib Impurity 19 impact the stability or shelf life of a pharmaceutical product?

Impurities like Nintedanib Impurity 19 can contribute to degradation of the active ingredient, leading to decreased stability and potentially reducing the shelf life of the product.

Is Nintedanib Impurity 19 considered harmful or toxic to humans?

Whether an impurity like Nintedanib Impurity 19 is harmful or toxic would depend on its specific properties and concentration, which would need to be evaluated through safety testing.

Are there regulatory limits or guidelines for acceptable levels of impurities like Nintedanib Impurity 19 in pharmaceutical products?

Regulatory agencies such as the FDA or EMA may have established limits or guidelines for impurities in pharmaceutical products, including Nintedanib Impurity 19, to ensure safety and quality standards are met.

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