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Imatinib Impurity 36

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For Research Use Only | Not For Clinical Use
CATAPB106261487
CAS106261-48-7
Structure
Molecular Weight234.3
Molecular FormulaC13H18N2O2

What is the molecular weight of Imatinib Impurity 36?

The molecular weight of Imatinib Impurity 36 is 234.3.

What is the molecular formula of Imatinib Impurity 36?

The molecular formula of Imatinib Impurity 36 is C13H18N2O2.

What is the CAS number of Imatinib Impurity 36?

The CAS number of Imatinib Impurity 36 is 106261-48-7.

How is Imatinib Impurity 36 classified based on its molecular formula?

Imatinib Impurity 36 is classified as a compound containing 13 carbon atoms, 18 hydrogen atoms, 2 nitrogen atoms, and 2 oxygen atoms.

What is the significance of identifying specific impurities like Imatinib Impurity 36 in pharmaceutical products?

Identifying specific impurities like Imatinib Impurity 36 is important for ensuring the purity, safety, and efficacy of pharmaceutical products.

How is Imatinib Impurity 36 detected and analyzed in pharmaceutical samples?

Imatinib Impurity 36 is typically detected and analyzed using analytical techniques such as chromatography and spectroscopy.

What are the potential sources of Imatinib Impurity 36 in pharmaceutical manufacturing processes?

Imatinib Impurity 36 may arise as a byproduct or impurity during the synthesis or purification of the active pharmaceutical ingredient.

How can the presence of Imatinib Impurity 36 impact the quality of pharmaceutical products?

The presence of Imatinib Impurity 36 can affect the stability, bioavailability, and overall quality of pharmaceutical products.

What measures can be taken to control or minimize the formation of Imatinib Impurity 36 during pharmaceutical production?

Stringent process controls, purification techniques, and analytical monitoring can be employed to control or minimize the formation of Imatinib Impurity 36.

In what ways can the identification and characterization of Imatinib Impurity 36 contribute to pharmaceutical research and development?

The identification and characterization of Imatinib Impurity 36 can lead to improved understanding of synthetic pathways, impurity profiles, and quality control methods in pharmaceutical research and development.

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