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Perospirone Impurity 7

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For Research Use Only | Not For Clinical Use
CATAPB1993362096
CAS1993362-09-6
Molecular Weight225.29
Molecular FormulaC12H19NO3

What is the product name of CAS 1993362-09-6?

The product name is Perospirone Impurity 7.

What is the molecular weight of Perospirone Impurity 7?

The molecular weight of Perospirone Impurity 7 is 225.29.

What is the molecular formula of Perospirone Impurity 7?

The molecular formula of Perospirone Impurity 7 is C12H19NO3.

What is the chemical structure of Perospirone Impurity 7?

The chemical structure of Perospirone Impurity 7 is composed of carbon, hydrogen, nitrogen, and oxygen atoms arranged in a specific configuration.

Why is it important to identify and classify impurities in pharmaceutical products?

It is important to identify and classify impurities in pharmaceutical products because impurities can affect the safety, efficacy, and stability of the drug.

How is Perospirone Impurity 7 classified in terms of its chemical composition?

Perospirone Impurity 7 is classified based on its molecular formula, which indicates the types and numbers of atoms present in the molecule.

What are the potential sources of impurities in pharmaceutical products?

Impurities in pharmaceutical products can come from raw materials, synthesis processes, degradation reactions, or environmental factors.

How can impurities affect the quality of a pharmaceutical product?

Impurities can affect the potency, stability, bioavailability, and safety of a pharmaceutical product, leading to potential health risks for patients.

How is Perospirone Impurity 7 detected and quantified in a pharmaceutical sample?

Perospirone Impurity 7 can be detected and quantified using analytical techniques such as HPLC, GC-MS, NMR spectroscopy, or mass spectrometry.

What are the regulatory requirements for controlling impurities in pharmaceutical products?

Regulatory authorities require pharmaceutical companies to establish and implement guidelines for identifying, monitoring, and controlling impurities in drug products to ensure patient safety and product quality.

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