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Paliperidone Impurity 10

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For Research Use Only | Not For Clinical Use
CATAPB1008796233
CAS1008796-23-3
Molecular Weight206.24
Molecular FormulaC11H14N2O2

What is the product name of CAS 1008796-23-3?

The product name is Paliperidone Impurity 10.

What is the molecular weight of Paliperidone Impurity 10?

The molecular weight is 206.24.

What is the molecular formula of Paliperidone Impurity 10?

The molecular formula is C11H14N2O2.

What is the specific role of Paliperidone Impurity 10?

Paliperidone Impurity 10 is a specific impurity related to the compound paliperidone.

How does the molecular structure of Paliperidone Impurity 10 differ from paliperidone?

The molecular structure of Paliperidone Impurity 10 is different from paliperidone, as it is an impurity of the compound.

What are the potential effects of Paliperidone Impurity 10 on the purity of paliperidone?

Paliperidone Impurity 10 may impact the purity of paliperidone and may require additional purification steps in the manufacturing process.

Are there established guidelines for the maximum allowable levels of Paliperidone Impurity 10 in paliperidone products?

It is likely that there are established guidelines for the maximum allowable levels of Paliperidone Impurity 10 in paliperidone products to ensure product quality and safety.

How is Paliperidone Impurity 10 detected and quantified in paliperidone samples?

Paliperidone Impurity 10 can be detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry.

Are there any known interactions between Paliperidone Impurity 10 and other drug substances?

There may be potential interactions between Paliperidone Impurity 10 and other drug substances if present in combination products or co-administered.

Is Paliperidone Impurity 10 monitored in pharmacovigilance efforts for paliperidone-containing medications?

Paliperidone Impurity 10 may be monitored in pharmacovigilance efforts to ensure the safety and efficacy of paliperidone-containing medications by assessing impurity levels and potential impacts on patients.

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