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Baclofen Impurity 9 HCl

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For Research Use Only | Not For Clinical Use
CATAPB03930
Synonyms4-amino-3-(4-methoxyphenyl)butanoic acid hydrochloride
Molecular Weight245.7
Molecular FormulaC11H15NO3·HCl

What is the molecular weight of Baclofen Impurity 9 HCl?

The molecular weight of Baclofen Impurity 9 HCl is 245.7.

Can you provide a synonym for Baclofen Impurity 9 HCl?

A synonym for Baclofen Impurity 9 HCl is 4-amino-3-(4-methoxyphenyl)butanoic acid hydrochloride.

What is the molecular formula of Baclofen Impurity 9 HCl?

The molecular formula of Baclofen Impurity 9 HCl is C11H15NO3·HCl.

What is the chemical composition of Baclofen Impurity 9 HCl?

The chemical composition of Baclofen Impurity 9 HCl consists of carbon, hydrogen, nitrogen, oxygen, and chlorine.

Is Baclofen Impurity 9 HCl a pure substance?

No, Baclofen Impurity 9 HCl is considered an impurity in the pharmaceutical compound Baclofen.

What is the significance of identifying Baclofen Impurity 9 HCl in pharmaceutical products?

Identifying Baclofen Impurity 9 HCl is important for quality control in the manufacturing of Baclofen to ensure purity and efficacy.

How does the molecular structure of Baclofen Impurity 9 HCl differ from Baclofen?

Baclofen Impurity 9 HCl contains an additional methyl group on the phenyl ring compared to the structure of Baclofen.

Are there specific testing methods for detecting Baclofen Impurity 9 HCl in pharmaceutical samples?

Yes, there are analytical techniques such as HPLC (High Performance Liquid Chromatography) and GC-MS (Gas Chromatography-Mass Spectrometry) used for the detection of Baclofen Impurity 9 HCl.

What is the role of hydrochloride in the molecular structure of Baclofen Impurity 9 HCl?

The hydrochloride salt form of Baclofen Impurity 9 enhances its solubility in water and aids in its stability for pharmaceutical applications.

How might the presence of Baclofen Impurity 9 HCl impact the safety and effectiveness of Baclofen as a medication?

The presence of impurities like Baclofen Impurity 9 HCl can affect the potency and purity of the pharmaceutical product, potentially leading to safety concerns and diminished therapeutic effects.

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