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Methyldopa EP Impurity A (Hydrochloride)

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For Research Use Only | Not For Clinical Use
CATAPB01484
Synonyms(S)-2-amino-3-(4-hydroxy-3-methoxyphenyl)-2-methylpropanoic acid hydrochloride
Molecular Weight261.7
Molecular FormulaC11H15NO4·HCl

What is the molecular weight of Methyldopa EP Impurity A (Hydrochloride)?

The molecular weight of Methyldopa EP Impurity A (Hydrochloride) is 261.7.

What is the molecular formula of Methyldopa EP Impurity A (Hydrochloride)?

The molecular formula of Methyldopa EP Impurity A (Hydrochloride) is C11H15NO4·HCl.

What is the synonym of Methyldopa EP Impurity A (Hydrochloride)?

(S)-2-amino-3-(4-hydroxy-3-methoxyphenyl)-2-methylpropanoic acid hydrochloride.

How is Methyldopa EP Impurity A (Hydrochloride) chemically represented?

Methyldopa EP Impurity A (Hydrochloride) is represented chemically as C11H15NO4·HCl.

What is the chemical structure of Methyldopa EP Impurity A (Hydrochloride)?

The chemical structure of Methyldopa EP Impurity A (Hydrochloride) is a derivative of methyldopa with a hydrochloride group.

In what form is Methyldopa EP Impurity A (Hydrochloride) typically found?

Methyldopa EP Impurity A (Hydrochloride) is typically found as a crystalline white powder.

What is the significance of the hydrochloride group in Methyldopa EP Impurity A?

The hydrochloride group in Methyldopa EP Impurity A helps stabilize the molecule and improve its solubility in aqueous solutions.

What is the role of Methyldopa EP Impurity A in pharmaceutical research?

Methyldopa EP Impurity A is used as a reference standard for the identification and quantification of impurities in Methyldopa formulations.

How does the molecular weight of Methyldopa EP Impurity A compare to that of Methyldopa?

The molecular weight of Methyldopa EP Impurity A (261.7) is slightly lower than that of Methyldopa (at 211.7).

Why is Methyldopa EP Impurity A important in pharmaceutical quality control?

Methyldopa EP Impurity A serves as a marker for assessing the purity and quality of Methyldopa preparations, ensuring they meet the required standards for use in pharmaceutical products.

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