Aztreonam Impurity 12

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For Research Use Only | Not For Clinical Use

CAT	APB02892
Synonyms	2-(((Z)-(1-(2-aminothiazol-4-yl)-2-(((2R,3R)-2-methyl-4-oxoazetidin-3-yl)amino)-2-oxoethylidene)amino)oxy)-2-methylpropanoic acid
Molecular Weight	355.37
Molecular Formula	C13H17N5O5S

What is the molecular weight of Aztreonam Impurity 12?

The molecular weight of Aztreonam Impurity 12 is 355.37.

What is the molecular formula of Aztreonam Impurity 12?

The molecular formula of Aztreonam Impurity 12 is C13H17N5O5S.

What are the synonyms of Aztreonam Impurity 12?

One of the synonyms is 2-(((Z)-(1-(2-aminothiazol-4-yl)-2-(((2R,3R)-2-methyl-4-oxoazetidin-3-yl)amino)-2-oxoethylidene)amino)oxy)-2-methylpropanoic acid.

Can Aztreonam Impurity 12 be used for medicinal purposes?

No, Aztreonam Impurity 12 is an impurity and not intended for medicinal use.

What is the chemical structure of Aztreonam Impurity 12?

Aztreonam Impurity 12 has a complex chemical structure, as represented by the molecular formula C13H17N5O5S.

How is Aztreonam Impurity 12 formed?

Aztreonam Impurity 12 is likely formed as a byproduct during the synthesis of the main compound, aztreonam.

Is Aztreonam Impurity 12 commonly found in pharmaceutical products?

No, Aztreonam Impurity 12 is considered an impurity and should be present in very small quantities in pharmaceutical products.

Are there any known health risks associated with Aztreonam Impurity 12?

The health risks of Aztreonam Impurity 12 would depend on the concentration present and the specific context of exposure.

How is Aztreonam Impurity 12 typically detected in pharmaceutical samples?

Aztreonam Impurity 12 may be detected using analytical techniques such as HPLC (High-Performance Liquid Chromatography) or LC-MS (Liquid Chromatography-Mass Spectrometry).

Does the presence of Aztreonam Impurity 12 impact the effectiveness of the main pharmaceutical product?

The presence of impurities like Aztreonam Impurity 12 can potentially affect the purity, stability, and efficacy of the main pharmaceutical product, which is why limits are set for impurity levels in drug formulations.

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