Open Ring Aztreonam Impurity

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For Research Use Only | Not For Clinical Use

CAT	APB02889
Synonyms	(Z)-2-(2-(2-aminothiazol-4-yl)-2-(((2-carboxypropan-2-yl)oxy)imino)acetamido)-3-(sulfoamino)butanoic acid
Molecular Weight	453.45
Molecular Formula	C13H19N5O9S2

What is the product name of the Open Ring Aztreonam Impurity?

The product name is Open Ring Aztreonam Impurity.

What are the synonyms for the Open Ring Aztreonam Impurity?

One of the synonyms is (Z)-2-(2-(2-aminothiazol-4-yl)-2-(((2-carboxypropan-2-yl)oxy)imino)acetamido)-3-(sulfoamino)butanoic acid.

What is the molecular weight of the Open Ring Aztreonam Impurity?

The molecular weight is 453.45.

What is the molecular formula of the Open Ring Aztreonam Impurity?

The molecular formula is C13H19N5O9S2.

What is the structure of the Open Ring Aztreonam Impurity?

The Open Ring Aztreonam Impurity has a complex chemical structure composed of thiazole, carboxypropan, and sulfoamino groups.

What are the potential impurities that could be present in the Open Ring Aztreonam Impurity?

Possible impurities could include related substances, degradation products, or reaction by-products.

How is the purity of the Open Ring Aztreonam Impurity typically determined?

Purity is often determined using analytical techniques such as HPLC or GC.

What is the significance of identifying and quantifying impurities in pharmaceuticals?

Identifying and quantifying impurities is crucial for ensuring the safety, efficacy, and quality of pharmaceutical products.

How might impurities impact the efficacy of a drug product?

Impurities could potentially affect the pharmacological activity of the drug, leading to unpredictable or adverse effects on patients.

What steps can be taken to minimize impurities during the synthesis and manufacturing of pharmaceutical products?

Process optimization, purification techniques, and strict quality control measures can help minimize impurities in pharmaceutical products.

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