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Tazobactam Acid Impurity 3

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For Research Use Only | Not For Clinical Use
CATAPB2570356748
CAS2570356-74-8
Molecular Weight328.34
Molecular FormulaC12H16N4O5S

What is the product name of CAS 2570356-74-8?

The product name is Tazobactam Acid Impurity 3.

What is the molecular weight of Tazobactam Acid Impurity 3?

The molecular weight is 328.34.

What is the molecular formula of Tazobactam Acid Impurity 3?

The molecular formula is C12H16N4O5S.

What is the CAS number for Tazobactam Acid Impurity 3?

The CAS number is 2570356-74-8.

What is the structure of Tazobactam Acid Impurity 3 based on its molecular formula?

The structure consists of 12 carbon atoms, 16 hydrogen atoms, 4 nitrogen atoms, 5 oxygen atoms, and 1 sulfur atom.

What is the significance of Tazobactam Acid Impurity 3 in pharmaceutical applications?

Tazobactam Acid Impurity 3 is an impurity that may be present in pharmaceutical formulations of tazobactam, indicating the presence of potential contaminants or degradation products.

How is Tazobactam Acid Impurity 3 typically detected in pharmaceutical samples?

Tazobactam Acid Impurity 3 can be detected using analytical techniques such as HPLC (High-Performance Liquid Chromatography) or LC-MS (Liquid Chromatography-Mass Spectrometry).

Is Tazobactam Acid Impurity 3 considered harmful in pharmaceutical formulations?

The presence of impurities, including Tazobactam Acid Impurity 3, in pharmaceuticals is generally undesirable as it may affect the efficacy, stability, or safety of the drug product.

Are there regulatory guidelines regarding the acceptable levels of Tazobactam Acid Impurity 3 in pharmaceutical products?

Regulatory authorities such as the FDA (Food and Drug Administration) provide guidelines on the maximum allowable levels of impurities, including Tazobactam Acid Impurity 3, in pharmaceutical products.

How can pharmaceutical manufacturers reduce the presence of Tazobactam Acid Impurity 3 in their products?

Manufacturers can implement rigorous quality control measures, purification processes, and storage conditions to minimize the formation and presence of impurities like Tazobactam Acid Impurity 3 in pharmaceutical formulations.

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