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Cefathiamidine Impurity 5

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For Research Use Only | Not For Clinical Use
CATAPB04623
Synonyms(6R,7R)-7-(2-bromoacetamido)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Molecular Weight335.17
Molecular FormulaC10H11BrN2O4S

What is the molecular weight of Cefathiamidine Impurity 5?

The molecular weight of Cefathiamidine Impurity 5 is 335.17.

What is the molecular formula of Cefathiamidine Impurity 5?

The molecular formula of Cefathiamidine Impurity 5 is C10H11BrN2O4S.

What is the synonym of Cefathiamidine Impurity 5?

The synonym of Cefathiamidine Impurity 5 is (6R,7R)-7-(2-bromoacetamido)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid.

What is the chemical structure of Cefathiamidine Impurity 5?

The chemical structure of Cefathiamidine Impurity 5 is a 1-azabicyclo[4.2.0]oct-2-ene derivative with a 2-bromoacetamido side chain.

How many carbon atoms are present in the molecular formula of Cefathiamidine Impurity 5?

There are 10 carbon atoms in the molecular formula of Cefathiamidine Impurity 5.

What functional groups are present in the molecular formula of Cefathiamidine Impurity 5?

Cefathiamidine Impurity 5 contains the functional groups carboxylic acid, amide, ketone, and bromide.

What is the stereochemistry of Cefathiamidine Impurity 5?

The stereochemistry of Cefathiamidine Impurity 5 is (6R,7R), indicating the configuration of the chiral centers in the molecule.

What is the role of Cefathiamidine Impurity 5 in pharmaceutical manufacturing?

Cefathiamidine Impurity 5 is an impurity that needs to be controlled and monitored in the production of the antibiotic Cefathiamidine.

How is Cefathiamidine Impurity 5 detected and quantified in pharmaceutical products?

Cefathiamidine Impurity 5 can be detected and quantified using analytical techniques such as HPLC (High-Performance Liquid Chromatography) or LC-MS (Liquid Chromatography-Mass Spectrometry).

What precautions should be taken to prevent the presence of Cefathiamidine Impurity 5 in pharmaceutical formulations?

Strict control measures during the manufacturing process, rigorous testing of raw materials, and regular monitoring of impurity levels are essential to prevent the presence of Cefathiamidine Impurity 5 in pharmaceutical formulations.

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