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Ceftriaxone Impurity E

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For Research Use Only | Not For Clinical Use
CATAPB58909561
CAS58909-56-1
Structure
Synonyms(6R,7R)-7-amino-3-(((2-methyl-5,6-dioxo-1,2,5,6-tetrahydro-1,2,4-triazin-3-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Molecular Weight371.39
Molecular FormulaC12H13N5O5S2

What is the product name of the compound with CAS number 58909-56-1?

The product name is Ceftriaxone Impurity E.

What are the synonyms of Ceftriaxone Impurity E?

One of the synonyms is (6R,7R)-7-amino-3-(((2-methyl-5,6-dioxo-1,2,5,6-tetrahydro-1,2,4-triazin-3-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid.

What is the molecular weight of Ceftriaxone Impurity E?

The molecular weight is 371.39.

What is the molecular formula of Ceftriaxone Impurity E?

The molecular formula is C12H13N5O5S2.

What is the chemical structure of Ceftriaxone Impurity E based on its molecular formula?

The chemical structure contains a bicyclic ring system with various functional groups attached.

How many nitrogen atoms are present in the molecular formula of Ceftriaxone Impurity E?

There are five nitrogen atoms in the molecular formula.

What is the significance of the sulfur atoms in the molecular structure of Ceftriaxone Impurity E?

The sulfur atoms play a role in the thioe- Ther and thioester functional groups present in the compound.

How is Ceftriaxone Impurity E related to the antibiotic ceftriaxone?

It is an impurity of ceftriaxone, meaning it is a byproduct or related compound formed during the synthesis or storage of ceftriaxone.

What is the potential impact of Ceftriaxone Impurity E on pharmaceutical formulations containing ceftriaxone?

It may affect the purity, stability, or efficacy of the pharmaceutical product if present in significant quantities.

How can the presence of Ceftriaxone Impurity E be detected and monitored in pharmaceutical samples?

Analytical techniques like HPLC (high-performance liquid chromatography) or NMR (nuclear magnetic resonance) can be used for detection and quantification of impurities in pharmaceutical samples.

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