Neohesperidin Dihydrochalcone EP Impurity A

N° de SZ CAT:	SZ-N104002
Número CAS	23643-71-2
Mol.F.	C20H28O13
Peso Molecular	476.4
Status de Fatura	Custom Synthesis
Rel. CAS No	200933-22-8 (Hydrate salt)

Disclaimer

SynZeal product information given on this website is as per the existing understanding while publishing the details on website. The customer is responsible for assessing the accuracy of the information at the time of actual purchase.

SynZeal will update these details as per new development or finding in product specification without further noticed.

Nome Químico: 1-[4-[[2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2,6-dihydroxyphenyl]ethanone (as per EP & USP)

Sinônimo: Phloroacetophenone Neohesperidoside (EP & USP) ; Neohesperidin Dihydrochalcone USP Related Compound A

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O[C@@H]1[C@@H](O[C@H]2[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O2)[C@H](OC3=CC(O)=C(C(C)=O)C(O)=C3)O[C@H](CO)[C@H]1O

Neohesperidin Dihydrochalcone EP Impurity A is chemically 1-[4-[[2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2,6-dihydroxyphenyl]ethanone (as per EP & USP). It is also known as Phloroacetophenone Neohesperidoside (EP & USP) ; Neohesperidin Dihydrochalcone USP Related Compound A. Neohesperidin Dihydrochalcone EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Neohesperidin Dihydrochalcone EP Impurity A can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Neohesperidin .

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

Neohesperidin Dihydrochalcone EP Impurity A

Contacts

Our Locations