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Chemical product profile

HONGKUN / PRODUCT DIRECTORY

4′-Demethylepipodophyllotoxin β-D-glucoside | CAS 23363-35-1

A stereodefined lignan β-D-glucoside investigated in cellular comparisons with etoposide and teniposide, with glycosidic identity, stereochemistry and assigned content guiding research and analytical qualification.

CAS23363-35-1
Molecular formulaC27H30O13
Molecular weight562.5 g/mol

Product overview

A β-D-glucosyl unit, stereodefined lignan framework, lactone and free phenolic hydroxyl distinguish this research and analytical compound. Its identity depends on both the sugar linkage and the lignan configuration. For comparative or quantitative work, specify the complete structure and the characterization and assigned-content data needed by the method.

Chemical identity

Chemical name
4′-Demethylepipodophyllotoxin β-D-glucoside
CAS number
23363-35-1
Molecular formula
C27H30O13
Molecular weight
562.5 g/mol

Application context

The glucoside has been investigated in cell-based comparisons with etoposide and teniposide and has an etoposide-related impurity-analysis context. For research comparisons, confirm the complete glycosidic and lignan identity. Quantitative method work requires appropriate separation from comparison compounds and an assigned content that accounts for water and residual solvents where applicable.

Chemistry and synthetic role

The β-D-glucosidic linkage joins the sugar unit to a stereodefined lignan framework carrying lactone and phenolic functions. Characterization for comparison studies should identify the glycosidic configuration and the lignan stereochemistry together.

Quality review

Establish glycoside and stereochemical identity

Confirm the β-D glucoside and the specified lignan configuration, rather than relying only on the podophyllotoxin family name.

Demonstrate separation for the intended analytical use

For etoposide-related testing, demonstrate chromatographic separation of this glucoside from the comparison compounds used in the method.

Review assigned content

Distinguish area purity from mass-based content. If quantitative use is planned, agree how water and residual solvents are treated in the assigned value.

Preparing a specification

State CAS 23363-35-1, the complete β-D-glucoside identity and the intended research or analytical use. For quantitative reference work, define characterization and content-assignment requirements, including the basis for water and solvent corrections where applicable.

Packaging and storage

Agree packaging, net weight and transport arrangements for the selected grade, quantity and destination. Confirm storage and handling conditions using the current SDS for the proposed material.

Documentation

Request complete glycosidic and stereochemical identification, a COA and a chromatographic method suited to the intended comparison. For quantitative use, confirm availability of content-assignment calculations and supporting water or residual-solvent data.

Procurement questions

Is this etoposide or teniposide?

No. It is a distinct lignan glucoside that has been studied in comparison with those compounds.

Which identity features matter for comparison work?

The β-D-glucosidic linkage and the specified lignan stereochemistry, supported by characterization of the proposed material.

What is needed for quantitative method work?

An assigned content on a stated basis, appropriate chromatographic separation and relevant water or residual-solvent corrections.

Technical sources
  1. PubChem CID 159949 — structure propertiesPubChem / NCBI
  2. PubChem CID 159949 — CAS and synonymsPubChem / NCBI
  3. Etoposide impurity 1, HY-136669MedChemExpress
  4. 4′-Demethylepipodophyllotoxin-beta-D-glucoside: a new podophyllotoxin derivative with VM-26-like and VP-16-213-like activitiesOriginal research paper indexed by PubMed / NLM