6,6-Bis(benzylthio)hexane-1,2,3,4,5-pentaol CAS 40733-07-1

Purity 97%+In StockPharmaceutical Standards
CAS No.40733-07-1
Molecular FormulaC20H26O5S2
Molecular Weight410.55 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6,6-Bis(benzylthio)hexane-1,2,3,4,5-pentaol CAS 40733-07-1 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 6,6-Bis(benzylthio)hexane-1,2,3,4,5-pentaol.

6,6-Bis(benzylthio)hexane-1,2,3,4,5-pentaol (CAS 40733-07-1), molecular formula C20H26O5S2 and molecular weight 410.55 g/mol, is a CATO reference standard with documented purity and traceability.

6,6-Bis(benzylthio)hexane-1,2,3,4,5-pentaol (C20H26O5S2) contains a flavonoid core, a sulfone group, a hydroxyl group, an ether linkage. The carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), 6,6-Bis(benzylthio)hexane-1,2,3,4,5-pentaol meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC20H26O5S2
Molecular Weight410.55 g/mol
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1968
Sulfur Atoms2

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Why CATO?