5H-Tribenzo[a,f,k]trindene, 10,15-dihydro-2,7,12-triiodo-5,5,10,10,15,15-hexamethyl- CAS 597554-77-3

Purity 97%+In StockPharmaceutical Standards
CAS No.597554-77-3
Molecular FormulaC33H27I3
Molecular Weight804.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5H-Tribenzo[a,f,k]trindene, 10,15-dihydro-2,7,12-triiodo-5,5,10,10,15,15-hexamethyl- CAS 597554-77-3 chemical structure

Description

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.

5H-Tribenzo[a,f,k]trindene, 10,15-dihydro-2,7,12-triiodo-5,5,10,10,15,15-hexamethyl- (CAS 597554-77-3) is a high-purity analytical reference standard with the molecular formula C33H27I3 and a molecular weight of 804.28 g/mol.

5H-Tribenzo[a,f,k]trindene, 10,15-dihydro-2,7,12-triiodo-5,5,10,10,15,15-hexamethyl- (C33H27I3) contains iodine substitution, a polycyclic aromatic system. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; 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).

CATO manufactures 5H-Tribenzo[a,f,k]trindene, 10,15-dihydro-2,7,12-triiodo-5,5,10,10,15,15-hexamethyl- under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC33H27I3
Molecular Weight804.28 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)19.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1984
Halogen ContentI-containing

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