2-Iodo-1,3,5-triisopropylbenzene CAS 2100-22-3

Purity 97%+In StockPharmaceutical Standards
CAS No.2100-22-3
Molecular FormulaC15H23I
Molecular Weight330.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Iodo-1,3,5-triisopropylbenzene CAS 2100-22-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 330.25 g/mol gives 2-Iodo-1,3,5-triisopropylbenzene distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 2-Iodo-1,3,5-triisopropylbenzene (CAS 2100-22-3), a certified reference material (molecular formula C15H23I, MW 330.25 g/mol) for analytical method development and quality control.

2-Iodo-1,3,5-triisopropylbenzene (C15H23I) contains iodine substitution, an aromatic ring 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

CATO manufactures 2-Iodo-1,3,5-triisopropylbenzene 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 FormulaC15H23I
Molecular Weight330.25 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Halogen ContentI-containing

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