4-(tert-Butyl)-2,6-diiodoaniline CAS 173282-39-8

Purity 97%+In StockPharmaceutical Standards
CAS No.173282-39-8
Molecular FormulaC10H13I2N
Molecular Weight401.03 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(tert-Butyl)-2,6-diiodoaniline CAS 173282-39-8 chemical structure

Description

CATO manufactures 4-(tert-Butyl)-2,6-diiodoaniline 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.

CATO supplies 4-(tert-Butyl)-2,6-diiodoaniline (CAS 173282-39-8), a certified reference material (molecular formula C10H13I2N, MW 401.03 g/mol) for analytical method development and quality control.

The molecular framework of 4-(tert-Butyl)-2,6-diiodoaniline (C10H13I2N) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, iodine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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.

Physical & Chemical Properties

Molecular FormulaC10H13I2N
Molecular Weight401.03 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2006
Halogen ContentI-containing
Nitrogen Atoms1

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