2-Chloro-1-iodoanthracene-9,10-dione CAS 10430-70-3

Purity 97%+In StockPharmaceutical Standards
CAS No.10430-70-3
Molecular FormulaC14H6ClIO2
Molecular Weight368.55 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Chloro-1-iodoanthracene-9,10-dione CAS 10430-70-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 368.55 g/mol gives 2-Chloro-1-iodoanthracene-9,10-dione distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 2-Chloro-1-iodoanthracene-9,10-dione (CAS 10430-70-3), a certified reference material (molecular formula C14H6ClIO2, MW 368.55 g/mol) for analytical method development and quality control.

The molecular framework of 2-Chloro-1-iodoanthracene-9,10-dione (C14H6ClIO2) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine/iodine substitution, a polycyclic aromatic system. 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC14H6ClIO2
Molecular Weight368.55 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1959
Halogen ContentCl/I-containing

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