2-Bromo-5-ethoxy-4-(2-hydroxyethoxy)benzaldehyde CAS 832133-67-2

Purity 97%+In StockPharmaceutical Standards
CAS No.832133-67-2
Molecular FormulaC11H13BrO4
Molecular Weight289.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Bromo-5-ethoxy-4-(2-hydroxyethoxy)benzaldehyde CAS 832133-67-2 chemical structure

Description

The molecular framework of 2-Bromo-5-ethoxy-4-(2-hydroxyethoxy)benzaldehyde (C11H13BrO4) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

2-Bromo-5-ethoxy-4-(2-hydroxyethoxy)benzaldehyde (CAS 832133-67-2), molecular formula C11H13BrO4 and molecular weight 289.12 g/mol, is a CATO reference standard with documented purity and traceability.

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-Bromo-5-ethoxy-4-(2-hydroxyethoxy)benzaldehyde 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 FormulaC11H13BrO4
Molecular Weight289.12 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentBr-containing

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