3-(2-hydroxy-ethoxy)-4-methoxy-benZaldehyde CAS 57643-36-4

Purity 97%+In StockPharmaceutical Standards
CAS No.57643-36-4
Molecular FormulaC10H12O4
Molecular Weight196.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(2-hydroxy-ethoxy)-4-methoxy-benZaldehyde CAS 57643-36-4 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 3-(2-hydroxy-ethoxy)-4-methoxy-benZaldehyde.

CATO supplies 3-(2-hydroxy-ethoxy)-4-methoxy-benZaldehyde (CAS 57643-36-4), a certified reference material (molecular formula C10H12O4, MW 196.20 g/mol) for analytical method development and quality control.

The molecular framework of 3-(2-hydroxy-ethoxy)-4-methoxy-benZaldehyde (C10H12O4) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, 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).

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.

As a certified reference material (CRM), 3-(2-hydroxy-ethoxy)-4-methoxy-benZaldehyde meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC10H12O4
Molecular Weight196.20 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1973

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