3-(4-(Tert-butyl)phenyl)acrylaldehyde CAS 86604-07-1

Purity 97%+In StockPharmaceutical Standards
CAS No.86604-07-1
Molecular FormulaC13H16O
Molecular Weight188.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-(Tert-butyl)phenyl)acrylaldehyde CAS 86604-07-1 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-(4-(Tert-butyl)phenyl)acrylaldehyde.

3-(4-(Tert-butyl)phenyl)acrylaldehyde (CAS 86604-07-1) is a high-purity analytical reference standard with the molecular formula C13H16O and a molecular weight of 188.27 g/mol.

3-(4-(Tert-butyl)phenyl)acrylaldehyde (C13H16O) contains a hydroxyl group, an ether linkage, an aromatic ring system. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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-(4-(Tert-butyl)phenyl)acrylaldehyde 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 FormulaC13H16O
Molecular Weight188.27 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1981

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