Phenol, 2-methoxy-4-(1-propen-1-yl)-, polymer with 2-methoxy-4-(2-propen-1-yl)phenol CAS 68928-73-4

Purity 97%+In StockPharmaceutical Standards
CAS No.68928-73-4
Molecular Formula2*C10H12O2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Phenol, 2-methoxy-4-(1-propen-1-yl)-, polymer with 2-methoxy-4-(2-propen-1-yl)phenol CAS 68928-73-4 chemical structure

Description

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system, Phenol, 2-methoxy-4-(1-propen-1-yl)-, polymer with 2-methoxy-4-(2-propen-1-yl)phenol is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 164.20 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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).

Phenol, 2-methoxy-4-(1-propen-1-yl)-, polymer with 2-methoxy-4-(2-propen-1-yl)phenol (CAS 68928-73-4) is a high-purity analytical reference standard with the molecular formula C10H12O2 and a molecular weight of 164.20 g/mol.

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), Phenol, 2-methoxy-4-(1-propen-1-yl)-, polymer with 2-methoxy-4-(2-propen-1-yl)phenol 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 Formula2*C10H12O2
Molecular Weight164.20 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1976

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