(E)-6-(4-Methoxyphenyl)hex-5-enoic acid CAS 81077-29-4

Purity 97%+In StockPharmaceutical Standards
CAS No.81077-29-4
Molecular FormulaC13H16O3
Molecular Weight220.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-6-(4-Methoxyphenyl)hex-5-enoic acid CAS 81077-29-4 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 (E)-6-(4-Methoxyphenyl)hex-5-enoic acid.

(E)-6-(4-Methoxyphenyl)hex-5-enoic acid (CAS 81077-29-4) is a high-purity analytical reference standard with the molecular formula C13H16O3 and a molecular weight of 220.26 g/mol.

Structurally, (E)-6-(4-Methoxyphenyl)hex-5-enoic acid (C13H16O3) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 220.26 g/mol, it falls into the medium-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), (E)-6-(4-Methoxyphenyl)hex-5-enoic acid 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 FormulaC13H16O3
Molecular Weight220.26 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1980

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