4-(3-Methoxyphenoxy)-3,6-dioxocyclohex-1-ene-1-carbaldehyde CAS CATO-C3D-5036

Purity 97%+In StockPharmaceutical Standards
CAS No.CATO-C3D-5036
Molecular FormulaC14H12O5
Molecular Weight260.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(3-Methoxyphenoxy)-3,6-dioxocyclohex-1-ene-1-carbaldehyde CAS CATO-C3D-5036 chemical structure

Description

The molecular framework of 4-(3-Methoxyphenoxy)-3,6-dioxocyclohex-1-ene-1-carbaldehyde (C14H12O5) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, a polycyclic aromatic system. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, 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).

4-(3-Methoxyphenoxy)-3,6-dioxocyclohex-1-ene-1-carbaldehyde (CAS CATO-C3D-5036), molecular formula C14H12O5 and molecular weight 260.24 g/mol, is a CATO reference standard with documented purity and traceability.

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), 4-(3-Methoxyphenoxy)-3,6-dioxocyclohex-1-ene-1-carbaldehyde 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 FormulaC14H12O5
Molecular Weight260.24 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present

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