Ethyl 2,4-dimethylfuran-3-carboxylate CAS 6148-33-0

Purity 97%+In StockPharmaceutical Standards
CAS No.6148-33-0
Molecular FormulaC9H12O3
Molecular Weight168.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 2,4-dimethylfuran-3-carboxylate CAS 6148-33-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 168.19 g/mol gives Ethyl 2,4-dimethylfuran-3-carboxylate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

Ethyl 2,4-dimethylfuran-3-carboxylate (CAS 6148-33-0), molecular formula C9H12O3 and molecular weight 168.19 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system, Ethyl 2,4-dimethylfuran-3-carboxylate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 168.19 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

CATO manufactures Ethyl 2,4-dimethylfuran-3-carboxylate under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC9H12O3
Molecular Weight168.19 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958

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