3-((1R,2R,3R)-3-Hydroxy-5-oxo-2-(3-oxooctyl)cyclopentyl)propanoic acid CAS 20675-85-8

Purity 97%+In StockPharmaceutical Standards
CAS No.20675-85-8
Molecular FormulaC16H26O5
Molecular Weight298.37 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-((1R,2R,3R)-3-Hydroxy-5-oxo-2-(3-oxooctyl)cyclopentyl)propanoic acid CAS 20675-85-8 chemical structure

Description

Based on its molecular formula C16H26O5, 3-((1R,2R,3R)-3-Hydroxy-5-oxo-2-(3-oxooctyl)cyclopentyl)propanoic acid contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 298.37 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).

3-((1R,2R,3R)-3-Hydroxy-5-oxo-2-(3-oxooctyl)cyclopentyl)propanoic acid (CAS 20675-85-8), molecular formula C16H26O5 and molecular weight 298.37 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.

CATO manufactures 3-((1R,2R,3R)-3-Hydroxy-5-oxo-2-(3-oxooctyl)cyclopentyl)propanoic acid 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 FormulaC16H26O5
Molecular Weight298.37 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at room temperature, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1962

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