6-Oxo-6-(9-Phenanthryl)hexanoic acid CAS 898766-34-2

Purity 97%+In StockPharmaceutical Standards
CAS No.898766-34-2
Molecular FormulaC10H8F2O3
Molecular Weight214.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Oxo-6-(9-Phenanthryl)hexanoic acid CAS 898766-34-2 chemical structure

Description

CATO manufactures 6-Oxo-6-(9-Phenanthryl)hexanoic 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.

6-Oxo-6-(9-Phenanthryl)hexanoic acid (CAS 898766-34-2) is a high-purity analytical reference standard with the molecular formula C10H8F2O3 and a molecular weight of 214.17 g/mol.

Structurally, 6-Oxo-6-(9-Phenanthryl)hexanoic acid (C10H8F2O3) contains a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, 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 214.17 g/mol, it falls into the medium-molecular-weight range. 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).

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

Physical & Chemical Properties

Molecular FormulaC10H8F2O3
Molecular Weight214.17 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing

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