(8-Phenylnaphthalen-1-yl)boronic acid CAS 181135-36-4

Purity 97%+In StockPharmaceutical Standards
CAS No.181135-36-4
Molecular FormulaC16H13BO2
Molecular Weight248.08 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(8-Phenylnaphthalen-1-yl)boronic acid CAS 181135-36-4 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 (8-Phenylnaphthalen-1-yl)boronic acid.

(8-Phenylnaphthalen-1-yl)boronic acid (CAS 181135-36-4), molecular formula C16H13BO2 and molecular weight 248.08 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C16H13BO2, (8-Phenylnaphthalen-1-yl)boronic acid contains a carboxylic acid group, a hydroxyl group, an ether linkage, a polycyclic aromatic system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 248.08 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC16H13BO2
Molecular Weight248.08 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2008

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Why CATO?