Copper, (4-bromo-3-hydroxy-2-naphthoato)(5-chloro-8-quinolinolato)- CAS 14040-00-7

Purity 97%+In StockPharmaceutical Standards
CAS No.14040-00-7
Molecular FormulaC20H11BrClCuNO4
Molecular Weight508.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Copper, (4-bromo-3-hydroxy-2-naphthoato)(5-chloro-8-quinolinolato)- CAS 14040-00-7 chemical structure

Description

As a certified reference material (CRM), Copper, (4-bromo-3-hydroxy-2-naphthoato)(5-chloro-8-quinolinolato)- 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.

Copper, (4-bromo-3-hydroxy-2-naphthoato)(5-chloro-8-quinolinolato)- (CAS 14040-00-7) is a high-purity analytical reference standard with the molecular formula C20H11BrClCuNO4 and a molecular weight of 508.21 g/mol.

Copper, (4-bromo-3-hydroxy-2-naphthoato)(5-chloro-8-quinolinolato)- (C20H11BrClCuNO4) contains a salt form, a flavonoid core, an amide group, a hydroxyl group, an ether linkage, chlorine/bromine substitution. Halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC20H11BrClCuNO4
Molecular Weight508.21 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature, 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961
Halogen ContentCl/Br-containing
Nitrogen Atoms1

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