3-quinolinecarboxylic acid, 6-bromo-4-hydroxy- 4-hydroxy-6-bromoquinoline-3-carboxylic acid 6 - Bromo - 4 - hydroxyquinoline - 3 - carboxylic acid 6-Bromo-4-hydroxy-quinoline-3-carboxylic acid 6-bromo-4-hydroxy-3-quinolinecarboxylic acid 6-bromo-4-hydroxyquinoline-3-carboxylic acid 98948-95-9 aurora 19699 buttpark 21\09-50 otava-bb bb7110950773 CAS 98948-95-9

Purity 97%+In StockPharmaceutical Standards
CAS No.98948-95-9
Molecular FormulaC10H16BrNO3
Molecular Weight278.14 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-quinolinecarboxylic acid, 6-bromo-4-hydroxy-
4-hydroxy-6-bromoquinoline-3-carboxylic acid
6 - Bromo - 4 - hydroxyquinoline - 3 - carboxylic acid
6-Bromo-4-hydroxy-quinoline-3-carboxylic acid
6-bromo-4-hydroxy-3-quinolinecarboxylic acid
6-bromo-4-hydroxyquinoline-3-carboxylic acid
98948-95-9
aurora 19699
buttpark 21\09-50
otava-bb bb7110950773 CAS 98948-95-9 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 278.14 g/mol gives 3-quinolinecarboxylic acid, 6-bromo-4-hydroxy- 4-hydroxy-6-bromoquinoline-3-carboxylic acid 6 - Bromo - 4 - hydroxyquinoline - 3 - carboxylic acid 6-Bromo-4-hydroxy-quinoline-3-carboxylic acid 6-bromo-4-hydroxy-3-quinolinecarboxylic acid 6-bromo-4-hydroxyquinoline-3-carboxylic acid 98948-95-9 aurora 19699 buttpark 21\09-50 otava-bb bb7110950773 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

3-quinolinecarboxylic acid, 6-bromo-4-hydroxy- 4-hydroxy-6-bromoquinoline-3-carboxylic acid 6 - Bromo - 4 - hydroxyquinoline - 3 - carboxylic acid 6-Bromo-4-hydroxy-quinoline-3-carboxylic acid 6-bromo-4-hydroxy-3-quinolinecarboxylic acid 6-bromo-4-hydroxyquinoline-3-carboxylic acid 98948-95-9 aurora 19699 buttpark 21\09-50 otava-bb bb7110950773 (CAS 98948-95-9), molecular formula C10H16BrNO3 and molecular weight 278.14 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 3-quinolinecarboxylic acid, 6-bromo-4-hydroxy- 4-hydroxy-6-bromoquinoline-3-carboxylic acid 6 - Bromo - 4 - hydroxyquinoline - 3 - carboxylic acid 6-Bromo-4-hydroxy-quinoline-3-carboxylic acid 6-bromo-4-hydroxy-3-quinolinecarboxylic acid 6-bromo-4-hydroxyquinoline-3-carboxylic acid 98948-95-9 aurora 19699 buttpark 21\09-50 otava-bb bb7110950773 (C10H16BrNO3) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 3.0, corresponding to approximately 3 ring(s) or double-bond equivalent(s). With a molecular weight of 278.14 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures 3-quinolinecarboxylic acid, 6-bromo-4-hydroxy- 4-hydroxy-6-bromoquinoline-3-carboxylic acid 6 - Bromo - 4 - hydroxyquinoline - 3 - carboxylic acid 6-Bromo-4-hydroxy-quinoline-3-carboxylic acid 6-bromo-4-hydroxy-3-quinolinecarboxylic acid 6-bromo-4-hydroxyquinoline-3-carboxylic acid 98948-95-9 aurora 19699 buttpark 21\09-50 otava-bb bb7110950773 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 FormulaC10H16BrNO3
Molecular Weight278.14 g/mol
AppearanceWhite to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
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)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1985
Halogen ContentBr-containing
Nitrogen Atoms1

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