2,6-Dibromo-3-methyl-4-nitrophenol CAS 14401-03-7

Purity 97%+In StockPharmaceutical Standards
CAS No.14401-03-7
Molecular FormulaC7H5Br2NO3
Molecular Weight310.93 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,6-Dibromo-3-methyl-4-nitrophenol CAS 14401-03-7 chemical structure

Description

2,6-Dibromo-3-methyl-4-nitrophenol (CAS 14401-03-7), molecular formula C7H5Br2NO3 and molecular weight 310.93 g/mol, is a CATO reference standard with documented purity and traceability.

2,6-Dibromo-3-methyl-4-nitrophenol (C7H5Br2NO3) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring system. It is notably hygroscopic, 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 2,6-Dibromo-3-methyl-4-nitrophenol 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 FormulaC7H5Br2NO3
Molecular Weight310.93 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO, water
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961
Halogen ContentBr-containing
Nitrogen Atoms1

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