2-Bromomethyl-isonicotinic acid methyl ester hydrobromide CAS 1956366-21-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1956366-21-4
Molecular FormulaC8H8BrNO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Bromomethyl-isonicotinic acid methyl ester hydrobromide CAS 1956366-21-4 chemical structure

Description

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

2-Bromomethyl-isonicotinic acid methyl ester hydrobromide (CAS 1956366-21-4), molecular formula C8H8BrNO2HBr and molecular weight 310.97 g/mol, is a CATO reference standard with documented purity and traceability.

2-Bromomethyl-isonicotinic acid methyl ester hydrobromide (C8H8BrNO2HBr) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

As a certified reference material (CRM), 2-Bromomethyl-isonicotinic acid methyl ester hydrobromide 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.

Physical & Chemical Properties

Molecular FormulaC8H8BrNO2 HBr
Molecular Weight310.97 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
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1996
Halogen ContentBr-containing
Nitrogen Atoms1

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