Dimethyl 2-(aminomethyl)benzylphosphonate oxalate CAS 1383133-20-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1383133-20-7
Molecular FormulaC10H16NO3P
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Dimethyl 2-(aminomethyl)benzylphosphonate oxalate CAS 1383133-20-7 chemical structure

Description

Dimethyl 2-(aminomethyl)benzylphosphonate oxalate (C10H16NO3PC2H2O4) contains a nitrogen-containing heterocyclic scaffold, an amide group, a phosphate ester group, a hydroxyl group, an ether linkage. It is notably hygroscopic, 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.

CATO supplies Dimethyl 2-(aminomethyl)benzylphosphonate oxalate (CAS 1383133-20-7), a certified reference material (molecular formula C10H16NO3PC2H2O4, MW 319.25 g/mol) for analytical method development and quality control.

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

As a certified reference material (CRM), Dimethyl 2-(aminomethyl)benzylphosphonate oxalate 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 FormulaC10H16NO3P C2H2O4
Molecular Weight319.25 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, 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; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms1

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