Eosin-5-maleimide CAS 150322-02-4

Purity 97%+In StockPharmaceutical Standards
CAS No.150322-02-4
Molecular FormulaC24H27Br4NO7
Molecular Weight761.09 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Eosin-5-maleimide CAS 150322-02-4 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 761.09 g/mol gives Eosin-5-maleimide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

Eosin-5-maleimide (CAS 150322-02-4) is a high-purity analytical reference standard with the molecular formula C24H27Br4NO7 and a molecular weight of 761.09 g/mol.

Eosin-5-maleimide (C24H27Br4NO7) contains a flavonoid core, 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. 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.

As a certified reference material (CRM), Eosin-5-maleimide 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 FormulaC24H27Br4NO7
Molecular Weight761.09 g/mol
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1999
Halogen ContentBr-containing
Nitrogen Atoms1

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