2-(5-Bromo-3-methylpentyl)isoindoline-1,3-dione CAS 10250-44-9

Purity 97%+In StockPharmaceutical Standards
CAS No.10250-44-9
Molecular FormulaC14H16BrNO2
Molecular Weight310.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(5-Bromo-3-methylpentyl)isoindoline-1,3-dione CAS 10250-44-9 chemical structure

Description

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

2-(5-Bromo-3-methylpentyl)isoindoline-1,3-dione (CAS 10250-44-9), molecular formula C14H16BrNO2 and molecular weight 310.19 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C14H16BrNO2, 2-(5-Bromo-3-methylpentyl)isoindoline-1,3-dione contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 310.19 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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

Physical & Chemical Properties

Molecular FormulaC14H16BrNO2
Molecular Weight310.19 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1959
Halogen ContentBr-containing
Nitrogen Atoms1

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