2-(6-Bromohexyl)-5-nitroisoindoline-1,3-dione CAS 140715-57-7

Purity 97%+In StockPharmaceutical Standards
CAS No.140715-57-7
Molecular FormulaC14H15BrN2O4
Molecular Weight355.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(6-Bromohexyl)-5-nitroisoindoline-1,3-dione CAS 140715-57-7 chemical structure

Description

Structurally, 2-(6-Bromohexyl)-5-nitroisoindoline-1,3-dione (C14H15BrN2O4) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 8.0, corresponding to approximately 8 ring(s) or double-bond equivalent(s). With a molecular weight of 355.18 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

2-(6-Bromohexyl)-5-nitroisoindoline-1,3-dione (CAS 140715-57-7), molecular formula C14H15BrN2O4 and molecular weight 355.18 g/mol, is a CATO reference standard with documented purity and traceability.

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), 2-(6-Bromohexyl)-5-nitroisoindoline-1,3-dione 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 FormulaC14H15BrN2O4
Molecular Weight355.18 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1997
Halogen ContentBr-containing
Nitrogen Atoms2

Related Bromohexyl Standards

Recommended Standards

Why CATO?