3,6,11,14-Tetrabromodibenzo[g,p]chrysene CAS 2127391-91-5

Purity 97%+In StockPharmaceutical Standards
CAS No.2127391-91-5
Molecular FormulaC26H12Br4
Molecular Weight643.99 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,6,11,14-Tetrabromodibenzo[g,p]chrysene CAS 2127391-91-5 chemical structure

Description

Structurally, 3,6,11,14-Tetrabromodibenzo[g,p]chrysene (C26H12Br4) contains bromine substitution, a polycyclic aromatic system. The molecule exhibits a degree of unsaturation (DBE) of 19.0, corresponding to approximately 19 ring(s) or double-bond equivalent(s). With a molecular weight of 643.99 g/mol, it falls into the high-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

3,6,11,14-Tetrabromodibenzo[g,p]chrysene (CAS 2127391-91-5), molecular formula C26H12Br4 and molecular weight 643.99 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.

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.

Physical & Chemical Properties

Molecular FormulaC26H12Br4
Molecular Weight643.99 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)19.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1997
Halogen ContentBr-containing

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