1,5-Bis(4-Allyldimethylammoniumphenyl)pentan-3-one, Dibromide

• CAT Number: R020601
• CAS Number: 402-40-4
• Molecular Formula: C27H38Br2N2O
• Molecular Weight: 566.42
• Purity: ≥95%
• Synonyms: 4,4’-(3-Oxo-1,5-pentanediyl)bis[N,N-dimethyl-N-2-propen-1-yl-benzenaminium Bromide
• Storage: -20°C
• IUPAC Name: [4-[5-[4-[dimethyl(prop-2-enyl)azaniumyl]phenyl]-3-oxopentyl]phenyl]-dimethyl-prop-2-enylazanium;dibromide
• InChI: InChI=1S/C27H38N2O.2BrH/c1-7-21-28(3,4)25-15-9-23(10-16-25)13-19-27(30)20-14-24-11-17-26(18-12-24)29(5,6)22-8-2;;/h7-12,15-18H,1-2,13-14,19-22H2,3-6H3;2*1H/q+2;;/p-2
• InChIKey: WKDURMTZOWGWTD-UHFFFAOYSA-L
• SMILES: C[N+](C)(CC=C)C1=CC=C(C=C1)CCC(=O)CCC2=CC=C(C=C2)[N+](C)(C)CC=C.[Br-].[Br-]

1,5-Bis(4-allyldimethylammoniumphenyl)pentan-3-one dibromide(CAT: R020601) is a cationic, quaternary ammonium compound featuring a symmetric bisphenyl structure linked by a ketone-containing pentane backbone. The presence of allyldimethylammonium groups at the para positions enhances its hydrophilicity and electrostatic interaction capabilities, making it valuable in molecular recognition, DNA/RNA binding, and supramolecular chemistry. Its dibromide counterions ensure solubility in aqueous media, supporting applications in biochemistry and materials science. This compound is also investigated for its antimicrobial activity, potential in drug delivery systems, and as a template in functional polymer synthesis. Its structural rigidity and amphiphilic nature offer versatility in both biological and synthetic research contexts.