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Benzyldodecyldimethylammonium Chloride Dihydrate

CAS No. 147228-80-6

Benzyldodecyldimethylammonium Chloride Dihydrate( —— )

Catalog No. M27530 CAS No. 147228-80-6

Benzyldodecyldimethylammonium chloride dihydrate is a quaternary ammonium compound (QAC).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Benzyldodecyldimethylammonium Chloride Dihydrate
  • Note
    Research use only, not for human use.
  • Brief Description
    Benzyldodecyldimethylammonium chloride dihydrate is a quaternary ammonium compound (QAC).
  • Description
    Benzyldodecyldimethylammonium chloride dihydrate is a quaternary ammonium compound (QAC). Benzyldodecyldimethylammonium chloride dihydrate can be used as a biocide to target antibiotic-resistant bacteria, such as methicillin-resistant Staphylococcus aureus (MRSA), multidrug-resistant (MDR) P. aeruginosa et. al. Benzyldodecyldimethylammonium chloride dihydrate, an antimicrobial agent, bacteriostatic or bactericidal properties depending on the concentration.(In Vitro):Benzyldodecyldimethylammonium chloride dihydrate interacts strongly with cell surfaces in a concentration-dependent manner, and binds by ionic and hydrophobic interactions to microbial membrane surfaces, as manifested by phenomena such as membrane disruption and loss of membrane integrity with consequent leakage of essential intracellular constituents, which promote significant and irreversible changes in the cell structure. Benzyldodecyldimethylammonium chloride dihydrate (0-40 mg/L; 0-24 hours) inhibits P. fluorescens with a MIC of 20 mg/L. At 5 mg/L, cells have the same growth behaviour as the control. At concentrations of 10 and 15 mg/L the growth profile is different from the control, and the cells start to grow only after 8 h of adaptation. At concentrations of ≥20 mg/L, BDMDAC inhibits cell growth.(In Vivo):Benzyldodecyldimethylammonium chloride dihydrate (1-10 μM; 2 hours) results in a dose-dependent changes in the percent population of dead rat thymocyte cells.
  • In Vitro
    Benzyldodecyldimethylammonium chloride dihydrate (1-10 μM; 2 hours) results in a dose-dependent changes in the percent population of dead rat thymocyte cells.Benzyldodecyldimethylammonium chloride dihydrate (0-40 mg/L; 0-24 hours) inhibits P. fluorescens with a MIC of 20 mg/L. At 5 mg/L, cells have the same growth behaviour as the control. At concentrations of 10 and 15 mg/L the growth profile is different from the control, and the cells start to grow only after 8 h of adaptation. At concentrations of ≥20 mg/L, BDMDAC inhibits cell growth.Benzyldodecyldimethylammonium chloride dihydrate interacts strongly with cell surfaces in a concentration-dependent manner, and binds by ionic and hydrophobic interactions to microbial membrane surfaces, as manifested by phenomena such as membrane disruption and loss of membrane integrity with consequent leakage of essential intracellular constituents, which promote significant and irreversible changes in the cell structure. Cell Viability Assay Cell Line:Rat thymocyte cells Concentration:0, 5, 10, 15, 20 and 40 mg/L Incubation Time:2 hours Result:Resulted in cell death.Cell Proliferation Assay Cell Line:Bacterial P. fluorescen Concentration:0, 5, 10, 15, 20 and 40 mg/L Incubation Time:2 hours Result:Inhibited bacterial growth in a time and dose dependent manner.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    Antibacterial
  • Recptor
    SKP2 E3 ligase|Apoptosis
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    147228-80-6
  • Formula Weight
    376.02
  • Molecular Formula
    C21H42ClNO2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (265.94 mM)
  • SMILES
    O.O.[Cl-].CCCCCCCCCCCC[N+](C)(C)Cc1ccccc1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Rico-Bautista E, Zhu W, Kitada S, Small Molecule-Induced Mitochondrial Disruption Directs Prostate Cancer Inhibition via UPR Signaling. Oncotarget. 2013 Jul 14.
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