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Chemical Compound Review

CHEBI:75293     methyl-trioctyl-azanium

Synonyms: NSC-221149, AC1L2HVB, CTK0J6788, NSC221149, 22061-11-6, ...
 
 
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Disease relevance of methyl-trioctyl-azanium

  • Factors influencing the potential use of Aliquat 336 for the in situ extraction of carboxylic acids from cultures of Pseudomonas putida [1].
  • Influence of a co-solvent (acetone) and ultrasonication on the acute toxicity of a quaternary amine (Aliquat 336) and an organophosphorus compound (HDEHP) to Daphnia magna [2].
 

High impact information on methyl-trioctyl-azanium

  • Optimal results were obtained in the presence of 0.005 M of NaOH (pH 11.70) in the SP, 1M of NaBr in the RP, 20% of Aliquat 336 in dihexyl ether as membrane impregnation solvent, stirring rate of 500 rpm and extraction time of 60 min [3].
  • The reactive extraction of phenylalanine with Aliquat 336: buffer co-extraction equilibrium and mass transfer kinetics [4].
  • The quaternary amine Aliquat 336 (trioctyl/decylmethylammonium entity), dissolved in octan-1-ol showed no inhibition on the growth of Pseudomonas putida, at least with respect to molecular toxicity [1].
  • Water numbers were determined for the TOMAC system, with values of approximately 10, and as a function of pH and ionic strength for CTAB for each of the mutant enzymes [5].
  • Experiments were carried out at different initial concentrations of Cu(II) (1.57-5 mol/m3), solution pH (3.0-8.0), HCHO concentrations (0-3 vol.%), Aliquat 336 concentrations (80-400 mol/m3), and temperatures (15-35 degrees C) [6].
 

Associations of methyl-trioctyl-azanium with other chemical compounds

  • The kinetics of epoxidation, including the characteristics of the catalyst and the effect of the amount of cocatalyst, agitation speed, quaternary ammonium salts, amount of Aliquat 336, amount of hydrogen peroxide, amount of chloroform, pH value, organic solvents, and temperature on the conversion of 1,7-octadiene were investigated in detail [7].
  • Protection by 2-methoxyethoxymethyl chloride (MEM-Cl) was achieved by phase transfer catalysis with Aliquat 336, subsequent removal of the protecting group was completed with Amberlyst 15 [8].
  • During the forward extraction process, it was revealed that a high value of solubilization of protein in Aliquat 336 reversed micelles could be achieved when four out of the six alkanes (cyclohexane, n-hexane, isooctane, n-octane) were used as the solvent for Aliquat 336 [9].
 

Analytical, diagnostic and therapeutic context of methyl-trioctyl-azanium

References

  1. Factors influencing the potential use of Aliquat 336 for the in situ extraction of carboxylic acids from cultures of Pseudomonas putida. Jaquet, A., Quan, L., Marison, I.W., von Stockar, U. J. Biotechnol. (1999) [Pubmed]
  2. Influence of a co-solvent (acetone) and ultrasonication on the acute toxicity of a quaternary amine (Aliquat 336) and an organophosphorus compound (HDEHP) to Daphnia magna. Berglind, R., Dave, G. Bulletin of environmental contamination and toxicology. (1981) [Pubmed]
  3. Extraction and preconcentration of salbutamol and terbutaline from aqueous samples using hollow fiber supported liquid membrane containing anionic carrier. Yamini, Y., Reimann, C.T., Vatanara, A., Jönsson, J.A. Journal of chromatography. A. (2006) [Pubmed]
  4. The reactive extraction of phenylalanine with Aliquat 336: buffer co-extraction equilibrium and mass transfer kinetics. Scarpello, J.T., Stuckey, D.C. Biotechnol. Bioeng. (2000) [Pubmed]
  5. Extraction of charged fusion proteins in reversed micelles: comparison between different surfactant systems. Forney, C.E., Glatz, C.E. Biotechnol. Prog. (1995) [Pubmed]
  6. Effect of formaldehyde on Cu(II) removal from synthetic complexed solutions by solvent extraction. Lin, S.H., Kao, H.C., Su, H.N., Juang, R.S. Journal of hazardous materials. (2005) [Pubmed]
  7. Ultrasound assisted phase-transfer catalytic epoxidation of 1,7-octadiene - a kinetic study. Wang, M.L., Rajendran, V. Ultrasonics sonochemistry (2007) [Pubmed]
  8. Facile protection of phenols and hydroxypyridines: key components of natural products--a new pathway to orellanine. Michelot, D., Meyer, M. Nat. Prod. Res. (2003) [Pubmed]
  9. Separation of alpha-amylase by reversed micellar extraction. Effect of solvent type and cosolvent concentration on the transfer process. Chang, Q.L., Chen, J.Y. Appl. Biochem. Biotechnol. (1997) [Pubmed]
  10. Isolation of specific tRNAs using an ionic-hydrophobic mixed-mode chromatographic matrix. Bischoff, R., McLaughlin, L.W. Anal. Biochem. (1985) [Pubmed]
 
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