1946
DOI: 10.1021/ja01209a013
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Quaternary Ammonium Salts as Germicides. II. Acetoxy and Carbethoxy Derivatives of Aliphatic Quaternary Ammonium Salts

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Cited by 21 publications
(9 citation statements)
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“…nificantly different in bactericidal activity(209).on September 8, 2020 by guest http://mmbr.asm.org/…”
mentioning
confidence: 98%
“…nificantly different in bactericidal activity(209).on September 8, 2020 by guest http://mmbr.asm.org/…”
mentioning
confidence: 98%
“…In other words, synergistic action of hydrophobic groups and hydrophilic ones of the surfactant ion makes it possess strong bactericidal activity. [35][36][37] The double-alky chains of gemini surfactant molecule can simultaneously interact with the cell lipid layer at the same time, enhancing the effectiveness of the sterilization, so bacteriostatic capability of G n Cl 2 are stronger than the corresponding single-chain surfactant. [38][39][40] Judging from Table 4, G 12 Cl 2 , G 14 Cl 2 , G 16 Cl 2 are all antibacterial to Escherchia, Staphylococcus aureus, and Pseudomonas aeruginosa, and the sterilization ability increases as the chain length at the same concentration.…”
Section: Bacteriostatic Capabilitymentioning
confidence: 99%
“…Le tensioactif utilisé est le bromure de benzyldodécyldiméthylammonium (BBDDA) CH 3 (CH^ (CH 3 ) 2 NCH 2 C 6 H 5 Br. Il a été synthétisé selon la méthode utilisée par (SHELTON et al, 1948).…”
Section: Matériau Utiliséunclassified