69696-98-6 Usage
Uses
Used in Organic Synthesis:
N,N,N,N'',N'',N''-Hexabutyl-1,6-hexanediaminium dibromide is used as a phase transfer catalyst for facilitating reactions that involve the transfer of a reactant from one phase to another, thereby improving the efficiency and selectivity of the reaction.
Used in Surfactant Industry:
N,N,N,N'',N'',N''-HEXABUTYL-1,6-HEXANEDIAMINIUM DIBROMIDE) serves as a surfactant, which helps in reducing the surface tension between two liquids or between a liquid and a solid, making it useful in various applications such as detergents, emulsifiers, and wetting agents.
Used in Antimicrobial Applications:
N,N,N,N'',N'',N''-Hexabutyl-1,6-hexanediaminium dibromide is utilized as an antimicrobial agent due to the presence of bromine atoms, which contribute to its ability to inhibit the growth of microorganisms, making it suitable for use in sanitizing and disinfecting products.
Used in Pharmaceutical Industry:
This versatile compound finds applications in the pharmaceutical field, where it can be used in the development of new drugs or as an intermediate in the synthesis of existing medications.
Check Digit Verification of cas no
The CAS Registry Mumber 69696-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,9 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69696-98:
(7*6)+(6*9)+(5*6)+(4*9)+(3*6)+(2*9)+(1*8)=206
206 % 10 = 6
So 69696-98-6 is a valid CAS Registry Number.
69696-98-6Relevant academic research and scientific papers
Refining the model to design α-chymotrypsin superactivators: The role of the binding mode of quaternary ammonium salts
Gabriele, Francesco,Goracci, Laura,Germani, Raimondo,Spreti, Nicoletta
, p. 20823 - 20833 (2020/12/28)
A number of quaternary ammonium salts with bulky hydrophobic moieties are known to provoke the superactivation of α-chymotrypsin (α-CT) in aqueous solution. In particular, benzyl-substituted ammonium and dicationic ammonium-based salts have recently emerged as promising classes of compounds to induce α-CT superactivation and stabilization. Preliminary in silico modelling suggested the α-CT residue tryptophan 215 to be the major anchor point of these additives. In order to achieve a broader knowledge of the enzyme-additive interactions and to validate the modelling studies, new ammonium-based additives were designed and tested. The hydrophobic interaction resulted in being critical to improving superactivation, with [(2,3,5,6-tetramethyl-p-phenylene)dimethylene]bis[triethylammonium bromide] (bisEDuEAB) resulting as the most effective quaternary ammonium superactivating agent studied so far. Finally, a general agreement between in silico outcomes and kinetic parameters was observed, and data interpretation is discussed based on the proposed α-CT/additive binding modes. This journal is
