51963-62-3 Usage
Uses
Used in Disinfectant and Sanitizer Products:
4-Ethoxy-N,N,N-trimethyl-4-oxo-1-butanaminium chloride is used as an active ingredient in disinfectants and sanitizers for its potent antibacterial properties. It helps to eliminate harmful microorganisms and contributes to maintaining a clean and hygienic environment.
Used in Healthcare Settings:
In healthcare facilities, 4-Ethoxy-N,N,N-trimethyl-4-oxo-1-butanaminium chloride is used as a disinfectant to reduce the risk of infections and the spread of diseases. Its ability to kill a wide range of bacteria makes it a valuable component in the fight against hospital-acquired infections.
Used in Food Industry:
4-Ethoxy-N,N,N-trimethyl-4-oxo-1-butanaminium chloride is used as a sanitizing agent in the food industry to ensure the cleanliness of surfaces and equipment. This helps to prevent contamination and maintain food safety standards.
Used in Household Cleaning Products:
4-Ethoxy-N,N,N-trimethyl-4-oxo-1-butanaminium chloride is also used in household cleaning products, such as all-purpose cleaners and surface disinfectants, to provide a powerful antibacterial action. It helps to keep homes clean and free from harmful bacteria.
Used in Water Treatment:
4-Ethoxy-N,N,N-trimethyl-4-oxo-1-butanaminium chloride can be used in water treatment processes to control the growth of bacteria and other microorganisms, ensuring the safety and quality of water supplies.
Check Digit Verification of cas no
The CAS Registry Mumber 51963-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,6 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51963-62:
(7*5)+(6*1)+(5*9)+(4*6)+(3*3)+(2*6)+(1*2)=133
133 % 10 = 3
So 51963-62-3 is a valid CAS Registry Number.
51963-62-3Relevant academic research and scientific papers
Exploiting neighboring-group interactions for the self-selection of a catalytic unit
Gasparini, Giulio,Prins, Leonard J.,Scrimin, Paolo
supporting information; experimental part, p. 2475 - 2479 (2009/02/06)
(Figure Presented) A good neighbor is better than a far-away friend: A tethering strategy is used to self-select groups that assist in the cleavage of a neighboring carboxylic ester moiety (see picture, TSA=transition-state analogue). A correlation is observed between the amplification at thermodynamic equilibrium and the catalytic efficiency.
Relationships between chemical structure and inhibition of human placental choline acetyltransferase by keto analogs of acetylcholine
Chaturvedi,Rowell,Sastry
, p. 657 - 660 (2007/11/05)
Seven keto analogs of acetylcholine were synthesized and evaluated as inhibitors of human placental choline acetyltransferase. Their potencies for inhibition of horse serum cholinesterase and stimulation of cholinergic receptors in the longitudinal ileal muscle of the guinea pig were investigated. The most potent and selective inhibitor of choline acetyltransferase was (2-benzoylethyl) trimethylammonium chloride with an I50 of 3x10-6M. It exhibited considerably low activities at muscarinic and nicotinic receptors and cholinesterases. Its high potency for inhibiting choline acetyltransferase was attributed to: its cationic terminal, a site for an electron acceptor interaction; an aryl moiety for hydrophobic and electron donor contributions; and a positive charge on the carbon atom adjacent to the benzene ring due to the presence of the carbonyl group, which interacts with the nucleophilic residue on the enzyme.
