24396-72-3 Usage
Description
N-dodecyl-benzenesulfonamide is a chemical compound that serves as a surfactant and emulsifier, commonly utilized in various industrial and consumer products. It is a sulfonamide derivative characterized by a dodecyl group attached to the benzene ring, which endows it with surfactant properties.
Uses
Used in Detergent and Cleaning Products Industry:
N-dodecyl-benzenesulfonamide is used as a surfactant and emulsifier for its ability to lower the surface tension of water, which enhances the wetting and spreading of liquids on surfaces. This property makes it a valuable component in the production of detergents, soaps, and cleaning products.
Used in Lubricants and Antifreeze Industry:
N-dodecyl-benzenesulfonamide is also utilized as an additive in certain lubricants and antifreeze formulations, where its surfactant properties contribute to improved product performance.
Used in Agricultural and Pesticide Products:
In the agricultural sector, N-dodecyl-benzenesulfonamide is employed in the formulation of pesticides and other related products, leveraging its surfactant and emulsifying characteristics to enhance the effectiveness of these products.
Safety Precautions:
It is important to handle N-dodecyl-benzenesulfonamide with care, as it can cause skin and eye irritation. Additionally, it is harmful if ingested or inhaled in large quantities, necessitating proper safety measures during its use and storage.
Check Digit Verification of cas no
The CAS Registry Mumber 24396-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,9 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24396-72:
(7*2)+(6*4)+(5*3)+(4*9)+(3*6)+(2*7)+(1*2)=123
123 % 10 = 3
So 24396-72-3 is a valid CAS Registry Number.
24396-72-3Relevant articles and documents
1,4-Aryl migration under copper(I) atom transfer conditions
Clark, Andrew J.,Coles, Stuart R.,Collis, Alana,Debure, Thomas,Guy, Collette,Murphy, Nicholas P.,Wilson, Paul
experimental part, p. 5609 - 5612 (2011/02/24)
Reaction of N-alkyl-N-(trichloroacetyl)arylsulfonamides with CuCl/amines leads to N-alkyl-N-(dichloroacetyl)-arylsulfonamides via reduction or N-alkyl-aryldichloroacetamides via 1,4-aryl migration with loss of SO2. The ratio of reduction to ary
