20466-47-1 Usage
Class of compound
Organosulfur compounds
2-(octylsulfonyl)ethanol belongs to a group of compounds that contain sulfur atoms bonded to carbon atoms.
Physical state
Colorless liquid
This chemical compound is in a liquid state and is colorless, meaning it does not have any visible color.
Odor
Characteristic sulfurous odor
2-(octylsulfonyl)ethanol has a distinct smell associated with sulfur, which can be detected at certain concentrations.
Industrial applications
Surfactant
As a surfactant, 2-(octylsulfonyl)ethanol helps to reduce the surface tension between liquids and solids, making it useful in various industrial processes.
Uses
Dispersing agent, emulsifier, and wetting agent
In the production of paints, coatings, and cleaning agents, 2-(octylsulfonyl)ethanol is used to improve the distribution of ingredients, mix different substances, and enhance the spreading of liquids on surfaces.
Antimicrobial properties
2-(octylsulfonyl)ethanol has the ability to inhibit the growth of microorganisms, making it useful in personal care and household cleaning products to provide additional cleaning power and protection.
Check Digit Verification of cas no
The CAS Registry Mumber 20466-47-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,6 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20466-47:
(7*2)+(6*0)+(5*4)+(4*6)+(3*6)+(2*4)+(1*7)=91
91 % 10 = 1
So 20466-47-1 is a valid CAS Registry Number.
20466-47-1Relevant articles and documents
REACTIONS OF OXIRANES WITH ALKYLTHIOLS
Chlebicki, Jan,Cichacz, Zbigniew
, p. 485 - 494 (2007/10/02)
Alkyl-2-hydroxyalkyl sulfides and their oxyalkylenated adducts were obtained in the reaction of oxirane or methyloxirane with C4-C12 alkylthiols in presence of basic or acidic catalysts.The sulfides were further oxidized to sulfoxides and sulfones.
Functional organic peroxides. XVII. Sulfonyl-containing dialkyl peroxides
Rakhimov, A. I.,Shatalin, Yu. V.,Baklanov, A. V.,Derzhinskii, A. R.,Konyushkin, L. D.,et al.
, p. 1708 - 1711 (2007/10/02)
High-boiling sulfonyl-containing dialkyl peroxides (initiators of cross-linking processes in saturated elastomers) are formed during the alkylation of tert-butyl hydroperoxides by 2-chloroethyl alkyl sulfones in the presence of alkali.Comparison of the kinetic parameters of the thermal decomposition of C8H17SO2CH2CH2OOC(CH3)3 and di-tert-butyl peroxide shows that the sulfonyl-containing fragment removed to the β position does not affect the thermal stability of the peroxide bond.The main reaction of the radical C8H17SO2CH2CH2O. generated during thermolysis is the abstraction of a hydrogen atom from the solvent.
