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A classic laboratory method involves Bouveault-Blanc reduction of ethyl laurate. [4] Dodecanol is used to make surfactants, which are used in lubricating oils, and pharmaceuticals. Millions of tons of sodium dodecylsulfate (SDS) are produced annually by sulfation of dodecyl alcohol: [6] SO 3 + CH 3 (CH 2) 10 CH 2 OH → CH 3 (CH 2) 10 CH 2 OSO 3 H
1-Dodecanol [2] 75.70 0.3750 Ethane: 5.562 0.0638 Ethanethiol: 11.39 0.08098 Ethanol: 12.18 0.08407 Ethyl acetate ... 1 J·m 3 /mol 2 = 1 m 6 ·Pa/mol 2 = 10 L 2 ...
2,3-Dimethyl-1-butanol; 3,3-Dimethyl-1-butanol This page was last edited on 27 March 2024, at 19:55 (UTC). Text is available under the Creative Commons Attribution ...
It is formed by the ethoxylation chemical reaction of dodecanol (lauryl alcohol) to give a material with 5 repeat units of ethylene glycol. Multilamellar vesicle formation [ edit ]
Although isooctanol (and the derived isooctyl prefix) is commonly used in industry to refer to 2-ethylhexanol and its derivatives, IUPAC naming conventions [21] dictate that this name is properly applied to another isomer of octanol, 6-methylheptan-1-ol. The Chemical Abstracts Service likewise indexes isooctanol (CAS# 26952-21-6) as 6 ...
After the FDA has banned red dye No.3, you may be wondering which drinks and candies contain it. Here's the full list—plus, when it'll be removed from shelves.
Every helpful hint and clue for Wednesday's Strands game from the New York Times.
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.