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2-Butoxyethanol is an organic compound with the chemical formula BuOC 2 H 4 OH (Bu = CH 3 CH 2 CH 2 CH 2). This colorless liquid has a sweet, ether -like odor, as it derives from the family of glycol ethers , and is a butyl ether of ethylene glycol .
Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: 184.3 3.69 –5.96 –5.87 K b & K f [1] Lauric acid: 298.9 44 –3.9
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.
2-Butoxyethanol acetate is used in a variety of industries as a solvent for nitrocellulose and multicolored lacquers, varnishes, enamels, and epoxy resin. It is useful as a solvent because of its high boiling point. It is also used in the manufacture of polyvinyl acetate latex. It is an ingredient in ink removers and spot removers. [2] [3]
Diethylene glycol butyl ether (2-(2-butoxyethoxy)ethanol) is the organic compound with the formula C 4 H 9 OC 2 H 4 OC 2 H 4 OH. A colorless liquid, it is common industrial solvent. It is one of several glycol ether solvents. It has low odour and high boiling point.
It is a liquid. [2] It has the formula C 6 H 12 O 3 and CAS Registry Number of 2516-93-0. [3] It is REACH registered with the EC number 677-344-8. [4] n-Butyl glycidyl ether is metabolized renally to this compound as is 2-butoxyethanol. [5] [6] Methods have been developed and papers published to detect the compound in urine and blood. [7] [8 ...
2-(2-Ethoxyethoxy)ethanol, also known under many trade names, is the organic compound with the formula CH 3 CH 2 OCH 2 CH 2 OCH 2 CH 2 OH. It is a colorless liquid. It is a popular solvent for commercial applications. [1] It is produced by the ethoxylation of ethanol (CH 3 CH 2 OH).
At room temperature, acetaldehyde (H 3 CC(O)H) is more stable than vinyl alcohol (H 2 C=CHOH) by 42.7 kJ/mol. [3] Vinyl alcohol gas isomerizes to the aldehyde with a half-life of 30 min at room temperature. [1] H 2 C=CHOH → H 3 CC(O)H The industrial synthesis of acetaldehyde (Wacker process) proceeds via the intermediacy of a vinyl alcohol ...