Ethylene glycol monoethyl ether

This colorless liquid has a mild and agreeable odor ond combines o low evoporotion rate with a strong solvent action. It is miscible In all proportions with acetone, benzene, carbon tetrachloride, ethyl ether, methanol and water. It has a powerful solvent action on nitrocellulose and alkyd resins and an extremely high dilution ratio with coal-tar hydrocarbons. This solvent will tolerate 4.9 times its own volume of toluene before the mixture will ceose to dissolve nitrocellulose, while butyl acetate will tolerate only 2.9 times its volume. [Pg.515]

Appeoronce water-nvhite Specific heat (average) cal./°C. 0.53 [Pg.515]

Cellosolve A trade name for ethylene glycol monoethyl ether. Also known as Oxitol. [Pg.86]

Glycol Ethers. The addition of one mole of ethylene oxide [75-21-8] to ethanol gives ethylene glycol monoethyl ether [109-86-4]. [Pg.415]

Butyl alcohol, ethylene glycol monoethyl ether, cyclohexanol, benzyl alcohol, diethylene glycol monobutyl ether, and dibutyl phthalate... [Pg.67]

Ethylene glycol monobutyl ether, see Butyl cellosolve Ethylene glycol monoethyl ether, see Cellosolve... [Pg.117]

In addition, water motion has been investigated in reverse micelles formed with the nonionic surfactants Triton X-100 and Brij-30 by Pant and Levinger [41]. As in the AOT reverse micelles, the water motion is substantially reduced in the nonionic reverse micelles as compared to bulk water dynamics with three solvation components observed. These three relaxation times are attributed to bulklike water, bound water, and strongly bound water motion. Interestingly, the overall solvation dynamics of water inside Triton X-100 reverse micelles is slower than the dynamics inside the Brij-30 or AOT reverse micelles, while the water motion inside the Brij-30 reverse micelles is relatively faster than AOT reverse micelles. This work also investigated the solvation dynamics of liquid tri(ethylene glycol) monoethyl ether (TGE) with different concentrations of water. Three relaxation time scales were also observed with subpicosecond, picosecond, and subnanosecond time constants. These time components were attributed to the damped solvent motion, seg-... [Pg.413]

Davidow (19), of the Food and Drug Administration, has described a colorimetric method applicable to technical chlordan. The method is based on the observation that when technical chlordan is heated with a mixture of diethanolamine and methanolic potassium hydroxide, a purple color is produced. When known amounts of this insecticide were added to cabbage, pears, and fresh and rancid rat fat, recoveries of 74 to 104% of the insecticide were obtained. However, because two crystalline isomers of chlordan isolated from the technical product do not give a colored reaction product with the reagent, further investigation of the method is being made. The red color obtained when technical chlordan is heated with pyridine, alcoholic alkali, and ethylene glycol monoethyl ether, as described by Ard (2), likewise fails with the crystalline isomers of this insecticide. [Pg.68]

Poisons. These were the phosphorofluoridates prepared by the Cambridge team of chemists (pp. 2-7), and eserine. Since the phosphorofluoridates slowly hydrolyse in water, stock solutions of these and of eserine were prepared in ethylene glycol monoethyl ether, and... [Pg.76]

Fluoro- and 2-hydroxy-2 -2"-fluoroethoxydiethyl ether were both toxic the former had a l.d. 50 of 15-20 mg./kg. and the latter of 30-40 mg. /kg. If the former is readily oxidized to the corresponding acid in the animal body, then we should expect it to be non-toxic in view of the non-toxicity of ethyl 2-fluoroethoxyacetate referred to above. It must be concluded then that the ether alcohols exert some toxic action per se. Ethylene glycol monoethyl ether, was examined physiologically but was found to be non-toxic,1 showing that the activity of 2-fluoro-2 -hydroxydiethyl ether was again closely associated with the 2-fluoroethoxy group in the molecule. [Pg.177]

Synonyms AI3-01236 BRN 1098271 CCRIS 2294 Cellosolve Cellosolve solvent Dowanol 8 Dowanol EGEE EINECS 203-804-1 Ektasolve EE Ethyl cellosolve Ethylene glycol ethyl ether Ethylene glycol monoethyl ether Glycol ether EE Glycol monoethyl ether Hydroxy ether Jeffersol EE NCI-C54853 NSC 8837 Oxitol Polysolv EE RCRA waste number U359 Solvid UN 1171. [Pg.550]

Synonyms Acetic acid, 2-ethoxyethyl ester AI3-01955 BRN 1748677 CCRIS 3286 Cello-solve acetate CSAC EGEEA EINECS 203-839-2 Ekasolve EE acetate solvent Ethoxy-acetate 2-Ethoxyethanol acetate Ethoxyethyl acetate P-Ethoxyethyl acetate 2-Ethoxyethyl ethanoate Ethylene glycol ethyl ether acetate Ethylene glycol monoethyl ether acetate Glycol ether EE acetate Glycol monoethyl ether acetate NSC 8658 Oxitol acetate Oxytol acetate Polysolv EE acetate UN 1172. [Pg.552]

Ethylene glycol monoethyl ether acetate [112-15-2] 44.0 0.44 Stephenson, 1993d ... [Pg.1247]

Ethylene glycol monobutyl ether, see 2-Butoxyethanol Ethylene glycol mono-/7-butyl ether, see 2-Butoxyethanol Ethylene glycol monoethyl ether, see 2-Ethoxyethanol Ethylene glycol monoethyl ether acetate, see 2-Ethoxyethyl acetate... [Pg.1486]

Synonyms Ethylene glycol monoethyl ether cellosolve EGEE 2-EE... [Pg.303]

Reproductive toxicity of ethylene glycol monoethyl ether tested by continuous breeding of CD-I mice. Environ Health Perspect 57 85-90, 1984... [Pg.304]

See also in sourсe #XX -- [ Pg.303 , Pg.304 , Pg.306 , Pg.447 , Pg.448 ]

See also in sourсe #XX -- [ Pg.364 ]

See also in sourсe #XX -- [ Pg.29 , Pg.81 ]

See also in sourсe #XX -- [ Pg.130 , Pg.131 ]

See also in sourсe #XX -- [ Pg.412 , Pg.413 , Pg.542 ]

See also in sourсe #XX -- [ Pg.162 ]

See also in sourсe #XX -- [ Pg.50 , Pg.190 ]

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