Glycol monoethyl ether, diethylen

Diethylene Glycol Monoethyl Ether Diethylene Glycol Monomethyl Ether Diethyleneimide Oxide Diethylene Imidoxide Di(Ethylene Oxide)... [Pg.42]

Diethylene Glycol Monomethyl Ether) (Diethylene Glycol Monoethyl Ether) (Diethylene Glycol Monobutyl Ether) (Diethylene Glycol Monohexyl Ether)... [Pg.513]

Dowanol EE Dowanol EM Diethylene Glycol Monoethyl Ether Diethylene Glycol Epichlorohydrin Epoxidized Drying Oils Epichlorohydrin Epoxidized Vegetable Oils... [Pg.143]

Diethylene Glycol Monobutyl Ether Diethylene Glycol Monoethyl Ether Diethylene Glycol Mononiethyl Ether Dipropylene Glycol Ethoxy Triglycol... [Pg.212]

Ethylene Glycol Ethyl Ether Ethylene Glycol Monoethyl Ether Diethylene Glycol Butyl Ether... [Pg.1669]

Diethylene glycol monoethyl ether [111-90-0] M 134.2, b 201.9", d 0.999, n 1.4273, n 1.4254. Ethylene glycol can be removed by extracting 250g in 750mL of benzene with 5mL portions of water, allowing for phase separation, until successive aqueous portions show the same volume increase. Dried, and freed from peroxides, as described for diethylene glycol mono-n-butyl ether. [Pg.203]

Caprylic acid, see Octanoic acid Caprylic alcohol, see 1-Octanol Carbitol, see Diethylene glycol monoethyl ether Carbolic acid, see Phenol Carbon disulphide Carbon monoxide Carbon oxysulphide, see Carbonyl sulphide... [Pg.202]

Ethynylation of 3j -hydroxy-16a-methyl-5a-androstan-17-one in a mixture of diethylene glycol dimethyl ether and diethylene glycol monoethyl ether in the presence of potassium hydroxide produces two isomeric 17-ethynyl derivatives. This result is not unexpected since molecular models suggest that the steric influence of the 13/ -methyl group is nearly offset by the 16a-methyl group. The presence of a 16a-acetoxy group in the estrone series also leads to the formation of epimeric 17-ethynyl compounds (61) and (62) on reaction with acetylenedimagnesium bromide. [Pg.66]

R. H. M. van Ingen and F. M. Nijssen, Determination of diethylene glycol monoethyl ether in flavors hy two-dimensional capillary gas cliromatography , J. High Resolut. Chromatogr. 12 484-485 (1989). [Pg.73]

For the preparation of an alcohol-free ethereal solution of diazomethane, the generating flask is charged with 35 ml of diethylene glycol monoethyl ether, 10 ml of ether, and a solution of 6 g of potassium hydroxide in 10 ml of water. The flask is heated in a water bath at 70°, and a solution of 21.4 g of Diazald in 140 ml of ether is added over 20 minutes with occasional shaking of the flask. The distillate is collected as above and the yield is the same. [Pg.155]

The solubility of latex in water can be improved by replacing the solvent used in the system. Initially, the water is removed and than a hydrophobic organic solvent is replaced by a hydrophilic solvent, which has a boiling point above 100 C. This last solvent can be ethylene glycol, diethyl ether of diethylene glycol, monoethyl ether of ethylene glycol, or polyethylene glycols. This treatment results in a pastelike composition that can be easily mixed with water and used as a final product. [Pg.69]

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

Dimethylbulane-2,3KJiol 15-Diethoxyethane 2-ButoxyethanoI 1,1-Diethoxyethane Diethylene glycol monoethyl ether Triethylene glycol... [Pg.476]

Fuel system icing inhibitors such as EGME (ethylene glycol monoethyl ether) and DEGME (diethylene glycol monoethyl ether) contain oxygen, but are added within controlled limits. [Pg.51]