Ethylene glycol monomethyl ether

Methyl acetate-methanol Minimum-hoiling azeotrope Ethylene glycol monomethyl ether Element of recovery system for alternative to production of methyl acetate hy reactive distillation alternative to azeotropic, pressure, swing distillation... [Pg.1315]

Ethylene dibromide (1,2-dibromoethane) Ethylene dichloride (1,2-dichloroethane) Ethylene glycol monomethyl ether acetate, see Methyl cellosolve acetate Ethylene oxide... [Pg.337]

Ethylene glycol monomethyl ether acetate (methyl cellosolve acetate)... [Pg.377]

Methyl butyl ketone, see 2-Hexanone Methyl cellosolve, see 2-Methoxyethanol Methyl cellosolve acetate, see Ethylene glycol monomethyl ether acetate... [Pg.380]

Ethylene glycol monomethyl ether, see Methyl cellosolve Ethylenimine, see Aziridine Ethylene oxide Ethyl ether... [Pg.117]

Solubilization of a graft copolymer comprising a hydrophobic poly(dodecyl-methacrylate) backbone and hydrophilic poly(ethylene glycol) monomethyl ether side chains in water/AOT/cyclohexane w/o microemulsions was rationalized in terms of the backbone dissolved in the continuous apolar phase and the side chains entrapped within the aqueous micellar cores [189],... [Pg.490]

Turanose Phenylosazone. A mixture of 4 g. of turanose, 2 ec. of water, and 1 co. of phenylhydrazine was warmed on the steam-bath until solution was complete. To the cooled solution was added 3.5 cc. of phenylhydrazine and 4 cc. of glacial acetic acid, and the mixture returned to the steam-bath for one hour. At the expiration of this time, 40 cc. of warm 60% alcohol was added and, upon cooling, a rapid crystallization of the osazone occurred. The osazone was recovered by filtration and washed with absolute alcohol followed by ether to yield 4.2 g. (69%) of lemon-yellow needles. The osazone is soluble in hot water and separates on cooling as jelly-like particles, but water is not a satisfactory solvent for its purification. It was recrystallized from 15 parts of 95% alcohol with good recovery, as needles which melted with decomposition at 200-205° and rotated [ ]d +24.5° - +33.0° (24 hours, constant value c, 0.82) in a mixture of 4 parts of pyridine, by volume, and 6 parts of absolute ethyl alcohol. In methyl cellosolve (ethylene glycol monomethyl ether) solution it rotated C< 3d" + 44.3°— + 48.5° (24 hours, constant value c, 0.80). [Pg.44]

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