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Ethylene glycol mono methyl ether

With triphenylphosphine and diisopropyl azodicarboxylate, various ether end groups can be attached, e.g., methoxy groups with methanol, 2-methoxyethoxy end groups with ethylene glycol mono methyl ether, etc. [Pg.145]

Hollow fiber UF membranes have been prepared from PPESK with a dry/ wet phase inversion technique. Ethylene glycol mono methyl ether, diethylene glycol, and methyl ethyl ketone were used as non-solvent additives and NMP was used as a solvent in membrane preparation. ... [Pg.260]

Ethylene glycol mono methyl ether, 145, 260 Ethylene propylene diene monomer, 316... [Pg.588]

Poly(ethylene glycol)dimethyl ether Poly(ethylene glycol)mono methyl ether Polypropylene oxide Poly(propylene glycol)... [Pg.278]

Starting materials 1,6-diisocyantohexane and poly(ethylene glycol mono methyl ether) PEGME, mol. wt. ave.-350,500,750,1900 and 5000- were obtained from Aldrich Co. Polyethyleneimines 6, 18, 200, and 1000 with Mn of 600, 1800, 10-20,000 and 50-100,000 respectively, were used as obtained. Simple amines were distilled before use. [Pg.164]

Ethers and alcohol ethers Ethers such as ethyl ether are excellent solvents for some of the natural resins, oils, and fats. The usual forms of ether used in protective coatings are alcohol ethers such as ethylene glycol mono methyl ether, known commonly as cellosolve. Cellosolve is a good solvent for many oils, gums, natural resins, and synthetic resins such as alkyds, ethyl-cellulose, nitro-cellulose, polyvinyl acetate, pol)Tvinyl butyryl, and phenolics. Cellosolve is a slow solvent that is used in many lacquers to improve flow-out and gloss. [Pg.614]

METHYL CELLOSOLVE ACETATE C,H,0, 2-Mcthoxycthyl Accttie, Glycol mono ncthyl ether toccate. Ethylene llycol mono-methyl ether occtoie Nitrates strong oxidizers, alkalies, and adds III I.I a.2... [Pg.225]

C6H140 3-methyl-1-pentanol 589-35-5 202.70 11.861 2 9067 C6H1402 ethylene glycol mono-sec-butyl ether 7795-91-7 208.52 19.605 2... [Pg.564]

Ethylene glycol mono-p-tolyl ether. See Methyl phenoxyethanol Ethylene glycol nonyl phenyl ether. See Nonoxynol-1... [Pg.1723]

Fig. 28, Chromatogram of glycol and chlorohydrin ethers in 50% dimethylformamide/ hexane (1) monomethyl-, monoethyl-, and mono-n-butyl ether of ethylene glycol, (2) monobutyl ether of diethylene glycol, (3) methyl, ethyl, /i-propyl, and /i-butyl alcohol, (4) a-dichlorohydrin, (5) ethylene chlorohydrin and 1,2-propylenechlorohydrin. Fig. 28, Chromatogram of glycol and chlorohydrin ethers in 50% dimethylformamide/ hexane (1) monomethyl-, monoethyl-, and mono-n-butyl ether of ethylene glycol, (2) monobutyl ether of diethylene glycol, (3) methyl, ethyl, /i-propyl, and /i-butyl alcohol, (4) a-dichlorohydrin, (5) ethylene chlorohydrin and 1,2-propylenechlorohydrin.
Homologous mono-alkyl ethers of ethylene glycol, such as monoethyl glycol (or 2-ethoxyethanol), HOC2H4OC2H5, form excellent solvents as they combine to a large extent the solvent properties of alcohols and ethers. The monoethyl and the monomethyl members have the technical names of ethyl cellosolve and methyl cellosolve respectively. Dioxan... [Pg.15]

Mono-alkyl ethers of ethylene glycol, ROCHjCHjOH. The mono methyl, ethyl and n-butyl ethers are inexpensive and are known as methyl cellosolve, cellosolve, and butyl cellosolve respectively. They are completely miscible with water, and are excellent solvents. The commercial products are purified by drying over anhydrous potassium carbonate or anhydrous calcium sulphate, followed by fractionation after... [Pg.170]

Mole-nots, see Strychnine Mollan 0, see Bis(2-ethylhexyl) phthalate Mondur TD, see 2,4-Toluene diisocyanate Mondur TD-80, see 2,4-Toluene diisocyanate Mondur TDS, see 2,4-Toluene diisocyanate Monobromobenzene, see Bromobenzene Monobromobenzol, see Bromobenzene Monobromoethane, see Ethyl bromide Monobromomethane, see Methyl bromide Monobromotrifluoromethane, see Bromotrifluoromethane Monobutylamine, see Butylamine Mono-n-butylamine, see Butylamine Monobutyl ethylene glycol ether, see 2-Butoxyethanol Monochlorbenzene, see Chlorobenzene Monochlorethane, see Chloroethane Monochloroacetaldehyde, see Chloroacetaldehyde Monochlorobenzene, see Chlorobenzene Monochlorodibromomethane, see Dibromochloromethane Monochlorodiphenyl oxide, see 4-Chlorophenyl phenyl ether... [Pg.1496]

In 1926, Berl and Bitter studied the action of sodium hydroxide and carbon disulfide upon ethylene glycol, glyceritol, and their methyl ethers, and concluded that, whilst one vacant hydroxyl group is essential for occurrence of esterification, the presence of additional free hydroxyl groups inhibits reactivity. They failed to achieve xanthation of even the mono-hydric compounds in the presence of an equimolar proportion of water, unless activated carbon was also added. By using various 0-methylated celluloses, they were able to demonstrate that, for maximum esterification, two free hydoxyl groups for each D-glucopyranose residue are necessary. [Pg.135]

ACETATE d ISOPROPYLE (French) (108-21-4) see isopropyl acetate. ACETATE de L ETHER MONO-METHYLIQUE de L ETHYLENE-GLYCOL (French) (110-49-6) see ethylene glycol monomethyl ether acetate. ACETATE de METHYLE (French) (79-20-9) see methyl acetate. [Pg.3]

See other pages where Ethylene glycol mono methyl ether is mentioned: [Pg.246]    [Pg.89]    [Pg.196]    [Pg.110]    [Pg.31]    [Pg.34]    [Pg.195]    [Pg.246]    [Pg.89]    [Pg.196]    [Pg.110]    [Pg.31]    [Pg.34]    [Pg.195]    [Pg.314]    [Pg.253]    [Pg.1113]    [Pg.1644]    [Pg.1644]    [Pg.1167]    [Pg.931]    [Pg.2122]    [Pg.359]    [Pg.75]    [Pg.664]    [Pg.874]    [Pg.245]    [Pg.365]    [Pg.874]    [Pg.397]    [Pg.505]    [Pg.1212]    [Pg.18]   


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Ether ethylene

Ethylene glycol ethers

Ethylene glycol-mono-methyl ether, acetate

Glycols/glycol ethers

Methyl Glycol

Methyl glycolate

Methyl, mono

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