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Ethyl glycollic ether

Glycollie Acid.—If a solution of 30 g. sodium glycollate in 38 cc. water is electrolyzed with a current strength of 1 amp., there are formed chiefly carbonic acid and formaldehyde,. besides a little carbon monoxide, formic acid, and oxygen (Miller and Hofer1). Walker2 obtained aldehyde in the electrolysis of the sodium salt of ethyl glycollic ether. [Pg.97]

Vinyl Ethers. The principal commercial vinyl ethers are methyl vinyl ether (methoxyethene, C H O) [107-25-5], ethyl vinyl ether (ethoxyethene, C HgO) [104-92-2], and butyl vinyl ether (1-ethenyloxybutane, C H 20) [111-34-2]. (See Table 8 for physical properties.) Others such as the isopropyl, isobutyl, hydroxybutyl, decyl, hexadecyl, and octadecyl ethers, as well as the divinyl ethers of butanediol and of triethylene glycol, have been offered as development chemicals (see Ethers). [Pg.114]

The manufacturing process for organo-soluble EHEC is similar to that for EC except that alkah cellulose reacts first with ethylene oxide to a low hydroxyethyl MS value of - 0.5 at a low temperature, - 50° C, followed by reaction of the ethyl chloride at a higher temperature. Additional by-products, which are removed during purification, include glycols and the reaction products of the glycols with ethyl chloride (glycol ethers). [Pg.278]

Grouping Acetone Ethane Ethyl-acetate Acetylene Ethyl amine Ethylene Acetaldehyde Ethyl glycol Crude oil Ethyl-ether Carbon disulphide Ethyl Nitrite... [Pg.179]

Solvents acetone, methyl ethyl ketone (MEK), toluene, xylene, glycol, ethers, alcohol defats and dries skin some may be absorbed may carry other components through skin high volatility, exposure possible irritation central nervous system depression (e.g. dizziness, loss of coordination) low to high toxicity, longterm effects... [Pg.145]

Diethylene glycol Diethylene glycol ether Di-(2 ethyl hexyl) phthalate Diethylenetriamine Difluorodibromomethane Difluorodichloromethane Diglycidyl ether of Bisphenol A Dihydrocapsaicin... [Pg.367]

Ethyl benzene Ethyl bromide 2-Ethyl butyl acrylate Ethyl chloride Ethyl ether Ethyl formate 2-Ethyl hexyl acrylate Ethyl iodide Ethyl propionate Ethyl propyl ether Ethyl sulfide Ethylene bromide Ethylene chloride Ethylene glycol Ethylidebe chloride Fluorobenzene Formic acid Freon-11 Freon-12 Freon-21 Freon-22 Freon-113 Glycerol, 100%... [Pg.484]

METHYL sec-BUTYL ETHER METHYL tert-BUTYL ETHER METHYL ISOBUTYL ETHER ETHYL PROPYL ETHER ETHYLENE GLYCOL MONOPROPYL NEOPENTYL GLYCOL... [Pg.37]

Uses. Nearly half the ethyl alcohol produced in petrochemical plants (not the stuff fermented for human consumption) is used as a chemical intermediate in the manufacture of ethyl acrylate, ethyl amines, ethyl acetate (when you pop the cap on nail polish remover, you smell ethyl acetate), ethylene chloride, glycol ethers, acetaldehyde, and acetic acid. However, you will see in the chapters on acetaldehyde and acetic acid, there are now more competitive routes than those based on ethyl alcohol. [Pg.197]

SBA is primarily used as feedstock for methyl ethyl ketone. Other uses include hydraulic fluids, industrial cleaning compounds, paint remover, and an extracting agent for oils, perfumes, and dyes. TBA is used mostly as feedstock to make methyl methacrylate and glycol ethers (by reaction with ethylene or propylene oxides.) TBA is also a coproduct with PO, as covered in Chapter 11. [Pg.208]

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]

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]

Synonyms Cellosolve acetate ethylene glycol monoethyl ether acetate EGEEA 2-ethoxy ethanol acetate 2-EEA EEA EEAc ethyl glycol acetate... [Pg.304]

Solvent Beverages Acetaldehyde Acetic Acid H Hi ethyl Filter Ethyl Acetate Glycol Ether... [Pg.13]

Ethylene glycol ethyl butyl ether Ethylene glycol monobutyl ether Ethylene glycol monoethyl ether (Cellosolve)... [Pg.219]

List B, giving examples of liquids where a degree of concentration is necessary before hazardous levels of peroxides will develop, includes several common solvents containing one ether function (diethyl ether, ethyl vinyl ether, tetrahydrofuran), or two ether functions (p-dioxane, 1,1 -diethoxyethane, the dimethyl ethers of ethylene glycol or diethylene glycol ), the secondary alcohols 2-propanol and 2-butanol, as well as the susceptible hydrocarbons propyne, butadiyne, dicyclopentadiene, cyclohexene and tetra- and deca-hydronaphthalenes. Checking stocks at 12 monthly intervals, with peroxidic samples being discarded or repurified, is recommended here [1],... [Pg.2523]

The selectivity of the Complex Formation is a very interesting subject, y - Cyclodextrin, (y - CD) has been found to form inclusion complexes with poly (methyl vinyl ether) (PMVE), poly(ethyl vinyl ether) (PEVE), and poly(n- propyl vinyl ether) (PnPVE) of various molecular weights to give stoichiometric compounds in crystalline states. However, a- cyclodextrin (a - CD) and (3 - Cyclodextrin ((3- CD) did not form complexes with poly (alkyl vinyl ether)s of any molecular weight, y -CD did not form complexes with the low molecular weight analogs, such as diethyl ether and trimethylene glycol dimethyl ether. [Pg.219]

Industrial uses of ethanol include solvents (especially for toiletries and cosmetics, coatings and inks, and detergents and household cleaners), and chemical intermediates (especially ethyl acrylate, vinegar, ethylamines, and glycol ethers). Most corn fermentation alcohol is used in fuel, industrial solvents and chemicals, and beverages. [Pg.217]

As many as 70 products were at one time produced commercially from ethanol. Some of these downstream products are butanol, 2-ethyl hexanol, crotonaldehyde, butyraldehyde, acetaldehyde, acetic acid, butadiene, sorbic acid, 2-ethylbutanol, ethyl ether, many esters, ethanol-glycol ethers, acetic anhydride, vinyl acetate, ethyl vinyl ether, even ethylene gas. Many of these products are now more economically made from other feedstocks such as ethylene for acetaldehyde and methanol-carbon monoxide for acetic acid. Time will tell when a revival of biologically-oriented processes will offer lower-cost routes to at least the simpler products. [Pg.58]

Since their commercial introduction in 1926, glycol ethers have become valuable as industrial solvents and chemical intermediates. Because glycol monoethers contain a -OCH2CH2OH group, they resemble a combination of ether and ethyl alcohol in solvent properties. The most common... [Pg.359]

Synthetic ethanol has the following uses as a chemical intermediate (for ethyl acetate, ethyl acrylate, glycol ethers, ethylamines, etc.), 30 percent in toiletries and cosmetics, 20 percent as a coatings solvent, 15 percent as a raw material for vinegar, 10 percent in household cleaners, 7 percent in detergents, 5 percent in pharmaceuticals, 5 percent in printing inks, 3 percent and in miscellaneous uses, 5 percent. [Pg.364]


See other pages where Ethyl glycollic ether is mentioned: [Pg.170]    [Pg.170]    [Pg.170]    [Pg.170]    [Pg.550]    [Pg.144]    [Pg.173]    [Pg.823]    [Pg.154]    [Pg.328]    [Pg.1467]    [Pg.309]    [Pg.216]    [Pg.31]    [Pg.297]    [Pg.334]    [Pg.891]    [Pg.380]    [Pg.390]    [Pg.393]    [Pg.823]    [Pg.192]    [Pg.274]    [Pg.75]    [Pg.112]    [Pg.23]   
See also in sourсe #XX -- [ Pg.97 ]




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DIETHYLENE GLYCOL ETHYL ETHER ACETATE66(Vol

Diethylene Glycol Ethyl Ether

Diethylene glycol mono ethyl ether

Diethylene glycol mono ethyl ether acetate

Ether ethylic

Ethers ethyl ether

Ethyl ether

Ethyl glycol

Ethyl glycolate

Ethylene Glycol Ethyl Ether

Ethylene Glycol Ethyl Hexyl Ether

Ethylene glycol mono ethyl ether

Glycol ethyl ether

Glycol ethyl ether

Glycolic acid ethyl ether

Glycols/glycol ethers

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