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Ethylene glycol monoacetate

The reaction is carried out over a supported metallic silver catalyst at 250—300°C and 1—2 MPa (10—20 bar). A few parts per million (ppm) of 1,2-dichloroethane are added to the ethylene to inhibit further oxidation to carbon dioxide and water. This results ia chlorine generation, which deactivates the surface of the catalyst. Chem Systems of the United States has developed a process that produces ethylene glycol monoacetate as an iatermediate, which on thermal decomposition yields ethylene oxide [75-21-8]. [Pg.433]

Ethylene glycol monoacetate 5-Chloro-2-methyl-4-isothiazolin-3-one or... [Pg.74]

Figure 5-2. Ethylene glycol monoacetate, formaldehyde, glutaraldehyde, lactic acid, iodoacetone, succinimide. Figure 5-2. Ethylene glycol monoacetate, formaldehyde, glutaraldehyde, lactic acid, iodoacetone, succinimide.
Photolytic. Grosjean (1997) reported a rate constant of 1.87 x lO " cm /molecule-sec at 298 K for the reaction of 2-ethoxyethanol and OH radicals in the atmosphere. Based on an atmospheric OH radical concentration of 1.0 x 10 molecule/cm , the reported half-life of methanol is 0.35 d (Grosjean, 1997). Stemmier et al. (1996) reported a rate constant of 1.66 x 10 " cm /molecule-sec for the OH radical-initiated oxidation of 2-ethoxyethanol in synthetic air at 297 K and 750 mmHg. Major reaction products identified by GC/MS (with their yields) were ethyl formate, 34% ethylene glycol monoformate, 36% ethylene glycol monoacetate, 7.8% and ethoxyacetaldehyde, 24%. [Pg.551]

Ethylene glycol diformate, see 1,4-Dioxane Ethylene glycol monoacetate, see 2-Ethoxyethanol Ethylene glycol monoformate, see 2-Ethoxyethanol Ethylene oxide, see 1,2-Dichloroethane, Ethylene dibromide... [Pg.1529]

Example the oxidation of acetaldehyde ethylene acetal to ethylene glycol monoacetate with Fe—M-polyphthalocyanines (M V, Cr, Cu, etc.) as catalysts 110>. [Pg.115]

When palladium-catalyzed acetoxylation is carried out in the presence of nitrate or nitrite ions, ethylene glycol monoacetate (EGMA) results as the major product of the reaction (equation 163).420... [Pg.366]

Ethylene glycol monoacetate, hi 16 Ethylene glycol monobutyl ether, b410 Ethylene glycol monoethyl ether, e34 Ethylene glycol monomethyl ether, m65 Ethylene glycol monomethyl ether acetate, m68 Ethylene iodide, d403 Ethylene iodohydrin, i35... [Pg.245]

In some of the studies on the vinyl acetate synthesis from ethylene, high boiling products were reported (9, 10, 24, 25, 26). These included ethylidene diacetate (III), ethylene glycol monoacetate (IV) and ethylene glycol diacetate (V). Little attention has been given to the reactions by which these products are formed. No dioxygenated products have been reported previously when higher olefins have been used. [Pg.99]

Fig. 22. Apparent mechanical water permeability Lp of sprayed CA latex films vs weight loss of teachable materials. Key ( ) diacetin ( ) diethyl tartrate ( ) ethylene glycol monoacetate (A) triethyl phosphate (O) trimethyl phosphate ( ) ethylene glycol diacetate + diethyl tartrate (A) ethylene glycol diacetate + trimethyl phosphate [135]... Fig. 22. Apparent mechanical water permeability Lp of sprayed CA latex films vs weight loss of teachable materials. Key ( ) diacetin ( ) diethyl tartrate ( ) ethylene glycol monoacetate (A) triethyl phosphate (O) trimethyl phosphate ( ) ethylene glycol diacetate + diethyl tartrate (A) ethylene glycol diacetate + trimethyl phosphate [135]...
Fig. 24. Release profiles of potassium chloride from osmotic tablets prepared by spraying a CA latex as a function of the plasticizer type and amount, and the coating temperature. Key (J) diethyl tartrate 120%, 50°C (2) diethyl tartrate 160%, 60°Q (J) trimethyl phosphate 160%, 60°C (4) ethylene glycol monoacetate 360%, 60 °C (5) ethylene glycol monoacetate 60%, 60 °C (6) organic solution, 35 °C (no plasticizer) [133]... Fig. 24. Release profiles of potassium chloride from osmotic tablets prepared by spraying a CA latex as a function of the plasticizer type and amount, and the coating temperature. Key (J) diethyl tartrate 120%, 50°C (2) diethyl tartrate 160%, 60°Q (J) trimethyl phosphate 160%, 60°C (4) ethylene glycol monoacetate 360%, 60 °C (5) ethylene glycol monoacetate 60%, 60 °C (6) organic solution, 35 °C (no plasticizer) [133]...
ETHYLENE GLYCOL MONOACETATE (542-59-6) C4H8O3 Combustible liquid (flash point 215 °F/102°C oc Fire Rating 1). Unless inhibited p-methoxyphenol is recommended), polymerization can occur, especially when heated. Violent reaction with strong... [Pg.468]

Formation of vinyl acetate by the reaction of ethylene with Pd(OAc)2 can be understood by the acetoxypalladation and )3-H elimination (path a). No hydride shift occurs because the acetoxy group is electron-attracting. In addition, ethylene glycol monoacetate (9) is formed as a nucleophilic addition product in the presence of nitrate anion (path b) [13]. Formation of glycol monoacetate is explained by the displacement of Pd-OAc with a nitrate anion, followed by hydrolysis of the nitrate ester. [Pg.30]

Dioxygenadon by nucleophilic addition to alkenes takes place in the presence of the nitrate anion. The reaction of ethylene with Pd(OAc>2 in the presence of LiN03 affords ethylene glycol monoacetate (9) [13]. [Pg.39]

See other pages where Ethylene glycol monoacetate is mentioned: [Pg.40]    [Pg.380]    [Pg.386]    [Pg.73]    [Pg.75]    [Pg.219]    [Pg.27]    [Pg.380]    [Pg.386]    [Pg.428]    [Pg.78]    [Pg.106]    [Pg.423]    [Pg.115]    [Pg.529]    [Pg.615]    [Pg.106]    [Pg.599]    [Pg.1076]    [Pg.2381]    [Pg.1061]    [Pg.2539]    [Pg.522]    [Pg.522]    [Pg.257]    [Pg.386]    [Pg.1131]    [Pg.2314]    [Pg.471]    [Pg.84]    [Pg.46]   
See also in sourсe #XX -- [ Pg.74 , Pg.75 ]

See also in sourсe #XX -- [ Pg.99 ]

See also in sourсe #XX -- [ Pg.148 , Pg.257 ]



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Glycol monoacetate

Monoacetalization

Monoacetate

Monoacetates

Monoacetic

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