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Diethyl ether phthalate

Diethylene triamine Diethyl ether, see Ethyl ether Di(2-ethylhexyl)phthalate, see Di-sec-octyl phthalate Diethyl ketone Diethyl phthalate Diethyl sulphate Difluorodibromomethane Diglycidyl ether (DGE)... [Pg.157]

Diethyl aniline, 54 Diethylcarbaniazine citrate, 54 Diethyl carbamyl chloride, 54 Diethyl chlorophosphate, 54 Diethylene triamine, 54 Diethyl ether, 54 Di(2-ethylhexyl) phthalate, 54 Diethyl ketone, 54 Diethyl-p-phenylenediamine, 54 Diethyl phthalate, 54 Diethylstilbestrol, 55 Diethyl sulfate, 55 Diethyl zinc, 55 Difluoromethane chloride, 55 Digitoxin, 55 Diglycidyl ether, 55 Digoxin, 55 Diisobutyl ketone, 55 Diisopropylamine, 55 Diisopropyl ether, 55 DIKAMIN , 2,4-D, 55 DIKONIRT , 2,4-D, 55 Dimefox, 55 Dimethoate, 55 3,3 -Dimethoxybenzidine, 55 n,n-Dimethylacetamide, 56 Dimethylamine, 56 4-Dimethylaminoazobenzene, 56 Dimethylaminoethanol, 56 n,n-Dimethyl aniline, 56 7,12-Dimethylbenz[a]anthracene, 56 3,3 -Dimethylbenzidine, 56... [Pg.330]

Diethylene dioxide, see 1.4-Dioxane Diethylene ether, see 1.4-Dioxane Diethylene oxide, see 1.4-Dioxane. Tetrahydrofuran Diethylene oximide. see Morpholine Diethyleneimid oxide, see Morpholine Diethyleneimide oxide, see Morpholine Diethylenimide oxide, see Morpholine IV.lV-Diethylethanamine. see Triethylamine Diethylethanolamine. see 2-Diethylaminoethanol IV.lV-Diethylethanolamine. see 2-Diethylaminoethanol Diethyl ether, see Ethyl ether Di(2-ethylhexyl) orthophthalate. see Bis(2-ethylhexyl) phthalate... [Pg.1476]

The vapor pressure, p, of a solvent at 25°C is an important quantity and varies considerably among common solvents, some being very volatile (n-pentane and diethyl ether) whereas others are quite nonvolatile (n-hexadecane and dibutyl phthalate). [Pg.52]

The vapour pressure, p, of a solvent at 25°C is an important quantity and varies considerably among common solvents, some being very volatile, such as n- pentane and diethyl ether, with p = 68.7 and 71.6 kPa, respectively at this temperature, whereas others are quite non-volatile, such as -hexadecane and dibutyl phthalate, with p = 2 x K>4 and 1 x K>5 kPa, respectively. The values of the vapour pressure of the solvents in our List at 25 °C (or where otherwise noted, for solvents not liquid at 25 °C), p/kPa in exponential notation ( E k = 10 /l), are shown in Table 3.1 and pertain to the saturation value,... [Pg.135]

Suzuki et al. [Ill] screened three solvents—methylene chloride, diethyl ether, and benzene—to determine their ability to produce optimum elution of phthalic acid monoesters sorbed on a styrene divinylbenzene polymer (Figure 2.40). The effect of elution solvent strength on the recovery of the free acid form of the monomethyl (MMP), ethyl (MEP), -propyl (MPRP), K-butyl (MBP), K-pentyl (MPEP), and -octyl (MOP) phthalates is compared. The phthalic acid monoesters are arranged in Figure 2.40 in the order of increasing number of carbons in the alkyl chain, which in turn is roughly correlated with an increase in hydrophobicity. [Pg.105]

Recovery using methylene chloride or diethyl ether as eluting solvents was 86% or more for the monoesters depicted in Figure 2.40, except for the monomethyl phthalate. Relative to benzene, the polar character of methylene chloride and diethyl ether improves the wetability of the apolar sorbent having polar water molecules sorbed to the surface. The reduced recovery of mono-methyl-phthalate using methylene chloride or diethyl ether is probably due to incomplete sorption (i.e., the breakthrough volume may have been exceeded) rather than to incomplete desorption, because the more hydrophobic components were more completely desorbed. [Pg.106]

Dichlorvos Diethyl ether Diethyl phthalate Diethylene glycol... [Pg.461]

A solution of 10.0 g (89.2 mmol) of 2-inethylcyclohexanone in 75 mL of dry diethyl ether and 126 mL of dry ethanol is added to 500 mL of liquid ammonia. Lithium (12 g) is added in small pieces over a 70 min-period. The blue color disappears after an additional 30 min. The ammonia is evaporated, 750 mL of a mixture of ice and water are added, and the mixture is acidified with hydrochloric acid, then extracted with four portions of diethyl ether. The organic layer is separated, dried, and most of the solvent is removed. The residue is distilled at atmospheric pressure and the fraction with bp 163-I66X is collected to give a water-white liquid yield 6.4g (63%) n 0 1.455 99% one component (by GC) mp (of the corresponding acid phthalate) 125 126 C. [Pg.670]

With alcohols, chlorine produces alkyl hypochlorites, which explode on exposure to sunlight or heat. Reaction of chlorine with formaldehyde, acetaldehyde, or diethyl ether is violent. Liquid chlorine reacts explosively with carbon disulfide, glycerol, dialkyl phthalates, polypropylene, wax, rubber, and linseed oil. [Pg.474]

Acetone, acetic acid, alcohols, diethyl ether, diols, ethylene chlorohydrin, glycol ethers, isobutyl phthalate, phenol, saturated hydrocarbons, trichloroethyl phosphate, tricresyl phosphate... [Pg.829]

N,N-Diethylaniline N,N-Diethylbenzenamine. See Diethyl aniline Diethyl 1,2-benzenedicarboxylate. See Diethyl phthalate Di(2-ethylbutyl) phthalate. See Dihexyl phthalate Diethyl Carbitol. See Diethylene glycol diethyl ether Diethyl Cellosolve. See Ethylene glycol diethyl ether... [Pg.1073]

In plastic Li-ion batteries, 20 wt% of dibulyl phthalate is added to the electrode composition to be molded and later to be extracted with diethyl ether. This results in the desired microporous electrode. ... [Pg.297]

Herbicides may be determined by specific extraction, esterification, and gas chromatographic conditions. Aqueous samples are extracted with diethyl ether and then esterified with either diazomethane or pentafluorobenzyl bromide. The derivatives are determined by GC with an electron capture detector. Compound identifications should be supported by GC-MS for the qualitative confirmation. Alkaline hydrolysis and subsequent solvent wash removes many chlorinated hydrocarbons and phthalates that might otherwise interfere with the electron capture analysis. [Pg.5050]

Ethanol 50-75 176 80 — — E E 2-5% Diethyl Ether, 05-0.2 H SO. Balance primarily water. Phthalate ester manufacturing. Agitation, by 1100 Ib./hr. flow, total days 146. [Pg.681]

Diethoxyoxanilide, 194 Diethylene glycol, 81 Diethylene glycol dibenzoate, 9 Di(ethylene glycol) methyl ether, 205 Diethylene glycol monomethyl ether, 206 Diethyl ether, 198, 216, 218 Di-2-ethylhexyl-l,2-cyclohexane diacid ester, 13 Di(2-ethylhexyl)phthalate, 239... [Pg.254]

Diethyl Benzene Diethyl Carbonate Diethyl Ether Diethyl Ketone Diethyl Malonate Diethyl Phthalate Diethylamine... [Pg.3475]


See other pages where Diethyl ether phthalate is mentioned: [Pg.111]    [Pg.120]    [Pg.111]    [Pg.120]    [Pg.105]    [Pg.2]    [Pg.314]    [Pg.670]    [Pg.2]    [Pg.303]    [Pg.170]    [Pg.1604]    [Pg.515]    [Pg.78]    [Pg.533]   


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Diethyl ether

Diethyl phthalate

Diethyl phthalates

Phthalates

Phthalation

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