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107-21-1 Ethyleneglycol

Triiodobenzoates. The derivatives enumerated above are unsatisfactory for alcohol - ethers, e.g., the mono-ethers of ethyleneglycol ( cellosolves ) and the mono-ethers of diethyleneglycol ( car-bitols ) (see Table 111,27). Crystalline derivatives of alcohol - ethers are readily obtained with 3 4 5-triiodobenzoyl chloride (for preparation, see Section VII,21), for example ... [Pg.265]

Successful results have been obtained (Renfrew and Chaney, 1946) with ethyl formate methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec.-butyl and iso-amyl acetat ethyleneglycol diacetate ethyl monochloro- and trichloro-acetates methyl, n-propyl, n-octyl and n-dodecyl propionates ethyl butyrate n-butyl and n-amyl valerates ethyl laurate ethyl lactate ethyl acetoacetate diethyl carbonate dimethyl and diethyl oxalates diethyl malonate diethyl adipate di-n-butyl tartrate ethyl phenylacetate methyl and ethyl benzoates methyl and ethyl salicylates diethyl and di-n-butyl phthalates. The method fails for vinyl acetate, ieri.-butyl acetate, n-octadecyl propionate, ethyl and >i-butyl stearate, phenyl, benzyl- and guaicol-acetate, methyl and ethyl cinnamate, diethyl sulphate and ethyl p-aminobenzoate. [Pg.393]

EGTA ethyleneglycol-bis(P-ami noethyl ether) -N,N -tetraacetic acid 5.4 10.9... [Pg.364]

Pyrazolines Imidazoles Thiazoles Oxadiazoles 1 -Phenylpyrazoles Purines Dioxolanes Ox azolines 10% Cyanethylated mannite on Celite 545. 5% OV-17 on Chromosorb W, AW-DMCS (H.P.). Carbowax 4000, dioleate on firebrick, 190 °C. Silicone grease on Chromosorb P. Apiezon L on firebrick C-22, 220 °C. 15% Hallcomid M-18 on firebrick. Carbowax 20M on Gas-Chrom P. Ethyleneglycol succinate on Diatoport-S. [Pg.32]

Ethers, esters, amides and imidazolidines containing an epithio group are said to be effective in enhancing the antiwear and extreme pressure peiformance of lubricants. Other uses of thiiranes are as follows fuel gas odorant (2-methylthiirane), improvement of antistatic and wetting properties of fibers and films [poly(ethyleneglycol) ethers of 2-hydroxymethyl thiirane], inhibition of alkene metathesis (2-methylthiirane), stabilizers for poly(thiirane) (halogen adducts of thiiranes), enhancement of respiration of tobacco leaves (thiirane), tobacco additives to reduce nicotine and to reduce phenol levels in smoke [2-(methoxymethyl)thiirane], stabilizers for trichloroethylene and 1,1,1-trichloroethane (2-methylthiirane, 2-hydroxymethylthiirane) and stabilizers for organic compounds (0,0-dialkyldithiophosphate esters of 2-mercaptomethylthiirane). The product of the reaction of aniline with thiirane is reported to be useful in the flotation of zinc sulfide. [Pg.184]

Dibutylcarbitol [di(ethyleneglycol)dibutyl ether] [112-73-2] M 218.3, b 125-130 /0.1mm, d 0.883, n 1.424. Freed from peroxides by slow passage through a column of activated alumina. The eluate was shaken with Na2C03 (to remove any remaining acidic impurities), washed with water, and stored with CaCl2 in a dark bottle [Tuck J Chem Soc 3202 1957]. [Pg.194]

Monodispersed poly (methyl methacrylate-ethyleneglycol dimethacrylate) is prepared by a multistep swelling and polymerization method. When a good solvent such as toluene is applied as a porogen, the seed polymer severely affects the pore structure, whereas no effects are observed with poor solvents, such as cyclohexanol, as a porogen, in comparison with the conventional suspension polymerization (68,69). [Pg.18]

Diacetylene reacts with ethyleneglycol in the presence of alkalis at 75-140°C to form a mixture of 2-(prop-2-ynyl)-l,3-dioxolane (36), 2-(propa-l,2-dienyl)-l,3-dioxolane (37), and 2-(prop-l-ynyl)-l,3-dioxolane (38) (1-5 h, yield 66%), the ratio of which depends on the experimental conditions (74ZOR953). [Pg.169]

An application of an LC-SFC system has been demonstrated by the separation of non-ionic surfactants consisting of mono- and di-laurates of poly (ethyleneglycol) (23). Without fractionation in the precolumn by normal phase HPLC (Figure 12.18 (a)) and transfer of the whole sample into the SFC system, the different homologues coeluted with each other. (Figure 12.18(b)). In contrast with prior fractionation by HPLC into two fractions and consequent analysis by SFC, the homologues in the two fractions were well resolved (Figures 12.18(c) and 12.18(d)). [Pg.324]

Phenyl ethyleneglycol Nitrated Products. Nitration of phenylethyleneglycol with mixed nitric-sulfuric acid gave an expl product, mp ca 85°, which was claimed to be 110% as powerful as TNT, as detd by the Trauzl test, and whose performance was intermediate between that of Tetryl and TNT (Ref 1)... [Pg.718]

Polyethylene Glycols. See in Vol 6, E252-L to E253-R under Ethyleneglycol Polymers Polyethyleneglycols or Polyglycols . [Pg.816]

With diblock copolymers, similar behavior is also observed. One component is enriched at the surface and depending on miscibility and composition a surface-induced ordered lamellar structure normal to the surface may be formed. Recent investigations include poly (urethanes) [111], poly(methoxy poly (ethyleneglycol) methacrylate)/PS [112] and PS/PMMA [113, 114]. In particular the last case has been extensively studied by various techniques including XPS, SIMS, NR and optical interferometry. PS is enriched at the surface depending on blockcopolymer composition and temperature. A well ordered lamellar structure normal to the surface is found under favourable conditions. Another example is shown in Fig. 6 where the enrichment of poly(paramethylstyrene), PMS(H), in a thin film of a di-... [Pg.381]

Ohya et al. reported poly(ethyleneglycol)-grafted chitosan nanoparticles as peptide drug carriers. The incorporation and release of insulin was dependent on the extent of the reaction of poly(ethyleneglycol) with chitosan [190]. [Pg.175]


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Diacetate ethyleneglycol

EGDN = ethyleneglycol dinitrate

Ether ethyleneglycol

Ethyleneglycol 1,2-Propanediol

Ethyleneglycol bis

Ethyleneglycol diacrylate

Ethyleneglycol dimethacrylate

Ethyleneglycol dimethacrylate EDMA)

Ethyleneglycol dimethyl ether

Ethyleneglycol dinitrate

Ethyleneglycol methacrylate phosphate

Ethyleneglycol molecular structure

Ethyleneglycol monobutyl ether

Ethyleneglycol monomethyl ether

Ethyleneglycol monomethylether

Ethyleneglycol mononitrate

Ethyleneglycol monophenyl ether

Ethyleneglycol polyesters

Ethyleneglycol solutions

Ethyleneglycol, treatment

Ethyleneglycol-functionalized

Formaldehyde-releasing compounds ethyleneglycol-hemiformals)

Glycols ethyleneglycol

Hydrotris(3,5-Dimethyl-l-pyrazolyl)borato oxomolybdenum(V)ethyleneglycolate LMoO(Eth-Gly)

I ethyleneglycol

Tetra-ethyleneglycol diacrylate

Tetra-ethyleneglycol dimethacrylate

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