Category: 112-59-4

Vapor-Liquid Equilibrium for Propylene Glycol + 2-(2-Hexyloxyethoxy)ethanol and 1-Methyl-2-pyrrolidone + 1-Methoxypropan-2-ol was written by Chylinski, Krzysztof;Fras, Zbigniew;Malanowski, Stanislaw K.. And the article was included in Journal of Chemical and Engineering Data in 2004.Synthetic Route of C10H22O3 The following contents are mentioned in the article:

The saturation pressures of propylene glycol at (393 to 423) K, 2-(2-hexyloxyetoxy)ethanol at (402 to 423) K, 1-methyl-2-pyrrolidone at (352 to 378) K, and 1-methoxypropan-2-ol at (347 to 378) K were measured by an ebulliometry method. The vapor-liquid equilibrium (P, T, x, y) was measured by an ebulliometry method for the system propylene glycol + 2-(2-hexyloxyethoxy)ethanol at (403.15, 413.15, and 423.15) K and for the system 1-methyl-2-pyrrolidone + 1-methoxypropan-2-ol at (353.15, 363.15, and 373.15) K. The exptl. vapor pressures were correlated with Antoine and association + equation of state (AEOS) equations, while the VLE was correlated with the AEOS equation of state for all the temperature intervals and with equations representing activity coefficients at specific particular isotherms. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Synthetic Route of C10H22O3).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Synthetic Route of C10H22O3

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Selection of frothers from residual organic reagents for copper-molybdenite sulfide flotation was written by Xia, Y. K.;Peng, F. F.. And the article was included in International Journal of Mineral Processing in 2007.Computed Properties of C10H22O3 The following contents are mentioned in the article:

Evaluation of potential organic frothers for copper-molybdenum sulfide mineral flotation was systematically studied. A frother characterization methodol. including parameters of the frothing system, namely, initial dynamic frothing index and initial dynamic froth collapse rate are used in the anal. of dynamic frothing of the reagent and in selection of potential frothers. Flotation tests using organic reagents as frothers for the ore are conducted to determine the metallurgical performance of the potential frothers. The metallurgical performance of the flotation is also used to confirm the potential frothers selected by using the parameters of the frothing system. The latter can also be used in the formulation of frother mixtures of the reagents to meet the desired frother property. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Computed Properties of C10H22O3).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Computed Properties of C10H22O3

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Microemulsion polymerization of styrene stabilized by sodium dodecyl sulfate and diethylene glycol monoalkyl ether was written by Chern, C. S.;Liu, C. W.. And the article was included in Colloid and Polymer Science in 2000.Recommanded Product: 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

The effects of diethylene glycol monoalkyl ether cosurfactants on the formation of an oil-in-water styrene (ST) microemulsion and the subsequent free radical polymerization were studied. Na dodecyl sulfate was used as the surfactant. The pseudo three-component phase diagram (macroemulsion, microemulsion and lamellar gel phases) was constructed for each cosurfactant. The primary parameters selected for the polymerization study are the concentrations of cosurfactant and styrene. The number of latex particles nucleated is much smaller than that of the microemulsion droplets initially present in the reaction system. Limited flocculation of the latex particles occurs to some extent during polymerization The diethylene glycol monoalkyl ether group tends to enhance the latex stability. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Recommanded Product: 2-(2-(Hexyloxy)ethoxy)ethanol).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Recommanded Product: 2-(2-(Hexyloxy)ethoxy)ethanol

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Liquid-Liquid Equilibria and Partitioning of o-Chlorophenol in Ethylene Glycol Monobutyl Ether + Water, Diethylene Glycol Monohexyl Ether + Water, and Poly(oxyethylene(4)) Lauryl Ether + Water was written by Lee, Hyun-Song;Lee, Huen. And the article was included in Journal of Chemical and Engineering Data in 1996.Electric Literature of C10H22O3 The following contents are mentioned in the article:

Liquid-liquid equilibrium of ethylene glycol monobutyl ether (C₄E₁) + water and diethylene glycol monohexyl ether (C₆E₂) + water at atm. pressure and measured for temperature ranges of 322.8 K and 273.2 K to 382.5 K, resp. The lower critical solution temperature (LCST) and upper critical solution temperature (UCST) of C₄E₁ + water were determined to be 322.8 K and 402.8 K, resp. The LCST of C₆E₂ + water is 273.2 K, while the corresponding UCST does not exist. The equilibrium compositions of o-chlorophenol partitioning in the top and bottom phases of the three binary C₄E₁ + water, C₆E₂ + water, and poly(oxyethylene(4)) lauryl ether (C₁₂E₄) + water mixtures were also measured. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Electric Literature of C10H22O3).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Electric Literature of C10H22O3

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Densities, excess molar volumes, speeds of sound, and isothermal compressibilities for {2-(2-hexyloxyethoxy)ethanol+ n-alkanol} systems at temperatures between (288.15 and 308.15)K was written by Pal, Amalendu;Gaba, Rekha. And the article was included in Journal of Chemical Thermodynamics in 2008.SDS of cas: 112-59-4 The following contents are mentioned in the article:

The densities, ρ and the speeds of sound, u, for {2-(2-hexyloxyethoxy)ethanol (C₆E₂) + methanol, + 1-propanol, + 1-pentanol, and + 1-heptanol} were measured as a function of composition using an Anton-Paar DSA 5000 densimeter at temperatures (288.15, 293.15, 298.15, 303.15, and 308.15) K and atm. pressure over the whole concentration range. The ρ and u values were used to calculate excess molar volumes, V ^E, and excess molar isentropic compressibility, K^E_S,m, resp. Also, thermal expansivity, α, partial molar volume, V i , and partial molar volume of the components at infinite dilution,^–V_i0 , were calculated The variation of these properties with composition and temperature of the mixtures are discussed in terms of mol. interactions. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4SDS of cas: 112-59-4).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.SDS of cas: 112-59-4

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Phase Equilibria on Eight Binary Mixtures was written by Giles, Neil F.;Wilson, Loren C.;Wilson, Grant M.;Wilding, W. Vincent. And the article was included in Journal of Chemical and Engineering Data in 1997.Computed Properties of C10H22O3 The following contents are mentioned in the article:

Vapor-liquid equilibrium are reported for the following five systems at two temperatures each: 2-(2-(hexyloxy)ethoxy)ethanol + 1,2-ethanediol; 2-(hexyloxy)ethanol + 1,2-propanediol; acetone cyanohydrin + acetone; acetone cyanohydrin + hydrogen cyanide; Pr mercaptan + butane. The system pressure and temperature were measured at several charge compositions along a given isotherm for each system. Equilibrium vapor- and liquid-phase compositions were derived from the measured PTx data using the Soave equation of state to represent the vapor phase and the Wilson or the van Laar activity coefficient model to represent the liquid phase. The solubility of oxygen in propylene oxide, nitrogen in propylene oxide, and methane in dichloromethane has been measured at three pressures at each of two or three temperatures This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Computed Properties of C10H22O3).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Computed Properties of C10H22O3

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Effect of chemical formulations for uranium decontamination by chemical gels was written by Jung, Chong-Hun;Choi, Wang-Kyu;Moon, Jei-Kwon. And the article was included in Asian Journal of Chemistry in 2016.Name: 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

A review. The decontamination and rheol. behaviors of chem. gels prepared in a Ce(IV)-HNO₃ or HNO₃ based solution for tile surfaces contaminated with uranium radionuclides were investigated. Gelling agents were prepared by adding PEG-based non-ionic coviscosifiers into a stable pyro Si viscosifier. Dispersion of gelling agents in a Ce(IV)-HNO₃ solution or HNO₃ solution produces a chem. decontamination gel. The order of removal percentage of uranium with various co-viscosifiers was diethylene glycol hexyl ether (DGHE) > tripropylene glycol dodecyl ether (TPGDDE) > tripropylene glycol Bu ether (TPGBE).This is considered to be due to the difference in the length of hydrophobic alkyl chains of coviscosifier and initial activity level of contaminated specimens. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Name: 2-(2-(Hexyloxy)ethoxy)ethanol).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Name: 2-(2-(Hexyloxy)ethoxy)ethanol

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Temperature Dependence of Emulsion Morphologies and the Dispersion Morphology Diagram. 3. Inversion Hysteresis Lines for Emulsions of Middle and Bottom Phases of the System C₆H₁₃(OC₂H₄)₂OH/n-Tetradecane/”Water” was written by Smith, Duane H.;Sampath, Ramanathan;Dadyburjor, Dady B.. And the article was included in Journal of Physical Chemistry in 1996.Reference of 112-59-4 The following contents are mentioned in the article:

The morphologies and phase volume fractions at which inversion occurred for (macro)emulsions formed by the middle-phase microemulsion (M) and water-rich bottom phase (B) were determined by means of elec. conductivity measurements for the amphiphile/oil/”water” system C₆H₁₃(OC₂H₄)₂OH/n-tetradecane/aqueous 10 mM NaCl at temperatures from 25 °C down to 12 °C, near the lower critical end-point temperature (T_lc =10.4 °C). The M/B and B/M morphologies and their inversion hysteresis lines conformed to the previously postulated dispersion morphol. diagram; i.e., within exptl. uncertainties, the two emulsion inversion lines in phase, volume-temperature space met at a “critical point” that coincided with the lower critical end point for the phases. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Reference of 112-59-4).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Reference of 112-59-4

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Frother function-structure relationship: Dependence of CCC95 on HLB and the H-ratio was written by Finch, James A.;Zhang, Wei. And the article was included in Minerals Engineering in 2014.Category: ethers-buliding-blocks The following contents are mentioned in the article:

Although the number and diversity of com. frothers has steadily increased to meet flotation industry demands, frother selection is still mainly empirical. As part of a general structure-property study, the paper presents a correlation between the critical coalescence concentration (CCC95) and H-ratio for surfactants used as flotation frothers. The CCC95 were determined in 0.8 m³ mech. flotation cell. The H-ratio was a substitution of hydrophile-lipophile balance (HLB) and determined through high resolution proton NMR (¹H NMR) spectrometry. A large data set, consisting of 45 surfactants from four frother families, was used to develop the correlation. It is shown that the H-ratio can substitute for HLB. The potential of NMR both to identify the frother family and to derive the H-ratio in predicting CCC95 for com. frothers is discussed. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Category: ethers-buliding-blocks).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Category: ethers-buliding-blocks

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Ether | (C2H5)2O – PubChem

Flotation of carbonaceous copper shale-quartz mixture with poly(ethylene glycol) alkyl ethers was written by Kowalczuk, Przemyslaw B.;Zaleska, Emilia;Danczak, Oliver. And the article was included in Transactions of Nonferrous Metals Society of China in 2015.Safety of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

The influence of different poly(ethylene glycol) alkyl ethers (C_nH_2n+1O(C₂H₄O)_mH, C_nE_m) on flotation of carbonaceous copper shale mixed with quartz as a gangue mineral was investigated. The results show that all of the ethers C₄E₁, C₄E₂, C₄E₃, C₂E₂, C₆E₂ investigated can be used for the flotation of carbonaceous copper shale. The best selectivity of separation in the flotation of the carbonaceous copper shale and quartz mixture is obtained with the C₄E₂ and C₂E₂ ethers. The obtained data can be used for developing separation of organic carbon present in carbonaceous shale at a rougher flotation stage on an industrial scale. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Safety of 2-(2-(Hexyloxy)ethoxy)ethanol).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Safety of 2-(2-(Hexyloxy)ethoxy)ethanol

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Ether – Wikipedia,
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