Tag: 100-200

Leick, Noemi et al. published their research in Dalton Transactions in 2022 | CAS: 112-49-2

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Ether is less polar than esters, alcohols or amines because of the oxygen atom that is unable to participate in hydrogen bonding due to the presence of bulky alkyl groups on both sides of the oxygen atom. But ether is more polar than alkenes. The unique properties of ethers (i.e., that they are strongly polar, with nonbonding electron pairs but no hydroxyl group) enhance the formation and use of many reagents. For example, Grignard reagents cannot form unless an ether is present to share its lone pair of electrons with the magnesium atom. Complexation of the magnesium atom stabilizes the Grignard reagent and helps to keep it in solution.Electric Literature of C8H18O4

Thermal stability and structural studies on the mixtures of Mg(BH4)2 and glymes was written by Leick, Noemi;Tran, Ba L.;Bowden, Mark E.;Gennett, Thomas;Autrey, Tom. And the article was included in Dalton Transactions in 2022.Electric Literature of C8H18O4 This article mentions the following:

Coordination complexes of Mg(BH4)2 are of interest for energy storage, ranging from hydrogen storage in BH4 to electrochem. storage in Mg based batteries. Understanding the stability of these complexes is crucial since storage materials are expected to undergo multiple charging and discharging cycles. To do so, we examined the thermal stabilities of the 1 : 1 mixtures of Mg(BH4)2 with different glymes by DSC-TGA, TPD-MS and powder XRD anal. Despite their structural similarities, these mixtures show diverse phase transitions, speciations and decomposition pathways as a function of linker length. In the experiment, the researchers used many compounds, for example, 2,5,8,11-Tetraoxadodecane (cas: 112-49-2Electric Literature of C8H18O4).

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Ether is less polar than esters, alcohols or amines because of the oxygen atom that is unable to participate in hydrogen bonding due to the presence of bulky alkyl groups on both sides of the oxygen atom. But ether is more polar than alkenes. The unique properties of ethers (i.e., that they are strongly polar, with nonbonding electron pairs but no hydroxyl group) enhance the formation and use of many reagents. For example, Grignard reagents cannot form unless an ether is present to share its lone pair of electrons with the magnesium atom. Complexation of the magnesium atom stabilizes the Grignard reagent and helps to keep it in solution.Electric Literature of C8H18O4

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Costero, Ana M. et al. published their research in Chemistry – An Asian Journal in 2010 | CAS: 5367-32-8

3-Methyl-4-nitroanisole (cas: 5367-32-8) belongs to ethers. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.COA of Formula: C8H9NO3

Chromo-Fluorogenic Detection of Nerve-Agent Mimics Using Triggered Cyclization Reactions in Push-Pull Dyes was written by Costero, Ana M.;Parra, Margarita;Gil, Salvador;Gotor, Raul;Mancini, Pedro M. E.;Martinez-Manez, Ramon;Sancenon, Felix;Royo, Santiago. And the article was included in Chemistry – An Asian Journal in 2010.COA of Formula: C8H9NO3 This article mentions the following:

A family of azo and stilbene derivatives (1-9) are synthesized, and their chromo-fluorogenic behavior in the presence of nerve-agent simulants, diethylchlorophosphate (DCP), diisopropylfluorophosphate (DFP), and diethylcyanophosphate (DCNP) in acetonitrile and mixed solution of water/acetonitrile (3:1 volume/volume) buffered at pH 5.6 with MES, is investigated. The prepared compounds contain 2-(2-N,N-dimethylaminophenyl)ethanol or 2-[(2-N,N-dimethylamino)phenoxy]ethanol reactive groups, which are part of the conjugated π-system of the dyes and are able to give acylation reactions with phosphonate substrates followed by a rapid intramol. N-alkylation. The nerve-agent mimic-triggered cyclization reaction transforms a dimethylamino group into a quaternary ammonium, inducing a change of the electronic properties of the delocalized systems that results in a hypsochromic shift of the absorption band of the dyes. Similar reactivity studies are also carried out with other “non-toxic” organophosphorus compounds, but no changes in the UV/Vis spectra were observed The emission behavior of the reagents in acetonitrile and water-acetonitrile 3:1 volume/volume mixtures is also studied in the presence of nerve-agent simulants and other organophosphorous derivatives The reactivity between 1-9 and DCP, DCNP, or DFP in buffered water-acetonitrile 3:1 volume/volume solutions under pseudo first-order kinetic conditions, using an excess of the corresponding simulant, are studied in order to determine the rate constants (k) and the half-life times (t1/2 = ln2/k) for the reaction. The detection limits in water/acetonitrile 3:1 volume/volume are also determined for 1-9 and DCP, DCNP, and DFP. Finally, the chromogenic detection of nerve agent simulants both in solution and in gas phase are tested using silica gel containing adsorbed compounds 1, 2, 3, 4, or 5 with fine results. In the experiment, the researchers used many compounds, for example, 3-Methyl-4-nitroanisole (cas: 5367-32-8COA of Formula: C8H9NO3).

3-Methyl-4-nitroanisole (cas: 5367-32-8) belongs to ethers. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.COA of Formula: C8H9NO3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Galkin, Maxim V. et al. published their research in ChemCatChem in 2014 | CAS: 3929-47-3

3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.Product Details of 3929-47-3

Mild Heterogeneous Palladium-Catalyzed Cleavage of β-O-4′-Ether Linkages of Lignin Model Compounds and Native Lignin in Air was written by Galkin, Maxim V.;Sawadjoon, Supaporn;Rohde, Volker;Dawange, Monali;Samec, Joseph S. M.. And the article was included in ChemCatChem in 2014.Product Details of 3929-47-3 This article mentions the following:

A mild and robust heterogeneous palladium-catalyzed C-O bond cleavage of 2-aryloxy-1-arylethanols using formic acid as reducing agent in air was developed. The cleaved products were isolated in 92-98% yield; and by slightly varying the reaction conditions, a ketone, an alc., or an alkane can be generated in near-quant. yield. This reaction is applicable to cleaving the β-O-4′-ether bond found in lignin polymers of different origin. The reaction was performed on a lignin polymer model to generate either the monomeric aryl ketone or alkane in a quant. yield. Moderate depolymerization was achieved with native lignin at similar reaction conditions. Mechanistic studies under kinetic control indicate that an initial palladium-catalyzed dehydrogenation of the alc. is followed by insertion of palladium to an enol equivalent A palladium-formato complex reductively cleaves the palladium-enolate complex to generate the ketone. In the experiment, the researchers used many compounds, for example, 3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3Product Details of 3929-47-3).

3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.Product Details of 3929-47-3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Hahn, Nathan T. et al. published their research in ACS Applied Energy Materials in 2020 | CAS: 112-49-2

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. Ethyl ether is an excellent solvent for extractions and for a wide variety of chemical reactions. It is also used as a volatile starting fluid for diesel engines and gasoline engines in cold weather. Dimethyl ether is used as a spray propellant and refrigerant. Methyl t-butyl ether (MTBE) is a gasoline additive that boosts the octane number and reduces the amount of nitrogen-oxide pollutants in the exhaust. The ethers of ethylene glycol are used as solvents and plasticizers.Formula: C8H18O4

Influence of Ether Solvent and Anion Coordination on Electrochemical Behavior in Calcium Battery Electrolytes was written by Hahn, Nathan T.;Driscoll, Darren M.;Yu, Zhou;Sterbinsky, George E.;Cheng, Lei;Balasubramanian, Mahalingam;Zavadil, Kevin R.. And the article was included in ACS Applied Energy Materials in 2020.Formula: C8H18O4 This article mentions the following:

The emergence of magnesium and calcium batteries as potential beyond Li ion energy storage technologies has generated significant interest into the fundamental aspects of alk. earth metal cation coordination in multivalent electrolytes and the impact of coordination on application-critical electrolyte properties such as solubility, transport, and electrochem. stability. Understanding these details in calcium electrolytes is of immediate importance due to recent, unprecedented demonstrations of reversible calcium metal electrodeposition in a limited number of ethereal solvent-based systems. In this work, we provide insight connecting Ca2+ coordination tendencies to important calcium battery electrolyte properties. Our results demonstrate a clear solvent:Ca2+ coordination strength trend across a series of cyclic ether and linear glyme solvents that controls the extent of ion association in solutions of “weakly” coordinating salts. We apply understanding gained from these results to rationalize relative anion:Ca2+ coordination tendencies and attendant Ca2+ coordination structures using two oxidatively stable anions of particular interest for current battery electrolytes. Armed with this understanding of solvent and anion interactions with Ca2+, we demonstrate and interpret differences in electrochem. calcium deposition behavior across several electrolyte exemplars with varying solvent and anion coordination strengths. Our findings demonstrate that solvents exhibiting especially strong coordination to Ca2+, such as triglyme, can inhibit reversible calcium deposition despite effective elimination of anion:Ca2+ coordination while solvents exhibiting more modest coordination strength, such as 1,2-dimethoxyethane, may enable deposition provided anion:Ca2+ coordination is substantially limited. These results reveal that the strength of coordination of both anion and solvent should be considered in the design of electrolytes for calcium batteries. In the experiment, the researchers used many compounds, for example, 2,5,8,11-Tetraoxadodecane (cas: 112-49-2Formula: C8H18O4).

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. Ethyl ether is an excellent solvent for extractions and for a wide variety of chemical reactions. It is also used as a volatile starting fluid for diesel engines and gasoline engines in cold weather. Dimethyl ether is used as a spray propellant and refrigerant. Methyl t-butyl ether (MTBE) is a gasoline additive that boosts the octane number and reduces the amount of nitrogen-oxide pollutants in the exhaust. The ethers of ethylene glycol are used as solvents and plasticizers.Formula: C8H18O4

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Chylinski, Krzysztof et al. published their research in Journal of Chemical and Engineering Data in 2004 | CAS: 112-59-4

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

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

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Xia, Y. K. et al. published their research in International Journal of Mineral Processing in 2007 | CAS: 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. 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

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

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Chern, C. S. et al. published their research in Colloid and Polymer Science in 2000 | CAS: 112-59-4

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

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

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Lee, Hyun-Song et al. published their research in Journal of Chemical and Engineering Data in 1996 | CAS: 112-59-4

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

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

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Pal, Amalendu et al. published their research in Journal of Chemical Thermodynamics in 2008 | 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

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, KES,m, resp. Also, thermal expansivity, α, partial molar volume, V i , and partial molar volume of the components at infinite dilution,–Vi0 , 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

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Giles, Neil F. et al. published their research in Journal of Chemical and Engineering Data in 1997 | CAS: 112-59-4

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

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

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem