Komarek, Karel et al. published their research in Scientific Papers of the University of Pardubice, Series A: Faculty of Chemical Technology in 1999 | 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. 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.Computed Properties of C10H22O3

The application of derivatization and retention indices system for identification of alkyl polyethylene glycol ethers by capillary gas chromatography was written by Komarek, Karel;Richter, Pavel. And the article was included in Scientific Papers of the University of Pardubice, Series A: Faculty of Chemical Technology in 1999.Computed Properties of C10H22O3 The following contents are mentioned in the article:

This study deals with the possibility of GC anal. of individual alkylpolyethylene glycol ethers (APEGEs) C4 – C10. The possibilities of derivatization reactions of these substances and the advantages of the derivative preparation are discussed. APEGEs were converted into three types of derivatives: acetates, trifluoroacetates and trimethylsilyl ethers. The retention indexes of individual oligomers of APEGEs and their derivatives for the column temperature programmed linearly were measured. The influence of an increase in the length of the chain in the alkyl or polyoxyethylene glycol part of mol. of non-derivatized APEGEs and their derivatives on the retention indexes was studied. 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. 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.Computed Properties of C10H22O3

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D’Arrigo, G. et al. published their research in European Physical Journal E: Soft Matter in 2003 | 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. 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.Product Details of 112-59-4

Small-angle neutron scattering studies of aqueous solutions of short-chain amphiphiles was written by D’Arrigo, G.;Giordano, R.;Teixeira, J.. And the article was included in European Physical Journal E: Soft Matter in 2003.Product Details of 112-59-4 The following contents are mentioned in the article:

The authors present small angle neutron scattering measurements on binary aqueous solutions of some short-chain amphiphiles (diols, triols, glycols and diglycols) at room temperature The spectra were analyzed in terms of the Teubner-Strey phenomenol. formula which allows to obtain a measure for the amphiphilicity strength of each system (amphiphilicity factor fa). In some systems, however, other models, valid for micellar solutions, give also a good representation of the spectra. As a result, independently of the type of hydrophilic group side (oxydrilic or oxirane), these systems cover the entire accessible amphiphilicity scale (-1 < fa < 1). Some disordered systems (fa > 1) presumably are able to form micelle-like aggregates. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Product Details of 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. 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.Product Details of 112-59-4

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Masaro, L. et al. published their research in Macromolecules in 1999 | 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. 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.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol

Self-Diffusion of End-Capped Oligo(ethylene glycol)s in Poly(vinyl alcohol) Aqueous Solutions and Gels was written by Masaro, L.;Zhu, X. X.. And the article was included in Macromolecules in 1999.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

We have studied the self-diffusion of a series of end-capped ethylene glycol and oligo(ethylene glycol)s in poly(vinyl alc.) aqueous solutions and gels by pulsed-gradient spin echo NMR spectroscopy. The end groups of the diffusants include small flexible groups (Me, Et, hexyl) and bulky rigid groups (tert-Bu and aromatic groups). The effect of the size and geometry of the end groups on the self-diffusion coefficients of the derivatives of ethylene glycol and of oligo(ethylene glycol)s is investigated. The diffusion data are analyzed with several phys. models of diffusion based on different phys. concepts to test their applicabilities. The variation of the parameters used in these diffusion models with the size and geometry of the diffusants is also discussed. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Quality Control 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. 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.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol

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Kowalczuk, Przemyslaw B. et al. published their research in Separation Science and Technology in 2018 | 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. 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.Recommanded Product: 112-59-4

Facile determination of foamability index of non-ionic and cationic frothers and its effect on flotation of quartz was written by Kowalczuk, Przemyslaw B.;Siedlarz, Marta;Szczerkowska, Sabina;Wojcik, Marta. And the article was included in Separation Science and Technology in 2018.Recommanded Product: 112-59-4 The following contents are mentioned in the article:

In this work, a facile method for determination of foaming properties of frothers was used. It was based on measuring the foam height in a flotation machine at different concentrations of frothers. Based on the foam height-concentration curve, a new foaming parameter, so-called concentration at half of the maximum foam height CMH, was proposed. Assessment and usefulness of CMH were shown in flotation of quartz. The concentration of amine at the critical contact angle CCA, at which amine starts to be a collector, was also determined The determined values of CCA were similar to CMH and were equal to 1.3, 0.14 and 0.03 mM for ButNH2, HexNH2 and OctNH2, resp. The values of CMH and CCA depended on the alkyl chain of frothers. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Recommanded Product: 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. 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.Recommanded Product: 112-59-4

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Mitrinovic, Dragoslav M. et al. published their research in Physical Review E: Statistical, Nonlinear, and Soft Matter Physics in 2001 | CAS: 112-59-4

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. Polyesters are important plastics, with monomers linked by ester moieties. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Synthetic Route of C10H22O3

X-ray study of oil-microemulsion and oil-water interfaces in ternary amphiphilic systems was written by Mitrinovic, Dragoslav M.;Williams, Scott M.;Schlossman, Mark L.. And the article was included in Physical Review E: Statistical, Nonlinear, and Soft Matter Physics in 2001.Synthetic Route of C10H22O3 The following contents are mentioned in the article:

X-ray reflectivity and diffuse scattering measurements are presented from the interfaces between oil-rich and microemulsion bulk phases and between oil-rich and water-rich phases in three-component microemulsion systems (consisting of water, alkane, and CiEj, where the last represents n-alkyl polyglycol ether with i = 4,6,10 and j = 1,2,4). The x-ray measurements are analyzed with a two-parameter fit that determines the interfacial roughness, varying from 25-160 Å, and the interfacial tension, varying from 1.4-0.03 mN/m, for these samples. Although a nonmonotonic profile at the oil-microemulsion interface is not observed, these measurements exclude the presence of oscillating profiles with repeat distances >500 Å. 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. 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. Polyesters are important plastics, with monomers linked by ester moieties. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Synthetic Route of C10H22O3

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Ether – Wikipedia,
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Cheng, Chi-Wen et al. published their research in Chemical Physics Letters in 2012 | CAS: 112-59-4

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. Polyesters are important plastics, with monomers linked by ester moieties. 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.Related Products of 112-59-4

Study of the reactive excited-state dynamics of delipidated bacteriorhodopsin upon surfactant treatments was written by Cheng, Chi-Wen;Lee, Yuan-Pern;Chu, Li-Kang. And the article was included in Chemical Physics Letters in 2012.Related Products of 112-59-4 The following contents are mentioned in the article:

The dynamics of the reactive excited-state of bacteriorhodopsin treated with various surfactants have been investigated through the measurement of pump-probe absorption spectra. Upon excitation of bR at 570 nm in the presence of ionic surfactants CTAB and SDS, the lifetime of the reactive excited-state of the all-trans protonated Schiff base, probed at 460 nm, was observed to increase up to 20%, whereas an insignificant change was observed upon addition of neutral surfactant C6E2. Measurements of steady-state absorption spectra, fluorescence, and CD indicated that the bR suspensions retain their trimeric configuration with partial delipidation. This removal of lipids causes a structural alteration and the varied excited-state dynamics. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Related Products of 112-59-4).

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. Polyesters are important plastics, with monomers linked by ester moieties. 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.Related Products of 112-59-4

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Ether – Wikipedia,
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Keefe, Melinda et al. published their research in CoatingsTech in 2011 | 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. 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.Name: 2-(2-(Hexyloxy)ethoxy)ethanol

Art and industry: novel approaches to the evaluation and development of cleaning systems for artists’ acrylic latex paints was written by Keefe, Melinda;Tucker, Christopher;Behr, Anastasia Mardilovich;Meyers, Greg;Reinhardt, Carl;Boomgaard, Tom;Peitsch, Cory;Ormsby, Bronwyn;Soldano, Alexia;Phenix, Alan;Learner, Thomas. And the article was included in CoatingsTech in 2011.Name: 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

A method has been developed to quantify and differentiate the cleaning efficacies of traditional and novel aqueous, aliphatic hydrocarbon solvent, and water-in-oil microemulsion-based cleaning systems using high throughput tools and methodol. Cleaning solutions with good cleaning efficacy were identified from all three classes of formulations by screening hundreds of formulations on the high throughput tools. 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 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. 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.Name: 2-(2-(Hexyloxy)ethoxy)ethanol

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Ether – Wikipedia,
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Frail, Paul R. et al. published their research in Chemistry of Materials 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. 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.Related Products of 112-59-4

Modulation of Dark Conductivity over a 1 × 10-12 to 1 × 10-5 S/cm Range Through Ancillary Group Modification in Amorphous Solids of Ethyne-Bridged (Porphinato)zinc(II) Oligomers was written by Frail, Paul R.;Susumu, Kimihiro;Huynh, Michael;Fong, Jennie;Kikkawa, J. M.;Therien, Michael J.. And the article was included in Chemistry of Materials in 2007.Related Products of 112-59-4 The following contents are mentioned in the article:

2- And 4-probe dark conductivity (DC) data obtained for thin-film and solid-state samples of undoped PZnn oligomers show that the measured DCs for these species span an impressively wide range. Sterically unencumbered PZnn oligomers enable augmented interchain electronic coupling in the solid state and provide electronically functional thin films via direct spin-casting. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Related Products 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. 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.Related Products of 112-59-4

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

Piekarski, H. et al. published their research in Journal of Thermal Analysis and Calorimetry in 2005 | 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. 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.Electric Literature of C10H22O3

Heat capacity of aqueous 2-(2-hexyloxyethoxy)ethanol solutions by DSC. Application of two-point scaling to pseudophases coexistence was written by Piekarski, H.;Tkaczyk, M.;Wasiak, M.. And the article was included in Journal of Thermal Analysis and Calorimetry in 2005.Electric Literature of C10H22O3 The following contents are mentioned in the article:

The sp. heat capacities of aqueous solutions of 2-(hexyloxyethoxy)ethanol have been measured from 2 to 55°C within the whole available composition range by DSC. Changes of specific, partial, and apparent molar heat capacities of investigated system were analyzed and considered as an effect of structural transformations. The two-point scaling theory was applied to the description of the binary mixtures properties in the pseudo-phase coexistence region. 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. 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. 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.Electric Literature of C10H22O3

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Ether – Wikipedia,
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Mathieu, Didier et al. published their research in Industrial & Engineering Chemistry Research in 2013 | 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.COA of Formula: C10H22O3

Power Law Expressions for Predicting Lower and Upper Flammability Limit Temperatures was written by Mathieu, Didier. And the article was included in Industrial & Engineering Chemistry Research in 2013.COA of Formula: C10H22O3 The following contents are mentioned in the article:

By analogy with recent models for flash point, the lower and upper flammability limit temperatures of organic compounds are represented as power law expressions in terms of fragment contributions. The predictive value of the resulting models compares well with recently published methods. A major advantage of the present approach is the fact it provides better insight into the relations between flammability limit temperatures and mol. structure. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4COA of Formula: 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.COA of Formula: C10H22O3

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