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

Wilding, W. V. et al. published their research in International DATA Series in 2003 | 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. 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-vapor equilibrium. 1,2-Ethanediol – 2-(2-hexyloxy)ethoxy)ethanol system was written by Wilding, W. V.. And the article was included in International DATA Series in 2003.Electric Literature of C10H22O3 The following contents are mentioned in the article:

The vapor pressures and the mole fractions of ethanediol in the liquid and in the vapor phase were calculated for the binary system 1,2-ethanediol/2-(2-hexyloxy)ethoxyethanol at T = 373.15 and 453.15 K. The data were reduced using the Wilson equation for the partial molar excess Gibbs energies. The standard deviations and azeotropic data are also given. 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 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. 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

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

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

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

Kamaura, Masahiro et al. published their research in Kidorui in 1998 | 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. 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.HPLC of Formula: 112-59-4

Preparation and catalytic activity of novel water-tolerant lanthanoid alkoxide complexes was written by Kamaura, Masahiro;Daikai, Kazuhiro;Hanamoto, Takeshi;Inanaga, Junji. And the article was included in Kidorui in 1998.HPLC of Formula: 112-59-4 The following contents are mentioned in the article:

We prepared novel water-resistant lanthanoid-lithium mixed alkoxide complexes by utilizing the high coordination number of lanthanoid ions in combination with polydentate ligands. The complexes are stable and effectively catalyze the Robinson-type reaction of 2-butanone with chalcone even in the presence of water (60 equiv to the catalyst). The terbium-lithium complex of polyethylene glycol was the most effective catalyst to the above reaction. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4HPLC of Formula: 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. 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.HPLC of Formula: 112-59-4

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

Gharagheizi, Farhad et al. published their research in Journal of Hazardous Materials in 2009 | 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.Name: 2-(2-(Hexyloxy)ethoxy)ethanol

Prediction of upper flammability limit percent of pure compounds from their molecular structures was written by Gharagheizi, Farhad. And the article was included in Journal of Hazardous Materials in 2009.Name: 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

In this study, a quant. structure-property relationship (QSPR) is presented to predict the upper flammability limit percent (UFLP) of pure compounds The obtained model is a five parameters multi-linear equation. The parameters of the model are calculated only from chem. structure. The average absolute error and squared correlation coefficient of the obtained model over all 865 pure compounds used to develop the model are 9.7%, and 0.92, resp. 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. 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.Name: 2-(2-(Hexyloxy)ethoxy)ethanol

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

Lim, Kyung-Hee et al. published their research in Colloids and Surfaces, A: Physicochemical and Engineering Aspects in 2005 | 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.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol

Temperature dependence of emulsion morphologies and the dispersion morphology diagram: Two-phase emulsions of the system C6H13(OC2H4)2OH/n-tetradecane/”water” was written by Lim, Kyung-Hee;Zhang, Wu;Smith, Gwynedd A.;Smith, Duane H.. And the article was included in Colloids and Surfaces, A: Physicochemical and Engineering Aspects in 2005.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

Using several different two-phase compositions of the pseudoternary amphiphile/oil/”water” system C6H13(OC2H4)2OH/n-tetradecane/aqueous 10 mM NaCl, it is shown by elec. conductometry that the temperature dependencies of the emulsion morphologies were consistent with predictions from the dispersion morphol. diagram, thus contradicting the phase inversion temperature (PIT) concept. 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. 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.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol

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

Finlay, Heather J. et al. published their research in Bioorganic & Medicinal Chemistry Letters in 2008 | CAS: 140715-61-3

N-(3-Methoxybenzyl)ethanamine (cas: 140715-61-3) 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. 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.Quality Control of N-(3-Methoxybenzyl)ethanamine

Pyrano-[2,3b]-pyridines as potassium channel antagonists was written by Finlay, Heather J.;Lloyd, John;Nyman, Michael;Conder, Mary Lee;West, Tonya;Levesque, Paul;Atwal, Karnail. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2008.Quality Control of N-(3-Methoxybenzyl)ethanamine The following contents are mentioned in the article:

The design and synthesis of a series of highly functionalized pyrano[2,3-b]pyridines is described. These compounds were assayed for their ability to block the IKur channel encoded by the gene hKV1.5 in patch-clamped L-929 cells. Six of the compounds in this series showed sub-micromolar activity, the most potent being 4-(4-ethylbenzenesulfonylamino)-3-hydroxy-2,2-dimethyl-3,4-dihydro-2H-pyrano[2,3-b]pyridine-6-carboxylic acid N-ethyl-N-phenylamide with an IC50 of 378 nM. This study involved multiple reactions and reactants, such as N-(3-Methoxybenzyl)ethanamine (cas: 140715-61-3Quality Control of N-(3-Methoxybenzyl)ethanamine).

N-(3-Methoxybenzyl)ethanamine (cas: 140715-61-3) 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. 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.Quality Control of N-(3-Methoxybenzyl)ethanamine

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

von Bergen, R. et al. published their research in Fluid Phase Equilibria in 1998 | 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. 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.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol

A lattice fluid approach to the concept of hydrophile lipophile balance: alkylethoxylated surfactants was written by von Bergen, R.;Rogel, E.. And the article was included in Fluid Phase Equilibria in 1998.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

The relation between hydrophile lipophile balance (HLB) and the parameters of a lattice fluid equation of state (Sanchez-Lacombe) are studied. The observed linear relation between the characteristic pressure (P*) and the HLB number, probably results from the fact that both parameters are connected to the cohesive energy d. (CED). The relation between the HLB number and the number of lattice sites occupied by the alkylethoxylated surfactants in the lattice fluid model are also studied. 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 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. 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.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol

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

Wang, Min et al. published their research in ACS Catalysis in 2018 | CAS: 2380-78-1

4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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. Related Products of 2380-78-1

Dealkylation of Lignin to Phenol via Oxidation-Hydrogenation Strategy was written by Wang, Min;Liu, Meijiang;Li, Hongji;Zhao, Zhitong;Zhang, Xiaochen;Wang, Feng. And the article was included in ACS Catalysis in 2018.Related Products of 2380-78-1 The following contents are mentioned in the article:

Lignin is a renewable and abundant aromatic polymer found in plants. We herein propose a “cutting tail” methodol. to produce phenol from lignin, which is achieved by combining Ru/CeO2 catalyst and CuCl2 oxidant via an oxidation-hydrogenation route. Phenol was obtained from separated poplar lignin with 13 wt % yield. Even raw biomass, such as poplar, birch, pine, peanut, bamboo willow, and straw, could be converted into phenol in 1-33 mg per g of biomass. This study involved multiple reactions and reactants, such as 4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1Related Products of 2380-78-1).

4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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. Related Products of 2380-78-1

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