Category: 112-59-4

A self-diffusion study of poly(ethylene-oxide) alkyl alcohols was written by Ambrosone, L.;Costantino, L.;D’Errico, G.;Vitagliano, V.. And the article was included in Journal of Solution Chemistry in 1997.Synthetic Route of C10H22O3 The following contents are mentioned in the article:

The self-diffusion coefficients of HDO and some surfactants in aqueous mixtures at different concentrations, below the critical micelle concentration, have been determined by means of the NMR, spin-echo pulsed field gradient method. The surfactant solutes chosen were ethylene glycol-pentyl alc., diethylene glycol-pentyl alc., ethylene glycol-hexyl alc., diethylene glycol-hexyl alc., triethylene glycol-hexyl alc., tetraethylene glycol-hexyl alc., pentaethylene glycol-hexyl alc. The interactions in solution are studied by analyzing the solute self-diffusion coefficients extrapolated to infinite dilution These values are compared with those of 1-alkanols. The slope of the self diffusion coefficients vs. the solute concentration are correlated with the microscopic friction coefficients A model for interpreting the exptl. data is suggested. 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 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 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. Synthetic Route of C10H22O3

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

Liquid-Liquid Equilibrium Phase Diagram and Density of Three Water + Nonionic Surfactant C_iE_j Binary Systems was written by Lai, Hsuan-Hong;Chen, Li-Jen. And the article was included in Journal of Chemical and Engineering Data in 1999.Application In Synthesis of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

Liquid-liquid equilibrium and d. data for three binary systems, water + C₆E₂, water + C₆E₃, and water + C₇E₃, ranging from their lower critical consolute solution temperature to 70 °C at atm. pressure are presented in this paper. (C_iE_j is the abbreviation of nonionic surfactant CH₃(CH₂)_i-1(OCH₂CH₂)_jOH). The exptl. results were correlated with the UNIQUAC model by fitting the UNIQUAC interaction parameters as a function of temperature Agreement between the calculated and exptl. data was excellent for all three systems. The lower critical consolute solution temperature, critical weight fraction, and critical d. were estimated by fitting the exptl. data to the critical scaling law. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Application In Synthesis 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. 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.Application In Synthesis of 2-(2-(Hexyloxy)ethoxy)ethanol

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Ether – Wikipedia,
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Surface structure and volatile characteristic of peanut proteins obtained through AOT reverse micelles was written by Zhao, Xiaoyan;Liu, Hongkai;Zhang, Xiaowei;Zhu, Haitao;Ao, Qiang. And the article was included in Colloids and Surfaces, B: Biointerfaces in 2019.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

This study provided the investigation of the surface structure and volatile compounds of peanut proteins obtained through aqueous buffer (AB) and reverse micelles (RMs) by X-ray diffraction (XRD), SEM (SEM), XPS and gas chromatog.-mass spectrometry (GC-MS). The results showed that RMs could modify the amorphous structure of peanut proteins and change the original structure. Significant differences were between the C, O, and N content in two type protein surfaces (P < 0.05). The O/C ratio from AB was higher than from RMs, but the N/C ratio was lower. These changes suggested that RMs could modify the surface morphol. and composition of peanut proteins. Untargeted profiling of volatile compounds showed that the volatile compounds of peanut proteins obtained by AB and RMs were major differences. Such finding suggested that RMs could contribute to improve the flavor properties of peanut protein. 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. 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.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol

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Nonionic microemulsions with chlorinated hydrocarbons for catalysis was written by Egger, H.;Sottmann, T.;Strey, R.;Valero, C.;Berkessel, A.. And the article was included in Tenside, Surfactants, Detergents in 2002.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

N-alkyl glycosides were found capable of solubilizing chlorinated oils into microemulsions. Interestingly, the ternary systems with such polar oils frequently used in organic syntheses show a temperature-dependent phase inversion within the exptl. window, which is absent with n-alkanes as the oil component. For comparison, the usefulness of the well-known class of n-alkyl polyglycol ethers is also examined The investigations show important differences in phase behavior, depending on whether the “hydrophobicity” of the oil is changed by altering the hydrocarbon chain length or the polarity. In addition, our studies reveal variations in the Krafft boundary of the glyco-surfactant systems using different chlorinated hydrocarbons. In a set of preliminary reaction experiments in these ternary micro-emulsions, the epoxidation of olefins with manganese dihydrosalen catalysts is 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 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 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. Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol

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

Aqueous solution behavior of cationic surfactant modulated by the presence of glycols and their ethers was written by Chavda, Suresh;Singh, Kulbir;Marangoni, D. Gerrard;Bahadur, Pratap. And the article was included in Bulletin of the Chemical Society of Japan in 2012.Electric Literature of C10H22O3 The following contents are mentioned in the article:

The effect of ethylene glycol (EG), diethylene glycol (DEG) and their monoalkyl (C₁-C₆) ethers (cellosolves and carbitols) and di-Me ethers (glymes and diglymes) on the micellar behavior of a cationic surfactant tetradecyltrimethylammonium bromide (TTAB) in aqueous solution was examined from elec. conductivity measurements. The effect of these additives on critical micelle concentration (CMC) and degree of counter ion dissociation (α) is evaluated. While both EG, DEG, their monomethyl/monoethyl ethers and di-Me ethers increased CMC and α, for monobutyl and monohexyl ethers a decrease in CMC was noticed at studied concentration For all ethers, the α values increased with concentration NOESY experiments confirmed the location of glycol ethers in micellar solution The results are discussed in terms of effect of ethers on water structure and solvent properties. 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. 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. Electric Literature of C10H22O3

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Ether – Wikipedia,
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Antiproliferative properties of Papaver rhoeas ovule extracts and derived fractions tested on HL60 leukemia human cells was written by Ovidi, Elisa;Masci, Valentina Laghezza;Garzoli, Stefania;Gambellini, Gabriella;Keita, Saran Vittoria;Zago, Daniele;Turchetti, Giovanni;Modesti, Lorenzo;Tiezzi, Antonio. And the article was included in Molecules in 2020.Computed Properties of C10H22O3 The following contents are mentioned in the article:

Papaver rhoeas plant is common in many regions worldwide and contributes to the landscape with its red flower. In the present study we first carried out morphol. investigation by optical and SEM of the ovules within the ovary. After ovules’ isolation we prepared extracts to test possible cytotoxic activities on HL60 leukemia human cells and investigated the extracts using thin-layer chromatog. (TLC) and gas-chromatog./mass spectrometry (GC-MS). P. rhoeas ovules showed an elongated, round shape and the presence of ordered sculptures on the ovule surface. The ovule extracts showed cytotoxic activity on HL60 human cells mainly found in some TLC-isolated spots. Compounds consisting of active spots were identified by GC-MS investigations. Our findings on the P. rhoeas ovule compounds open perspectives for further investigations of TLC-isolated spots on other human cancer cell lines. 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. 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.Computed Properties of C10H22O3

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Predicting Flash Points of Pure Compounds and Mixtures with COSMO-RS was written by Reinisch, Jens;Klamt, Andreas. And the article was included in Industrial & Engineering Chemistry Research in 2015.Related Products of 112-59-4 The following contents are mentioned in the article:

Flash point (FP) is an important parameter to assess chem. compound safety. Many empirical approaches have been developed to predict FP based on mol. structure, sometimes involving a large number of descriptors and resulting in class-specific equations. This work demonstrated that a satisfying, rather general prediction of saturation pressure at the FP can be achieved using only mol. surface area. This relation in conjunction with any exptl. or computational method to calculate temperature-dependent vapor pressures allows for the FP predictions. In a second step, chem. mixture FP were calculated using COSMO-RS activity coefficients Using the proposed method, FP were calculated without needing data typically generated in experiments (normal b.p., combustion enthalpy), although exptl. pure-compound FP and vapor pressure data can still be used to increase prediction quality. 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. 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.Related Products of 112-59-4

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Thermophysical and bionotox properties of solvo-surfactants based on ethylene oxide, propylene oxide and glycerol was written by Queste, Sebastien;Michina, Youlia;Dewilde, Anny;Neueder, Roland;Kunz, Werner;Aubry, Jean-Marie. And the article was included in Green Chemistry in 2007.Application In Synthesis of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

Thermophys. and bionotox properties of a new class of natural solvo-surfactants, glycerol 1-monoethers, were investigated in comparison with widespread but harmful glycol ethers. Vapor pressures and heats of vaporization were measured between 25 °C and 50 °C, and calculated thanks to two group contribution methods. Evaporation rates and Hansen parameters, evaluated from TGA measurements and group contributions resp., were compared as well. Bionotox properties, i.e. cytotoxicity, irritating power and biodegradability, were evaluated exptl. Glycerol 1-monoethers turned out to be less volatile than glycol derivatives, but contrary to the latter they will not be considered as VOCs. Toxicities and irritating powers are equivalent and increase with increasing alkyl chain length, i.e. with increasing amphiphilicity. Glycerol ethers are degradable at lower concentrations compared to glycol compounds, which is related to their higher interfacial activity. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Application In Synthesis 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. 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.Application In Synthesis of 2-(2-(Hexyloxy)ethoxy)ethanol

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

The effect of glycols and their ethers on micellar behavior of cetyltrimethylammonium tosylate was written by Padasala, Shailesh;Chavda, S.;Ray, Debes;Aswal, Vinod K.;Bahadur, Pratap. And the article was included in Journal of Molecular Liquids in 2017.Category: ethers-buliding-blocks The following contents are mentioned in the article:

The effect of glycols viz., ethylene glycol (EG), diethylene glycol (DEG) propylene glycol (PG), dipropylene glycol (DPG) and their monoalkyl ethers on the morphol. features of cetyltrimethylammonium tosylate (CTAT) micelle was examined from viscosity and small angle neutron scattering (SANS) measurements. EG and DEG, and their short chain ethers showed an initial increase in viscosity followed by a decrease while long chain PG, DPG and their ethers showed a monotonous decrease in viscosity. SANS results support the viscosity behavior. These trends are explained on the basis of hydrophobicity of the additives that determines its location in the micelle exerting an effect on micelle morphol. The critical micelle concentrations (CMCs) of CTAT determined tensiometrically for selected systems are also reported. This study helps in fine tuning of rheol. of micellar systems in the presence of gycols and their ethers often used with surfactant systems. 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, 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.Category: ethers-buliding-blocks

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

Alkyl polyglucosides as hydrotropes was written by Matero, Anna;Mattsson, Asa;Svensson, Martin. And the article was included in Journal of Surfactants and Detergents in 1998.Name: 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

The hydrotropic effect of different alkyl polyglucosides (APG) was studied and compared with a model hydrotrope, toluol-4-sulfonic acid. The effect was assessed by 2 different methods: (i) as the cloud point elevation of a solution containing different nonionic surfactants upon addition of the hydrotrope and (ii) the destabilization of liquid crystalline phases in a ternary system. The effect of the hydrophobic alkyl group length was opposite in the 2 methods. APG with intermediate alkyl chain lengths (octyl and decyl) was very effective in elevating the cloud point, while APG with a short (butyl) group was the most efficient in destabilizing liquid crystalline phases in the system of water, sodium dodecyl sulfate and pentanol. Effects on phase behavior and cloud point elevation with addition of an APG are highly dependent on its structure. However, the correlation between structural effects as observed in the 2 methods requires further study. 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. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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.Name: 2-(2-(Hexyloxy)ethoxy)ethanol

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Ether – Wikipedia,
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