Category: 112-59-4

Combinatorial libraries of diamidopyridine-derived ‘tweezer’ receptors and sequence selective binding of peptides was written by Arienzo, Rosa;Kilburn, Jeremy D.. And the article was included in Tetrahedron in 2002.Related Products of 112-59-4 The following contents are mentioned in the article:

A library of diamidopyridine derived tweezer receptors with peptidic side-arms has been prepared Screening experiments with the library and a dye-labeled tripeptide L-Glu-L-Ser-L-Val-OH showed excellent selectivity (strong binding of the dye-labeled guest to ∼0.2% of resin-bound library members was observed) and led to the identification of a tweezer receptor structure, which was shown to bind the tripeptide with good selectivity over related tripeptide sequences. Analogous screening experiments with the side-chain protected tripeptide L-Glu(O^tBu)-L-Ser(^tBu)-L-Val-OH, showed little selectivity for any particular library member. The results are discussed in relation to previous screening experiments, using the same tripeptide guests, with related tweezer receptor libraries, which differ by one methylene in the separation of the diamidopyridine unit from the peptidic side-arms of the tweezer receptors. 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 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. 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

Study on the change of aroma compounds in hops with different drying methods was written by Xia, Na;Reyanggu, Abula;Munire, Abudukelim. And the article was included in Shipin Gongye Keji in 2013.Synthetic Route of C10H22O3 The following contents are mentioned in the article:

Effects of drying methods on volatile components of hops were determined by solid phase microextraction-gas chromatog.-mass spectrometry (SPME-GC-MS). There were 41 kinds of volatile components identified in fresh hops, including nine kinds of alcs., three kinds of aldehydes, seven kinds of esters, five kinds of ketones, three kinds of alkenes, seven kinds of organic acid, seven kinds of other ingredients, and the olefins accounted for 58.54% of the total relative content. Compared with fresh hops, there was an increase of two kinds of components in hops of factory hot air drying, accounted for 0.57% of the total peak area, and a decrease of eleven kinds, accounted for 3.69% of the total peak area, there was an increase of two kinds of components in hops of ambient air drying, accounted for 0.53% of the total peak area, and a decrease of eight kinds, accounted for 1.5% of the total peak area, the volatile constituents species and quantity were similar to that of fresh hops, and air drying could reduce the loss of hops volatile components. 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 typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. 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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Bacteriorhodopsin O-state photocycle kinetics: a surfactant study was written by Chu, Li-Kang;El-Sayed, Mostafa A.. And the article was included in Photochemistry and Photobiology in 2010.Safety of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

The spectroscopy and dynamics of interaction between the O intermediate of bacteriorhodopsin (bR) and several surfactants (cetrimonium bromide [CTAB], sodium dodecyl sulfate [SDS] and diethylene glycol mono-n-hexyl ether [C6E2]) were investigated using steady-state UV-VIS spectrometry, CD spectroscopy and time-resolved absorption techniques. The steady-state spectral results show that bR can retain its trimeric state without severe damage in the molar concentration ratio of C6E2/bR ranging up to 4000. Time-resolved observations indicate that the rise and decay rates and transient populations of the O state can be increased in the presence of nonionic surfactant C6E2; however, these studies indicate the opposite phenomenon in the presence of the ionic surfactants CTAB and SDS. The observed 40% enhancement in the transient population of the O intermediate state that results from treatment of C6E2 is proposed to result from an expanding bR structure, which leads to more effective proton pumping efficiency in the photosynthetic system of bR. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Safety of 2-(2-(Hexyloxy)ethoxy)ethanol).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. 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.Safety of 2-(2-(Hexyloxy)ethoxy)ethanol

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Densities, excess molar volumes, speeds of sound, and isothermal compressibilities for 2-(2-hexyloxyethoxy)ethanol + n-alkylamine at temperatures between 288.15 K and 308.15 K was written by Pal, Amalendu;Gaba, Rekha;Sharma, Sanjay. And the article was included in Journal of Chemical & Engineering Data in 2008.Electric Literature of C10H22O3 The following contents are mentioned in the article:

The densities, ρ, and the speeds of sound, u, for binary liquid mixtures containing 2-(2-hexyloxyethoxy)ethanol (C₆E₂) and n-butylamine (BA), dibutylamine (DBA), and tributylamine (TBA) have been measured as a function of composition using a vibrating tube densimeter and sound analyzer Anton-Paar model DSA-5000 at temperatures (288.15, 293.15, 298.15, 303.15, and 308.15) K and atm. pressure. The ρ and u values were used to calculate excess molar volumes, V^E_m, and excess molar isentropic compressibility, K^E_S,m, resp. The V^E_m and K^E_S,m values are shown to be neg. for all the mixtures over the entire composition range. Both V^E_m and K^E_S,m become more neg. for all the mixtures with the rise of temperature The change of V^E_m and K^E_S,m with composition and temperature are discussed with a view to understand mol. interactions present in alkoxyethanol-alkylamine mixtures 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. 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.Electric Literature of C10H22O3

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

Hydrogen sulfide (H₂S) releasing capacity of isothiocyanates from Moringa oleifera Lam was written by Wang, Xiangshe;Liu, Yunjiao;Liu, Xingdi;Lin, Yi;Zheng, Xueqin;Lu, Yuyun. And the article was included in Molecules in 2018.Name: 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

Moringa oleifera Lam. is rich in phytochem. compounds especially glucosinolates (GSs) and isothiocyanates (ITCs), which are active compounds for cancer chemoprevention benefits of Brassicaceae vegetables. In this study, we determined the total contents of GSs and ITCs and their specific profiles in different Moringa tissues including seeds, stems, leaves and roots. Seeds (seeds with shell and seed kernel) showed significantly higher levels of total GSs and ITCs than that of other Moringa tissues. The hydrogen sulfide (H₂S) releasing capacity of total ITCs extracted from different Moringa tissues was determined by lead (II) acetate assay in 24-well plates. The H₂S releasing capacity of different Moringa tissues were evaluated and compared. Moringa seeds showed the highest H2S releasing capacity, followed by roots, leaves and stems. Our results suggest that Moringa based foods may exhibit health benefits due to its GSs and ITCs contents that are the precursors for H₂S, in addition to the recognized action mechanisms of ITCs. 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, including apples, durians, pears, bananas, pineapples, and strawberries. 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.Name: 2-(2-(Hexyloxy)ethoxy)ethanol

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

Capillary gas chromatography-mass spectrometry of lower oxyethylenated aliphatic alcohols was written by Komarek, Karel;Pitthard, Vaclav;Kostrubanicova, Eva;Skvarenina, Stanislav;Hoffmann, Jaromir. And the article was included in Journal of Chromatography A in 1997.COA of Formula: C10H22O3 The following contents are mentioned in the article:

Capillary gas chromatog.-mass spectrometric (CGC-MS) anal. was carried out on alkylpoly(ethylene glycol) ethers, derived from ethoxylation of C₄-C₁₀ alcs., both as synthetic mixtures and as residues in water after their biodegradation MS was used for the acquisition of spectra and for the recording of retention times and the areas of eluted components. Especially, alkylpoly(ethylene glycol) ethers were identified by a combination of electron impact (EI) mass spectra and by correlating their relative retention times with the structure of the mols. Using these correlations, the length of both the poly(ethylene glycol) part and the alkyl part of a mol. were determined Retention times of the eluted components were used for calculation of the relative retention characteristics. The peak areas were used to determine the concentration decreases of individual components as a function of the degradation time. Alkylpoly(ethylene glycol) ethers were analyzed in both the non-derivatized form and after their conversion to trimethylsilyl derivatives and acetates. 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. 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. 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.COA of Formula: C10H22O3

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

Electroconductometric determination of completely engulfing Maxwell-type three-phase emulsions was written by Lee, Jong-Moon;Lim, Kyung-Hee. And the article was included in Journal of Industrial and Engineering Chemistry (Seoul, Republic of Korea) in 2003.Electric Literature of C10H22O3 The following contents are mentioned in the article:

The completely engulfing Maxwell-type morphol. of 3-phase emulsions was determined by the elec. method in which elec. conductivities of the emulsions were measured at various relative amounts of the equilibrium phases and fit to the conductivity equations of this morphol. The Maxwell-type 3-phase emulsions can be regarded as (i) the drops as 2-phase emulsions were dispersed in the continuous 3rd phase from the standpoint of the morphol. and (ii) the drops of one phase are dispersed in the continuous phase as emulsions composed of the other 2 phases from the standpoint of the way the 3-phase emulsions are prepared Previously the Maxwell-type morphol. could not be determined by the elec. method because the equation for the case (i) was used. However, the conductivities calculated by the equation for the case (ii) were in excellent agreement with the measured ones and the Maxwell-type morphol. could be determined This result implies that elec. conductivity behavior of completely engulfing Maxwell-type 3-phase emulsions should be examined from the way they are formed. 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. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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

Prediction of flash points of pure organic compounds: Evaluation of the DIPPR database was written by Alibakhshi, A.;Mirshahvalad, H.;Alibakhshi, S.. And the article was included in Process Safety and Environmental Protection in 2017.Recommanded Product: 112-59-4 The following contents are mentioned in the article:

The flash point is one of the most important flammability properties of compounds for the design of inherently safe processes. Many models have been developed to predict the flash point using the DIPPR database. However, for only 740 of the 1628 organic compounds available in the DIPPR database, the data for both flash point and normal b.p. were exptl. determined For the other compounds, at least one of these properties was predicted and therefore is not appropriate for model development. The present study introduces a model to predict the flash points of pure organic compounds using their mol. structures and normal b.ps. The new model exploits the equality of the relative errors observed for the normal b.p. and flash point values predicted using the Joback method. Consequently, the relative error of the predicted normal b.ps. can be used as a scaling factor to modify the predicted flash points. The ability of the model to evaluate the accuracy of a database was investigated. The ratio of the relative error of the predicted flash point to the relative error of the predicted normal b.p. obtained using the Joback method was proposed as a measure to evaluate the accuracy of flash point data. 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. 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. Recommanded Product: 112-59-4

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

Mechanism of stereoselective production of trans-1-decalone by electrochemical catalysis in microemulsions was written by Gao, Jianxin;Njue, Christopher K.;Mbindyo, Jeremiah K. N.;Rusling, James F.. And the article was included in Journal of Electroanalytical Chemistry in 1999.Recommanded Product: 112-59-4 The following contents are mentioned in the article:

Microemulsions made from water, oil and surfactant are attractive alternatives to organic solvents for mediated electrochem. synthesis. Cyclization of 2-(4-bromobutyl)-2-cyclohexen-1-one (1) to 1-decalone (2) mediated by an electrochem. generated cobalt(I) complex favored the trans- form over cis-1-decalone by ∼93:7 in microemulsions, but poorer stereoselectivity was obtained in organic solvents. Microemulsion composition, surfactant type (cationic or anionic), or chirality of the mediator did not significantly influence the trans/cis ratio of 1-decalone. Selective formation of trans-1-decalone in microemulsions is attributed to equilibration of isomers via keto-enol tautomerization catalyzed by hydroxide ions formed by coelectrolysis of water during the reaction. Trans-1-decalone was efficiently produced in 2 h electrolyzes in microemulsions with large volume fractions of water. Organic solvents with trace amounts of water gave little stereoselectivity in similar periods, but longer equilibration times produced larger proportions of trans-1-decalone. 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 typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. 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

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

Measurement and Prediction of the Molar Heat Capacities of Liquid Polyoxyethylene Glycol Monoalkyl Ethers (C_nE_m) was written by Goralski, Pawel;Tkaczyk, Mariola. And the article was included in Journal of Chemical & Engineering Data in 2015.Safety of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

The saturation heat capacities of eleven polyoxyethylene glycol monoalkyl ethers (C_nE_m) were measured by the calorimetric (DSC) method. The measurements were performed within the temperature range of (275.15 to 339.15) K by Micro DSCIII (Setaram) calorimeter. Assuming that the molar heat capacity (C_p,m) shows an additive character, the contributions to the C_p,m values of particular functional groups forming the compounds of C_nE_m series were calculated Two models differing in the manner of mol. division into functional groups, i.e., first- and second-order additivity group contribution approach, were used. In the latter, not only the type of functional group but also its position and the closest neighborhood was taken into account. The average deviations between the exptl. values of C_p and those estimated on the basis of the group contributions do not exceed 0.4 % for the compound of the series under investigation. The group contributions determined in this study make it possible to predict the molar heat capacity of monoethers C_nE_m within the temperature range of (270 to 350) K with an average error below 1 %. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Safety of 2-(2-(Hexyloxy)ethoxy)ethanol).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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.Safety of 2-(2-(Hexyloxy)ethoxy)ethanol

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