Category: 112-59-4

Permeation properties of surface modified nanofiltration membrane was written by Park, Hyung-Kiu;Jang, Gyung-Gug;Tak, Tae-Moon. And the article was included in Memburein in 2004.Electric Literature of C10H22O3 The following contents are mentioned in the article:

In this study, we prepared nanofiltration membrane by applying the interfacial polymerization method as a way of manufacturing composite membranes. We have examined the effects of various preparation factors such as monomer concentration and composition, thermal curing condition, post treatment condition. In addition to preparation conditions, we also monitored the effects of operation conditions such as feed solution concentration and operation pressure on the permeation properties of the resulting nanofiltration membrane. We intended to increase the permeation rate of nanofiltration membrane by the enlargement of effective surface area using additives during interfacial polymerization step. With increasing monomer concentration, the membrane permeation rate decreased while maintaining almost constant rejection. With respect to curing conditions, increasing the curing temperature decreased both permeation rate and rejection. 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 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.Electric Literature of C10H22O3

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

Corresponding States Method for Estimation of Upper Flammability Limit Temperature of Chemical Compounds was written by Gharagheizi, Farhad;Ilani-Kashkouli, Poorandokht;Mohammadi, Amir H.. And the article was included in Industrial & Engineering Chemistry Research in 2012.Name: 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

The accuracy and predictability of predictive methods to determine chem. species flammability characteristics are critically important in the chem. industry. This work continued applying the gene expression programming math. strategy to modify existing thermophys. property correlations available in the literature to: optimize the number of independent parameters; amplify the generality; and improve accuracy and predictability. This work presented a simple corresponding states model to predict the upper flammability limit temperature for 1462 organic compounds from 76 chem. families. Correlation parameters included critical temperature and compound acentric factor. Obtained statistical parameters including average absolute relative deviation of results from the DIPPR 801 database values (1.7, 1.8, and 1.7% for training, optimization, and prediction sets, resp.) demonstrated improved accuracy of presented correlations. 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 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.Name: 2-(2-(Hexyloxy)ethoxy)ethanol

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

Effect of chain length in ethoxylated and sulfonate surfactants upon the limiting diffusion coefficients in water at 25.0°C was written by Ortona, Ornella;D’Errico, Gerardino;Ciccarelli, Donato;Vitagliano, Vincenzo. And the article was included in Physical Chemistry Chemical Physics in 2000.Application In Synthesis of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

Limiting diffusion coefficients of ethoxylated surfactants of general formula CH₃(CH₂)_p-1(OCH₂CH₂)_qOH (C_pE_q) and sulfonate surfactants of formula CH₃(CH₂)_p-1SO₃^– Na⁺(C_pSO₃Na) were measured at 25°C by the Taylor dispersion technique. The series C₆E_q, with 0≤q≤5, was studied to evaluate the effect of the length of ethoxylic chain, (-OCH₂CH₂-)_q, on the mobility of the surfactant, the series C_pE₅ with 0≤p≤8 was studied to evaluate the effect of the length of the hydrophobic group, (-CH₂-)_p. The series C_pSO₃Na was also studied to compare the exptl. results with the intradiffusion coefficients obtained by the NMR-PGSE technique and with the data computed by the Nernst-Hartley equation. 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. 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.Application In Synthesis of 2-(2-(Hexyloxy)ethoxy)ethanol

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

Microwave-assisted synthesis of silver nanoprisms/nanoplates using a “modified polyol process” was written by Darmanin, Thierry;Nativo, Paola;Gilliland, Douglas;Ceccone, Giacomo;Pascual, Cesar;De Berardis, Barbara;Guittard, Frederic;Rossi, Francois. And the article was included in Colloids and Surfaces, A: Physicochemical and Engineering Aspects in 2012.Safety of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

In this paper, we report a novel, efficient and versatile process to produce high concentrations of silver nanoprisms, while controlling their size (prism height) and size dispersity, using a “modified polyol process” (microwave-assisted process). If the formation of silver spherical particles, nanocubes or nanowires has already been reported using the classical polyol process (reduction of AgNO₃ by ethylene glycol and in presence of PVP), here we show that the production of silver nanoprisms/nanoplates is possible by a careful choice in the process parameters and in particular in the reducing agent (ethylene glycol should be replaced by a reducing agent containing only one hydroxyl reducing group such as ethylene glycol monoalkyl ethers). The synthesis, characterization, the influence of parameters and the mechanism of formation are discussed in order to correlate the operational conditions with the shape and the dimension of the nanoparticles. 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, including apples, durians, pears, bananas, pineapples, and strawberries. 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.Safety of 2-(2-(Hexyloxy)ethoxy)ethanol

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

Synthesis of acyclic quaternary ammonium compounds containing ω-alkoxyethyl and 2-hydroxyethyl substituents at the nitrogen atom was written by Tcarkova, K. V.;Belus, S. K.;Artyushin, O. I.;Kharlamov, A. V.;Bondarenko, N. A.. And the article was included in Russian Chemical Bulletin in 2015.Recommanded Product: 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

A series of acyclic sym. quaternary ammonium chlorides Me₂(HOCH₂CH₂)N⁺(CH₂CH₂O)_nR Cl^– (n = 1, R = n-C₉H₁₉; n = 2, R = n-C₆H₁₃; n = 3, R = n-C₃H₇) was synthesized by alkylation of the corresponding tertiary amines Me₂N(CH₂CH₂O)_nR with ethylene chlorohydrin in a two-phase system, using water as a solvent. The tertiary amines were synthesized in a heterogeneous system organic phase-aqueous phase, using an aqueous solution of Me₂NH and a solid alkali. The intermediate monoethers of ethylene, di and triethylene glycol were obtained in high yield via a phase-transfer alkylation in dioxane, using solid KOH. The proton and carbon atom signals in the NMR spectra of the synthesized amines and ammonium chlorides were assigned based on the data of heteronuclear correlations (¹H, ¹³C). 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. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. 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.Recommanded Product: 2-(2-(Hexyloxy)ethoxy)ethanol

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

Anchoring vs Bridging: New Findings on Polymer Additives in Bicontinuous Microemulsions was written by Maccarrone, Simona;Allgaier, Juergen;Frielinghaus, Henrich;Richter, Dieter. And the article was included in Langmuir in 2014.Electric Literature of C10H22O3 The following contents are mentioned in the article:

We show for the first time the effect of telechelic polymers as additives in bicontinuous microemulsions. We combined macroscopic observations of the phase behavior with microscopic measurements of the structure by small-angle neutron scattering (SANS) to recover the two elastic moduli, κ and κ̅, namely the bending rigidity and saddle-splay modulus. On the basis of these results, we could classify the effect of telechelic polymers along with confinement, expressed as the ratio of the polymer end-to-end distance R_ee and the oil-water domain size d. Their unique property to anchor at two points in the membrane (bridging) acts like a switch from antibooster to booster of the surfactant efficiency (between low and ultralow confinement). In the region of medium confinement, all telechelic polymers are in the bridging configuration and we have a maximum of the boosting effect, while at high confinement, the reversed behavior is found where anchoring and/or bridging do not play any role anymore. 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 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. 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.Electric Literature of C10H22O3

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

The effect of solder paste residues on RF signal integrity was written by Turbini, Laura J.;Smith, Brian A.;Brokaw, James;Williams, John;Gamalski, Jurgen. And the article was included in Journal of Electronic Materials in 2000.Synthetic Route of C10H22O3 The following contents are mentioned in the article:

Wireless devices such as pagers and cellular phones are becoming common consumer items. These products require low loss RF signal propagation which is affected by material choices and processing conditions. This paper examines the effect of a series of no-clean solder pastes on signal integrity using an RF test circuit which sends a broadband signal through a gallium arsenide antenna switch and measures its transmission using a network analyzer. The test circuit also measures signal leakage. This paper reports on two different test vehicles, one that uses a 900 MHz antenna switch, and the other that uses a 2.0 GHz antenna switch. The transmission and leakage readings were taken daily for 16-21 days while the test vehicles were under accelerated aging conditions of 85°C and 85% RH. Average values for the readings for each solder paste were plotted to provide comparison among the pastes. The comparison data clearly distinguish solder pastes that provide consistency throughout the test period from those which do not. 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. 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.Synthetic Route of C10H22O3

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

Gene expression programming strategy for estimation of flash point temperature of non-electrolyte organic compounds was written by Gharagheizi, Farhad;Ilani-Kashkouli, Poorandokht;Farahani, Nasrin;Mohammadi, Amir H.. And the article was included in Fluid Phase Equilibria in 2012.Reference of 112-59-4 The following contents are mentioned in the article:

The accuracy and predictability of correlations and models to determine the flammability characteristics of chem. compounds are of drastic significance in various chem. industries. In the present study, the main focus is on introducing and applying the gene expression programming (GEP) math. strategy to develop a comprehensive empirical method for this purpose. This work deals with presenting an empirical correlation to predict the flash point temperature of 1471 (non-electrolyte) organic compounds from 77 different chem. families. The parameters of the correlation include the mol. weight, critical temperature, critical pressure, acentric factor, and normal b.p. of the compounds The obtained statistical parameters including root mean square of error of the results from DIPPR 801 data (8.8, 8.9, 8.9 K for training, optimization and prediction sets, resp.) demonstrate improved accuracy of the results of the presented correlation with respect to previously-proposed methods available in open literature. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Reference of 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.Reference of 112-59-4

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

Memantine nanoemulsion: a new approach to treat Alzheimer’s disease was written by Kaur, Atinderpal;Nigam, Kuldeep;Srivastava, Sukriti;Tyagi, Amit;Dang, Shweta. And the article was included in Journal of Microencapsulation in 2020.Formula: C10H22O3 The following contents are mentioned in the article:

A nanoemulsion loaded with memantine for intranasal delivery to bypass the blood-brain barrier for the treatment of Alzheimer disease. The nanoemulsion was prepared using homogenisation and ultrasonication methods. The developed nanoemulsion was characterised, in vitro release and antioxidant potential was analyzed. The in vivo studies were carried out by radiolabelling the memantine with technetium pertechnetate. The finalised NE showed particle-size of ~11 nm and percentage transmittance of ~99%. The in vitro release studies showed 80% drug release in simulated nasal fluid. The nanoemulsion showed 98% cell viability and antioxidative assays confirmed that the encapsulation of memantine in a nanoemulsion sustained its antioxidative potential. Gamma images and biodistribution results also confirmed higher uptake of formulation with %radioactivity of 3.6 ± 0.18%/g at 1.5 h in brains of rats administered intranasally. The developed nanoemulsion could be used as a potential carrier of memantine for a direct nose to brain delivery. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Formula: 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.Formula: C10H22O3

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

Synthesis of sulfated oligosaccharide glycosides having high anti-HIV activity and the relationship between activity and chemical structure was written by Katsuraya, Kaname;Nakashima, Hideki;Yamamoto, Naoki;Uryu, Toshiyuki. And the article was included in Carbohydrate Research in 1999.SDS of cas: 112-59-4 The following contents are mentioned in the article:

Sulfated laminara-oligosaccharide glycosides having high anti-human immunodeficiency virus (HIV) activities were synthesized from laminara-tetraose, -pentaose and -hexaose. The oligosaccharide glycosides were synthesized by treating peracetylated β-oligosaccharides with various alcs. and Lewis acid catalysts. The effects of the number of glucose residues and the alkyl chain-length on anti-HIV activity were examined The anti-HIV activity of sulfated dodecyl laminara-pentaosides and -hexaosides increased with increasing degree of sulfation (DS) and the pentaoside having an almost fully-sulfated saccharide portion had the highest activity, whereas for the hexaoside a somewhat lower DS manifested the highest activity. Sulfated laminara-oligosaccharide glycosides having fluoroalkyl-containing aglycons of high hydrophobicity showed potent inhibitory effects against HIV infection. In contrast, hydrophilic substituents containing oligo(ethyleneoxy) groups as aglycons in the sulfated oligosaccharides did not show high anti-HIV activity. 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. 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.SDS of cas: 112-59-4

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