Truong, H. T. et al. published their research in Separation and Purification Technology in 2013 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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 763-69-9

Dehydration of reactive industrial mixtures by pervaporation: An innovative approach in acrylic esters processes was written by Truong, H. T.;Rode, S.;Roizard, D.;Mouzon-Pelletier, S.;Tretjak, S.. And the article was included in Separation and Purification Technology in 2013.Related Products of 763-69-9 The following contents are mentioned in the article:

This work demonstrates for the first time in open literature the dehydration by pervaporation of reactive mixtures encountered in the synthesis of Et acrylate. These mixtures contained, together with water and ethanol, highly reactive monomers, i.e., acrylic acid and Et acrylate. Among com. available membranes, the Pervap#1201 of Sulzer Chemtech and the Zeolite-T of Mitsui were identified as promising membranes. As Pervap#1201 clearly performed better, it was selected for detailed pervaporation investigations. The total permeation flux of Pervap#1201 varied from 0.05 to 1.2 kg m-2 h-1 and the water permeance varied from 360 to 1700 GPU depending on the mass fraction of water in the feed (0.02-0.15) and the operating temperature (65-95 °C). Its separation factor (β) toward water was greater than 4000 and the selectivity (α) was greater than 200. Permeate is essentially composed of water (0.99 mass fraction), ethanol (<0.007), acrylic acid (0.002) and Et acrylate (0.001). The permeate fluxes were modeled using the solution-diffusion approach and the estimated values showed good agreement with exptl. values. The chem. stability of the Pervap#1201 membrane was investigated using continuous pervaporation experiments Importantly, the performance of Pervap#1201 was demonstrated to be very stable, even after six months of immersion in a reaction mixture Considering the pervaporation performances and the membrane stability in the presence of acrylic derivatives, the use of the Pervap#1201 membrane in the coupling reaction-esterification of Et acrylate appears to be very promising for industrial application. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Related Products of 763-69-9).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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 763-69-9

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Spanik, I. et al. published their research in Uchenye Zapiski Kazanskogo Universiteta, Seriya Estestvennye Nauki in 2014 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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 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. Category: esters-buliding-blocks

A comparative study of various sample preparation procedures for characterization of organic compounds in brandy was written by Spanik, I.;Vyviurska, O.;Makysova, K.. And the article was included in Uchenye Zapiski Kazanskogo Universiteta, Seriya Estestvennye Nauki in 2014.Category: esters-buliding-blocks The following contents are mentioned in the article:

This paper describes the composition of volatile compounds in 19 different wine distillates was studied by gas chromatog. (GC) coupled with flame ionization (FID) or mass-spectrometric (MS) detector. The studied samples were divided into two groups depending on the way of their production and geog. region. The effect of various sample treatment procedures on final composition of volatiles was investigated in details. The effectiveness of direct injection, headspace, solid phase extraction (SPE), solid phase microextraction (SPME) and liquid-liquid extraction (LLE) was compared. Moreover, the effect of exptl. conditions of preconcentration methods such as type of sorbent, temperature, time or solvent removal procedure was studied in details. The repeatability of particular sample preparation procedure was evaluated by comparison of peak areas for randomly selected compounds obtained from 4 parallel measurements. It was shown that the most suitable sample treatment procedure in terms of repeatability is SPE followed by direct injection and headspace. LLE and SPME provide higher variability of peak areas, thus utilization of internal standard for quantification is recommended. On the contrary, the most suitable sample treatment procedure in terms of the number of different type of compounds is liquid-liquid extraction into CH2Cl2. By this method, more than 240 compounds have been extracted from wine distillates produced by classical technol. Furthermore, SPME has shown different selectivity which allows one to determine compounds that could not be extracted by other studied sample preparation methods. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Category: esters-buliding-blocks).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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 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. Category: esters-buliding-blocks

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Wang, Haiying et al. published their research in Energy & Fuels in 2019 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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.Recommanded Product: Ethyl 3-ethoxypropanoate

Production of Aryl Oxygen-Containing Compounds by the Pyrolysis of Bagasse Alkali Lignin Catalyzed by LaM0.2Fe0.8O3 (M = Fe, Cu, Al, Ti) was written by Wang, Haiying;Han, Hongjing;Sun, Enhao;Han, Yejun;Zhang, Yanan;Li, Jinxin;Chen, Yanguang;Song, Hua;Zhao, Hongzhi;Kang, Yue. And the article was included in Energy & Fuels in 2019.Recommanded Product: Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

A series of LaM0.2Fe0.8O3 (M = Fe, Cu, Al, Ti) samples synthesized by the sol-gel method were used to catalyze the pyrolysis of bagasse alkali lignin (BAL) to produce aryl oxygen-containing compounds The effects of doping metal ions in the B-site of LaFeO3 were investigated by X-ray diffraction, SEM, Brunauer-Emmett-Teller, and X-ray photoelectron spectrometer. Furthermore, the catalytic pyrolysis performances of the perovskites were evaluated by thermogravimetric anal. and the fixed-bed microreactor, and the gaseous and liquid pyrolysis products were analyzed by GC and gas chromatog./mass spectrometry (GC/MS), resp. The results indicated that the perovskites have a cubic crystal phase, porous structure, and large sp. surface area. After doping Cu, Al, and Ti ions in the B-site of perovskites, the grain sizes were refined, the performance of catalyzing BAL pyrolysis was improved, and the yields of liquid pyrolysis products increased by 24.1-39.1%. The selectivities of CO2 and CO in gaseous products decreased by 5.8-16.3 and 26.0-34.8%, resp., which resulted from the inhibition of decarboxylation and decarbonylation. The total selectivities of target products, i.e., aryl oxygen-containing compounds (including phenolics, guaiacols, syringols, and phenylates) obtained from BAL pyrolysis catalyzed using perovskites were all greater than 74 wt %, which was higher than that obtained from the pyrolysis of pure BAL (62 wt %) in the absence of catalyst. After 5 cycles of redox reaction, the perovskite still showed a well-maintained structural and catalytic stability. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Recommanded Product: Ethyl 3-ethoxypropanoate).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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.Recommanded Product: Ethyl 3-ethoxypropanoate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Stoyanova-Slavova, Iva B. et al. published their research in Environmental Toxicology and Chemistry in 2014 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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. 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.SDS of cas: 763-69-9

Partial least square and k-nearest neighbor algorithms for improved 3D quantitative spectral data-activity relationship consensus modeling of acute toxicity was written by Stoyanova-Slavova, Iva B.;Slavov, Svetoslav H.;Pearce, Bruce;Buzatu, Dan A.;Beger, Richard D.;Wilkes, Jon G.. And the article was included in Environmental Toxicology and Chemistry in 2014.SDS of cas: 763-69-9 The following contents are mentioned in the article:

A diverse set of 154 chems. that included US Food and Drug Administration-regulated compounds tested for their aquatic toxicity in Daphnia magna were modeled by a 3-dimensional quant. spectral data-activity relationship (3D-QSDAR). Two distinct algorithms, partial least squares (PLS) and Tanimoto similarity-based k-nearest neighbors (KNN), were used to process bin occupancy descriptor matrixes obtained after tessellation of the 3D-QSDAR space into regularly sized bins. The performance of models utilizing bins ranging in size from 2 ppm × 2 ppm × 0.5 Å to 20 ppm × 20 ppm × 2.5 Å was explored. Rigorous quality-control criteria were imposed: 100 randomized 20% hold-out test sets were generated and the average R2test of the resp. models was used as a measure of their performance, and a Y-scrambling procedure was used to identify chance correlations. A consensus between the best-performing composite PLS model using 0.5 Å × 14 ppm × 14 ppm bins and 10 latent variables (average R2test = 0.770) and the best composite KNN model using 0.5 Å × 8 ppm × 8 ppm and 2 neighbors (average R2test = 0.801) offered an improvement of about 7.5% (R2test consensus = 0.845). Projection of the most frequently occurring bins on the standard coordinate space indicated that the presence of a primary or secondary amino group-substituted aromatic systems-would result in an increased toxic effect in Daphnia. The presence of a second aromatic ring with highly electroneg. substituents 5 Å to 7 Å apart from the first ring would lead to a further increase in toxicity. Environ Toxicol Chem 2014;33:1271-1282. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9SDS of cas: 763-69-9).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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. 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.SDS of cas: 763-69-9

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Cao, Shurui et al. published their research in International Journal of Environmental Analytical Chemistry in 2020 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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 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. Formula: C7H14O3

Development of a method based on thermal desorption-gas chromatography/mass spectrometry for the determination of 103 volatile organic compounds in mattresses was written by Cao, Shurui;Wen, Yao;Xi, Cunxian;Li, Xianliang;Zhang, Lei;Wang, Guomin;Shang, Jingchuan. And the article was included in International Journal of Environmental Analytical Chemistry in 2020.Formula: C7H14O3 The following contents are mentioned in the article:

A sensitive and reliable method based on environment test chamber coupled with thermal desorption and gas chromatog.-mass spectrometry (ETC-TD-GC/MS) was developed and validated for the determination of 103 volatile organic compounds (VOCs) emitted from mattresses. In the study, two com. sorbent tubes were compared in terms of adsorption efficiency towards the target analytes. The result illustrated that the multisorbent tubes containing Carbopack C, Carbopack B and Carboxen 1000 had better performance than Tenax TA tubes owing to their large surface area, low capacity for water and high temperature stability, which allowed a wide range of VOCs to be absorbed, especially for VOCs with low b.ps. and small mols. To achieve the optimum conditions for the anal., several thermal desportion parameters were accurately investigated. Under the optimal conditions, the method showed good linearities, with correlation coefficients ranging from 0.9982 to 0.9999 and the method detection limits and method quantification limitsfor target compounds in the range of 0.006 ∼ 0.561μg/m3 and 0.020 ∼ 1.870μg/m3, resp. In order to evaluate the performance of the developed method on real samples, various mattresses from different manufacturers were analyzed. All mattress samples were found to emit VOCs and the values of area-specific emission rate (SERs) for total target compounds were in the range of 90.25 ∼ 288.63μg/m2·h. Moreover, the SERs of VOCs were influenced by the type of sponge materials and mattress fabric layers. The study demonstrated that the method is sensitive, accurate and well-suited for the determination of VOCs emitted from mattresses. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Formula: C7H14O3).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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 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. Formula: C7H14O3

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Forero G., Luis A. et al. published their research in Fluid Phase Equilibria in 2014 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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 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: 763-69-9

A modified Patel-Teja cubic equation of state. Part II: Parameters for polar substances and its mixtures was written by Forero G., Luis A.;Velasquez J., Jorge A.. And the article was included in Fluid Phase Equilibria in 2014.Recommanded Product: 763-69-9 The following contents are mentioned in the article:

In this work, the parameters of the equation of state formed by the Patel-Teja pressure-volume-temperature relationship and the alpha function of Heyen have been estimated for 184 polar substances. To obtain the parameters of the proposed model, pseudo-exptl. data have been generated using the DIPPR correlations for vapor pressure and liquid d. The proposed model in conjunction with the Wong-Sandler mixing rules and the NRTL activity model have been used to describe the vapor liquid equilibrium of some complex mixtures Three kinds of binary systems have been analyzed and they are those of the type: polar substance/aromatic, polar substance/n-alkane and polar substance/n-alkanol. Based on the homologous series concept, generalized expressions for the binary interaction parameters in the Wong-Sandler-NRTL mixing rules were developed in order to correlate vapor-liquid equilibrium at low pressures for the selected mixtures For n-alkanes and aromatic compounds, the acentric factor has been used to generalize the binary interaction parameters for mixtures with a polar substance and these kinds of compounds In the case of systems composed by a polar substance and an alc., the reduced dipole moment of the alcs. is used to develop the generalized expressions. Ninety-two binary mixtures were analyzed and a relative average absolute deviation of 1.21% was estimated for the bubble pressure. Finally, the model was validated by predicting binary vapor-liquid equilibrium at high pressures and for ternary mixtures In both cases, the results are satisfactory. The average absolute deviations in bubble pressure are 2.34% for high pressure predictions and 1.15% for ternary mixtures This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Recommanded Product: 763-69-9).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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 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: 763-69-9

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Perestrelo, Rosa et al. published their research in Molecules in 2018 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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.Computed Properties of C7H14O3

Establishment of the volatile signature of wine-based aromatic vinegars subjected to maceration was written by Perestrelo, Rosa;Silva, Catarina L.;Silva, Pedro;Camara, Jose S.. And the article was included in Molecules in 2018.Computed Properties of C7H14O3 The following contents are mentioned in the article:

The flavoring of vinegars with aromatic fruits and medicinal herbs is a practice with increasing trend mostly in countries with oenol. tradition, resulting in a product of improved quality and consumer attractiveness. This study was directed towards the evaluation of the impact of the maceration process on the volatile signature of wine-based aromatic vinegars (WBAVs). The evaluation was performed using solid phase microextraction (SPME) combined with gas chromatog. combined with mass spectrometry (GC-MS). Exptl. parameters influencing headspace solid (HS)-SPME extraction efficiency, were optimized using an univariate exptl. design. The best results were achieved using a polydimethylsiloxane (PDMS) fiber, 10 mL of vinegar sample, at 50 °C for 30 min of extraction This way One hundred and three volatile organic compounds (VOCs), belonging to different chem. families including Et esters (37), higher alcs. (20), fatty acids (10), terpenoids (23), carbonyl compounds (six), lactones (five) and volatile phenols (two), were identified in wine vinegar (control) and WBAV. As far as we know, 34 of these VOCs are reported for the first time in macerated vinegars. Higher alcs. and lactones are the major chem. families in WBAV macerated with apple, whereas terpenoids are predominant in WBAV macerated with banana. The obtained data represent a suitable tool to guarantee the authenticity and genuineness of WBAV, as well as to promote the production of WBAV with improved sensorial and organoleptic properties. To the best of our knowledge, there are no reported studies dealing with the volatile signature of WBAV enriched with banana, passion fruit, apple and pennyroyal. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Computed Properties of C7H14O3).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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.Computed Properties of C7H14O3

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Majumdar, Partha et al. published their research in Polymer in 2006 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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.Related Products of 763-69-9

Influence of solvent composition and degree of reaction on the formation of surface micro-topography in a thermoset siloxane-urethane system was written by Majumdar, Partha;Webster, Dean C.. And the article was included in Polymer in 2006.Related Products of 763-69-9 The following contents are mentioned in the article:

The effects of solvent composition and degree of reaction prior to film formation leading to the formation of a biphasic micro-topog. surface in a crosslinked siloxane-urethane coating system were explored. For the solvent composition study, a D-optimal mixture design study was carried out using Me n-amyl ketone (MAK), toluene, Et 3-ethoxy propionate (EEP), Bu acetate (BA) and iso-Pr alc. (IPA) as solvents. The study revealed that the presence of slow evaporating solvents MAK, EEP and the absence of fast evaporating solvent IPA in the solvent composition with a minimal amount of BA favored formation of a structured surface. Control over the domain size could be obtained by varying the MAK:EEP ratio in solvent compositions having a fixed amount of BA. The effect of mixing time on the formation of surface domains was studied. At short mixing times (<2 h) and long mixing times (>7 h), no surface phase separation is observed, while at intermediate times a window’ was found where surface microdomains of similar size are generated. Doubling the level of catalyst halves the mixing time required to generate surfaces with microdomains. SEM studies with energy dispersive x-ray mapping and dynamic mech. anal. (DMA) were done in order to understand the development of the phases in the PDMS-polyurethane system. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Related Products of 763-69-9).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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.Related Products of 763-69-9

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Ma, Qiulin et al. published their research in Energy Conversion and Management in 2021 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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.Application In Synthesis of Ethyl 3-ethoxypropanoate

Production of upgraded biocrude from hydrothermal liquefaction using clays as in situ catalysts was written by Ma, Qiulin;Wang, Kui;Sudibyo, Hanifrahmawan;Tester, Jefferson W.;Huang, Guangqun;Han, Lujia;Goldfarb, Jillian L.. And the article was included in Energy Conversion and Management in 2021.Application In Synthesis of Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

Hydrothermal liquefaction (HTL) is a thermochem. process that converts biomass into biocrude. HTL suffers from low yields of water-insoluble biocrude with high oxygen contents and low heating values. Inexpensive clay minerals including montmorillonite, dolomite, kaolinite and sand were used to upgrade HTL biocrude as in situ acid-base catalysts. Batch tests were performed using starch with 5 wt% clay minerals at 300°C for 1 h. Bio-oil was fractionated into water-soluble and water-insoluble parts to explore potential catalytic mechanisms by analyzing the fractional distribution, elemental composition and chem. composition Higher carbon recoveries in the bio-oil fraction (approaching 60%) occurred with clay-catalyzed HTL. Energy recovery of both bio-oil fractions increased by approx. 22% for all clays. A base-catalyzed pathway inhibits char formation from catalytic HTL, with dolomite approaching a char yield as low as 3%. Chromatog. anal. of heavy and light oils from both fractions showed that dolomite and montmorillonite play a catalytic effect via base and acid pathways on upgrading biocrude. Clay-catalyzed HTL modified the b.p. distributions by producing more 100-300°C middle temperature distillates. Overall, catalytic HTL with clay minerals enhanced the heating value and energy recovery of bio-oils. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Application In Synthesis of Ethyl 3-ethoxypropanoate).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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.Application In Synthesis of Ethyl 3-ethoxypropanoate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Rios-Reina, Rocio et al. published their research in Food Research International in 2019 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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.HPLC of Formula: 763-69-9

A comparative study of the volatile profile of wine vinegars with protected designation of origin by headspace stir bar sorptive extraction was written by Rios-Reina, Rocio;Segura-Borrego, M. Pilar;Garcia-Gonzalez, Diego L.;Morales, M. Lourdes;Callejon, Raquel M.. And the article was included in Food Research International in 2019.HPLC of Formula: 763-69-9 The following contents are mentioned in the article:

The characteristic volatile profile of the Spanish Vinagre de Jerez (VJ), Vinagre de Condado de Huelva (VC) and Vinagre de Montilla-Moriles (VMM) protected designation of origin (PDO) wine vinegars has been studied and compared for the first time by headspace stir bar sorptive extraction-gas chromatog.-mass spectrometry (HSSE-GC-MS). The possible markers of each category and PDO were assessed. Acetates were the majority group in all vinegars, while ketones, C13-norisoprenoids and volatile phenols showed significant differences between the three PDOs. Anal. of variance (ANOVA), heatmap and partial least squares-discriminant anal. (PLS-DA) were performed. According to these results, 1-heptanol, Me nonanoate, 2-methylbutanoic acid, 2,2,6-trimethyl-cyclohexanone, trans-2-decenal, eucalyptol and α-terpineol, were the most significant compounds for differentiating of VC, diacetyl and acetoin, Et 3-ethoxypropanoate, 2- and 3-heptanone, 2-methyl-1-hexadecanol, 1-octen-3-ol, p-Cresol and camphene for VMM; and β-damascenone, 5-hydroxymethylfurfural, 3-heptanol, trans-2-hexen-1-ol and trans-2-hexen-1-yl acetate for VJ. Classification results showed that 100% of PDO samples were correctly classified, reaffirming the utility of the volatile profiles for classifying and authenticating wine vinegar PDOs. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9HPLC of Formula: 763-69-9).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. 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.HPLC of Formula: 763-69-9

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics