Category: 763-69-9

Investigation of achromatic micro polarizer array for polarization imaging in visible-infrared band was written by Li, Peng;Kang, Guoguo;Vartiainen, Ismo;Wang, Fangzhou;Liu, Ying;Tan, Xiaodi. And the article was included in Optik (Munich, Germany) in 2018.Recommanded Product: Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

The design and fabrication of a micro polarizer array (MPA) for polarization imaging is described for visible-IR region. The MPA, composed of 1280 × 1024 elements, is designed to be integrated directly onto the CMOS chip. Each micro polarizer consists of a 200-nm-period Al wire grating with the dimension of 5.2 μm × 5.2 μm, and the performance of gratings with finite number of periods and gradient ridge-length has been thoroughly investigated. The grating ridge of each polarizer orients four different directions offset by 45°, which determines different polarization directions correspondingly. Initial test and experiment for the MPA are performed and the crosstalk caused by diffraction is discussed. 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. 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 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.Recommanded Product: Ethyl 3-ethoxypropanoate

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

Evolution of aromatic compounds in grape wines fermented with and without the addition of ginkgo biloba leaf extract during aging was written by Zhang, Guodong;Qi, Yulin;Hu, Boran. And the article was included in Shipin Kexue (Beijing, China) in 2010.Formula: C7H14O3 The following contents are mentioned in the article:

The present study aimed to analyze and compare the evolution of aromatic compounds in grape wines fermented with and without the addition of Ginkgo biloba leaf extract during aging. The aromatic compounds in grape wines were extracted by the solvent extraction method, analyzed by GC-MS and identified by the computer search technique. Totally 32 compounds were separated, among which 29 were identified, mainly including aldehydes, alcs., esters, and furans. There was an obvious difference in aromatic compounds between both freshly fermented grape wines. However, the difference became unobvious after 1 yr of aging and both aged grape wines exhibited similar kind and amount of aromatic compounds 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. 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.Formula: C7H14O3

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

Effect of solvent composition on the formation of microtopographical siloxane-urethane surface was written by Majumdar, Partha;Webster, Dean C.. And the article was included in PMSE Preprints in 2005.Safety of Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

The effect of solvent composition on the formation of microtopog. surface domains in a crosslinked siloxane-urethane coating system was explored using five different solvents. A D-optimal mixture design study was carried out using Me n-amyl ketone (MAK), toluene, Et 3-ethoxypropionate (EEP), Bu acetate (BA) and iso-Pr alc. (IPA). The study revealed that presence of slow evaporating solvents MAK, EEP and absence of fast evaporating solvent IPA in the solvent composition with min. amount of BA would favor formation of a structured surface. Vapor pressure and solubility parameter of the solvent compositions for structured surface were lower than the vapor pressure and solubility parameter of the solvent compositions for non-structured surface. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Safety of Ethyl 3-ethoxypropanoate).

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. Safety of Ethyl 3-ethoxypropanoate

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

Pd(II)-catalyzed acetalization of terminal olefins with electron-withdrawing groups in supercritical carbon dioxide: selective control and mechanism was written by Wang, Zhao-Yang;Jiang, Huan-Feng;Ouyang, Xiao-Yue;Qi, Chao-Rong;Yang, Shao-Rong. And the article was included in Tetrahedron in 2006.Safety of Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

Pd(II)-catalyzed acetalization of terminal olefins with electron-withdrawing groups was carried out smoothly in supercritical CO₂ under O atm. when polystyrene-supported benzoquinone (PS-BQ) or Cu^II (Cu^I) chloride was employed as cocatalyst. The higher selectivity was achieved, without any chlorinated byproduct detected, when using PS-BQ instead of Cu^II (or Cu^I) chloride. PS-BQ could be recycled with excellent catalytic activity remaining after each simple filtration. Cl ion is a promoter. The different acetalization mechanisms were revealed by the subtle relation of Cl ion and benzoquinone (BQ) to the catalytic activity of PdCl₂/PS-BQ, Pd^II-CuCl₂ or Pd(OAc)₂/PS-BQ. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Safety of Ethyl 3-ethoxypropanoate).

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. 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.Safety of Ethyl 3-ethoxypropanoate

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

GC-MS determination of residual amounts of volatile organic compounds in solidified paint with accelerated solvent extraction was written by Ma, Teng-zhou;Chen, Jun-shui;Cheng, Yu-xiao;Ma, Ming;Zhang, Lin;Shen, Bo. And the article was included in Lihua Jianyan, Huaxue Fence in 2013.Computed Properties of C7H14O3 The following contents are mentioned in the article:

Residual amounts of 7 volatile organic compounds, i.e., toluene, ethylbenzene, xylene, hexamethylacetone, 3-ethoxypropionate, 6-methyl-2-heptanone and benzylalc. in solidified paint were determined by GC-MS. The sample was crushed and extracted (by ASE) thrice with acetone consecutively, at 50°C for 3 min in each extraction HP-5MS column was used for separation Linear relationships between values of peak area and mass concentration of the 7 volatile organic compounds were kept in definite ranges, with detection limits (3S/N) in the range of 0.01-1.35μg. Using blank sample as matrix, test for recovery was made by standard addition method, and values of recovery obtained were in the range of 84.4%-104%, with values of RSD’s (n = 6) in the range of 0.80%-13%. 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. 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. Computed Properties of C7H14O3

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

Novel photoacid generators for chemically amplified resists was written by Asakura, Toshikage;Yamato, Hitoshi;Matsumoto, Akira;Murer, Peter;Ohwa, Masaki. And the article was included in Journal of Photopolymer Science and Technology in 2003.Safety of Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

Recently the authors developed new class of non-ionic oxime sulfonate PAG. The compounds generate various kinds of sulfonic acids, such as n-propane, n-octane, camphor and p-toluene sulfonic acid under deep-UV exposure and trifluoromethanesulfonic acid under ArF exposure and are applicable for the corresponding chem. amplified (CA) photoresists. The application-relevant properties of the compounds such as solubility in propylene glycol monomethyl ether acetate (PGMEA), Et lactate, Et 3-ethoxypropionate, and 2-heptanone, UV absorption, thermal stability with or without poly(4-hydroxystyrene) (PHS), volatility, performance in model resist formulations were evaluated. In addition, the microlithog. simulation based on the results of DRM results of the trifluoromethanesulfonate was also studied. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Safety of 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. 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.Safety of Ethyl 3-ethoxypropanoate

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

Tracking steel corrosion in halide solutions with a pH stimuli responsive polymer was written by Hanna, Joshua S.;Rawlins, James W.. And the article was included in Proceedings of the International Waterborne, High-Solids, and Powder Coatings Symposium in 2012.Quality Control of Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

In situ and non-invasive corrosion monitoring was accomplished using a simple spectroscopic technique in combination with a recently synthesized fluorescent pH stimuli responsive polymer. The characterization protocol quantified the relative standard deviation of the average fluorescence intensity over the entire steel substrate to quantify the onset of corrosion using up to 1536 data points. Statistically relevant data for coated substrates exposed to a series of different environments were able to provide a corrosivity ranking at a high level of confidence. In this paper, the methods and capability of the combined approach were confirmed to correlate corrosion severity vs. different halide salts, matching trends already established in literature with time to initiate corrosion. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Quality Control of Ethyl 3-ethoxypropanoate).

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. 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.Quality Control of Ethyl 3-ethoxypropanoate

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

Effects of the ether oxygen atom in alkyl side chains on the physical properties of piperidinium ionic liquids was written by Nokami, T.;Yamashita, T.;Komura, T.;Handa, N.;Shimizu, M.;Yamaguchi, K.;Domi, Y.;Usui, H.;Sakaguchi, H.;Itoh, T.. And the article was included in Faraday Discussions in 2018.Related Products of 763-69-9 The following contents are mentioned in the article:

Various types of piperidinium ionic liquids (ILs) equipped with an oxygen atom-containing alkyl side chain on the pos. charged nitrogen atom were systematically synthesized and their phys. properties investigated. The thermal stability, viscosity, electrochem. window, and ion conductivity were influenced significantly by changing the position of the oxygen atom in the alkyl chain. Although the lowest viscosity was recorded for 1-((2-methoxyethoxy)methyl)-1-methylpiperidin-1-ium bis(trifluoromethylsulfonyl)amide ([PP_1MEM][Tf₂N]), 1-methyl-1-(2-propoxyethyl)piperidin-1-ium bis(trifluoromethylsulfonyl)amide ([PP_1PE][Tf₂N]) can be recommended as the best IL as an electrolyte due to its low viscosity and high thermal and electrochem. stability among the seven ILs tested. 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 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. 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.Related Products of 763-69-9

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

Characteristics of Gases Emitted from Chicken Manure Wastewater and Potential Effects on Human Health was written by Fakkaew, Krailak;Kongkratoke, Sitang;Tantrakarnapa, Kraichat;Polprasert, Chongrak;Sudsandee, Suntorn. And the article was included in Environmental Science and Pollution Research in 2022.Name: Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

Hazardous and odorous gas emissions from chicken manure wastewater are a public preoccupation. Odor composition measurements are crucial steps to provide appropriate air pollution control measures and design strategies to minimize the human health impact. In this study, chicken manure wastewater samples were extensively analyzed in a closed system by a portable handheld gas detector to characterize the odor and chem. compositions A portable detector was calibrated prior to sampling. The total number of 153 chem. compounds found in the chicken manure wastewater samples had various olfactory characteristics, including strong, pleasant, and odorless smells. Depending on the route of exposure, most of these chem. compounds could cause human health effects, such as irritation, burns, and severe symptoms including carcinogenic. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Name: Ethyl 3-ethoxypropanoate).

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. 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.Name: Ethyl 3-ethoxypropanoate

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

Catalytic Olefin Hydroalkoxylation by NanoParticles of Pollucite was written by Zamanian, Sara;Kharat, Ali Nemati. And the article was included in Australian Journal of Chemistry in 2015.Safety of Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

The catalytic hydroalkoxylation of α,β-unsaturated esters, nitriles, and ethers with aliphatic and aromatic alcs. over pollucite using thermal and microwave-assisted methods was investigated. To study the effect of the alc. structures on the mechanism of the hydroalkoxylation reaction, different alcs., such as methanol to butanol, cyclohexanol, phenol, and 2-ethylhexanol were used. The activities of pollucite, in contrast to other basic solids, were scarcely affected by the presence of air and moisture. The correlation between alc. acidity and reaction activity is discussed. The prepared pollucite was characterized by X-ray diffraction, volumetric nitrogen adsorption surface area anal., and CO2 temperature-programmed desorption. SEM anal. revealed that the size of the modified nano catalyst particles was under 40nm. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Safety of Ethyl 3-ethoxypropanoate).

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. 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.Safety of Ethyl 3-ethoxypropanoate

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