Category: 115-84-4

Facilitated transport of boric acid by 1,3-diols through supported liquid membranes was written by Bachelier, N.;Chappey, C.;Langevin, D.;Metayer, M.;Verchere, J.-F.. And the article was included in Journal of Membrane Science in 1996.Reference of 115-84-4 The following contents are mentioned in the article:

Boric acid is transported selectively by 1,3-diols from an aqueous source phase into an alk. aqueous receiving phase through an organic solvent (o-dichlorobenzene) phase. Measurements of the transport rates were made by using a U-tube apparatus The process was adapted to liquid membranes supported on polypropylene films. The factors which influence the stability of the supported liquid membrane are discussed. Assuming that the transport of the neutral 1:1 diol-boric acid complex within the organic phase is diffusion-limited, a model is proposed that realistically represents the fluxes of boric acid as a function of the initial concentrations of boric acid and diol. The exptl. diffusion coefficients were determined and agreed satisfactorily with the calculated values. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Reference of 115-84-4).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Reference of 115-84-4

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Influence of ozone and ultraviolet combination on volatile flavor and functional components of dried Goji was written by Gong, Yuan;Liu, Dun-hua. And the article was included in Shipin Yu Fajiao Gongye in 2015.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Volatile compounds in Gojis treated by ozone and UV combination and untreated ones were extracted and analyzed by solid phase micro-extraction and gas chromatog. mass spectrometry. The relative contents of volatile compounds were tested. Thee were 46 volatile compounds identified which accounted for 64.02% of the total amount of elution components in untreated Goji; 51 volatile compounds were identified which was 70.73% of the total amount of elution components in ozone and UV combined dried Goji. Compared with the untreated ones, the ozone and UV treated Gojis were higher in the quantities and relative content of volatile components and in the functional ingredients flavonoid content increased slightly, polysaccharides and carotenoids declined at different degrees. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Influence of ozone and ultraviolet combined treatment on the volatile flavor and functional components of dried Lycium barbarum was written by Gong, Yuan;Liu, Dun-hua;Wang, Xu;Xu, Meng-xia;Liao, Ruo-yu. And the article was included in Shipin Keji in 2015.Category: alcohols-buliding-blocks The following contents are mentioned in the article:

Volatile compounds in ozone and UV combined treatment and untreated Lycium barbarum were extracted and analyzed by solid phase micro-extraction and gas chromatog. mass spectrometry and determined the relative contents of volatile compounds Totally 52 volatile compounds were identified accounted for 70.25% of the total amount of elution components in untreated Lycium barbarum. Totally 60 volatile compounds were identified accounted for 82.54% of the total amount of elution components in ozone and UV combined dried Lycium barbarum, the quantities and relative content of volatile components in the multi-class were increased and the functional ingredients in flavonoid content increased slightly, polysaccharides, carotenoids have declined of different degrees. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Category: alcohols-buliding-blocks).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Category: alcohols-buliding-blocks

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Partial Molar Volumes and Partial Molar Isentropic Compressions of Selected Branched Diols at Infinite Dilution in Water at Temperatures T = (278 to 318) K and Atmospheric Pressure was written by Cibulka, Ivan;Hnedkovsky, Lubomir. And the article was included in Journal of Chemical & Engineering Data in 2013.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Speed of sound and d. data for dilute aqueous solutions of four branched diols derived from propane-1,3-diol (2-methyl-2-propylpropane-1,3-diol, 2,2-diethylpropane-1,3-diol, and 2-ethyl-2-butylpropane-1,3-diol) and 3-methylpentane-1,5-diol were obtained using the Anton Paar DSA 5000 vibrating-tube densimeter and sound analyzer in the temperature range from (278.15 to 318.15) K and at atm. pressure. Standard molar isentropic compressions and standard molar volumes were evaluated from the measured data. Present data were combined with those obtained previously for related solutes, and relations to the structures of solute mols. are discussed. The predictions of standard molar volumes based on the group contribution approach were tested and analyzed. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Quality Control of 2-Butyl-2-ethylpropane-1,3-diol).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. The oxygen atom of the strongly polarized O―H bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol

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Alcohol – Wikipedia,
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Properties of coatings based on carbamate functional binders was written by . And the article was included in Proceedings of the Annual Meeting Technical Program of the FSCT in 2002.HPLC of Formula: 115-84-4 The following contents are mentioned in the article:

The use of a crosslinkers in a coating formulation is carefully selected since it influences the performance characteristics of a fully formulated paint. The use of single component (1K) melamine-crosslinked systems generally has the advantage of better hardness development, solvent resistance, and ease of use, compared to similarly crosslinked 2 component (2K) polyisocyanate-based systems. In studies of crosslink densities of films prepared from oligomeric urethane polyols, probably the methoxymethyl groups of melamine resins could react with urethane groups (i.e. secondary carbamate groups) as well as reacting with hydroxyl groups. A 1K solvent-borne system using carbamate-functional polymers are evaluated for performance characteristics. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4HPLC of Formula: 115-84-4).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.HPLC of Formula: 115-84-4

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Analysis of volatile components in Pu-er tea by SPME-GC-MS was written by Luo, Fa-mei;Zhan, Jia-fen;Luo, Zheng-gang;Jiang, Dong-hua;Du, Ping;Jiang, Jing;Zhang, Xian-jun. And the article was included in Linchan Huaxue Yu Gongye in 2010.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Volatile components from two kinds of Pu-er tea, namely raw tea and ripe tea by two different fermentation processes were extracted by solid phase micro-extraction(SPME) and qual. analyzed by gas chromatog./mass spectrometry (GC-MS). The result showed that 60 volatile compounds were identified from two kinds of Pu-er tea, including 44 from raw tea and 43 from ripe tea and 27 from both of them. The main volatile compounds of raw tea were 1, 2, 3-trimethoxybenzene, epoxylinalool, veratrole, linalool oxide, β-linalool, α-terpineol, etc. The main volatile compounds of ripe tea were 5-methyl-2-hexaone, tetrahydrolinalool, linalool oxide, β-linalool, iso-Bu ether, α-terpineol, etc. There are significant differences among component and content in raw tea and ripe tea on account of fermentation difference. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Inhibitory properties of 1,3-propanediols in cutting fluids was written by Bennett, E. O.;Gannon, J. E.;Bennett, D. L.. And the article was included in Tribology International in 1983.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Preservative properties and compatibility studies of 1,3-propanediol-based cutting fluid additives are reported for a number of compounds Compatibilities of some of the title preservatives with EDTA  [60-00-4] are reported; in addition, compatibilities are also given for 2-nitro-2-ethyl-1,3-propanediol (I) [597-09-1] with other cutting fluid preservatives, a number of alkanolamines and amines, and a number of com. cutting fluids. I was compatible with EDTA, showed no antagonism with other preservatives (except for Triadine 10  [72103-18-5]), combined well with C_2-4 alkanolamines and butylamines, and generally improved inhibition of a number of com. fluids. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

A statistical comparison of high-performance glycols in polyester resins for coatings was written by Golob, Dennis J.;Odom, Thomas A. Jr.;Whitson, Russell L.. And the article was included in Polymeric Materials Science and Engineering in 1990.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

High-solids enamel formulations containing polyesters based on >1 glycols [2-butyl-2-ethyl-1,3-propanediol (I), 1,4-cyclohexanedimethanol (II), hydroxypivalyl hydroxypivalate (III), 2,2,4-trimethyl-1,3-pentanediol (IV), and neopentyl glycol(V)] plus melamine were evaluated for various characteristics. Relative rankings were (property, highest glycol given): cure, II; flexibility I; hardness, II; hydrolytic stability, II; processability, II; stain and chem. resistance, III and IV; viscosity, I and III and IV and V. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Quality Control of 2-Butyl-2-ethylpropane-1,3-diol).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Polyols based on isocyanates and melamines and their applications in 1K and 2K coatings was written by Yahkind, A. L.;Paquet, D. A.;Parekh, D. V.;Stine, C. L.;van der Ven, L. G. J.. And the article was included in Progress in Organic Coatings in 2010.Computed Properties of C9H20O2 The following contents are mentioned in the article:

Polyurethane polyols (PUPOs) and melamine polyols (MEPOs), invented by AkzoNobel Coatings, offer valuable alternatives to the commonly used polyester and acrylic polyols and new formulating tools for the development of novel coatings. The resin chem. is based on the predominantly selective reactivity of α,β- and α,γ-diols with commonly used polyisocyanate and melamine formaldehyde crosslinkers. The resulting low mol. weight, hydroxyl functional resins are suitable for use in low VOC coatings. By choosing the appropriate crosslinker, diol, and modifier, the chem. structures of these resins can be altered to obtain the desired properties of the coatings. Synthesis methods for novel PUPOs and MEPOs and properties of one component and two component coatings containing them are described. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Computed Properties of C9H20O2).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Computed Properties of C9H20O2

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Synthesis and Enzymatic Degradation of Soft Aliphatic Polyesters was written by Buchholz, Viola;Agarwal, Seema;Greiner, Andreas. And the article was included in Macromolecular Bioscience in 2016.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Novel aliphatic enzymically degradable polyesters with short alkyl side chains for tuning crystallinity are presented in this work. The intrinsic problem of aliphatic polyesters is their brittleness and tendency to crystallize. This was modulated by the synthesis of random copolyesters based on aliphatic linear monomers, adipic acid, 1,5-pentanediol and monomers with aliphatic branches, such as 2-butyl-2-ethyl-1,3-propanediol by polycondensation. The resulting copolyesters were crystalline, wax-like or had liquid texture with varied mech. properties and enzymic degradability depending upon the copolymer composition Such polyesters are of significant interest for a wide range of possible applications such as controlled drug delivery, agricultural applications and as packing materials. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Name: 2-Butyl-2-ethylpropane-1,3-diol).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Name: 2-Butyl-2-ethylpropane-1,3-diol

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts