Category: 115-84-4

Synthetic ester lubricants was written by Barnes, R. S.;Fainman, M. Z.. And the article was included in Lubrication Engineering in 1957.Safety of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Phys. properties and coefficients of friction were determined for esters of neopentyl glycol, tri(hydroxymethyl)ethane, tri(hydroxymethyl)propane, pentaerythritol, 2-butyl-2-ethyl-1,3-propanediol, and 2,2,4-trimethyl-1,3-pentanediol with n-C₉, n-C₁₀, n-C₁₄ and n-C₁₈ acids from natural sources, highly branched acids obtained by the Oxo process, and mixed normal and branched acids obtained by caustic extraction of the liquid product from CO hydrogenation. Study of the thermal decomposition at 260° of selected esters indicated that its rate is generally greatly increased by H in the β position. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Safety of 2-Butyl-2-ethylpropane-1,3-diol).

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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Safety of 2-Butyl-2-ethylpropane-1,3-diol

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Alcohol – Wikipedia,
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Desymmetrization of Diols by Phosphorylation with a Titanium-BINOLate Catalyst was written by Ouellette, Erik T.;Lougee, Marshall G.;Bucknam, Andrea R.;Endres, Paul J.;Kim, John Y.;Lynch, Emma J.;Sisko, Elizabeth J.;Sculimbrene, Bianca R.. And the article was included in Journal of Organic Chemistry in 2021.COA of Formula: C9H20O2 The following contents are mentioned in the article:

The desymmetrization of ten prochiral diols by phosphoryl transfer with a titanium-BINOLate complex is discussed. The phosphorylation of nine 1,3-propane diols is achieved in yields of 50-98%. Enantiomeric ratios as high as 92:8 are achieved with diols containing a quaternary C-2 center incorporating a protected amine. The chiral ligand, base, solvent, and stoichiometry are evaluated along with a nonlinear effect study to support an active catalyst species that is oligomeric in chiral ligand. The use of pyrophosphates as the phosphorylating agent in the desymmetrization facilitates a user-friendly method for enantioselective phosphorylation with desirable protecting groups (benzyl, o-nitrobenzyl) on the phosphate product. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4COA of Formula: C9H20O2).

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. 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.COA of Formula: C9H20O2

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Alcohol – Wikipedia,
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Evaluation of mosquito repellents was written by Bar-Zeev, M.;Ben-Tamar, D.. And the article was included in Mosquito News in 1971.Recommanded Product: 115-84-4 The following contents are mentioned in the article:

A method for evaluating repellents by using rabbits is described. The repellent effect of 279 compounds was tested against Culex pipiens molestus. Eighty-seven of these compounds were also tested against Aedes aegypti. The most effective compound against both species was 2-ethoxy-N,N-diethylbenzamide (I). Two compounds, 1,1-dimethylpropyl m-chlorocarbanilate and l-ethylpropyl m-chlorocarbanilate, were highly effective against C. pipiens molestus but not A. aegypti; an addnl. 6 compounds were particularly effective against C. pipiens molestus: sec-Bu N,N-diisopropylsuccinamate, N-n-amyl-3,6-endo-methylene-4-cyclohexene-1,2-dicarboximide, Et β-benzoylacrylate, 2-(dicyclohexylamino)ethanol, N-hexyl-butyramide, and I. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Recommanded Product: 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.Recommanded Product: 115-84-4

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New polyester intermediates for powder coatings was written by Johnson, Larry K.;Sade, William T.. And the article was included in Proceedings of the Waterborne, High-Solids, and Powder Coatings Symposium in 1991.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

All-aliphatic powder coatings for improved UV resistance could be prepared using 1,4-cyclohexanedicarboxylic acid as the sole diacid component if the formulation contained a glass temperature (T_g)-enhancing glycol such as hydrogenated bisphenol A. The melt viscosities of polyesters for powder coatings could be reduced by the incorporation of 1,3-cyclohexanedicarboxylic acid. Hydroxypivalyl hydroxypivalate reduced both the T_g and melt viscosity of resins into which it was incorporated as a partial replacement for neopentyl glycol. The use of 2-butyl-2-ethyl-1,3-propanediol had an effect on the T_g that was less than predicted based on its structure. 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. 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. 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.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol

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Materials for protection against biting insects was written by Travis, B. V.;Smith, Carroll N.. And the article was included in J. Forestry in 1950.Reference of 115-84-4 The following contents are mentioned in the article:

The following compounds were effective against mosquitoes and flies and harmless to the human skin: dimethyl phthalate; di-Me bicyclo[2.2.1]-5-heptene-2,3-dicarboxylate (I); Indalone (n-butyl mesityl oxide oxalate); 6-12 (2-ethyl-1,3-hexane diol); and 2-phenoxyethyl acetate. 2-Butyl-2-ethyl-1,3-propanediol was effective for clothing applications. Against chiggers the above compounds are satisfactory but benzyl or benzyl benzoate are preferable. Most effective against ticks were, in order of preference: N-butylacetanilide, hexyl mandelate, Indalone, I, 2-butyl-2-ethyl-1,3-propanediol, diethyl phthalate, and benzyl benzoate. The 1st compound is too toxic for skin applications. Directions for use are given. 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. 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. 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.Reference of 115-84-4

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Test for the comparison of glass-resin adhesion in laminates, application to glass-polyene ester laminates was written by Zalmanski, Alain. And the article was included in Bulletin de la Societe Chimique de France in 1970.Formula: C9H20O2 The following contents are mentioned in the article:

The adhesion of glass fibers to the polyester matrix in the reinforced laminates was determined by measuring the difference between the bending resistance of the reinforced laminate and the pure resin. The glass fiber content, type of the resin, the modifying diacid, the unsaturation mode of the polyester, and the type of the glycols and monomers used were the main parameters affecting adhesion. An improvement in adhesion was observed when using a polyester containing ∼25% maleic anhydride; modifying with tetrahydro- or hexahydrophthalic anhydride; using neopentyl glycol or 1,3-butylene glycol; and the partial replacing of styrene with Me methacrylate, ethylene glycol dimethacrylate, or chlorostyrene. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Formula: C9H20O2).

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.Formula: C9H20O2

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Anticonvulsant activity of 2,2-disubstituted 1,3-propanediols in electroshock seizures was written by Berger, F. M.. And the article was included in Proceedings of the Society for Experimental Biology and Medicine in 1951.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

cf. C.A. 45, 265a. Compounds studied were, 2,2-dimethyl-, 2,2-diethyl-, 2,2-dipropyl-, 2-butyl-, 2,2-dibutyl-, 2-ethyl-2-methyl-, 2-isopropyl-2-methyl-, 2-propyl-2-methyl-, 2-butyl-2-methyl-, 2-butyl-2-ethyl-, 2-ethoxy-2-ethyl-, 2-ethyl-2-phenyl-, 2-phenyl-, 2,2-diphenyl-, 2-phenoxy-2-phenyl-, and 2,2-dibenzyl-1,3-propanediol. All compounds in suitable doses protected mice against electroshock convulsion. The mol. configuration favorable for maximum activity is the presence of a quaternary C atom to which 1 or 2 Ph radicals are attached. Several of the compounds were about as potent as mephenesin. The most potent (the diphenyl derivative) was about 1/6 as potent as Na phenobarbital. 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. 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Name: 2-Butyl-2-ethylpropane-1,3-diol

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Equilibrium of boron extraction with 2-butyl-2ethyl-1,3-propanediol in 2-ethylhexanol was written by Kwon, TaeOk;Kawano, Yuka;Toorisaka, Eiichi;Takanashi, Hirokazu;Yamagishi, Toshio;Hirata, Makoto;Hano, Tadashi. And the article was included in Solvent Extraction Research and Development, Japan in 2004.HPLC of Formula: 115-84-4 The following contents are mentioned in the article:

Boron extraction equilibrium was investigated by using 2-butyl-2-ethyl-1,3-propane-diol (BEPD) dissolved in 2-ethylhexanol (EH) as the organic solvent at various boric acid concentrations, extractant concentrations and pH values. The distribution ratio of boron increased with the initial concentration of BEPD in the organic phase for all boron concentrations examined in this study. At each BEPD concentrations, the distribution ratio of boron was constant with minimal effect of boron concentration The effect of pH on boron extraction with BEPD in EH was also examined, and the results verified the fact that boron extraction with BEPD in 2-ethylhexanol was effective in acidic and weakly alk. media (pH < 9), but at pH values above 8 boron was stripped from the organic phase. 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. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.HPLC of Formula: 115-84-4

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Influence of side group contents of polycarbonate glycol on aggregation structures and mechanical properties of polyurethane elastomers was written by Kojio, Ken;Furukawa, Mutsuhisa;Motokucho, Suguru;Mizokami, Motonori;Yoshinaga, Kohji. And the article was included in Nippon Gomu Kyokaishi in 2012.SDS of cas: 115-84-4 The following contents are mentioned in the article:

Polycarbonate (PC) glycol synthesized from 1,6-hexanediol and 2-butyl-2-ethyl-1,3-propanediol (BEPD) with various ratios were employed to control the mech. property of PC-glycol-based polyurethane elastomers (PUEs). The PUEs were synthesized from PC-glycol, 4,4′-diphenylmethane diisocyanate and 1,4-butanediol by a one-shot method. The degree of microphase separation became weaker with an increase in the BEPD content. This trend results in a decrease in Young’s modulus due to the lack of the formation of crystallized hard segment domains in the PUEs. Tensile strength and strain at break decreased and increased with increasing BEPD content, resp. This result clearly suggests that Bu and Et groups of the BEPD part suppressed the packing of the soft segment under elongation. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4SDS of cas: 115-84-4).

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. 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.SDS of cas: 115-84-4

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Alcohol – Wikipedia,
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Differential multicomponent spectrophotometry-spectrophotometric method for determination of benzyl benzoate and N-butyl acetanilide in clothing impregnant M-1960 was written by Beroza, Morton. And the article was included in Anal. Chem. in 1953.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

The differential multicomponent spectrophotometric analysis of Hiskey and Firestone (C.A. 46, 11013d) is modified to allow its use in systems that do not follow Beer’s law. Essentially the method involves the determination of absorbency differences between a solution containing known ingredients and one containing almost the same concentration of those ingredients. Analysis of the mixture by the absolute method permits a solution (saturated solution) of approx, equal concentration of pure materials to be prepared The differences in absorbancies of these two solutions are determined at chosen wave lengths and used to determine the final concentration When the system does not follow Beer’s law then known amounts of each substituent must be added to the saturated solution 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts