Mazet, Michel et al. published their research in Bulletin de la Societe Chimique de France in 1969 | CAS: 115-84-4

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. 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.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol

Neopentylic rearrangement of 2,2-disubstituted-1,3-propanediols in acid was written by Mazet, Michel. And the article was included in Bulletin de la Societe Chimique de France in 1969.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

The dehydration and substituent migration rates (Yvernault, Th. and Mazet, M., 1969), of 2,2-dihydrocarbyl-1,3-propanediols were studied in H2SO4. The reaction occurred by a synchronic ionization-migration mechanism. The substituents had a steric effect. The rates increased with the mol. weight of one of the substituents, and were higher for aryl, as compared to alkyl groups. 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. 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. 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.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Yvernault, Theophile et al. published their research in Comptes Rendus des Seances de l’Academie des Sciences in 1969 | CAS: 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. 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.Synthetic Route of C9H20O2

Determination of characteristic factors of the rate of migration of a group between vicinal carbon atoms was written by Yvernault, Theophile;Mazet, Michel. And the article was included in Comptes Rendus des Seances de l’Academie des Sciences in 1969.Synthetic Route of C9H20O2 The following contents are mentioned in the article:

The total 1st order rate constants for the rearrangement of HOCH2CR1RCH2OH to HOCH2CR(OH)CH2R1 (R and R1 are Me, Et, Pr, Bu, Bz, and Ph) were determined by azeotropic distillation The migration rate appears, as a 1st approximation, to be the product of 2 independent factors: the migratory power of the group, and an assistance factor of the adjacent group. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Synthetic Route of 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. 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.Synthetic Route of C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Anonymous et al. published their research in Research Disclosure in 1993 | CAS: 115-84-4

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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol

Improved hydrolytic stability of amine-neutralized polyester resin dispersions using 2-butyl-2-ethyl-1,3-propanediol was written by Anonymous. And the article was included in Research Disclosure in 1993.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Use of 5-100 mol% replacement of one or more diol monomers with 2-butyl-2-ethyl-1,3-propanediol (I) resulted in an improvement of hydrolytic stability of polyester dispersion as measured by decrease in pH of the dispersions after storage for 28 days at 125F (52°). I also reduced viscosity of the dispersion. 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. 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

He, Tao et al. published their research in Tuliao Gongye in 2014 | CAS: 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. 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.Category: alcohols-buliding-blocks

Preparation of carboxyl-terminated polyester resin for two-component matting superdurable weather resistant powder coatings was written by He, Tao;Gu, Yuxin;Xie, Jing;Lin, Xien;Ruan, Deliang;Liang, Baorong. And the article was included in Tuliao Gongye in 2014.Category: alcohols-buliding-blocks The following contents are mentioned in the article:

This article has described the preparation of a carboxyl-terminated polyester resin based on isophthalic acid for two-component matting super durable powder coatings. The prepared powder coating showed a matting effect with only 21∼26 gloss. The coating was featured by its lower gloss, smooth appearance and outstanding weather durability. 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. 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. 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.Category: alcohols-buliding-blocks

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Acree, Fred Jr. et al. published their research in Journal of Economic Entomology in 1962 | 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. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Application of 115-84-4

Quantitative gas chromatography of insect repellent mixture M-1960 was written by Acree, Fred Jr.;Beroza, Morton. And the article was included in Journal of Economic Entomology in 1962.Application of 115-84-4 The following contents are mentioned in the article:

Repellents in the M-1960 clothing impregnant, 2-butyl-2-ethyl-1,3-propanediol, N-butylacetanilide, and benzyl benzoate, can be analyzed quant. by gas chromatography. The analyses are conducted at 225° using 200 γ of each repellent on an 8-foot column of 5% Dow-Corning Silicone 550 on Haloport-F with a thermal conductivity detector. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Application of 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. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Application of 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Niu, Xiao-xue et al. published their research in Xiandai Tuliao Yu Tuzhuang in 2021 | CAS: 115-84-4

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.Application of 115-84-4

Influencing factors of leveling performance in β-hydroxyalkylamide powder coatings was written by Niu, Xiao-xue. And the article was included in Xiandai Tuliao Yu Tuzhuang in 2021.Application of 115-84-4 The following contents are mentioned in the article:

Polyester resin powder coatings are welcomed by people because of its four significant characteristics of high efficiency, environmental protection, high performance and economy, but its application in certain fields is limited due to their leveling performance is slightly inferior to solvent-based coatings. Therefore, the influence of factors such as acid value, viscosity, acidolytic agent type and additives on the leveling performance of β-hydroxyalkylamide powder coatings were discussed. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Application of 115-84-4).

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.Application of 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Gilbert, I. H. et al. published their research in Journal of Economic Entomology in 1957 | CAS: 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. 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.Name: 2-Butyl-2-ethylpropane-1,3-diol

Evaluation of repellents against mosquitoes and deer flies in Oregon was written by Gilbert, I. H.. And the article was included in Journal of Economic Entomology in 1957.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Field studies with repellents were conducted against Aedes communis, A. dorsalis (I), and Chrysops discalis. Diethyltoluamide was twice as effective as standard M 2020 [dimethylphthalate 40%, dimethyl carbate 30%, and ethyl hexanediol 30%] (II). The ortho and meta isomers of N,N-diethyltoluamide were 40% more effective against I than M 2020 (II). EtOH solutions or sprays were about equal in effectiveness. All new mixtures gave better protection than II against all species of mosquitoes. 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. 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. 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.Name: 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Schleyer, Paul von Rague et al. published their research in Journal of the American Chemical Society in 1961 | CAS: 115-84-4

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. 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.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol

Thorpe-Ingold hypothesis of valency deviation. Intramolecular H-bonding in 2-substituted propane-1,3-diols was written by Schleyer, Paul von Rague. And the article was included in Journal of the American Chemical Society in 1961.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

The Thorpe-Ingold hypothesis of valency deviation was examined by determination of the spectral shifts near 3 μ due to intramol. H-bonding in propane-1,3-diols. Results obtained indicated C-C-C angles appreciably larger than 109.5° in cyclopropane-1,1-dimethanol and propane-1,3-diol and slightly spread angles in cyclobutene-1,1-dimethanol and 2-monoalkyl substituted propane-1,3-diols. The method was not applicable to 1,3-diols with bulky substituents because of adverse steric effects. 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. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Vandevoorde, Paul et al. published their research in European Coatings Journal in 2005 | 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. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Computed Properties of C9H20O2

Making solid gains. Novel acrylic and polyester polyols reduce VOCs in solvent-borne urethanes was written by Vandevoorde, Paul;van Gaans, Ad. And the article was included in European Coatings Journal in 2005.Computed Properties of C9H20O2 The following contents are mentioned in the article:

High solids, solvent-borne polyurethanes offer excellent performance, but volatile organic compound (VOC) concentrations must be reduced to 420 g/L to produce compliant coatings. Different types of acrylic and polyester polyols were synthesized and their effect on coating properties was examined The combination of a low mol. weight acrylic polyol and a polyester-reactive diluent allowed hard clearcoats to be produced with low VOC content, even at low spraying viscosity. 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. 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. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Computed Properties of C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Cao, Yongyi et al. published their research in Guangdong Huagong in 2015 | CAS: 115-84-4

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. 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.Name: 2-Butyl-2-ethylpropane-1,3-diol

Synthesis of high-boiling water resistance polyester used for outdoor powder coatings was written by Cao, Yongyi;Chen, Guomin. And the article was included in Guangdong Huagong in 2015.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

The paper modifies the polyester resin which is used for general outdoor engineering with 2-ethyl-2-butyl-1, 3-propanediol (BEPD) as monomer, discuss the effect of BEPD to the glass transition temperature, viscosity, boiling water resistance, weathering resistance and mech. behavior of coatings. By the means of adjust the branching degree, use amount of catalyzer, the prepared resin has nice boiling water resistance and weather resistance. 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. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.Name: 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts