Category: 115-84-4

Use of spiro-orthosilicates as blocked polyol/reactive diluent in high solids PUR clearcoats for car refinish applications was written by van den Berg, Keimpe J.;van Oorschot, Ren;van der Ven, Leo G. J.. And the article was included in Pitture e Vernici, European Coatings in 2006.SDS of cas: 115-84-4 The following contents are mentioned in the article:

Spiro-orthosilicates, prepared from tetra-Et orthosilicate and a diol (2-butyl-2-ethyl-1,3-propanediol or 2-ethyl-1,3-hexanediol), were used as latent reactive diluent in two-pack polyurethane coatings. A fast curing and long pot life was achieved due to the latency in the can. Spiro-orthosilicates hydrolyze with moisture forming a diol and a polysiloxane. Kinetic data on hydrolysis and curing are given. The formation of polysiloxane was characterized by solid state Si NMR. The spiro-orthosilicates based films were tested as clearcoat for refinishing of automobiles. The coatings showed good stability after many car washes. 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. 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. 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.SDS of cas: 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Use of spiro-orthosilicates as blocked polyols/reactive diluents in high-solid PUR clear coats for car refinish applications was written by van den Berg, K. J.;van Oorschot, R.;van der Ven, L. G. J.. And the article was included in Surface Coatings International in 2006.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Spiro-orthosilicates, prepared from tetra-Et orthosilicate and a diol (2-butyl-2-ethyl-1,3-propanediol or 2-ethyl-1,3-hexanediol), were used as latent reactive diluent in two-pack polyurethane coatings. A fast curing and long pot life was achieved due to the latency in the can. Spiro-orthosilicates hydrolyze with moisture forming a diol and a polysiloxane. Kinetic data on hydrolysis and curing are given. The formation of polysiloxane was characterized by solid state Si NMR. The spiro-orthosilicates based films were tested as clearcoat for refinishing of automobiles. The coatings showed good stability after many car washes. 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. 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.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Solubility of crystalline β-diols in water was written by Putnina, A.. And the article was included in Latvijas PSR Zinatnu Akademijas Vestis, Kimijas Serija in 1990.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Solubilities (weight per cent) of crystalline β-diols determined by refractometry at 25° are: 2-tert-butyl-1,3-propanediol 7.9; 2,2-diethyl-1,3-propanediol 4.68; 1-(3-bromophenyl)-2,2-dimethyl-1,3-propanediol 0.20; 1,3-decanediol 0.19; 1,3-dodecanediol 0.11; 2-ethyl-2-butyl-1,3-propanediol 1.4 weight%. Values determined by gas chromatog. are: 3-phenyl-2,2-dimethyl-1,3-propanediol 0.89; 2,2-dipropyl-1,3-propanediol 0.77; 2,2,5-trimethyl-1,3-hexanediol 0.58; 1-touyl-1-phenyl-1,3-propanediol 0.21; 2,2-diisobutyl-1,3-propanediol 0.056 weight%. An empirical equation for calculating β-diol solubility is proposed. 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. 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.Name: 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Vapor Pressures and Enthalpies of Vaporization of a Series of the 1,3-Alkanediols was written by Verevkin, Sergey P.. And the article was included in Journal of Chemical & Engineering Data in 2007.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Molar enthalpies of vaporization of a series of six 1,3-alkanediols were obtained from the temperature dependence of the vapor pressure measured by the transpiration method. A large number of the primary exptl. results on temperature dependences of vapor pressures have been collected from the literature and have been evaluated in order to derive vaporization enthalpies at the reference temperature 298.15 K. The exptl. enthalpies of vaporization were checked for internal consistency. New exptl. results together with those selected from the literature have been recommended for thermochem. calculations 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. 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

Separation of fission and corrosion products from boric acid solutions by solvent extraction was written by Narbutt, J.;Olza, J.;Przybylowicz, Z.;Siekierski, S.. And the article was included in Journal of Radioanalytical Chemistry in 1979.Formula: C9H20O2 The following contents are mentioned in the article:

Extractive purification of H₃BO₃ [10043-35-3] from radioactive corrosion and fission products dissolved in aqueous solutions modeling PWR coolants was studied. Aliphatic 1,3-diols containing 8 and 9 C atoms/mol. were used as extractants for H₃BO₃. The behavior of some representative corrosion and fission products as well as various factors affecting their distribution between the organic and aqueous phases were also investigated. Conditions for the effective separation of H₃BO₃ from most of the radioactive contaminants are presented. 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. 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. 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.Formula: C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

New intermediates for the paint and coatings industries was written by Petersen, Leslie. And the article was included in Kemia – Kemi in 1996.Safety of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Neste Oxo, a part of Neste’s chems. division, serves the paint and surface coatings industry with a range of products. The Nexcoat family of coating intermediates are targeted at the fast-growing market for polyester-based coating. Nexcoat 600 (neopentyl glycol) is used in saturated polyesters for powder coating and polyester-based binders. Nexcoat 700 (2-butyl-2-ethyl-1,3-propanediol) serves some of the same markets but provides improved properties, including higher solubility in hydrocarbons, lower viscosity, lower water absorption, excellent hydrolytic stability, and improved flexibility. 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. 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.Safety of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Partial molar volumes of organic solutes in water. XXV. Branched aliphatic diols at temperatures (298 to 573) K and pressures up to 30 MPa was written by Cibulka, Ivan. And the article was included in Journal of Chemical Thermodynamics in 2014.Product Details of 115-84-4 The following contents are mentioned in the article:

Densities of dilute aqueous solutions of three 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 of 3-methylpentane-1,5-diol measured over the temperature range from (298 to 573) K and at pressures up to 30 MPa using a flow vibrating-tube densimeter are reported. 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. Predictions of standard molar volumes based on group contribution approach were tested and analyzed. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Product Details 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Product Details of 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Tests with repellents against the American dog tick was written by Cole, M. M.;Lloyd, Geo. W.. And the article was included in Journal of Economic Entomology in 1955.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Di-Bu adipate (I) repelled 86% of Dermacentor variablis when applied at the rate of 2 g. per sq. ft. of trouser cloth. Percentage repellence of mixts of equal parts of 2-butyl-2-ethyl-1,3-propanediol (II), benzyl benzoate (III), and N-butylacetanilide (IV) was 93%, equal parts of II, III, and IV with 1% lindane 89% equal parts of I, II, and IV 86%, equal parts of N-butyl-4-cyclohexene-1,2-dicarboximide (V), undecenoic acid (VI) and IV 83%, equal parts of II, III, and N-propylacetanilide 76%, equal parts of II, IV, and VI 75%, equal parts of I, II, and III 73%, equal parts of II, IV, and V 72%, and equal parts of II, III, and N-isopropylacetanilide 65%. 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

Ultraviolet and infrared spectrophotometric analysis of an insect-repellent mixture was written by Sassaman, Warren A.;Cohen, S. P.. And the article was included in Applied Spectroscopy in 1954.Computed Properties of C9H20O2 The following contents are mentioned in the article:

A spectrophotometric procedure employing measurements in both the ultraviolet and infrared regions was developed to determine the concentrations of N-butylacetanilide, benzyl benzoate, 2-ethyl-2-butyl-1,3-propanediol, and Tween 80, in a mixture containing only these 4 components. The first 2 components have relatively strong absorptivities in the ultraviolet at 227.5 and 280.3 millimicrons, while the latter 2 have absorption bands at the infrared wave lengths, 8.99 and 9.60 microns. By substituting the absorptivities at these wave lengths in a set of 4 simultaneous equations, the percentage of each component in an insect-repellent mixture is calculated 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. 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. 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

Corn earworm moth repellents was written by Roberts, James E.;Rolston, L. H.. And the article was included in J. Kansas Entomol. Soc. in 1958.Related Products of 115-84-4 The following contents are mentioned in the article:

The following materials tested in cages exhibited significant repellency against corn earworm moth oviposition: N-butylacetanilide, dimethyl phthalate, 2-butyl-2-ethyl-1,3-propanediol, Tat (75% dimethyl phthalate and 25% dimethylbicycloheptenedicarboxylate), and undecenoic acid. Little or no repellency was exhibited by N-ethylacetanilide, dibutyl adipate, benzyl benzoate, hexyl benzoate, caprylic acid, diphenyl carvonate, cinnamic acid, 2-phenylcyclohexanol, 2,3,4,5-bis (Δ²-butenylene) tetrahydrofurfural, butoxypolypropylene glycol, 2-ethyl-1,3-hexanediol, dibutyl phthalate, isobornyl thiocyanoacetate, and N,N-diethyl-m-toluamide. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Related Products of 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. 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.Related Products of 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts