Category: 115-84-4

QSPR Flash Point Prediction of Solvents Using Topological Indices for Application in Computer Aided Molecular Design. [Erratum to document cited in CA151:127086] was written by Patel, Suhani J.;Ng, Dedy;Mannan, M. Sam. And the article was included in Industrial & Engineering Chemistry Research in 2010.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

The neural network algorithms are modified as is the data in the tables. 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. 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

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Field tests of selected repellents against the American dog tick was written by Cole, Moses M.;Lloyd, George W.. And the article was included in Journal of Economic Entomology in 1951.COA of Formula: C9H20O2 The following contents are mentioned in the article:

Dibutyl adipate, a mixture of 2-butyl-2-ethyl-1,3-propanediol (I), benzyl benzoate (II), and N-butylacetanilide (III), a mixture of N-butyl-4-cyclohexane-1,2-dicarboximide (IV), undecylenic acid (V), and III, and a mixture of IV, V, I, III, and II gave 97-99.6% repellency against Dermacentor variabilis. 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. 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. 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.COA of Formula: C9H20O2

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

All-purpose repellent mixtures as clothing treatments against chiggers was written by Gilbert, I. H.;Gouck, H. K.. And the article was included in Florida Entomologist in 1953.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

A mixture containing benzyl benzoate 29.7, butylacetanilide 29.7, 2-butyl-2-ethyl-1,3-propanediol 29.7, and lindane 1.0% applied at the rate of 3.6 g./sq. ft. of cloth was the most effective repellant of 11 reported. With an average of 4 soap and water washings, 100% protection was maintained. 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. 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. 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.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Control of the pine root color weevil was written by Finnegan, R. J.;Stewart, K. E.. And the article was included in Journal of Economic Entomology in 1962.Safety of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Ethylene dichloride was effective in killing the larvae of Hylobius radicis, but failed to prevent reinfestation. Lindane and dieldrin applied as water emulsions directly to the ground around the base of the trees effectively controlled the insect for at least 4 years. 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. 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.Safety of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Transformations of diols and cyclic ethers. XXXI. Dehydration of 1,3-diols on metal catalysts was written by Bartok, Mihaly;Molnar, Arpad. And the article was included in Acta Chimica Academiae Scientiarum Hungaricae in 1973.Formula: C9H20O2 The following contents are mentioned in the article:

It has been exptl. confirmed that the transformation of the diols with the accompanying formation of oxo compounds can be observed not only on the vicinal diols but, with a change in the exptl. conditions, on certain types of 1,3-diols too. 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. 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.Formula: C9H20O2

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Synthesis of ester oils was written by Asinger, Friedrich;Fell, Bernhard;Pfeifer, Josef;Iqbal, Abul F. M.. And the article was included in Erdoel & Kohle, Erdgas, Petrochemie in 1970.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Viscosity and pour point data were reported for esters made from trimethyladipic acid or 1,10-decanedioic acid with various polyfunctional or monofunctional alcs. The latter included hydrogenation products from Versatic Acid 911. 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. 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

Organic treatment of titanium dioxide pigments was written by Luginsland, Hans Hermann. And the article was included in FATIPEC Congress in 1987.COA of Formula: C9H20O2 The following contents are mentioned in the article:

The use of neopentyl glycols, trimethylolalkanes, and amino glycols to improve the dispersibility of TiO₂ and the brightness of paints containing the pigments was discussed. 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. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. 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.COA of Formula: C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Gas chromatography of insect repellents was written by Acree, Fred Jr.;Beroza, C. Morton. And the article was included in Journal of Economic Entomology in 1962.HPLC of Formula: 115-84-4 The following contents are mentioned in the article:

Thirteen insect repellents (aromatic amides, esters, and branched chain diols) were separated on either Carbowax 20 M, Silicone 550, or Tide. A column of 15% Carbowax 20 M on acid-washed Columpak at a temperature of 246° was most satisfactory. Approx. 0.2 mg. of each repellent was sufficient for an analysis in an instrument using a thermal conductivity detector and a recorder having a 2.5-my. full span. 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. 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. 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.HPLC of Formula: 115-84-4

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Study on boiling water resistance of polyester resin for TGIC powder coating was written by Luo, Yi;Xie, Jing;Li, Yong;Liu, Liang;Shi, Yuan-tang;Chen, Li. And the article was included in Xiandai Tuliao Yu Tuzhuang in 2017.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

The effect of different amount of 2-butyl-2-ethyl-1,3-propanediol (BEPD), isophthalic acid (PIA) and additives on the boiling water resistance, mech. behavior of powder coatings were discussed. The boiling water resistance was analyzed with contact angle and scanning electron microscope. The results showed that the increasing BEPD and PIA was helpful to improve the water boiling resistance performance. 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Publication was written by Anonymous. And the article was included in Research Disclosure in 1999.Recommanded Product: 115-84-4 The following contents are mentioned in the article:

Environmental concerns have resulted in reduced sulfur content in diesel fuels. As a consequence of hydrotreating processes also the amount of lubricating compounds has decreased. Poor lubricity can lead to wear problems especially in rotary pumps. The wear can be prevented by providing lubricity additives in the fuel. Reformulated diesel fuel of the winter grade characteristics was used in this study. 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. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. 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.Recommanded Product: 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts