Category: 115-84-4

Cure of secondary carbamate groups by melamine-formaldehyde resins was written by Higginbottom, H. P.;Bowers, G. R.;Ferrell, P. E.. And the article was included in Journal of Coatings Technology in 1999.Synthetic Route of C9H20O2 The following contents are mentioned in the article:

Crosslink densities of films prepared from oligomeric urethane polyols suggested that the methoxymethyl groups of melamine-formaldehyde resins (I) could react with urethane groups (i.e., secondary carbamate groups) as well as reacting with hydroxyl groups. Co-reactants that contain secondary carbamate groups and no hydroxyl groups have been prepared with several types of backbone structures. Cure of such co-reactants by I resins has been studied using a gradient oven with determination of impact resistance, solvent resistance, and hardness. Several formulations from these cure profile sets have been selected for crosslink d. determinations by dynamic mech. anal. Crosslink densities of cured films are consistent with complete conversion of secondary carbamate groups at temperatures only slightly higher than those used for cure of hydroxyl groups. The -OH groups on certain acrylic polyols were converted to secondary carbamate groups. The original acrylic and the converted acrylic were both cured with I resins. Acid resistance was much better for films prepared from the acrylic that contained secondary carbamate groups. 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. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Synthetic Route of C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Role of graphene oxide and functionalized graphene oxide in protective hybrid coatings was written by Alrashed, Maher M.;Soucek, Mark D.;Jana, Sadhan C.. And the article was included in Progress in Organic Coatings in 2019.Category: alcohols-buliding-blocks The following contents are mentioned in the article:

This work evaluates the performance of hybrid coatings of polyurethane/polysiloxane filled with graphene oxide as replacement of chromate conversion coatings for protection of 2024-T3 aluminum alloys. The polysiloxanes in the hybrid coating form strong covalent bonds with the metal surfaces and inhibit corrosion, polyurethanes provide mech. and optical properties, and graphene oxide and isocyanate-treated graphene oxide particles reduce oxygen and moisture diffusion through the coatings. The corrosion performance evaluated using electrochem. impedance spectroscopy and filiform corrosion test indicates the following trends. The hybrid coatings filled with isocyanate-treated graphene oxide particles show lower resistance to corrosion compared to hybrid coatings without graphene oxide, although oxygen diffusion and water vapor transmission are reduced by resp. 50% and 10% in the presence of only 0.67 weight% graphene oxide. It is revealed that graphene oxide and isocyanate-treated graphene oxide particles promote polysiloxane condensation on particle surfaces, thereby effectively reducing a part of polysiloxanes that form continuous corrosion-protective layers on the aluminum alloy surface. 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. 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.Category: alcohols-buliding-blocks

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Synthesis and properties of hyperbranched polyesters with diol as a core monomer was written by Wang, Yong;Zhu, Yan-an;Kong, Xia;Qu, Jin-qing. And the article was included in Gaoxiao Huaxue Gongcheng Xuebao in 2013.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

The third generation hyperbranched polyesters (HBPs) were synthesized by the pseudo-one step method with 2, 2-bis(hydroxyl-methyl) propionic acid as AB₂ monomer, p-toluene sulfonic acid as catalyst, in which 2-butyl-2-ethyl-1, 3-propanediol (BEPD, HBP-1), 1, 4-butanediol (BDO, HBP-2), and neopentyl glycol (NPG, HBP-3) were used as the core monomers, resp. The structures and mol. weights of HBPs were characterized with FT-IR, NMR and GPC as well as their intrinsic viscosities were also given. The film properties of HBPs cured by the toluene diisocyanate adduct were tested. The thermal stability of cured HBPs films were also examined by thermogravimetric anal. (TGA). It was found that HBPs are successfully synthesized and HBP-1 displays the highest branching degree up to 0.55. The GPC measured mol. weights of HBPs approach to the theor. values, and HBP-1 exhibits the lowest polydispersity index up to 1.68. HBPs are soluble in strong polar solvents and insoluble in non-polar solvents and HBP-1 displays better solubility and lower intrinsic viscosity up to 4.24 mL·g^-1. The cured HBPs films exhibit good thermal stability, adhesion, flexibility, and high hardness. 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. 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

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Polyalcohols – important raw materials for the resin and paint industry was written by Soerensen, Kent. And the article was included in Faerg och Lack Scandinavia in 1992.Product Details of 115-84-4 The following contents are mentioned in the article:

A review with 12 references The most common polyalcs., their application in the resin and paint industry, their contribution to the properties of the resins and paints, especially alkyd resins, polyesters, and acrylic monomers, and their structure-property relationship are presented. Together with actual market prices, these data will allow the paint chemist to find the optimum formulation for performance and cost more rapidly, and avoid using unsuitable polyalcs., thereby decreasing the number of experiments and thus costs. The topics include: introduction; the significance of chem. structure (type of hydroxyl group, side groups, neo-structure, functionality); description of different polyalcs. [pentaerythritol (I), trimethylolpropane (II), glycerin, di-pentaerythritol, di-trimethylolpropane, alkoxylates of I and II, neopentylglycol, monoethyleneglycol, propyleneglycol, dimethylolpropionic acid, allyl ethers, and other polyalcs. (2-Et-2-Bu-1,3-propanediol, 1,6-hexanediol, 1,4-butanediol, 2,2,4-trimethyl-1,3-pentanediol, 1,4-cyclohexanediethanol, trimethylolethane, hydroxypivalyl hydroxypivalate, and cyclic II formal)]. 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. 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.Product Details of 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Comprehensive evaluation on volatile components in ozone and ultraviolet combined treatment Lycium barbarum based on principal component analysis was written by Gong, Yuan;Wang, Xu;Liao, Ruo-yu;Xu, Meng-xia;Liu, Dun-hua. And the article was included in Shipin Gongye Keji in 2015.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

In order to study on the effects of volatile components in ozone and UV combined treatment Lycium barbarum, the volatile components in samples with different processing methods were extracted by headspace-solid and anal. by gas chromatog. mass spectrometry (GC-MS). The anal. and evaluation on the volatile components by the principal components anal. (PCA) and cluster anal. (CA). The results indicated that seventy-eight volatile components were identified from Lycium barbarum with different processing methods, including 14 kinds of esters, 21 kinds of alcs., 16 kinds of olefins, 15 kinds of ketones, 5 kinds of aldehydes, 3 kinds of acids, 4 kinds of ethers and HCAS. Ten volatile components were common to these Lycium barbarum samples. PCA anal. identified 42 main volatile components. Combining with clustering anal. comprehensive evaluation that the flavor of volatile components descending order was after of combined treatment of Ozone and UV drying Lycium barbarum>after of combined treatment of Ozone and UV and vacuum dried Lycium barbarum>dried Lycium barbarum>fresh Lycium barbarum. 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. 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.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

High-Capacity Digital Polymers: Storing Images in Single Molecules was written by Laurent, Eline;Amalian, Jean-Arthur;Parmentier, Marie;Oswald, Laurence;Al Ouahabi, Abdelaziz;Dufour, Florent;Launay, Kevin;Clement, Jean-Louis;Gigmes, Didier;Delsuc, Marc-Andre;Charles, Laurence;Lutz, Jean-Francois. And the article was included in Macromolecules (Washington, DC, United States) in 2020.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

High-capacity digital poly(phosphodiester)s were synthesized by stepwise automated phosphoramidite chem. Coding libraries containing either 4 or 8 phosphoramidite monomers of different mass were used to encode the polymers, thus enabling storage densities of 2 or 3 bits/monomer, resp. In addition, a monomer containing a cleavable alkoxyamine and nucleotide mass tags enabling fragment identification were included in the chains to allow their decryption by electrospray pseudo-MS³ sequencing. As a proof of concept, black and white images with sizes ranging from 80 to 144 pixels were encoded in single polymer chains and decoded by mass spectrometry. Six different polymers were prepared in this work; three with the 4-monomer alphabet and three with the 8-monomer alphabet. In all cases, uniform macromols. were obtained and deciphered. Yet, the bulkiest monomers of the 8-symbol alphabet required optimized protocols for uniform polymer synthesis. A macromol. storage capacity of 144 bits per chain was obtained in this work, which is the highest capacity ever attained for a synthetic informational polymer. 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

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Compatibility of arthropod repellents with certain functional finishes of cotton uniform fabric was written by Markarian, Haig;Pratt, John J. Jr.;DeMorco, Carlo G.;Gouck, Harry K.. And the article was included in Journal of Economic Entomology in 1968.Reference of 115-84-4 The following contents are mentioned in the article:

The compatibility of various insect repellents in combination with 2 water repellents, 2 detoxicants for chem. warfare agents, and a fire retardant impregnated into a standard Army cotton cloth was studied. The water repellant, Quarpel, increased the stability of the insect repellents, M-1960 [30% 2-butyl-2-ethyl-1,3-propanediol, 30% N-butylacetanilide, 30% benzyl benzoate, 10% poly(oxyethylene)(20)sorbitan monooleate] and benzyl benzoate to washing and showed a slightly increased stability of deet to rinsing. However all 3 of the insect repellents decreased the water repellency of Quarpel and removed the water repellency of a quaternary ammonium compound Effectiveness of a detoxicant for chem. warfare agents was enhanced when combined with either M-1960 or deet. Duration of effective mosquito repellency of M-1960 was decreased by the detoxicant for chem. warfare agents, while duration of effective tick repellency was increased. A fire retardant slightly enhanced the stability of M-1960 to washing but decreased its duration of effective mosquito and tick repellency. Fire retardancy was not affected. 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. 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. 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

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Aroma components of Zijuan tea processed by four different methods was written by Chen, Bao;Jiang, Dong-hua;Luo, Fa-mei;Man, Hong-ping;Luo, Zheng-gang;Hu, Yan-ping;Yang, Liu-xia. And the article was included in Xiandai Shipin Keji in 2013.Application of 115-84-4 The following contents are mentioned in the article:

The aroma components of Zijuan tea processed by different methods (sun-dry tea, baked green tea, black tea and fermented tea) were extracted by solid phase micro-extraction (SPME), quantified by gas chromatog./mass spectrometry (GC-MS) and quantified by area normalization method. The results showed that 146 compounds were identified from different processed Zijuan Tea, including 81 compounds from sun-dry tea, 80 from baked green tea, 68 from black tea, 69 from fermented tea, and 30 from all the samples tested. The main aroma compounds of sun-dry tea were l-Octen-3-ol, 2-ethyl-Hexanol, Hotrienol, and β-Terpineol, etc. The main aroma compounds of baked green tea were linalool, 2-ethyl-hexanol, benzyl alc., l-octen-3-ol, etc. The main aroma compounds of black tea were linalool, epoxylinalol, cis-linalool oxide, and benzyl alc. The main aroma compounds of fermented tea were 1, 2, 3-trimethoxybenzene, epoxylinalol, cis-linalool oxide, and 2-ethyl-hexanol. In summary, there were significant differences in composition and content of aroma compounds of different processed Zijuan tea extracted by SPME. 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. 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.Application of 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

A rapid method for screening and evaluating mosquito repellents was written by Bar-Zeev, Micha. And the article was included in Bulletin of Entomological Research in 1962.Safety of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Candidate repellents are rapidly screened and evaluated by comparing them with a standard repellent or with each other. Mosquitoes are confined in a Petri dish covered with mosquito gauze and the bottom is lined with 2 semicircular filter papers, 1 of which is treated with a standard repellent and the other with a test compound The dish is placed in an apparatus through which passes a low stream of air. Counts are taken every 30 sec. on and above the halves of the dish, which is jarred after every 2nd count to change the position of the insects; a total of 40 counts is taken. The index of reaction is the mean excess of position records for the candidate over those for the standard. In tests against Aedes aegypti, the repellency of N,N-diethyl-m-toluamide and of O-chloro-N,N-diethylbenzamide did not differ, but each significantly exceeded that of di-Me phthalate (DMP). The loss of repelleney of DMP with time was approx. linear. DMP was superior to ethyl-1,3-hexanediol, Pr N,N-diethylsuccinamate, and indalone, and equal to dimethyl carbate, hexyl mandelate, and 2-butyl-2-ethyl-1,3-propanediol. 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. 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. 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.Safety of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Equilibrium behavior of boric acid extracted by aliphatic 1,3-diols was written by Xiong, Yan;Bao, Zongbi;Xing, Huabin;Su, Baogen;Yang, Yiwen;Ren, Qilong. And the article was included in Huagong Xuebao (Chinese Edition) in 2012.SDS of cas: 115-84-4 The following contents are mentioned in the article:

Solvent extraction based on aliphatic 1,3-diols is a promising technique for the recovery of boric acid from salt lake brine. In this work, two diols, 2-ethyl-1,3-hexanediol (EHD) and 2-butyl-2-ethyl-1,3-propanediol (BEPD) were selected as extractants and toluene was used as diluents. The effects of extractant concentration, pH of brine, initial boric acid concentration, magnesium chloride concentration, and temperature on the distribution coefficients of boric acid were systematically investigated. Distribution coefficients of boric acid up to 9.43 and 8.25 were obtained from the boric acid aqueous solutions with the initial concentration of 0.0185 mol·L^-1 when using toluene containing 0.4 mol·L^-1 EHD and BEPD, resp., as organic phases at 303.15 K. Higher extractant concentration or lower pH is favorable to the extraction However, the distribution coefficients decrease gradually with the increase of boric acid concentration and temperature The extraction of boric acid with aliphatic 1,3-diols is an exothermic process. The salting-out effect of magnesium chloride enhances the extraction performance. 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. 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. 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.SDS of cas: 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts