Category: 115-84-4

Evaluation of repellents against mosquitoes in Panama was written by Gilbert, I. H.;Gouck, H. K.. And the article was included in Florida Entomologist in 1955.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Protection time for skin applications of dimethyl phthalate (I) is 304 min. Protection time in min. for other compounds and mixtures is allyl mandelate 387; 1-(o-methoxyphenyl)-3-buten-1-ol 366; propyl mandelate 362; α-tert-butylpiperonyl alc. 361; o-ethoxy-N,N-diethylbenzamide (II) 356; N,N-diethyl-m-toluamide 349; amyl mandelate 344; N,N-diethyl-o-toluamide 332; dimethyl carbate (III) 318; 2-ethyl-1,3-hexanediol (IV) 313; propyl ester of N,N-diethylsuccinamic acid (V) 311; o-chloro-N,N-diethylbenzamide (VI) 308; 2-[2-(2-butoxyethoxy)ethoxy]ethyl senecioate 291; citral-malonic acid condensate Number 1 259; 60% I, 20% IV, and 20% indalone 328; 50% IV and 50% II 346; 40% I, 30% IV, and 30% V 325; 40% IV, 30% V, and 30% VI 318; 40% I, 30% IV, and 30% III 305; 16% I, 12% IV, 12% III, 10% ZnO, 10% Delta Prime (VII), 0.75% Veegum (VIII), 3% Span 80 (IX), 2% Tween 80 (X), and 34.25% H₂O 195; and 16% I, 12% IV, 12% III, 10% ZnO, 10% VII, 2.4% IX, 1.6% X, 0.25% VIII, 1.75% Pluronic F-68, and 34% H₂O 180. Addition of a few percent of α-cyano-2-furanacrylate to I and II of the above mixtures slightly increases protection time. 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. 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.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Determination of acid value, hydroxyl value and water content in reactions between dicarboxylic acids and diols using near-infrared spectroscopy and non-linear partial least squares regression was written by Heikka, Riitta A.;Immonen, Kirsi T.;Minkkinen, Pentti O.;Paatero, Erkki Y. O.;Salmi, Tapio O.. And the article was included in Analytica Chimica Acta in 1997.HPLC of Formula: 115-84-4 The following contents are mentioned in the article:

A predictive calibration model based on non-linear partial least squares (PLS) regression was developed to describe the relationship between the near-IR (NIR) reflectance spectra and the acid value, hydroxyl value, and water content in polyesterification of dicarboxylic acids with diols. Two dicarboxylic acids and six diols were tested in different combinations with one dicarboxylic acid and one diol at a time. Reactions were carried out isothermally in a laboratory scale semi-batch reactor at 140-190°. NIR spectrometry offered a fast in-line method for monitoring and controlling the polyesterification reaction. A predictive model which related all the NIR spectra and the measured acid values was developed. Calibration of the NIR spectra and the hydroxyl value succeeded in experiments in which the hydroxyl value was determined The measured water content and the NIR spectra could not be calibrated with the same model for different dicarboxylic acid and diol combinations. Principal component anal. (PCA) was used to classify the NIR spectra. The spectra could be classified according to the dicarboxylic acid and diol used in the experiment 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. 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. 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

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Thermomechanical Formation-Structure-Property Relationships in Photopolymerized Copper-Catalyzed Azide-Alkyne (CuAAC) Networks was written by Baranek, Austin;Song, Han Byul;McBride, Mathew;Finnegan, Patricia;Bowman, Christopher N.. And the article was included in Macromolecules (Washington, DC, United States) in 2016.Computed Properties of C9H20O2 The following contents are mentioned in the article:

Bulk photopolymerization of a library of synthesized multifunctional azides and alkynes was carried out toward developing structure-property relationships for CuAAC-based polymer networks. Multifunctional azides and alkynes were formulated with a copper catalyst and a photoinitiator, cured, and analyzed for their mech. properties. Material properties such as the glass transition temperatures (T_g) show a strong dependence on monomer structure with T_g values ranging from 41 to 90 °C for the series of CuAAC monomers synthesized in this study. Compared to the triazoles, analogous thioether-based polymer networks exhibit a 45-49 °C lower T_g whereas analogous monomers composed of ethers in place of carbamates exhibit a 40 °C lower T_g. Here, the formation of the triazole moiety during the polymerization represents a critical component in dictating the material properties of the ultimate polymer network where material properties such as the rubbery modulus, crosslink d., and T_g all exhibit strong dependence on polymerization conversion, monomer composition, and structure postgelation. 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. 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.Computed Properties of C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

A Bartonella Effector Acts as Signaling Hub for Intrinsic STAT3 Activation to Trigger Anti-inflammatory Responses was written by Sorg, Isabel;Schmutz, Christoph;Lu, Yun-Yueh;Fromm, Katja;Siewert, Lena K.;Bogli, Alexandra;Strack, Kathrin;Harms, Alexander;Dehio, Christoph. And the article was included in Cell Host & Microbe in 2020.Product Details of 115-84-4 The following contents are mentioned in the article:

Chronically infecting pathogens avoid clearance by the innate immune system by promoting premature transition from an initial pro-inflammatory response toward an anti-inflammatory tissue-repair response. STAT3, a central regulator of inflammation, controls this transition and thus is targeted by numerous chronic pathogens. Here, we show that BepD, an effector of the chronic bacterial pathogen Bartonella henselae targeted to infected host cells, establishes an exceptional pathway for canonical STAT3 activation, thereby impairing secretion of pro-inflammatory TNF-α and stimulating secretion of anti-inflammatory IL-10. Tyrosine phosphorylation of EPIYA-related motifs in BepD facilitates STAT3 binding and activation via c-Abl-dependent phosphorylation of Y₇₀₅. The tyrosine-phosphorylated scaffold of BepD thus represents a signaling hub for intrinsic STAT3 activation that is independent from canonical STAT3 activation via transmembrane receptor-associated Janus kinases. We anticipate that our findings on a mol. shortcut to STAT3 activation will inspire new treatment options for chronic infections and inflammatory diseases. 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. 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.Product Details of 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

BEPD (2-butyl-2-ethyl-1, 3-propanediol): A branched diol for high performing polyesters for coil coatings was written by Sorensen, Kent;Bernquist, Henrik;Ramakrishnan, S.;Saindane, Bhushan. And the article was included in Paintindia in 2013.HPLC of Formula: 115-84-4 The following contents are mentioned in the article:

Coil coating pre-coated metal, is a growing coating technol. due to its economic and sustainable advantages. The coating not only needs to be flexible enough so that it can be post-formed, but also give hardness, weather resistance, corrosion protection and be decorative. Polyesters are the workhorse resin for coil coatings and offer an economical coating with a very good performance balance overall, but the level of performance also depends on the monomer composition used. BEPD is an attractive choice here for achieving high quality polyesters due to its neo-structure and large bulky side-groups. The absence of βhydrogens improves the stability of the polyester when exposed to environmental factors and it also improves the thermal stability. Bulky side-groups protect the ester bonds against hydrolysis, break the crystallinity tendency without sacrificing the performance, introduce flexibility and give some lower viscosity to the coatings. The bulky side-groups do not give any prolonged esterification time as might have been expected. In this paper BEPD is compared with other glycols, e.g., neopentylglycol in coil polyesters. 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. 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. 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

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

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

Outdoor exposure and accelerated weathering of polyurethane/polysiloxane hybrid coatings was written by Gao, Tongzhai;He, Zhouying;Hihara, Lloyd H.;Mehr, Hamideh Shokouhi;Soucek, Mark D.. And the article was included in Progress in Organic Coatings in 2019.Computed Properties of C9H20O2 The following contents are mentioned in the article:

Two Polyurethane/polysiloxane hybrid coatings were compared using both real time exposure and accelerated weathering. The urethane coatings were differentiated by oligoesters selection with one being derived from cyclohexane diacids (CHDA) and 2-butyl-2-ethyl-1,3-propanediol (BEPD) and the other adipic acid (AA), isophthalic acid (IPA), 1,6-hexanediol (HD), and trimethylol propane (TMP). Three sites in Hawaii, Campbell Industrial Park (CIP), Kilauea Volcano, and Marine Corp Base Hawaii (MCBH), were selected for the outdoor exposure test with the increasing severity of the environment. After weathering, the coatings were analyzed by Fourier transform IR spectroscopy (FTIR) and solid state ¹³C NMR (NMR), Dynamic mech. anal. (DMA) and differential scanning calorimetry (DSC), and Scanning electronic microscopy (SEM). Urethanes based on cycloaliphatic oligoesters exhibited much better appearance compared to the aromatic-based polyesters. A degradation of both the carbamate and ester functionality was observed spectroscopically which was accompanied by an increase in Tg, and erosion of the surface of the coatings. It was found that the accelerated weathering test conducted in weatherometer provides harsher conditions than the three outdoor exposure tests (marine, volcano, and industrial park), while marine is the harshest among the three outdoor exposure sites. 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. 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. 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.Computed Properties of C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts