Category: 115-84-4

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

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