Category: 115-84-4

Field tests with mosquito and sand-fly repellents in Alaska was written by Applewhite, K. H.;Smith, Carroll N.. And the article was included in Journal of Economic Entomology in 1950.HPLC of Formula: 115-84-4 The following contents are mentioned in the article:

In field tests with 10 repellents (25% solutions) applied to the human skin, Pr N,N-diethylsuccinamate (I) was most effective against Aedes flavescens and I and di-Me phthalate (II) were equally effective and superior to the other repellents against a mixed population of Aedes species. Cream preparations containing 20% of each of the 10 repellents were slightly less effective than the 25% solutions The repellents tested in addition to I and II were: Mixture 6-2-2 (I 60%, 2-ethyl-1,3-hexanediol 20%, Indalone 20%); 2-ethyl-1,3-hexanediol; 4-(p-methoxyphenyl)-5-methyl-1,3-dioxane; Indalone; 2,2′-thiodiethanol diacetate; pentamethylene propionate; Et β-phenylhydracrylate; 2-ethyl-2-nitro-1,3-propanediol butyraldehyde, 2-ethyl-2-nitro-1,3-propanediol acetal. Thirty-five materials known to have mosquito-repellent properties were applied to cotton stockings in acetone solution at 3 g./sq. ft. of cloth (6.6 g./stocking). The impregnated stockings were subjected to wear and rinsing (cold water) tests. Materials which withstood 4 or more rinsings and 16 h. of wear were: hexyl mandelate (superior); Indalone; 2,2-[(2-ethylhexyloxy)ethoxy]-ethanol; cyclohexanepropionic acid; α,α,α-trichloro-N-(2-chloroethyl)acetamide; N-butylhexahydrophthalimide; N-butyl-1,2,3,6-tetrahydrophthalimide; caprylic acid; allyl α,β-epoxy-β-phenylbutyrate; isobornyl 4-morpholineacetate. Repellents applied to face masks as a protection against sand flies (Culicoides tristriatulus) failed. 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. 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.HPLC of Formula: 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Tandem Synthesis of Ultra-High Molecular Weight Drag Reducing Poly-α-Olefins for Low-Temperature Pipeline Transportation was written by Nifant’ev, Ilya E.;Tavtorkin, Alexander N.;Vinogradov, Alexey A.;Korchagina, Sofia A.;Chinova, Maria S.;Borisov, Roman S.;Artem’ev, Grigory A.;Ivchenko, Pavel V.. And the article was included in Polymers (Basel, Switzerland) in 2021.Product Details of 115-84-4 The following contents are mentioned in the article:

Ultra-high mol. weight poly-α-olefins are widely used as drag reducing agents (DRAs) for pipeline transportation of oil and refined petroleum products. The synthesis of polyolefin DRAs is based on low-temperature Ziegler-Natta (ZN) polymerization of higher α-olefins. 1-Hexene based DRAs, the most effective at room temperature, typically lose DR activity at low temperatures The use of 1-hexene copolymers with C8-C12 linear α-olefins appears to offer a solution to the problem of low-temperature drag reducing. The present work aims to develop two-stage synthesis of polyolefin DRAs that is based on selective oligomerization of ethylene in the presence of efficient chromium/aminodiphosphine catalysts (Cr-PNP), followed by polymerization of the olefin mixtures, formed at oligomerization stage, using efficient titanium-magnesium ZN catalyst. We have shown that oligomerization of ethylene in α-olefin reaction media proceeds faster than in saturated hydrocarbons, providing the formation of 1-hexene, 1-octene, and branched C10 and C12 olefins; the composition and the ratio of the reaction products depended on the nature of PNP ligand. Oligomerizates were used in ZN polymerization ‘as is’, without addnl. treatment. We assume that faster solubility and more efficient solvation of the polyolefins, prepared using ‘tandem’ ethylene-based process, represent an advantage of these type polymers over conventional poly(1-hexene) and linear α-olefin-based polymers when used as ‘winter’ DRAs. 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. 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. 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

Pressurized liquid extraction technique for the analysis of pesticides, PCBs, PBDEs, OPEs, PAHs, alkanes, hopanes, and steranes in atmospheric particulate matter was written by Clark, Adelaide E.;Yoon, Subin;Sheesley, Rebecca J.;Usenko, Sascha. And the article was included in Chemosphere in 2015.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

An anal. method has been developed for the pressurized liquid extraction (PLE) of a wide range of semi-volatile organic compounds (SVOCs) from atm. particulate matter. Approx. 130 SVOCs from eight compound classes were selected as mol. markers of (1) agricultural activity (30 current and historic-use pesticides), (2) industrial activity (18 PCBs), (3) consumer products and building materials (16 PBDEs, 11 OPEs), and (4) motor vehicle exhaust (22 PAHs, 16 alkanes, 9 hopanes, 8 steranes). Currently, there is no anal. method validated for the extraction of all eight compound classes in a single automated technique. The extraction efficiencies of varying solvents and solvent combinations at high temperatures and pressures were examined Extracts were concentrated and analyzed by gas chromatog. coupled with mass spectrometry. The optimized PLE method utilized methylene chloride:acetone (2:1 volume/volume) at 100 °C with three (5 min) static cycles, flush volume of 80%, and a 100 s N₂ purge. Spike and recovery experiments (n = 7) provided average percent recoveries for pesticides, PCBs, PBDEs, OPEs, PAHs, alkanes, hopanes, and steranes of 88.8 ± 4.0%, 86.9 ± 2.6%, 83.8 ± 2.9%, 101 ± 6%, 90.3 ± 6.1%, 74.4 ± 8.8%, 104 ± 8%, and 86.5 ± 8.6%, resp. The developed method was applied to atm. particulate matter samples collected in the greater Houston, TX metropolitan area. Ambient concentrations of eight classes of compounds (92 SVOCs) were reported in pg m^-3. 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. 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.Name: 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Effect of pigmentation on polyurethane/polysiloxane hybrid coatings was written by Gao, Tongzhai;Maya-Visuet, Enrique;He, Zhouying;Castaneda-Lopez, Homero;Zvonkina, Irina J.;Soucek, Mark D.. And the article was included in Journal of Applied Polymer Science in 2016.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Rutile TiO₂ was formulated into polyurethane/polysiloxane hybrid coatings in order to investigate the influence of pigmentation on the inorganic phase of the hybrid coatings. Two urethanes were prepared from the isocyanurate of hexane diisocyanate (HDI), alkoxysilane modified HDI, and tetra-Et orthosilicate (TEOS) oligomers, with oligoesters derived from either cyclohexane diacids (CHDA) and 2-butyl-2-ethyl-1,3-propanediol (BEPD) or adipic acid (AA), isophthalic acid (IPA), 1,6-hexanediol (HD), and trimethylol propane (TMP). The oligoesters were spectroscopically characterized using GPC, FT-IR, and NMR. Chem. interaction between the TiO₂ and the sol-gel precursor was investigated using solid-state ²⁹Si NMR and XPS. The morphol., mech., viscoelastic, thermal properties of the pigmented coatings are evaluated as a function of pigmentation volume concentration (PVC). Using AFM and SEM, the pigment was observed to be well dispersed in the polymer binder. The thermal stability, the tensile modulus, and strength of the coatings were enhanced with increasing PVC, whereas the pull-off adhesion and flexibility (elongation-at-break) were reduced with increasing PVC. Finally, the pigmented coatings were evaluated by electrochem. impedance spectroscopy (EIS) and the results showed that 10 wt % of the pigment improved the corrosion resistance of the entire coating system. © 2015 Wiley Periodicals, Inc. Appl. Polym. Sci. 2016, 133, 42947. 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. 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. 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.Name: 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Nanoscale wetting and fouling resistance of functionalized surfaces: Computational approach was written by Yiapanis, George;Maclaughlin, Shane;Evans, Evan J.;Yarovsky, Irene. And the article was included in Langmuir in 2014.COA of Formula: C9H20O2 The following contents are mentioned in the article:

A computational modeling methodol. has been developed and employed to characterize the nanoscale wettability and antifouling properties of functionalized hard and deformable surfaces, with a specific focus on poly(ethylene glycol) grafted substrates and their resistance to graphitic carbons. Empirical evidence suggests that the antifouling behavior of polyethylene PEG is associated with two main mechanisms: steric repulsions and hydration via formation of a structured water layer. However, there is also little attention paid to the contribution of steric repulsion vs surface hydration. We examine these two mechanisms through a combination of in silico contact angle and force measurements at the nanoscale level. We investigate the properties of the grafted functional chains and the underlying substrate, responsible for resisting surface deposition of graphitic contaminants in aqueous solution Our results reveal that the fouling-release efficiency is enhanced when PEG chains are grafted onto hard hydrophilic substrates such as silica in contrast to deformable polymer substrates where surface modifications are effectively mitigated during interfacial contact with a hard contaminant. We conclude that the contribution of steric repulsion vs surface hydration to the antifouling ability of surfaces is strongly dependent on the nanoscale structure and deformability of the substrate. This generic method can be applied to examine individual contribution of steric repulsions and surface hydration to antifouling performance of grafted chains. 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. 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.COA of Formula: C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Effect of monomer structure on crystallization and glass transition of flexible copolyesters was written by Pan, Chengqian;Lu, Jing;Wu, Binshuang;Wu, Linbo;Li, Bo-Geng. And the article was included in Journal of Polymers and the Environment in 2017.Electric Literature of C9H20O2 The following contents are mentioned in the article:

Amorphous flexible (co)polyesters with low glass transition temperature (T_g) are very desirable in impact modification of biodegradable brittle polymers and synthesis of biodegradable elastomers. However, most flexible polyesters and binary copolyesters made from linear diacid(s) and diol(s) are crystalline polymers. In order to investigate the effect of monomer structure on the crystallization and T_g of such copolyesters, novel ternary or multiple flexible copolyesters containing various structural units were designed and synthesized in this study, and characterized with ¹HNMR, GPC, DSC, WAXD, TGA and tensile testing. Introducing aromatic diacid (especially asym. one) or short-chain branched diol is favorable to depress copolyester crystallization, and leads to higher T_g at the same time. From easily crystallized to fully amorphous copolyesters with low T_g were successfully synthesized by adopting different combination of structural units. In addition, the existence of aromatic structural unit in copolyesters is helpful to improve their tensile properties. Graphical Abstract: Flexible copolyesters containing various structural units were designed and synthesized. Introducing asym., rigid aromatic or short-chain branched unit is favorable to depress copolyester crystallization, and leads to higher T_g at the same time. Crystalline to fully amorphous copolyesters with low enough T_g have been successfully synthesized by adjusting the structural units. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Electric Literature 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Electric Literature of C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Evaluations of repellents for Hippelates eye gnats was written by Axtell, Richard C.. And the article was included in Journal of Economic Entomology in 1967.Category: alcohols-buliding-blocks The following contents are mentioned in the article:

Twenty chemicals or combinations of chemicals were evaluated for their repellency toward H. pusio with turntables in the field. Some of the materials were also tested against H. bishoppi and H. pallipes. The most effective repellents for H. pusio were: Triple Mix (63.8% di-Me phthalate + 18.8% Indalone (butyl 3,4-dihydro-2,2-dimethyl-4-oxo-2H-pyran-6-carboxylate) + 17.3% ethylhexanediol), MGK (McLaughlin Gormley King Co.) Formula 5780 (75% ethylhexanediol + 4% MGK 264 (N-2-ethylhexyl)-5-norbornene-2,3-dicarboximide) + 1% MGK Repellent 11 (1,5a,6,9,9a,9b-hexahydro-4a-(4H)-dibenzofurancarboxaldehyde) + 1% MGK Repellent 326 (di-Pr 2,5-pyridinedicarboxylate)), butyl-acetanilide, and butylethylpropanediol. Less repellency was shown by TMPD (2,2,4-trimethyl-1,3-pentanediol) + 8% di-Me phthalate, TMPD, and ethylhexanediol. Other materials exhibited little or no repellency. H. bishoppi was generally repelled by those chemicals which were effective against H. pusio but some exceptions indicated definite differences in the sensory responses of these 2 species. Limited tests indicated that a repellent that is effective against H. pusio is not necessarily effective against H. pallipes. Four repellents applied to human skin were tested for their effectiveness against caged laboratory-reared gnats. The frequency of gnat landings on the treated skin of the forearms was used as the index of effectiveness. The repellency of deet, Triple Mix, and ethylhexanediol declined to 50% of the initial level in about 110 min. and TMPD in about 60 min. 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. 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.Category: alcohols-buliding-blocks

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Study of the infrared spectrophotometry and intramolecular hydrogen bonding in the structures of 1,3-glycols was written by Buc, Henri;Neel, Jean. And the article was included in Compt. Rend. in 1961.SDS of cas: 115-84-4 The following contents are mentioned in the article:

cf. Kuhn, CA 53, 9044b. In order to study the intensity of intramol, interaction between hydroxyl groups in poly(vinyl alcohol) a systematic examination of infrared absorption near 3600 cm.^-1 for 11 different 1,3-glycols, a 1,3,5-triol, and 7 alcohols was undertaken. All spectra were obtained in CCl₄ solution at 25° (unless otherwise stated) using a LiF prism (first 6 spectra) or a CaF₂ prism. Data for each compound, the free OH frequency ν1, the bonded OH frequency, ν2, the ratio of optical densities τ = D₂/D₁, the difference in frequencies Δν = ν1 – ν2, and Δμ’ the difference in frequency of the OH involved in the chelation, follow: 1,3-propanediol, 3635, 3557, 0.46, 78, -; PrOH, 3634, -, -, -, -; dl-1,3-butanediol, 3628, 3550, 0.92, 78, 84; BuOH, 3634, -, -, -, -; sec-BuOH, 3626, -, -, -, -; tert-BuOH, 3619, -, -, -, -; 1,3-propanediol, 3636, 3557, 0.45, 79, -; 2,2-dimethyl-1,3-propanediol, 3629, 3545, 0.50, 94, -; 2,2-diethyl-1,3-propanediol, 3639, 3545, 0.52, 94, -; 2-methyl-2-propyl-1,3-propanediol, 3639, 3545, 0.55, 94, -; 2-ethyl-2-butyl-1,3-propanediol, 3638, 3546, 0.51, 92, -; β-2,4-pentanediol, 3626, 3532, 1.52, 94, -; β-2,4-pentanediol, 3626, 3532, 0.81, 94, -; dl-2-methyl-2,4-pentanediol, 3614 (shoulder at 3628), 3529, 1.83, 85, 95; 2-pentanol, 8625, -, -, -, -; 1,5-pentanediol (65°), 3636, 3541, 0.09, 95, -; dl-1,3,5-pentanetriol, 3633 (shoulder at 3640), 3531, 1.07, 102, 105; 1-pentanol (65°), 3636, -, -, -, -; 3-pentanol (65°), 3632, -, -, -, -. 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. 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. 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.SDS of cas: 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

New materials for use as insect repellents was written by Smith, C. N.. And the article was included in Proceedings of the Annual Meeting, Chemical Specialties Manufacturers Association in 1950.SDS of cas: 115-84-4 The following contents are mentioned in the article:

Recent investigations of insect repellents for the U.S. Dept. of Defense have involved treatments for skin and clothing. Skin treatments in Alaska showed Pr N,N-diethylsuccinamate and dimethyl cis-bicyclo-[2.2.1]-5-heptene-2,3-dicarboxylate to be most effective against mixed populations of several species of Aedes mosquitoes. Compounds which were outstanding in clothing treatments against several species of mosquitoes included 2-butyl-2-ethyl-1,3-propanediol, N-butyl-1,2,3,6-tetrahydrophthalimide, α-butoxy-N-cyclohexylacetamide, Indalone, hexyl mandelate, Repellent 612, and dimethyl phthalate. N-butyl-, N-propyl-, and N-isopropylacetanilide, and N,N-dibutylaceto- and α-butoxy-N-cyclohexylacetamide were 90-100% effective against the lone star tick, Amblyomma americanum. Benzyl benzoate was effective against cat fleas, Ctenocephalides felis; hexyl mandelate and N-butyl- and N-prophylacetanilide were effective against rat fleas, Xenopsylla cheopis; hendecylic acid was effective against both. A mixture containing 30% each of 2-butyl-2-ethyl-1,3-propanediol, N-butylacetanilide, benzyl benzoate and 10% Tween 80 emulsifier, tested at 3.2 active ingredients/sq. ft. of cloth, was more effective against 3 species of mosquitoes than any individual repellent, was about equal to the best individual repellent against ticks, and only slightly less effective than the best against fleas; toxicity and skin-irritation tests are under way. The most practical materials for area control of chiggers are toxaphene, chlordan, and benzene hexachloride; for personal protection, benzyl benzoate. 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. 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. 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

Vapor Pressure, Heat Capacity, and Density along the Saturation Line: Measurements for Benzenamine, Butylbenzene, sec-Butylbenzene, tert-Butylbenzene, 2,2-Dimethylbutanoic Acid, Tridecafluoroheptanoic Acid, 2-Butyl-2-ethyl-1,3-propanediol, 2,2,4-Trimethyl-1,3-pentanediol, and 1-Chloro-2-propanol was written by Steele, W. V.;Chirico, R. D.;Knipmeyer, S. E.;Nguyen, A.. And the article was included in Journal of Chemical and Engineering Data in 2002.COA of Formula: C9H20O2 The following contents are mentioned in the article:

This paper reports measurements made within DIPPR² Project 821 for the 1995 Project Year. Vapor pressures were measured to a pressure limit of 270 kPa or lower decomposition point using a twin ebulliometry apparatus for the nine compounds listed in the title. Liquid-phase densities along the saturation line were measured for each compound over a range of temperatures (ambient to a maximum of 523 K). A differential scanning calorimeter was used to measure two-phase (liquid + vapor) heat capacities for each compound in the temperature region ambient to the critical temperature or lower decomposition point. Where possible, the critical temperature and critical d. for each compound were determined exptl. The results of the measurements were combined to derive a series of thermophys. properties including critical temperature, critical d., critical pressure, acentric factor, enthalpies of vaporization (restricted to within ± 50 K of the temperature region of the exptl. determined vapor pressures), enthalpies of fusion if solid at 310 K, solubility parameters, and heat capacities along the saturation line. Vapor-pressure representations were derived for each compound All measured and derived values were compared with those obtained in a search of the literature. Recommended critical parameters are listed for each of the compounds studied except 1-chloro-2-propanol. The compounds studied were benzenamine, butylbenzene, sec-butylbenzene, tert-butylbenzene, 2,2-dimethylbutanoic acid, tridecafluoroheptanoic acid, 2-butyl-2-ethyl-1,3-propanediol, 2,2,4-trimethyl-1,3-pentanediol, and 1-chloro-2-propanol. 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 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.COA of Formula: C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts