Category: 115-84-4

Influence of the glycol component in dibenzoate plasticizers on the properties of plasticized PVC films was written by Wardzinska, Elzbieta;Penczek, Piotr. And the article was included in Journal of Applied Polymer Science in 2005.Computed Properties of C9H20O2 The following contents are mentioned in the article:

A series of glycol dibenzoates was synthesized by transesterification of glycols with Me benzoate. PVC films were prepared from suspension grade PVC and the dibenzoates at a constant content of the dibenzoates. The mech. properties of the films were measured. In addition, the extractability and the absorption of various liquids was determined The effect of the structure of the glycol component in the dibenzoates on the mech. properties of the films and the plasticizing efficiency was investigated. Neopentyl glycol dibenzoate exhibits the highest plasticizing effect, followed by triethylene and ethylene glycol dibenzoates and the 2-(n-butyl)-2-ethyl-1,3-propanediol derivative It was found that the ether linkages in the dibenzoates mainly contribute to the plasticization of PVC. 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. 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.Computed Properties of C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Triple triangle glycol study was written by Eastman. And the article was included in Pitture e Vernici in 1991.Application of 115-84-4 The following contents are mentioned in the article:

The effect of incorporating 2-butyl-2-ethyl-1,3-propanediol (I), hydroxypivalyl hydroxypivalate (II), 2,2-dimethyl-1,3-propanediol (III), 2,2,4-trimethyl-1,3-pentanediol (IV), and(or) 1,4-cyclohexanedimethanol (V) into a polyester high-solids enamel were demonstrated. I and II demonstrated good synergism with other glycols, III gave good overall performance and was used as a reference, IV provided good hydrolytic and stain resistance but was the poorest in processing and had a poor hardness/flexibiility ratio, and V offered good salt spray and humidity resistance and was the fastest processing glycol with its main disadvantage being high solution viscosity and organic volatiles. 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. 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.Application of 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Efficacy of the clothing impregnants M-2065 and M-2066 against terrestrial leeches in North Borneo was written by Walton, Boyce C.;Traub, Robert;Newson, Harold D.. And the article was included in American Journal of Tropical Medicine and Hygiene in 1956.Safety of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

cf. Traub, et al., Nature 169, 667(1952). Impregnation of clothing with M-1960 (N-butylanilide 30, 2-butyl-2-ethyl-1,3-propanediol 30, benzylbenzoate 30, Tween 80 (I) 10%), M-2065 (C₁₀H₂₁CO₂H) (II) 29, N-propylacetanilide (III) 29, N-butyl-4-cyclohexene-1,2-carboximide (IV) 29, lindane (V) 3, and I 10%), or M-2066 (II, III, and IV, 29.66 each, V 1, I 10%) allowed an attachment of a maximum of 1 Haemadipsa zeylonica subagilis or H. picta during 0.5-h. wear while untreated clothing collected more than 14 and native dress averaged 9-22 leeches. Incomplete protection was given after 4, none after 6 washings of the uniforms. Most of the leeches going through treated uniforms had not fed while more than 50% of those in untreated uniforms had fed. Impregnated socks were an effective protection for scantily clad people. 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. 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.Safety of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Mechanism of chromic acid oxidation. III. The oxidation of diols was written by Kwart, Harold;Ford, J. A. Jr.;Corey, G. C.. And the article was included in Journal of the American Chemical Society in 1962.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

cf. CA 54, 6505a; 56, 7111c. The earlier interpretations of Rocek (CA 54, 13833a) and Favre (CA 53, 18084d) of the rates of chromic acid oxidation of diols were found to be misleading, in view of conformational and structural effects which govern the reactivity. The occurrence of cyclic chromate esters as intermediates in the oxidation of certain diol structures but not of others was inferred from rate data obtained for a variety of bicyclic, alicyclic, and acyclic 1,2- and 1,3-diols. In this fashion also, the geometric requirements for such cyclic chromate ester formation were found to be similar to those deduced earlier for boric acid complexing with diols. It was suggested that the formation of esters by interaction of chromic acid with alcs. was quite analogous to ester formation with boric rather than sulfuric acid, as claimed by Rocek. 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. 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.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

New CO₂-philic propane derivatives: design, synthesis and phase behavior in supercritical carbon dioxide was written by Li, Yalin;Yang, Hai-Jian;Zhou, Tao. And the article was included in Current Organic Chemistry in 2013.Formula: C9H20O2 The following contents are mentioned in the article:

Three new potent CO₂-philic propane derivatives, i.e. 1,3-bis(3-chloropropionyloxy)-2,2-diethylpropane, 1,3-bis(3-chloropropionyloxy)-2-butyl-2-ethylpropane, and 1,3-bis(3-chloropropionyloxy)-2-methyl-2-propylpropane, were designed and synthesized. Their structures were characterized by NMR, FTIR, and elemental anal. Phase behavior of the three compounds was investigated at temperatures ranging from 313 K to 333 K and pressures from 9.1 MPa to 16.1 MPa in supercritical carbon dioxide, the solubility differences were discussed. The exptl. solubility data were calculated and correlated by the two d.-based models: Bartle and Chrastil, and satisfied agreements were obtained. Addnl., the partial molar volumes V₂ for each compound were also estimated in the supercritical phase using the theory developed by Kumar and Johnston. 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

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Synthesis of some 1,1,1-tris(hydroxymethyl)alkanes was written by Weibull, Bengt;Matell, Magnus. And the article was included in Acta Chemica Scandinavica in 1962.Application of 115-84-4 The following contents are mentioned in the article:

By condensing 0.4 mole aldehyde with 3 moles HCHO in 500 ml. 1:1 aqueous EtOH and adding 0.4 mole KOH in 200 ml. 1:1 aqueous EtOH dropwise with cooling, the following 1,1,1-tris(hydroxymethyl)alkanes [R of RC(CH₂-OH)₃, % yield, b.p.(mm.), and m.p. (crystallization solvent), resp., given] were prepared: C₅H₁₁, 61, 160-2° (1.5), 64-5.5°(CCl₄); C₆H₁₃, -, – (-), 68-70° (CHCl₃); C₈H₁₇, 65, 190-200° (1.5), 73.5-5° (ligroine); C₉H₁₉, 47, 187-90° (1), 77-9° (ligroine); C₁₀H₂₁, 45, 180-6° (0.3), 79.5-81° (ligroine); and C₁₂H₂₅, 51, 200-20° (2.5), 83-8° (ligroine). Similarly prepd, was 3,3-bis(hydroxymethyl)heptane, 83, 136-43° (8), 40-2.5° (-). 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

Polymeric plasticizers. Preparation and characterization of a series of terminated polyesters was written by Koroly, Joseph E.;Beavers, Ellington M.. And the article was included in Industrial and Engineering Chemistry in 1953.Category: alcohols-buliding-blocks The following contents are mentioned in the article:

The general schematic structure for terminated polyesters L-G-(-A-G-)_n-L, where A represents a dibasic acid, L a mono-basic acid, G a dihydric alc., and n is the number of repeating units, is the basis of preparation of a polymeric plasticizer series. The monobasic acid of the reported study is lauric; the dibasic acids are succinic, adipic, sebacic, glutaric, thiodipropionic, azelaic, and γ-methyl-γ-acetylpimelic; the glycols are 1,2-propylene, ethylene, trimethylene, 1,3-butylene, 2,2-dimethyl-1,3-propanediol, and 2-ethyl-2-butylpropanediol; and the values of n are 1-10. The rate and degree of completion of the first reaction stage, which was direct esterification, was characterized by determination of the acid number; and that of the second reaction stage, which was polymerization by trans-esterification, was characterized by melt viscosity of the reaction mixture 20 references. 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. 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. 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.Category: alcohols-buliding-blocks

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Formation of neutral complexes of boric acid with 1,3-diols in organic solvents and in aqueous solution was written by Bachelier, Nicolas;Verchere, Jean-Francois. And the article was included in Polyhedron in 1995.HPLC of Formula: 115-84-4 The following contents are mentioned in the article:

From solubility measurements in organic media and extraction experiments, the values of the stability constants of neutral 1:1 complexes (HBL) formed between boric acid (HB) and 1,3-diols (L) were obtained in aqueous solution (K_cw) and in organic solvents (K_cs). The values of the partition coefficients of the diols (P_L) and (P_HBL) between H₂O and the organic solvents also were calculated Generally, the addition of a diol to an aqueous solution of borax is accompanied by a decrease of pH due to the prevailing formation of borate species but, in the case of 2-methyl-2,4-pentanediol, the pH increased, in agreement with the formation of a single neutral complex. A modification of a previous potentiometric procedure yields simultaneously the values of the stability constants of the neutral and anionic complexes in aqueous solution 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. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. 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

Study on extracting boron from underground brine by 2-butyl-2-ethyl-1,3-propanediol was written by Peng, Hao-ran;Shi, Hao;Zeng, Ying;Guo, Li;Jiang, Yun-jiang. And the article was included in Huagong Kuangwu Yu Jiagong in 2015.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Study was carried out of extracting boron from underground brine in Pingluo, Sichuan using 2-butyl-2-ethyl-1,3-propanediol (BEPDO) as extractant, and chloroform as diluents. The condition experiments show that the optimal concentration of extractant was 1.0 mol/L, the ratio of organic phase to brine was 1:1, the extraction time was 10 min, and through a two-stage extraction, the extraction rate reached 98.56% while the extraction capacity reached 44.25 g/L (in terms of H₃BO₃). In the stripping process, sodium hydroxide was used as stripping agent. The stripping rate reaches 95.49% under the optimal conditions: 0.3 mol/L sodium hydroxide, 8 min stripping time, ratio of organic phase to stripping agent 1:1, two-stage stripping. The recovery of boric acid reaches 94.87% after two-stage extracting and two-stage stripping under optimal conditions. 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Comparative tests for glass-resin bonds in laminates. Applications tounsaturated polyester-glass laminates was written by Zalmanski, Alain. And the article was included in Revue Generale des Caoutchoucs & Plastiques in 1970.Formula: C9H20O2 The following contents are mentioned in the article:

The difference between the bonding strengths of glass-polyester laminates and those of component polyesters prepared from copolymers of maleic, fumaric, itaconic, or citraconic anhydride; phthalic or isophthalic acids or hydrogenated analogs or adipic, succinic, anthracenesuccinic, or methacrylic acid or their anhydrides; propylene glycol, neopentyl glycol (I), or 1,3-butylene diglycol (II), etc.; and styrene, Me methacrylate (III), ethylene glycol dimethacrylate (IV), chlorostyrene (V), and (or) other vinyl monomers were a measure of the adhesion of the laminates. Best results were observed for polyesters prepared from ∼25% maleic anhydride; tetrahydrophthalic or anthracenesuccinic acid; I or II; and from styrene partially replaced by III, IV, or V. Improvement of adhesion is accompanied by improved phys.-chem. characteristics, especially weatherability. 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 weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. 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.Formula: C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts