Category: 5444-75-7

A unique benzoate plasticizer for reducing viscosity and fusion temperature was written by Bohnert, T.;Stanhope, B.;Gruszecki, K.;Pitman, S.;Elsworth, V.. And the article was included in Annual Technical Conference – Society of Plastics Engineers in 2000.COA of Formula: C15H22O2 The following contents are mentioned in the article:

Plastisol viscosity reduction and control is an important property specification in many PVC plastisol formulations. 2-Ethylhexyl benzoate plasticizer is under development that functions as a viscosity reducer. It also is a high solvating plasticizer in standard plastisol systems. Data are presented on the effect of the new benzoate plasticizer on phthalate- and other benzoate-containing plastisols and vinyl sheet properties. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7COA of Formula: C15H22O2).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. COA of Formula: C15H22O2

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Unique benzoate plasticizer for reducing viscosity and fusion temperature was written by Bohnert, T.;Stanhope, B.;Gruszecki, K.;Pitman, S.;Elsworth, V.. And the article was included in Journal of Vinyl & Additive Technology in 2000.Application In Synthesis of 2-Ethylhexyl benzoate The following contents are mentioned in the article:

Plastisol viscosity reduction and control is an important property specification in many vinyl plastisol formulations. 2-Ethylhexyl benzoate plasticizer is under development that functions as a viscosity reducer for PVC. It also is a highly solvating plasticizer in standard plastisol systems. Data are presented on the effects of the new benzoate plasticizer on the properties of phthalate- and benzoate-containing plastisols and vinyl sheet for flooring. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Application In Synthesis of 2-Ethylhexyl benzoate).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Application In Synthesis of 2-Ethylhexyl benzoate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Rapid and ecofriendly esterification of alcohols with 2-acylpyridazinones was written by Kim, Bo Ram;Sung, Gi Hyeon;Ryu, Ki Eun;Kim, Jeum-Jong;Yoon, Yong-Jin. And the article was included in Bulletin of the Korean Chemical Society in 2013.Electric Literature of C15H22O2 The following contents are mentioned in the article:

Atom-economical esterification is of great importance in green chem. The authors demonstrated the catalyst and additive free esterification of alcs. by their reaction with 2-acyl-4,5-dichloropyridazin-3(2H)- ones without solvent at 100°. Aliphatic and aromatic alcs. were converted into the corresponding esters in good to excellent yields. It is noteworthy that the reaction is solvent-free, atom-economic, easy-workup, and rapid and that the process is inexpensive. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Electric Literature of C15H22O2).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Electric Literature of C15H22O2

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Analysis of component composition of volatile compounds of field sow thistle (Sonchus Arvensis L.) leaves using the method of gas chromatography with mass-detection was written by Delyan, Eugene. And the article was included in Pharma Innovation in 2016.Computed Properties of C15H22O2 The following contents are mentioned in the article:

Gas chromatog. mass spectrometry (GC-MS) anal. revealed the presence of 26 compounds in leaves of field sow thistle Nutt. In GC-MS anal., some of the phytocomponents screened were phytol, pentacosane, 1,2-benzenedicarboxylic acid, bis (2-methylpropyl) ester. The compounds were identified by comparing their retention time and peak area with that of literature and by interpretation of mass spectra. Many of them have antioxidant, anti-inflammatory, antimicrobial and anticancer actions. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Computed Properties of C15H22O2).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Computed Properties of C15H22O2

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Catalytic reactions in microwave reactors was written by Pipus, Goran;Plazl, Igor;Koloini, Tine. And the article was included in Recents Progres en Genie des Procedes in 1999.Related Products of 5444-75-7 The following contents are mentioned in the article:

Esterification of benzoic acid with 2-ethylhexanol was studied in a microwave reactor. The reaction was homogeneously catalyzed with sulfuric acid. The microwave reactor operated at atm. pressure with reflux equipment. Kinetic parameters were exptl. determined under conventional heating. Conversions of the esterification were calculated on the basis of the measured temperatures and kinetic parameters. The operating conditions of the stirred tank reactor allowed to almost complete esterification in 20 min. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Related Products of 5444-75-7).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Related Products of 5444-75-7

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

A model for the pressure dependence of diffusion in condensed matter was written by Kapoor, Kamal;Kumari, Rashmi;Dass, Narsingh;Kumar, Rajendra. And the article was included in Pramana in 2006.Synthetic Route of C15H22O2 The following contents are mentioned in the article:

In the present paper, a model has been used to develop a simple relation to study the pressure dependence of self-diffusion in solids and liquids that has two adjustable parameters. The computation done in each substance is found to be in very good agreement with the exptl. data. It is interesting to note that the present relation is also capable of giving the activation volume in solids and liquids The activation volume computed in the solids is found to be in very good agreement with the data available. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Synthetic Route of C15H22O2).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Synthetic Route of C15H22O2

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Benzyl derivatives was written by Sipes, I. G.;DiNovi, M.;Larsen, J. C.;Renwick, A. G.. And the article was included in WHO Food Additives Series in 2011.Recommanded Product: 5444-75-7 The following contents are mentioned in the article:

The Committee evaluated eight addnl. flavoring agents belonging to the group of benzyl derivatives that was previously evaluated. The structural feature common to all members of the group is a primary oxygenated functional group bonded directly to a benzene ring or a functional group metabolized to a benzyl alc. or benzoic acid derivative Generally, the Committee concluded that these eight flavoring agents, which are additions to the group of benzyl derivatives evaluated previously, would not give rise to safety concerns at current estimated dietary exposures. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Recommanded Product: 5444-75-7).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: 5444-75-7

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Variable-pressure infrared studies on the molecular flexibility of the model lubricant 2-ethylhexyl benzoate (EHB) was written by Whitley, Andrew;Yarwood, Jack;Gardiner, Derek J.. And the article was included in Journal of the Chemical Society, Faraday Transactions in 1993.Application of 5444-75-7 The following contents are mentioned in the article:

A liquid-phase high-pressure IR study of the model lubricant 2-ethylhexyl benzoate (EHB) between 0 and 40 kbar (at ambient temperature) is reported. Changes in band position and bandwidth were interpreted in terms of in-chain and lateral chain interactions with a net increase in the importance of repulsive potentials and an increase in the distribution of mol. environments. Although changes in the proportion of gauche conformers in the hydrocarbon chain would be expected at higher densities, evidence of such changes were difficult to find in the IR spectrum. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Application of 5444-75-7).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Application of 5444-75-7

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Periplocain A, a New Naphthalene Derivative from Periploca aphylla Growing in Saudi Arabia was written by Al Musayeib, Nawal M.;Al-Massarani, Shaza M.;Amina, Musarat;El Dib, Rabab A.;Mohamed, Gamal A.;Ibrahim, Sabrin R. M.. And the article was included in Helvetica Chimica Acta in 2016.Recommanded Product: 5444-75-7 The following contents are mentioned in the article:

Periplocain A (I), a new naphthalene derivative together with four known compounds: 2-ethylhexyl benzoate, quercetin-3-O-α-L-rhamnopyranoside, quercetin-3-O-β-D-glucopyranoside and quercetin-3-(6-O-α-L-rhamnopyranosyl-β-D-glucopyranoside) were isolated from the AcOEt fraction of the aerial parts of Periploca aphylla (Asclepiadaceae). Their structures were established by multiple spectroscopic methods in addition to HR-ESI-MS and by comparison with literature data. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Recommanded Product: 5444-75-7).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Recommanded Product: 5444-75-7

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Characteristic chemical components of the essential oil from white kwao krua (Pueraria mirifica) was written by Yagi, Nobuo;Nakahashi, Hiroshi;Kobayashi, Tomohiro;Miyazawa, Mitsuo. And the article was included in Journal of Oleo Science in 2013.Category: esters-buliding-blocks The following contents are mentioned in the article:

The components of the essential oil from the roots of Pueraria mirifica were analyzed by capillary gas chromatog.-mass spectrometry (GC-MS). Eighty-two components, representing 88.5% of the total oil, were identified by GC-MS. The main component of the oil was 2-pentylfuran, followed by hexanal and hexadecanol. With regard to the odor components from the essential oil of P. mirifica as determined by gas chromatog.-olfactometry and aroma extract dilution anal., it was revealed that phenylacetaldehyde and (2E)-nonenal imparted the green odor of the oil, and geraniol contributed to the sweet odor. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Category: esters-buliding-blocks).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Category: esters-buliding-blocks

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics