Category: 5444-75-7

Infrared characterization of MgCl₂ supported Ziegler-Natta catalysts with monoester and diester as a modifier. [Erratum to document cited in CA120:135220] was written by Yang, C. B.;Hsu, C. C.;Park, Y. S.;Shurvell, H. F.. And the article was included in European Polymer Journal in 1994.Application In Synthesis of 2-Ethylhexyl benzoate The following contents are mentioned in the article:

The errors were not reflected in the abstract or the index entries. 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. 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. 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 In Synthesis of 2-Ethylhexyl benzoate

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

Gas chromatographic-mass spectrometric identification of impurities in recycled 2-ethylhexanol of di-2-ethylhexyl phthalate plasticizer production was written by Pleshkova, A. P.;Volkovich, S. V.. And the article was included in Zhurnal Analiticheskoi Khimii in 1993.Product Details of 5444-75-7 The following contents are mentioned in the article:

GC-MS with electron impact ionization and chem. ionization and involving separation on capillary columns was used to identify many impurities in recycled 2-ethylhexanol of di-2-ethylhexyl phthalate plasticizer production This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Product Details 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. 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.Product Details of 5444-75-7

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

Sunscreen compositions containing a combination of a linear ultraviolet radiation-absorbing polyether and other ultraviolet-screening compounds was written by Anonymous. And the article was included in IP.com Journal in 2016.Computed Properties of C15H22O2 The following contents are mentioned in the article:

Sunscreen composition including a combination of a linear UV radiation absorbing polyether that includes a covalently bound UV-chromophore, and at least one non-polymeric UV-screening compounds 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. 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. 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.Computed Properties of C15H22O2

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

Sunscreen compositions containing a combination of a linear ultraviolet radiation-absorbing polyether and other ultraviolet-screening compounds was written by Anonymous. And the article was included in IP.com Journal in 2016.Recommanded Product: 5444-75-7 The following contents are mentioned in the article:

Sunscreen composition including a combination of a linear UV radiation absorbing polyether that includes a covalently bound UV-chromophore, and at least one non-polymeric UV-screening compounds 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. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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. Recommanded Product: 5444-75-7

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

Oxidation of benzyl ethers by ammonium chlorochromate was written by Chen, Mifeng;Ding, Li;Cai, Kun;Rui, Yiwei;Wang, Junwen. And the article was included in Huaxue Shiji in 1996.Related Products of 5444-75-7 The following contents are mentioned in the article:

Ammonium chlorochromate (NH₄Cl·CrO₃) can selectively oxidize benzyl ethers to the corresponding benzoates in high yields in the mixed solvent of DMF and HOAc. The oxidation condition is mild, the product is easily separated and the starting material can be recovered. 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 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.Related Products of 5444-75-7

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

Comment on “Photodegradation Pathways of Nonabrominated Diphenyl Ethers, 2-Ethylhexyltetrabromobenzoate and Di(2-ethylhexyl)tetrabromophthalate: Identifying Potential Markers of Photodegradation” was written by Rayne, Sierra;Forest, Kaya. And the article was included in Environmental Science & Technology in 2009.Quality Control of 2-Ethylhexyl benzoate The following contents are mentioned in the article:

A polemic in response to Davis and Stapleton [Environ. Sci. Technol. 2009,43(15), 5739-5746] in which the authors confused proton transfer and hydrogen transfer processes in the photolysis of nonabrominated di-Ph ethers, 2-ethylhexyl tetrabromobenzoate, and bis(ethylhexyl) phthalate. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Quality Control of 2-Ethylhexyl benzoate).

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. 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. Quality Control of 2-Ethylhexyl benzoate

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

Esterification of Dicarboxylic Acids with 2-Ethylhexanol under Supercritical Conditions was written by Khamzin, Yu. A.;Imashev, U. B.;Udalova, E. A.;Shiriyazdanov, R. R.;Maksotov, E. K.;Davletshin, A. R.;Imasheva, M. U.;Makhmutova, O. N.;Telyashev, E. G.. And the article was included in Russian Journal of Physical Chemistry B in 2017.Reference of 5444-75-7 The following contents are mentioned in the article:

A study of esterification process of dicarboxylic acids with 2-ethylhexanol under supercritical conditions is presented. It was shown that the esterification reaction can be carried via out without a catalyst. The esters formed with greater rate and selectivity. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Reference 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. 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.Reference of 5444-75-7

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

Benzoate plasticizers for reducing plastisol viscosity and fusion temperature was written by Bohnert, T.;Stanhope, B.;Gruszecki, K.;Pitman, S.;Elsworth, V.. And the article was included in Polymers & Polymer Composites in 2000.HPLC of Formula: 5444-75-7 The following contents are mentioned in the article:

2-Ethylhexyl benzoate has the capability of lowering PVC plastisol viscosity while also performing as a highly solvating plasticizer. This unique combination is illustrated in both phthalate and benzoate containing plastisols and the properties of both the plastisol and the final sheet are presented. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7HPLC of Formula: 5444-75-7).

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. HPLC of Formula: 5444-75-7

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

Selective oxidation of benzyl ethers with ammonium chlorochromate in the dry state was written by Chen, Mi-Feng;Ding, Li;Cai, Kun;Liu, Liang-Xian;Liu, Feng. And the article was included in Youji Huaxue in 1995.Product Details of 5444-75-7 The following contents are mentioned in the article:

A new application of ammonium chlorochromate (I) as an efficient oxidant for benzyl ethers was reported. Without solvent, benzyl ethers are selectively oxidized by I to the corresponding benzoates in satisfactory yields. E.g., oxidation of PhCH₂OMe with I at 70° for 21 h gave 72% BzOMe. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Product Details 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. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Product Details of 5444-75-7

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

Versatile and sustainable alcoholysis of amides by a reusable CeO₂ catalyst was written by Siddiki, S. M. A. Hakim;Touchy, Abeda Sultana;Tamura, Masazumi;Shimizu, Ken-ichi. And the article was included in RSC Advances in 2014.COA of Formula: C15H22O2 The following contents are mentioned in the article:

CeO₂-catalyzed esterification between an equivalent molar ratio of primary amides and alcs. under neutral conditions, which provided the first versatile reusable catalytic system for direct alcoholysis of amides to esters with wider scope and 67 times higher turnover number (TON) than previous catalytic systems was reported. 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. 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. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.COA of Formula: C15H22O2

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