Lajko, Gyula et al. published their research in Biomedical Chromatography in 2016 | CAS: 2361926-29-4

(1R,2R)-Ethyl 2-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate (cas: 2361926-29-4) 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. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Quality Control of (1R,2R)-Ethyl 2-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate

High-performance liquid chromatographic enantioseparation of fluorinated cyclic β3-amino acid derivatives on polysaccharide-based chiral stationary phases. Comparison with nonfluorinated counterparts was written by Lajko, Gyula;Orosz, Timea;Kiss, Lorand;Forro, Eniko;Fueloep, Ferenc;Peter, Antal;Ilisz, Istvan. And the article was included in Biomedical Chromatography in 2016.Quality Control of (1R,2R)-Ethyl 2-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate The following contents are mentioned in the article:

The stereoisomers of five fluorinated cyclic β3-amino acid derivatives and their nonfluorinated counterparts were separated on chiral stationary phases containing as chiral selectors cellulose tris-(3,5-dimethylphenyl carbamate), cellulose tris-(3-chloro-4-methylphenyl carbamate), cellulose tris-(4-methylbenzoate), cellulose tris-(4-chloro-3-methylphenyl carbamate), amylose tris-(3,5-dimethylphenyl carbamate) or amylose tris-(5-chloro-2-methylphenyl carbamate). The enantioseparations were carried out in normal-phase mode with n-hexane/alc./alkylamine mobile phases in the temperature range 5-40 °C. The effects of the mobile phase composition, the nature and concentration of the alc. and alkylamine additives, the structures of the analytes and temperature on the separations were investigated. Thermodn. parameters were calculated from plots of ln a vs. 1/T. The Δ(ΔH°) values ranged between -5.0 and +1.6 kJ/mol, while Δ(ΔS°) varied between -12.6 and +5.7 J/mol/K. The enantioseparation was enthalpically controlled, the retention factor and the separation factor decreasing with increasing temperature, but entropically controlled separation was also observed The elution sequence was determined for all of the investigated analytes. This study involved multiple reactions and reactants, such as (1R,2R)-Ethyl 2-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate (cas: 2361926-29-4Quality Control of (1R,2R)-Ethyl 2-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate).

(1R,2R)-Ethyl 2-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate (cas: 2361926-29-4) 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. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Quality Control of (1R,2R)-Ethyl 2-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate

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

Balthazar, Celso F. et al. published their research in Journal of Dairy Science in 2021 | CAS: 2198-61-0

Isopentyl hexanoate (cas: 2198-61-0) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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 of 2198-61-0

Effect of probiotic Minas Frescal cheese on the volatile compounds profile and metabolic profile assessed by nuclear magnetic resonance spectroscopy and chemometric tools was written by Balthazar, Celso F.;Guimaraes, Jonas T.;Silva, Ramon;Filho, Elenilson G. A.;Brito, Edyr S.;Pimentel, Tatiana C.;Rodrigues, Sueli;Esmerino, Erick A.;Silva, Marcia Cristina;Raices, Renata S. L.;Granato, Daniel;Duarte, Maria Carmela K. H.;Freitas, Monica Q.;Cruz, Adriano G.. And the article was included in Journal of Dairy Science in 2021.Application of 2198-61-0 The following contents are mentioned in the article:

This study aimed to evaluate the effect of Lacticaseibacillus casei 01 as a probiotic culture on the production of volatile organic compounds and metabolic profile of Minas Frescal cheese. Lactose (α-lactose and β-lactose), fatty acids (unsaturated and saturated), citric acid, tryptophan, and benzoic acid were the main compounds Compared with the control cheese, probiotic cheese was characterized by the highest concentration of tryptophan and presented a higher number of volatile acids. The control cheese was characterized by the highest concentration of benzoic acid and fatty acids, resulting in a higher number of volatile alcs. and esters. No differences were observed for α-lactose, β-lactose, and citric acid contents. A clear separation of probiotic and control Minas Frescal cheese was obtained using 1H NMR spectra, demonstrating that the addition of probiotic culture altered the metabolic profile of Minas Frescal cheese. Overall, the findings suggested that the addition of probiotic culture promoted the proteolysis in the fresh cheeses, decreased the lipolysis, and altered the volatile compounds Furthermore, NMR spectroscopy coupled to chemometrics tools could be used to differentiate probiotic and conventional cheeses. This study involved multiple reactions and reactants, such as Isopentyl hexanoate (cas: 2198-61-0Application of 2198-61-0).

Isopentyl hexanoate (cas: 2198-61-0) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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 of 2198-61-0

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

Lu, Guangzhao et al. published their research in Journal of Materials Chemistry in 2020 | CAS: 2253-73-8

Isopropylisothiocyanate (cas: 2253-73-8) 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 2253-73-8

Saturated red iridium(III) complexes containing a unique four-membered Ir-S-C-N backbone: mild synthesis and application in OLEDs was written by Lu, Guangzhao;Yao, Jingwen;Chen, Zhanxiang;Ma, Dongge;Yang, Chuluo. And the article was included in Journal of Materials Chemistry in 2020.Product Details of 2253-73-8 The following contents are mentioned in the article:

New Ir(III) cyclometalated complexes (4tfmpiq)2Ir(tiptha), (4tfmpiq)2Ir(phdiptha), (4tfmpiq)2Ir(fphdiptha) and (4tfmpiq)2Ir(ipdptha) (4tfmpiq = 4-(4-(trifluoromethyl)phenyl)isoquinoline, tiptha = 1,1,3-triisopropylthiourea, phdiptha = 1,1-diisopropyl-3-phenylthiourea, fphdiptha = 3-(4-fluorophenyl)-1,1-diisopropylthiourea, ipdptha = 3-isopropyl-1,1-diphenylthiourea) containing a unique four-membered ring Ir-S-C-N backbone were facilely synthesized under mild conditions. By introducing different substituents such as iso-Pr, Ph, 4-fluorophenyl, diisopropylamine and diphenylamine on the thiourea ancillary ligands, not only the S-C-N ligands can be extensively derived, but also the emission colors (λpeak = 627-636 nm) and photoluminescence quantum efficiencies (ΦP = 38.0-42.0%) can be regulated. Employing these complexes as emitters, the organic light emitting diodes (OLEDs) exhibited good performances with a maximum external quantum efficiency (EQEmax) of 13.1% for saturated red emission with CIE coordinates of (0.68, 0.32). These results demonstrate the great potential of the S-C-N ancillary ligands for developing new Ir(III) complexes towards OLED applications. This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Product Details of 2253-73-8).

Isopropylisothiocyanate (cas: 2253-73-8) 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 2253-73-8

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

Lu, Guangzhao et al. published their research in Journal of Materials Chemistry in 2020 | CAS: 2253-73-8

Isopropylisothiocyanate (cas: 2253-73-8) 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.Application of 2253-73-8

Saturated red iridium(III) complexes containing a unique four-membered Ir-S-C-N backbone: mild synthesis and application in OLEDs was written by Lu, Guangzhao;Yao, Jingwen;Chen, Zhanxiang;Ma, Dongge;Yang, Chuluo. And the article was included in Journal of Materials Chemistry in 2020.Application of 2253-73-8 The following contents are mentioned in the article:

New Ir(III) cyclometalated complexes (4tfmpiq)2Ir(tiptha), (4tfmpiq)2Ir(phdiptha), (4tfmpiq)2Ir(fphdiptha) and (4tfmpiq)2Ir(ipdptha) (4tfmpiq = 4-(4-(trifluoromethyl)phenyl)isoquinoline, tiptha = 1,1,3-triisopropylthiourea, phdiptha = 1,1-diisopropyl-3-phenylthiourea, fphdiptha = 3-(4-fluorophenyl)-1,1-diisopropylthiourea, ipdptha = 3-isopropyl-1,1-diphenylthiourea) containing a unique four-membered ring Ir-S-C-N backbone were facilely synthesized under mild conditions. By introducing different substituents such as iso-Pr, Ph, 4-fluorophenyl, diisopropylamine and diphenylamine on the thiourea ancillary ligands, not only the S-C-N ligands can be extensively derived, but also the emission colors (λpeak = 627-636 nm) and photoluminescence quantum efficiencies (ΦP = 38.0-42.0%) can be regulated. Employing these complexes as emitters, the organic light emitting diodes (OLEDs) exhibited good performances with a maximum external quantum efficiency (EQEmax) of 13.1% for saturated red emission with CIE coordinates of (0.68, 0.32). These results demonstrate the great potential of the S-C-N ancillary ligands for developing new Ir(III) complexes towards OLED applications. This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Application of 2253-73-8).

Isopropylisothiocyanate (cas: 2253-73-8) 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.Application of 2253-73-8

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

Kim, Minhyo et al. published their research in LWT–Food Science and Technology in 2022 | CAS: 31566-31-1

Glyceryl monostearate (cas: 31566-31-1) 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. 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.Recommanded Product: Glyceryl monostearate

Utilization of oleogels with binary oleogelator blends for filling creams low in saturated fat was written by Kim, Minhyo;Hwang, Hong-Sik;Jeong, Sungmin;Lee, Suyong. And the article was included in LWT–Food Science and Technology in 2022.Recommanded Product: Glyceryl monostearate The following contents are mentioned in the article:

The binary blends of candelilla wax (CDW) and glycerol monostearate (GMS) at varying ratios were utilized to prepare canola oil oleogels whose feasibility as a shortening replacer in filling creams was evaluated. The blending ratio of 60:40 (CDW-60:GMS-40) generated oleogels with the highest hardness and the lowest melting temperature The replacement of shortening with CDW-60:GMS-40 oleogel produced filling creams with textural properties similar to those of the shortening one. These textural properties could alleviate the oil separation from the filling creams. The level of saturated fatty acids in the filling creams prepared with oleogels was distinctly reduced from 36.17% to 10.30%. The tomog. anal. demonstrated that the filling creams prepared with 100% GMS oleogel (CDW-0:GMS-100) exhibited a better aerated structure than those with CDW-60:GMS-40 oleogel, implying that the proportions of GMS in the oleogels pos. contributed to the aerated structure of the filling creams. The morphol. properties of the filling creams were linearly correlated with the sp. gr. (Pearson correlation coefficients >0.98) and seemed to be affected primarily by the level of saturated fatty acids (specifically, stearic and palmitic acids) of the oleogels. This study involved multiple reactions and reactants, such as Glyceryl monostearate (cas: 31566-31-1Recommanded Product: Glyceryl monostearate).

Glyceryl monostearate (cas: 31566-31-1) 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. 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.Recommanded Product: Glyceryl monostearate

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

Nguyen, Hoang Chinh et al. published their research in Energy Conversion and Management in 2018 | CAS: 1731-94-8

Methyl nonadecanoate (cas: 1731-94-8) 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.Formula: C20H40O2

Enzymatic production of biodiesel from insect fat using methyl acetate as an acyl acceptor: Optimization by using response surface methodology was written by Nguyen, Hoang Chinh;Liang, Shih-Hsiang;Chen, Shang-Sian;Su, Chia-Hung;Lin, Jhih-Huei;Chien, Chien-Chung. And the article was included in Energy Conversion and Management in 2018.Formula: C20H40O2 The following contents are mentioned in the article:

Black soldier fly larvae (BSFL) are oleaginous insects that can assimilate organic waste for fat accumulation, and thus serve as an alternative feedstock for biodiesel production In lipase-catalyzed transesterification, enzymes are deactivated by excess methanol. To address this obstacle, Me acetate is suggested as an alternative acyl acceptor to methanol. In this study, Me acetate was first used in the enzymic production of biodiesel with BSFL as a triglyceride source. The interesterification of BSFL fat with Me acetate was catalyzed using Novozym 435 as an efficient immobilized lipase. Response surface methodol. was used to optimize the reaction and establish a reliable math. model for prediction. A maximum biodiesel yield of 96.97% was reached at a reaction time of 12 h, molar ratio of Me acetate to fat of 14.64: 1, enzyme loading of 17.58%, and temperature of 39.5 °C. Under these optimal reaction conditions, Novozym 435 could be reused for up to 20 cycles without loss in enzyme activity. The properties of BSFL biodiesel were also investigated and all met the European standard EN 14214. This study indicates that the enzymic interesterification of BSFL fat with Me acetate is a promising and ecofriendly method for green fuel production This study involved multiple reactions and reactants, such as Methyl nonadecanoate (cas: 1731-94-8Formula: C20H40O2).

Methyl nonadecanoate (cas: 1731-94-8) 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.Formula: C20H40O2

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

Delgado de la Torre, M. Pilar et al. published their research in Journal of the Science of Food and Agriculture in 2014 | CAS: 1731-94-8

Methyl nonadecanoate (cas: 1731-94-8) 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.Electric Literature of C20H40O2

Comparative profiling analysis of woody flavouring from vine-shoots and oak chips was written by Delgado de la Torre, M. Pilar;Priego-Capote, Feliciano;Luque de Castro, M. Dolores. And the article was included in Journal of the Science of Food and Agriculture in 2014.Electric Literature of C20H40O2 The following contents are mentioned in the article:

BACKGROUNDWoody liquid flavourings extracted from different varieties of vine shoots and oak chips have been characterized by gas chromatog.-mass spectrometry to compare the profile of compounds as potential contributors to the organoleptical properties of wine and spirits aged in oak barrels. Oak chips are frequently added to barrels to accelerate the ageing process, while vine shoots are produced in high amounts in wine-producing countries. RESULTSThe extracts were isolated by superheated liquid extraction (SHLE) after optimization of extraction variables. The SHLE protocol was performed using ethanol-water mixtures (pH 3) at 220 °C for 60 min. Compounds were identified using NIST databases, and the resulting profile was used as a dataset for qual. and semi-quant. comparison between extracts obtained from different varieties of vine shoots and oak chips. CONCLUSIONStatistical anal. enabled demonstration of the similarity among extracts from vine shoots and oak wood, providing the first study on this subject. The special role of phenols and furanic derivatives has been described. This study is the first stage for characterization of vine shoots as a byproduct with potential for use in the oenol. field. © 2013 Society of Chem. Industry. This study involved multiple reactions and reactants, such as Methyl nonadecanoate (cas: 1731-94-8Electric Literature of C20H40O2).

Methyl nonadecanoate (cas: 1731-94-8) 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.Electric Literature of C20H40O2

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

Singh, Dheer et al. published their research in Chromatographia in 2014 | CAS: 1731-94-8

Methyl nonadecanoate (cas: 1731-94-8) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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.Quality Control of Methyl nonadecanoate

Response Factor Correction for Estimation of Ester Content in Biodiesel was written by Singh, Dheer;Chopra, Anju;Kumar, Ravindra;Sastry, M. I. S.;Patel, M. B.;Basu, B.. And the article was included in Chromatographia in 2014.Quality Control of Methyl nonadecanoate The following contents are mentioned in the article:

EN 14103 is generally used for quantification of ester content in biodiesel free of heptadecanoate ester (C17:0) or Me nonadecanoate (C19:0), which are employed as internal standards Ester content obtained by EN 14103 method did not match with theor. value of biodiesel, as the method did not take care of response factors of each component to compensate for changes in detector sensitivities. In this study, the whole range of fatty acid (C6-C24:1) Me esters were taken into consideration for the calculation of the ester content. Me nonadecanoate (C19:0) was used as an internal standard The response factors of both the saturated and unsaturated Me esters in the range C6-C24:1 were estimated and found in the range 0.97-1.16. The ester content was calculated after applying the response factors of each Me ester. The results obtained by this method agreed well with the theor. value as compared to estimated value using EN14103 method. The results obtained from this method also show good correlation (R2 = 0.98) with 1H-NMR method. Further, this method does not depend on nature of biodiesel feed stock and is applicable to all Me biodiesel samples obtained from different raw materials. This study involved multiple reactions and reactants, such as Methyl nonadecanoate (cas: 1731-94-8Quality Control of Methyl nonadecanoate).

Methyl nonadecanoate (cas: 1731-94-8) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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.Quality Control of Methyl nonadecanoate

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

Liu, Yunjiao et al. published their research in Current Research in Food Science in 2021 | CAS: 112-14-1

Octyl acetate (cas: 112-14-1) 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 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. Name: Octyl acetate

The potential of spent coffee grounds hydrolysates fermented with Torulaspora delbrueckii and Pichia kluyveri for developing an alcoholic beverage: The yeasts growth and chemical compounds modulation by yeast extracts was written by Liu, Yunjiao;Lu, Yuyun;Liu, Shao Quan. And the article was included in Current Research in Food Science in 2021.Name: Octyl acetate The following contents are mentioned in the article:

This study evaluated the effects of yeast extracts (YE) addition (0% and 0.25%, w/v) on the no-volatile and volatile compounds of spent coffee grounds (SCG) hydrolyzates fermented with single-cultures of two non-Saccharomyces wine yeasts, Torulaspora delbrueckii and Pichia kluyveri. The added YE improved the growth of both T. delbrueckii and P. kluyveri, especially P. kluyveri, resulting in higher ethanol production (1.98% vs 1.47%, volume/volume) by the latter yeast. In addition, the added YE did not impact on most of the alkaloids production regardless of yeast type, while significantly decreasing the contents of chlorogenic, and caffeic acids in SCG hydrolyzates fermented with P. kluyveri. Furthermore, more odor-active compounds such as acetate esters and 2-phenylethyl alc. were produced when YE was added, and P. kluyveri generated significantly higher amounts of esters compared to that of T. delbrueckii. Moreover, YE addition showed a more noticeable effect on the fermentation performance of P. kluyveri relative to that of T. delbrueckii. These findings indicated the potential of SCG hydrolyzates fermented with evaluated non-Saccharomyces yeasts and may expand the applications on utilizing SCG to develop new value-added alc. products. This study involved multiple reactions and reactants, such as Octyl acetate (cas: 112-14-1Name: Octyl acetate).

Octyl acetate (cas: 112-14-1) 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 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. Name: Octyl acetate

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

Ahmed, Shahnawaz et al. published their research in Journal of Integrative Agriculture in 2019 | CAS: 112-14-1

Octyl acetate (cas: 112-14-1) 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. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Product Details of 112-14-1

Chemical composition, antioxidant activity and GC-MS analysis of juice and peel oil of grapefruit varieties cultivated in India was written by Ahmed, Shahnawaz;Rattanpal, H. S.;Gul, Khalid;Dar, Rouf Ahmad;Sharma, Akash. And the article was included in Journal of Integrative Agriculture in 2019.Product Details of 112-14-1 The following contents are mentioned in the article:

Citrus family especially Grapefruit, has attained considerable attention due to the presence of a number of essential components that have cardiovascular and anti-hypertensive properties. The juice and essential oil extracted from eight recently released grapefruit cultivars were used to study physicochem. and antioxidant properties. The total soluble solids (TSS), titratable acidity (TA) and pH of juice samples extracted from various grapefruit varieties differed significantly. The refractive index, sp. gr. and optical rotation values for the oil varied from 1.473 to 1.396, 0.863 to 0.847 and +93 to +86, resp. The percent 2,2-diphenyl-1-picrylhydrazyl radical activity (% DPPH activity) and ferric reducing antioxidant power (FRAP) values for grapefruit juice and peel oil varied from 24.06 to 18.79, 2.91 to 1.44 mmol g-1 and 84.87 to 74.73, 7.76 to 5.73 mmol g-1, resp. There were significant differences in physicochem., antioxidant properties and volatile profiles of extracted juice and oil. The oil exhibited higher DPPH and FRAP values than the juice. Among different components identified which accounted for over 99% of the volatile fraction, limonene, myrcene, and benzopyran were major components in all oil samples. This study involved multiple reactions and reactants, such as Octyl acetate (cas: 112-14-1Product Details of 112-14-1).

Octyl acetate (cas: 112-14-1) 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. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Product Details of 112-14-1

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