Cerkowniak, Magdalena et al. published their research in Biomedical Chromatography in 2018 | CAS: 1731-94-8

Methyl nonadecanoate (cas: 1731-94-8) 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. Computed Properties of C20H40O2

Application of headspace solid-phase microextraction followed by gas chromatography coupled with mass spectrometry to determine esters of carboxylic acids and other volatile compounds in Dermestes maculatus and Dermestes ater lipids was written by Cerkowniak, Magdalena;Bogus, Mieczyslawa I.;Wloka, Emilia;Stepnowski, Piotr;Golebiowski, Marek. And the article was included in Biomedical Chromatography in 2018.Computed Properties of C20H40O2 The following contents are mentioned in the article:

A constant problem in veterinary medicine, human healthcare, agriculture, forestry and horticulture is the large number of pests, and the lack of effective methods to combat them which cause no harm to the rest of the environment. It is recommended and desired to reduce the use of chems. and increase the use of agents based on knowledge acquired in the fields of biol., chem. and agrochems. To learn the defense mechanisms of insects we should consider not only the site of their physiol. ability to protect against external factors (cuticle), but also the possibility of chem. protection, formed by all compounds on the surface and in the body of insects. In this study, a procedure was developed to determine the esters of carboxylic acids in insect lipids. Headspace solid-phase microextraction was followed by gas chromatog. coupled with gas spectrometry. First, the best conditions were selected for the anal. to obtain the best chromatog. separation An RTx-5 column was used for this purpose. Polydimethylsiloxane/divinylbenzene (PDMS/DVB) and polyacrylate fibers were used to isolate acid esters. PDMS/DVB fiber achieved the best conditions for the extraction; the extraction time was 50 min, the extraction temperature was 105°C and the desorption time was 10 min at 230°C. These solid-phase microextraction conditions were used to analyze volatile compounds extracted from insects belonging to the Dermestidae family. This study involved multiple reactions and reactants, such as Methyl nonadecanoate (cas: 1731-94-8Computed Properties of C20H40O2).

Methyl nonadecanoate (cas: 1731-94-8) 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. Computed Properties of C20H40O2

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

Dowek, Sahar et al. published their research in International Journal of Pharmacy and Pharmaceutical Sciences in 2020 | CAS: 1731-94-8

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

Antibacterial, antioxidant and phytochemical screening of palestinian mallow, Malva Sylvestris L was written by Dowek, Sahar;Fallah, Seema;Basheer-Salimia, Rezq;Jazzar, Mohannad;Qawasmeh, Abdel. And the article was included in International Journal of Pharmacy and Pharmaceutical Sciences in 2020.Formula: C20H40O2 The following contents are mentioned in the article:

Objective: To evaluate antibacterial, antioxidant activities, the existence of the major secondary metabolites, and volatile compounds in methanolic extracts from M. sylvestris leaves. Methods: Antibacterial activity was assessed using a well diffusion method. Antioxidant activity was assessed using ABTS•+and DPPH• free radical scavenging assays. Phytochem. screening for secondary metabolites and volatile compounds were done following standard techniques and gas chromatog.-mass spectrometry (GC-MS). Results: Methanolic extracts exhibited moderate antibacterial activity compared with the pos. control against the gram-neg. Klebsiella pneumoniae and the gram-pos. bacteria′s Staphylococcus aureus by 47.2 and with 47.1% resp. The average percentage of scavenging was 97.82 ± 0.05 and 79.49 ± 0.4 for ABTS•+ and DPPH•, correspondingly. Total phenols were quant. estimated and found to be 78.9 ± 9.55 mg GAE/g. Phytochem. screening assays revealed the presence of a wide range of phytochem. groups such as alkaloids flavonoids, phenols, tannins, quinones, saponins, steroids, tannins, terpenoides with at least sixteen volatile compounds detected in the plant. Conclusion: The present study confirmed the antioxidant activity of the methanolic extract of M. sylvestris and the existence of is the volatile compounds (phytol), which mediate, even partially, the antioxidant and the claimed analgesic activity of the plant. 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 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. 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. Formula: C20H40O2

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

Laskar, Ikbal Bahar et al. published their research in RSC Advances in 2018 | CAS: 1731-94-8

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

Waste snail shell derived heterogeneous catalyst for biodiesel production by the transesterification of soybean oil was written by Laskar, Ikbal Bahar;Rajkumari, Kalyani;Gupta, Rajat;Chatterjee, Sushovan;Paul, Bappi;Rokhum, Lalthazuala. And the article was included in RSC Advances in 2018.Recommanded Product: Methyl nonadecanoate The following contents are mentioned in the article:

A waste snail shell (Pila spp.) derived catalyst was used to produce biodiesel from soybean oil at room temperature for the first time. The snail shell was calcined at different temperatures of 400-1000 °C. The synthesized catalysts underwent XRD, SEM, TEM, EDS, FTIR, XRF, TG/DTA and N2 adsorption-desorption isotherm (BET) anal. The major component CaO was determined at a calcination temperature of 900 °C as depicted in the XRD results. 100% conversion of soybean oil to Me ester biodiesel was obtained, as confirmed by 1H NMR. A biodiesel yield of 98% was achieved under optimized reaction conditions such as a calcination temperature of 900 °C, a catalyst loading of 3 wt%, a reaction time of 7 h and a methanol to oil ratio of 6 : 1, and biodiesel conversion was confirmed by FT-NMR and IR spectroscopies. A total of 9 fatty acid Me esters (FAMEs) were identified in the synthesized biodiesel by the retention time and fragmentation pattern data of GC-MS anal. The catalyst was recycled 8 times without appreciable loss in its catalytic activity. A high biodiesel yield of 98% was obtained under these optimized conditions. The catalyst has the advantage of being a waste material, therefore it is easily prepared, cost free, highly efficient, biogenic, labor effective and environmentally friendly, making it a potential candidate as a green catalyst for low cost production of biodiesel at an industrial scale. This study involved multiple reactions and reactants, such as Methyl nonadecanoate (cas: 1731-94-8Recommanded Product: Methyl nonadecanoate).

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

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

Xu, Zhongping et al. published their research in Scientific Reports in 2016 | CAS: 1731-94-8

Methyl nonadecanoate (cas: 1731-94-8) 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. 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. Safety of Methyl nonadecanoate

Metabolic engineering of cottonseed oil biosynthesis pathway via RNA interference was written by Xu, Zhongping;Li, Jingwen;Guo, Xiaoping;Jin, Shuangxia;Zhang, Xianlong. And the article was included in Scientific Reports in 2016.Safety of Methyl nonadecanoate The following contents are mentioned in the article:

Cottonseed oil is recognized as an important oil in food industry for its unique characters: low flavor reversion and the high level of antioxidants (Vitamin) as well as unsaturated fatty acid. However, the cottonseed oil content of cultivated cotton (Gossypium hirsutum) is only around 20%. In this study, we modified the accumulation of oils by the down-regulation of phosphoenolpyruvate carboxylase 1 (GhPEPC1) via RNA interference in transgenic cotton plants. The qRT-PCR and enzyme activity assay revealed that the transcription and expression of GhPEPC1 was dramatically down-regulated in transgenic lines. Consequently, the cottonseed oil content in several transgenic lines showed a significant (P < 0.01) increase (up to 16.7%) without obvious phenotypic changes under filed condition when compared to the control plants. In order to elucidate the mol. mechanism of GhPEPC1 in the regulation of seed oil content, we quantified the expression of the carbon metabolism related genes of transgenic GhPEPC1 RNAi lines by transcriptome anal. This anal. revealed the decrease of GhPEPC1 expression led to the increase expression of triacylglycerol biosynthesis-related genes, which eventually contributed to the lipid biosynthesis in cotton. This result provides a valuable information for cottonseed oil biosynthesis pathway and shows the potential of creating high cottonseed oil germplasm by RNAi strategy for cotton breeding. This study involved multiple reactions and reactants, such as Methyl nonadecanoate (cas: 1731-94-8Safety of Methyl nonadecanoate).

Methyl nonadecanoate (cas: 1731-94-8) 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. 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. Safety of Methyl nonadecanoate

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

Nugroho, Aji et al. published their research in Journal of Food Science and Technology in 2022 | CAS: 1731-94-8

Methyl nonadecanoate (cas: 1731-94-8) 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. 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.Application of 1731-94-8

Antioxidant and antibacterial activities in 21 species of Indonesian sea cucumbers was written by Nugroho, Aji;Harahap, Iskandar Azmy;Ardiansyah, Ardi;Bayu, Asep;Rasyid, Abdullah;Murniasih, Tutik;Setyastuti, Ana;Putra, Masteria Yunovilsa. And the article was included in Journal of Food Science and Technology in 2022.Application of 1731-94-8 The following contents are mentioned in the article:

Sea cucumbers are marine organisms with uses in food, cosmetics, and medicine. This study aimed to identify Indonesian sea cucumbers with high antioxidant and antibacterial activities. Twenty-one sea cucumber species were used for this study. Antioxidant capacity was evaluated using the 2,2-diphenyl-β-picrylhydrazine assay. Antibacterial activity was assessed using the disk diffusion assay, whereas the resazurin-based assay was employed to determine the min. inhibitory concentration (MIC) and min. bactericidal concentration (MBC). Volatile compounds possibly related to the biol. activity of sea cucumbers were analyzed via gas chromatog.-mass spectrometry (GC-MS). Holothuria atra had the strongest antioxidant capacity (IC50 = 14.22 ± 0.87 μg μL-1). Stichopus vastus displayed the best antibacterial activity against Staphylococcus aureus, whereas Stichopus ocellatus extract was most potent against Vibrio cholerae. Holothuria albiventer, which controlled Bacillus subtilis most effectively while also being active against S. aureus and V. cholerae, was the optimal antimicrobial species. H. albiventer and Actinopyga echinites inhibited B. subtilis growth at 12.5 μg μL-1. The MBC tests indicated that the antibacterial activities of sea cucumbers at the MIC were bacteriostatic, rather than bactericidal, in nature. GC-MS anal. uncovered long-chain fatty acids that might be associated with the antibacterial activities of sea cucumbers. This study involved multiple reactions and reactants, such as Methyl nonadecanoate (cas: 1731-94-8Application of 1731-94-8).

Methyl nonadecanoate (cas: 1731-94-8) 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. 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.Application of 1731-94-8

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

Heidari, Mahsa et al. published their research in Journal of Food Science and Technology in 2020 | CAS: 1731-94-8

Methyl nonadecanoate (cas: 1731-94-8) 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. 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.Name: Methyl nonadecanoate

Discrimination between vegetable oil and animal fat by a metabolomics approach using gas chromatography-mass spectrometry combined with chemometrics was written by Heidari, Mahsa;Talebpour, Zahra;Abdollahpour, Ziba;Adib, Nooshin;Ghanavi, Zohre;Aboul-Enein, Hassan Y.. And the article was included in Journal of Food Science and Technology in 2020.Name: Methyl nonadecanoate The following contents are mentioned in the article:

Adulteration of olive oil with the other cheap oils and fats plays an important role in economics and has nutritional benefits. In this work, metabolite profiling was performed using gas chromatog.-mass spectrometry to identify and quantify animal fat (lard) adulteration in vegetable oil (olive oil). Principal component anal. could correctly identify and clustering olive oil, sunflower oil, sesame oil, lard, and adulterated samples through the changes in their fatty acid Me esters (FAMEs) profile. A targeted metabolomics method was then optimized and validated through construction of calibration curves of known FAMSs in olive oil and lard. The method was presented high linearity (R2 > 0.96) and good intra and inter day accuracy and precision (79-101 and 86-102% and 2-7 and 3-7, resp.) for determination of FAMEs. Afterwards the absolute concentration and relative percentage of FAMEs were successfully determined in 12 com. olive oils and 3 lards samples. Me myristate, Me palmitate, Me oleate, and Me stearate were selected as discriminant markers to identify and quantify lard adulteration even at a low level of lard (5%weight/weight), with errors less than 2% in the comparison of the absolute or relative concentrations of FAMEs using several statistical methods. The proposed methodol. allowed us to quantify the FAMEs simultaneously and also could predict small amount of lard in the adulterated olive oil samples. This study involved multiple reactions and reactants, such as Methyl nonadecanoate (cas: 1731-94-8Name: Methyl nonadecanoate).

Methyl nonadecanoate (cas: 1731-94-8) 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. 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.Name: Methyl nonadecanoate

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

Dharmalingam, Babu et al. published their research in Materials Today: Proceedings | CAS: 1731-94-8

Methyl nonadecanoate (cas: 1731-94-8) 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. 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.Computed Properties of C20H40O2

Prediction of split injection strategy assisted diesel engine combustion, performance and emission characteristics fuelled waste frying oil methyl ester through central composite design was written by Dharmalingam, Babu;Deepakkumar, R.;Bhattacharya, Kasturi;Paulraj Gundupalli, Marttin;Sriariyanun, Malinee. And the article was included in Materials Today: Proceedings.Computed Properties of C20H40O2 The following contents are mentioned in the article:

The objective of this study is to use response surface methodol. to forecast the performance, combustion, and emission characteristics of an advanced injection strategy-assisted diesel engine running on waste frying oil Me ester. The experiment was carried out on a diesel engine using a high-pressure fuel injection system. The main injection timing ranges varied from 16 to 24 °CA bTDC, whereas the post-injection ranges from -6 °CA bTDC to 6 °CA aTDC. The injection quantity for the main and post injections quantity varied from 70 % to 90 %, 10 % to 30 %, and the injection pressure is set at 500 bar. Experiments were carried out using a design matrix developed by the design of experiments At 100 % load, B100-90 %-10 % obtained the highest BTE of 33.87 % and the lowest fuel consumption of 0.268 kg/kW-hr. At the main injection timing of 22 °CA and post-injection timing of -4 °CA, D100-80 %-20 % achieved the lowest unburned hydrocarbon, Smoke emission of 13 ppm, and 1.613 FSN resp. The point prediction approach was used to forecast the combustion and emission parameters of a diesel engine, and the predicted results were in good agreement with the exptl. results. Furthermore, when compared to advance injection timing for biodiesel fuel, retarded injection timing reduces nitric oxide emission. The Split injection strategy is one of the most effective techniques to reduce soot and NOx emissions while maintaining diesel engine efficiency. This study involved multiple reactions and reactants, such as Methyl nonadecanoate (cas: 1731-94-8Computed Properties of C20H40O2).

Methyl nonadecanoate (cas: 1731-94-8) 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. 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.Computed Properties of C20H40O2

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

Krishnamoorthi, M. et al. published their research in Applied Energy in 2020 | 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

Experimental, numerical and exergy analyses of a dual fuel combustion engine fuelled with syngas and biodiesel/diesel blends was written by Krishnamoorthi, M.;Sreedhara, S.;Prakash Duvvuri, Pavan. And the article was included in Applied Energy in 2020.Electric Literature of C20H40O2 The following contents are mentioned in the article:

This work investigates the effects of addition of syngas and biodiesel on a reactivity controlled compression ignition (RCCI) engine fuelled with diesel. SEM (SEM) of exhaust particulate matter has been done to obtain particulate matter (PM) morphol. Energy and exergy analyses have been performed to observe energy and availability shares, and to provide directions for the energy recovery systems. Closed cycle combustion simulations have been performed to complement the exptl. results and for an improved understanding of in-cylinder dynamics. Based on the initial study, used cooking oil based biodiesel blend (B20, 20% biodiesel) has been chosen in experiments The optimal operating conditions for syngas/diesel and syngas/B20 in RCCI mode for different operating parameters have been investigated. Injection pressure, injection timing and pre-injection mass ratio have been modified to get improved combustion efficiency at mid-load. Syngas/diesel mode with an injection timing of 19° before top dead center (bTDC) shows slightly higher brake thermal efficiency (BTE) with 22% and 77% lower oxides of nitrogen (NOx) and PM resp. as compared to conventional diesel combustion. In syngas/B20 mode, a maximum BTE of 24% has been observed for the case with a pre-injection at 50° bTDC with 30% mass fraction and 18° bTDC main injection timing. Syngas/diesel shows a reduction in primary soot particle count by about 67% and contains larger aggregates as compared to neat diesel. 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

Liu, Tie-Yuan et al. published their research in Planta in 2019 | CAS: 1731-94-8

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

Comparative metabolite profiling of two switchgrass ecotypes reveals differences in drought stress responses and rhizosheath weight was written by Liu, Tie-Yuan;Chen, Mo-Xian;Zhang, Youjun;Zhu, Fu-Yuan;Liu, Ying-Gao;Tian, Yuan;Fernie, Alisdair R.;Ye, Nenghui;Zhang, Jianhua. And the article was included in Planta in 2019.Formula: C20H40O2 The following contents are mentioned in the article:

The aim of this work is to reveal the potential metabolites involved in rhizosheath formation under drought stress conditions. Panicum virgatum L. (switchgrass), which belongs to the Poaceae family, is an important biofuel and fodder crop in drought areas. Five switchgrass ecotypes (cv. Alamo, cv. Blackwake, cv. Summer, cv. Cave-in-Rock and cv. Kanlow) have a broad range of rhizosheath weight under drought conditions. GC-MS was used to determine the primary metabolites in the shoots and roots of selected ecotypes under drought stress conditions. The change trends of root hair length and d., lateral root number and related gene expression were consistent with rhizosheath weight in Alamo and Kanlow under drought and watered conditions. For root morphol. parameters, Alamo grew deeper than Kanlow, while Kanlow exhibited higher values for other parameters. In this study, the levels of amino acids, sugars and organic acids were significantly changed in response to drought stress in two switchgrass ecotypes. Several metabolites including amino acids and sugars in the large soil-sheathed roots of Alamo and Kanlow were significantly increased compared to small or no soil-sheathed roots of Alamo and Kanlow. Difference in rhizosheath size is reflected in the plant internal metabolites under drought stress conditions. Our results highlight the importance of using metabolite profiling and provide a better understanding of rhizosheath formation at the cellular level. 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 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.Formula: C20H40O2

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

Zhao, Wei et al. published their research in International Journal of Food Science and Technology in 2022 | CAS: 1731-94-8

Methyl nonadecanoate (cas: 1731-94-8) 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. 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. Related Products of 1731-94-8

Antioxidant activity assessment of Yingjisha sweet almond oil was written by Zhao, Wei;Wang, Liwen;Yang, Fan;Zhang, Ning;Fan, Jiahuan;Qin, Shini;Shao, Tong;Xu, Xianao;Yan, Shiyin;Guo, Hongxing;Li, Jianying;Zhao, Hui. And the article was included in International Journal of Food Science and Technology in 2022.Related Products of 1731-94-8 The following contents are mentioned in the article:

Sweet almond is one of the main cash crops in Yingjisha, Xinjiang Autonomous Region, China. The composition of sweet almond oil (SAO) was analyzed by gas chromatog.-mass spectrometry (GC-MS). SAO′s antioxidant activities were investigated by measuring its scavenging ability with 1,1-diphenyl-2-picrylhydrazyl (DPPH), 2,2′-Azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), hydroxyl radical scavenging assay and 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (Trolox) equivalent antioxidant capacity (TEAC) assay. Furthermore, in vivo antioxidant capacity was assessed using Saccharomyces cerevisiae model stimulated by hydrogen peroxide (H2O2) and carbon tetrachloride (CCl4). The results showed that SAO was mainly composed of Me oleate (21.28%), Me stearate (18.55%) and Me palmitate (14.1%). In vitro antioxidant test results showed that compared with the scavenging three free radicals capacity of 1 mmol L-1 Trolox, the SAO needed to reach 5 mg mL-1, 20 mg mL-1 and less than 20 mg mL-1, resp. In vivo experiments showed that SAO rescued the survival and inhibited intracellular oxidation and lipid peroxidation of Saccharomyces cerevisiae exposed to H2O2 and CCl4. Addnl., our results showed that the catalase encoded by the Gsh1 gene may be involved in the mechanism of action of SAO against intracellular oxidation These findings suggest that SAO possesses antioxidant capacities, and it is recommended to develop dietary antioxidants based on SAO. This study involved multiple reactions and reactants, such as Methyl nonadecanoate (cas: 1731-94-8Related Products of 1731-94-8).

Methyl nonadecanoate (cas: 1731-94-8) 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. 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. Related Products of 1731-94-8

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