Category: 2425-77-6

Hu, Shuangling;Chen, Qinghua;Guo, Fei;Wang, Mingle;Zhao, Hua;Wang, Yu;Ni, Dejiang;Wang, Pu published 《(Z)-3-Hexen-1-ol accumulation enhances hyperosmotic stress tolerance in Camellia sinensis》 in 2020. The article was appeared in 《Plant Molecular Biology》. They have made some progress in their research.Quality Control of 2-Hexyl-1-decanol The article mentions the following:

Volatile components in fresh leaves are involved in the regulation of many stress responses, such as insect damage, fungal infection, high temperature Here, we found that 7-day hyperosmotic treatment specifically led to the accumulation of (Z)-3-hexen-1-ol, (E)-2-hexenal and Me salicylate. (Z)-3-hexen-1-ol pretreatment dramatically enhanced the hyperosmotic stress tolerance of tea plants and decreased stomatal conductance, whereas (E)-2-hexenal and Me salicylate pretreatments did not exhibit. qRT-PCR anal. revealed that exogenous ABA induced the expressions of related enzyme genes, and (Z)-3-hexen-1-ol could up-regulate the expressions of many DREB and RD genes. Moreover, exogenous (Z)-3-hexen-1-ol tremendously induced the expressions of specific LOX and ADH genes within 24 h. Taken together, hyperosmotic stress induced (Z)-3-hexen-1-ol accumulation in tea plant via LOX, HPL and ADH genes, (Z)-3-hexen-1-ol could dramatically enhance the hyperosmotic stress tolerance via the decrease of stomatal conductance and MDA, accumulation of ABA and proline, activation of DREB and RD gene expressions. Key message: Hyperosmotic stress induced (Z)-3-hexen-1-ol accumulation in Camellia sinensis via up-regulation of most LOX, HPL and ADH genes, while (Z)-3-hexen-1-ol could dramatically enhance the hyperosmotic stress tolerance via the decrease of stomatal conductance, accumulation of proline, activation of DREB and RD gene expressions, and probably pos. feedback regulation of LOXs and ADHs. To complete the study, the researchers used 2-Hexyl-1-decanol (cas: 2425-77-6) .

2-Hexyl-1-decanol(cas: 2425-77-6) may be employed as an organic solvent to study the extraction of non-polar acidic drugs from human plasma by parallel artificial liquid membrane extraction (PALME). Quality Control of 2-Hexyl-1-decanol

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Safety of 2-Hexyl-1-decanol《Bithieno[3,4-c]pyrrole-4,6-dione-Mediated Crystallinity in Large-Bandgap Polymer Donors Directs Charge Transportation and Recombination in Efficient Nonfullerene Polymer Solar Cells》 was published in 2020. The authors were Zhao, Jiaji;Li, Qingduan;Liu, Shengjian;Cao, Zhixiong;Jiao, Xuechen;Cai, Yue-Peng;Huang, Fei, and the article was included in《ACS Energy Letters》. The author mentioned the following in the article:

Solution-processed nonfullerene bulk-heterojunction (BHJ) polymer solar cells (PSCs), which are composed of polymer donors and organic acceptors, are proven to manifest promising performance and long-term stability. In this concise contribution, bithieno[3,4-c]pyrrole-4,6-dione (BiTPD), which is a TPD derivative but presents a large planar structure and strong electron-withdrawing ability, was used to construct a large-bandgap polymer donor PBiTPD. Results show that the polymer donor PBiTPD realized power conversion efficiency (PCE) as high as 14.2% in fullerene-free BHJ solar cells. Larger ionization potential value, more favorable face-on backbone orientation, and stronger crystallinity were concurrently obtained in PBiTPD. Correspondingly, improved and more balanced charge transportation; less nongeminate and trap-assisted recombination losses; and thus high fill factor (FF) of 67%, short-circuit c.d. (Jsc) of 25.6 mA·cm^-2, and high open-circuit voltage (Voc) of 0.83 V were concurrently achieved in PBiTPD-based devices. PBiTPD does clear the way for a novel and promising class of large-bandgap polymer donor candidates.2-Hexyl-1-decanol (cas: 2425-77-6) were involved in the experimental procedure.

2-Hexyl-1-decanol(cas: 2425-77-6) has been shown to inhibit the growth of b16 mouse melanoma cells, suggesting it may be useful for treating skin cancer.Safety of 2-Hexyl-1-decanol This fatty acid also has transport properties and can form hydrogen bonds with other molecules.

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Adeleye, Temitope Adewumi;Ajiboye, Clement Odunayo;Ojah, Emmanuel Onah;Okesanjo, Toyin Patrick;Moronkola, Dorcas Olufunke published 《Composition and antioxidant potential of leaf and stem essential oils from Nigerian Indigofera spicata Forssk》. The research results were published in《Journal of Medicinal Plants Research》 in 2021.Synthetic Route of C16H34O The article conveys some information:

The chem. compositions and antioxidant evaluation of the essential oils (EOs) obtained by hydrodistillation from the leaf and stem of Indigofera spicata Forssk (Fabaceae) grown in Nigeria have been studied. The EOs were analyzed using gas chromatog. coupled with mass spectrometry (GC-MS) and the antioxidant potential was determined using 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging ability method. The essential oils from the leaf and stem obtained in 0.007% and 0.009% yield have been found to contain 18 and 17 compounds resp. 13 compounds identified in the stem EOs make 90.2% of it. Sesquiterpenes (49.2%) and alcs. (30.7%) are dominant classes of compounds in the leaf EOs, with the most abundant compounds as caryophyllene (38.2%), humulene (6.2%) and m-eugenol (27.5%). Whereas esters (47.2%), and monoterpenoids (20.8%) dominate the stem essential oils with major constituents as linalyl acetate (23.9%), α-terpinyl acetate (12.8%), 3,5,5-trimethyhexyl acetate (9.4%), and linalool (20.8%). Common to both EOs were linalool, (leaf, 1.9%) caryophyllene (stem 5.9%), linanyl acetate (leaf, 2.5%). Comparison of the composition pattern of the leaf and stem EOs of I. spicata revealed significant qual. and quant. differences. Monoterpenes, sesquiterpenoid, diterpenoid, epoxide and ether were exclusive to the leaf oil while saturated, unsaturated hydrocarbons and anhydride were found only in the stem oil. The IC₅₀ values of antioxidant evaluations show the leaf EO (36.97μg/mL) has more potential than the stem oil (39.89μg/mL) and comparable to that of the controls Vitamin C and Butylhydroxyl Anisole with IC₅₀ values 24.20 and 24.21μg/mL resp. Most of these identified compounds have been known for various pharmacol. activities such as antioxidant, antitumor, anti-inflammatory, even as fragrances and the antioxidant potential of the oils justify the ethno-medicinal uses of I. spicata. The experimental procedure involved many compounds, such as 2-Hexyl-1-decanol (cas: 2425-77-6) .

2-Hexyl-1-decanol(cas: 2425-77-6) is a fatty acid that is found in the essential oils of plants and has been shown to have fungicidal properties.Synthetic Route of C16H34O It has also been shown to inhibit the growth of Candida glabrata when used as a cationic surfactant.

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Chen, Zhao;Li, Yuanli;Liu, Xiaomin;Cui, Zhenggang published 《Dialkyl Sulfobetaine Surfactants Derived from Guerbet Alcohol Polyoxypropylene-Polyoxyethylene Ethers for SP Flooding of High Temperature and High Salinity Reservoirs》. The research results were published in《Journal of Surfactants and Detergents》 in 2021.Electric Literature of C16H34O The article conveys some information:

Dialkyl hydroxypropyl sulfobetaine (HSB) surfactants, C16GA-(PO)5-(EO)3-HSB and C24GA-(PO)10-(EO)10-HSB, were synthesized from Guerbet alcs. (GA) polyoxypropylene-polyoxyethylene (PO-EO) ethers and their behaviors in surfactant-polymer (SP) flooding of high temperature and high salinity reservoirs were examined and compared with their anionic hydroxypropyl sulfonate (HS) counterparts, C16GA-(PO)5-(EO)3-HS and C24GA-(PO)10-(EO)10-HS. The PO-EO chain embedded improves their aqueous solubility, and the sulfobetaines show better salt resistance than sulfonates. For a reservoir condition of total salinity 19,640 mg L-1 and 60-80°C, C16GA-(PO)5-(EO)3-HSB alone can reduce crude oil/connate water interfacial tension (IFT) to ultralow at 0.25-5 mM, which can be further widened to 0.1-5 mM by mixing with dodecylhexyl (C12+6) glyceryl ether hydroxypropyl sulfobetaine (C12+6GE-HSB), a slightly hydrophobic surfactant. C24GA-(PO)10-(EO)10-HSB is more hydrophobic for the specified reservoir condition, however, by mixing with hexadecyl di-Me hydroxypropyl sulfobetaine (C16HSB), a hydrophilic surfactant, ultralow IFT can also be achieved at a total concentration of 0.25-5 mM. The anionic counterparts can also reduce IFT to ultralow by mixing with C12+6GE-HSB and C16HSB, resp. Moreover, the optimum binary mixture, C16GA-(PO)5-(EO)3-HSB/C12+6GE-HSB at a molar fraction ratio of 0.6/0.4, can keep the neg. charged solid surface water-wet (θw = 12-23°) in a wide concentration range, and can still achieve ultralow IFT after stored at 90°C for 90 days (initially 5 mM), which overall are favor of improving oil displacement efficiency at high temperature and high salinity reservoir conditions. The experimental procedure involved many compounds, such as 2-Hexyl-1-decanol (cas: 2425-77-6) .

2-Hexyl-1-decanol(cas: 2425-77-6) is a fatty acid that is found in the essential oils of plants and has been shown to have fungicidal properties.Electric Literature of C16H34O It has also been shown to inhibit the growth of Candida glabrata when used as a cationic surfactant.

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Pojmanova, Petra;Ladislavova, Nikola;Skerikova, Veronika;Kania, Patrik;Urban, Stepan published 《Human scent samples for chemical analysis》 in 2020. The article was appeared in 《Chemical Papers》. They have made some progress in their research.SDS of cas: 2425-77-6 The article mentions the following:

This study is focused on finding an optimal preparation of the human scent samples for their detailed chem. anal. in connection with the possible forensic identifications of human individuals in the future. At the present time, the scent identification of people is carried out nearly exclusively using specially trained dogs. It is assumed that the human scent contains a certain group of compounds which allows the identification of people, the so-called human scent signature; however, its chem. composition is completely unknown, as of now. The principal problem of human scent studies consists in the very low concentrations of thousands of the scent compounds, whereas their relative concentrations are usually dramatically different. It seems to be obvious that the most appropriate anal. technique for these thousands of different chem. compounds is GC/MS. However, it is also necessary to find the most suitable sorbent material for human scent collection, an extraction solvent, and a pre-concentration technique. The selection of the appropriate gas chromatog. method is also important to achieve the optimal resolution of the targeted compounds Of course, in the first instance, it is necessary to decide what it means “the most suitable” for human scent chem. anal.2-Hexyl-1-decanol (cas: 2425-77-6) were involved in the experimental procedure.

2-Hexyl-1-decanol(cas: 2425-77-6) is a branched alcohol. It is one of the constituent of the essential oil, extracted from the roots of Adiantum flabellulatum. SDS of cas: 2425-77-6

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Ye, Xianfeng;Chen, Yang;Ma, Shiyun;Yuan, Tian;Wu, Yaxuan;Li, Yingxuan;Zhao, Yuqiang;Chen, Shuying;Zhang, Yiwen;Li, Liuyan;Li, Zhoukun;Huang, Yan;Cao, Hui;Cui, Zhongli published 《Biocidal effects of volatile organic compounds produced by the myxobacterium Corrallococcus sp. EGB against fungal phytopathogens》. The research results were published in《Food Microbiology》 in 2020.HPLC of Formula: 2425-77-6 The article conveys some information:

Myxobacteria have excellent biocontrol activity against various phytopathogens due to their rich spectrum of secondary metabolites and active predatory characteristics. In this study, the mycelial growth of Fusarium oxysporum f. sp. cucumerinum (FOC) was found to be significantly inhibited by volatile compounds (VOCs) produced by Corallococcus sp. EGB. A total of 32 compounds were identified among the VOCs produced by strain EGB, of which isooctanol exhibited the highest antifungal activity, with dosages of 3.75 and 4.0μL/plate being sufficient to suppress FOC and Penicillum digitatum, resp. Isooctanol was found to damage the cell wall and cell membranes of FOC and P. digitatum. Apoptosis-like cell death of FOC and P. digitatum induced by isooctanol was observed subsequently due to the accumulation of reactive oxygen species (ROS). The transcription level of genes related to cell wall integrity (CWI) pathway and redox reactions were significantly upregulated by 15- to 40-fold, indicating the stress caused by isooctanol. Postharvest storage experiments showed that the disease severity of post-harvest oranges infected with P. digitatum could be significantly reduced by isooctanol at 114.2μL/L. The experimental procedure involved many compounds, such as 2-Hexyl-1-decanol (cas: 2425-77-6) .

2-Hexyl-1-decanol(cas: 2425-77-6) is a fatty acid that is found in the essential oils of plants and has been shown to have fungicidal properties.HPLC of Formula: 2425-77-6 It has also been shown to inhibit the growth of Candida glabrata when used as a cationic surfactant.

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Wang, Yingying;Qin, Hongmei;Wang, Mei;Li, Yuxiang;Sun, Daotong;Yang, Jianye published 《Research of synthesis and properties of benzthiadiazole-based non-covalent conformational locking small molecule》 in 2021. The article was appeared in 《Gongneng Cailiao》. They have made some progress in their research.Reference of 2-Hexyl-1-decanol The article mentions the following:

In recent years, fused-ring compounds have achieved remarkable results in the field of organic optoelectronic materials. In this paper, two novel benzothiadiazole (BT)-based conjugated non-covalently bonded ring small mol. compounds with the electron-absorbing groups fluorine and cyano group as ending-group, namely BT2T-IC and BT2T-IC4F, were synthesized successfully by Still coupling and Knoevengel condensation reaction, resp. On the one hand, SO and OH can be used to form non-covalent bond conformation lock in mols. to promote the planarity of mols. On the other hand, intramol. charge transfer can be enhanced by increasing the electron-lack of the end group. Under the synergistic action, the spectral absorption of the two new small mol. compounds is broadened to the near IR region, which is conducive to obtaining a wide spectral response. Their mol. structures were characterized by NMR, and their photophysics and electrochem. properties were investigated by d. functional theory (DFT) calculations, UV-vis absorption spectroscopy and cyclic voltammetry experiments The experimental procedure involved many compounds, such as 2-Hexyl-1-decanol (cas: 2425-77-6) .

2-Hexyl-1-decanol(cas: 2425-77-6) is a fatty acid that is found in the essential oils of plants and has been shown to have fungicidal properties.Reference of 2-Hexyl-1-decanol It has also been shown to inhibit the growth of Candida glabrata when used as a cationic surfactant.

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Name: 2-Hexyl-1-decanol《Plant extracts effectiveness to extend bison meat shelf life》 was published in 2020. The authors were Sood, Vipasha;Tian, Wenchao;Narvaez-Bravo, Claudia;Arntfield, Susan D.;Gonzalez, Argenis Rodas, and the article was included in《Journal of Food Science》. The author mentioned the following in the article:

The effectiveness of plant extracts (0.05% rosemary and 0.08% oregano) to extend shelf life of bison strip loin steaks in terms of color stability and consumer acceptability was studied. Steaks treated with oregano presented lower oxygen consumption, higher metmyoglobin-reducing activity (MRA), decreased lipid oxidation, and provided a stable red color with less discoloration during the retail display period than the control and rosemary treated steaks (P < 0.05). Results from consumer sensory evaluation indicated that treated steaks under study were not significantly different from the control (P > 0.05) based on palatability attributes and acceptability. However, rosemary treated steaks were more desirable and palatable than their oregano counterparts (P < 0.05). Overall, plant extracts, particularly oregano, can improve color stability of bison steaks due to its antioxidants properties and ability to increase MRA capacity in fresh bison meat without posing any neg. impact on its sensory attributes. Practical Application : This study will provide valuable information to the bison meat industry on how to offer a more consistent and acceptable product (in terms of palatability and color) to consumers using plant-based natural antioxidants, without diminishing the palatability of their products. This technol. can offer two more days of shelf life in retail overwrap packaging, consequently, opening the possibility for the bison industry to expand its market with a potential to reduce retail losses due to poor color stability and early browning (i.e., stock out, markdowns, and waste due to expired display life). And 2-Hexyl-1-decanol (cas: 2425-77-6) was used in the research process.

2-Hexyl-1-decanol(cas: 2425-77-6) may be employed as an organic solvent to study the extraction of non-polar acidic drugs from human plasma by parallel artificial liquid membrane extraction (PALME). Name: 2-Hexyl-1-decanol

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Yada, Shiho;Yoshioka, Yuiko;Ohno, Masashi;Koda, Toshinari;Yoshimura, Tomokazu published 《Adsorption and aggregation properties of homogeneous polyoxyethylene alkyl ether- and ester-type nonionic surfactants with multi-branched double chains》 in 2022. The article was appeared in 《Colloids and Surfaces, A: Physicochemical and Engineering Aspects》. They have made some progress in their research.Electric Literature of C16H34O The article mentions the following:

Homogeneous polyoxyethylene (EO) alkyl ether- and ester-type nonionic surfactants with multi-branched double chains were newly synthesized. Their adsorption and aggregation properties were investigated through cloud point, surface tension, and small-angle X-ray scattering measurements, and compared to those of homogeneous EO alkyl ether- and ester-type nonionic surfactants with sym. and asym. linear double chains as well as a conventional surfactant with a linear single chain. The surface tension at the critical micelle concentration for the multi-branched double-chain type decreased considerably to 27.9-28.8 mN m^-1 despite having a large hydrophilic group of EO12 when multi-branched Me groups with low surface energy were used as the hydrophobic groups of the surfactants. In the temperature vs. concentration phase diagrams, the regions of lamellar liquid crystals were more extensive for the linear double-chain surfactants because of the small interfacial curvature induced by the steric hindrance of the multi-branched chains. To complete the study, the researchers used 2-Hexyl-1-decanol (cas: 2425-77-6) .

2-Hexyl-1-decanol(cas: 2425-77-6) may be employed as an organic solvent to study the extraction of non-polar acidic drugs from human plasma by parallel artificial liquid membrane extraction (PALME). Electric Literature of C16H34O

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HPLC of Formula: 2425-77-6《Polymeric ionic liquid absorbents for n-butanol recovery from aqueous solution》 was published in 2022. The authors were Biro, Robert;Daugulis, Andrew J.;Parent, J. Scott, and the article was included in《AIChE Journal》. The author mentioned the following in the article:

A wide-ranging study of imidazolium-based polymeric ionic liquids (PILs) as absorbents in two-phase partitioning bioreactor applications is presented, with a particular focus on the removal of n-butanol from dilute aqueous solutions The study begins with a description of the synthesis and phase transition temperatures of poly(1-vinyl-3-alkylimidazolium) bromides bearing alkyl groups of different lengths, architecture, and composition, as well as analogs bearing various inorganic and carboxylate anions. Knowledge of polymer structure is used to generate insight into the solute affinity of each PIL, as quantified by the measurements of n-butanol partition coefficient (PC_BuOH) and n-butanol/water selectivity (α_b/w). These equilibrium experiments are extended to create a complete P[(VC_12-linIm)(Br)]/n-BuOH/water ternary phase diagram that is used to propose a streamlined n-butanol recovery process. The experimental procedure involved many compounds, such as 2-Hexyl-1-decanol (cas: 2425-77-6) .

2-Hexyl-1-decanol(cas: 2425-77-6) is a branched alcohol. It is one of the constituent of the essential oil, extracted from the roots of Adiantum flabellulatum. HPLC of Formula: 2425-77-6

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