Droesbeke, Martijn A. et al. published their research in Green Chemistry in 2020 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Quality Control of 3,7-Dimethyloctan-1-ol

Biosourced terpenoids for the development of sustainable acrylic pressure-sensitive adhesives via emulsion polymerisation was written by Droesbeke, Martijn A.;Simula, Alexandre;Asua, Jose M.;Du Prez, Filip E.. And the article was included in Green Chemistry in 2020.Quality Control of 3,7-Dimethyloctan-1-ol The following contents are mentioned in the article:

The increasing regulations and restrictions in favor of a biobased and sustainable community could potentially harm the strong economic position of the polymer industry, which still heavily relyies on crude oil. The adhesive industry, in particular, is looking for more renewable alternatives and more environmentally friendly synthesis routes. In this work, (meth)acrylate derivatives of terpenoids, namely tetrahydrogeraniol, citronellol, menthol and isoborneol are introduced in the synthesis of waterborne pressure-sensitive adhesives (PSA) based on acrylic latexes via emulsion polymerization This industrially implemented setting enables the preparation of five different formulations with high biobased content with a renewable carbon content ranging from 70 to 100%. The biobased PSAs are found to be comparable in terms of tack, peel strength and shear resistance to a benchmark petroleum-derived com. product. They show good adhesion properties on steel, glass and polyethylene surfaces. Moreover, the various formulations displayed different mech. and adhesion properties, which make them attractive for a wide range of applications. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Quality Control of 3,7-Dimethyloctan-1-ol).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Quality Control of 3,7-Dimethyloctan-1-ol

Referemce:
Alcohol – Wikipedia,
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Li, Guolin et al. published their research in Nature Communications in 2020 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Electric Literature of C10H22O

Transition-metal-free formal cross-coupling of aryl methyl sulfoxides and alcohols via nucleophilic activation of C-S bond was written by Li, Guolin;Nieves-Quinones, Yexenia;Zhang, Hui;Liang, Qingjin;Su, Shuaisong;Liu, Qingchao;Kozlowski, Marisa C.;Jia, Tiezheng. And the article was included in Nature Communications in 2020.Electric Literature of C10H22O The following contents are mentioned in the article:

A transition-metal-free cross-coupling strategy utilizing aryl(heteroaryl) Me sulfoxides R1S(O)Me (R1 = Ph, 4-NCC6H4, 2-naphthyl, 3-pyridyl, 2-benzimidazolyl, etc.) and alcs. R2OH (R2 = Me, i-Pr, 2-cyclohexylethyl, 1-adamantylmethyl, etc.) to afford alkyl aryl(heteroaryl) ethers R1OR2 is reported. Two drug mols. were successfully prepared using this protocol as a key step and emphasized its potential utility in medicinal chem. A DFT computational study suggests that the reaction proceeds via initial addition of the alkoxide to the sulfoxide. This adduct facilitates further intramol. addition of the alkoxide to the aromatic ring wherein charge on the aromatic system is stabilized by the nearby potassium cation. Rate-determining fragmentation then delivers Me sulfenate and the aryl or heteroaryl ether. This study establishes the feasibility of nucleophilic addition to an appended sulfoxide as a means to form a bond to aryl(heteroaryl) systems and this modality is expected to find use with many other electrophiles and nucleophiles leading to new cross-coupling processes. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Electric Literature of C10H22O).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Electric Literature of C10H22O

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Alcohol – Wikipedia,
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Naicker, Letisha et al. published their research in ChemCatChem in 2022 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.COA of Formula: C10H22O

Influencing the Product Distribution in Citral Hydrogenation Using Ionic Liquid Modified Cu Catalysts was written by Naicker, Letisha;Schorner, Markus;Kremitzl, Daniel;Friedrich, Holger B.;Haumann, Marco;Wasserscheid, Peter. And the article was included in ChemCatChem in 2022.COA of Formula: C10H22O The following contents are mentioned in the article:

This work shows the effect of selected ionic liquids on the catalytic performance of a Cu/Al2O3 catalyst towards citral hydrogenation. The Cu/Al2O3 was prepared using a combination of wet impregnation and strong electrostatic interaction technique. The catalyst was coated with three ionic liquids, namely: [C4C1Pyrr][OTf], [C2C1C1Im][NTf2], and [C2C1Im][NTf2] resulting in Cu-based SCILL catalysts (solid catalyst with an ionic liquid layer). The fresh and used SCILL catalysts were characterized using FT-IR spectroscopy and thermal gravimetric anal. All Cu-SCILL catalysts were stable throughout the liquid-phase reactions with no leaching of ionic liquid being detectable by means of TGA. All ionic liquids investigated prevented the formation of undesired isopulegol compared to the 30% isopulegol selectivity obtained over the bare Cu/Al2O3 catalyst. The Cu-SCILL (coated with 15 weight% [C2C1Im][NTf2]) increased the selectivity towards geraniol and nerol by 340%. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8COA of Formula: C10H22O).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.COA of Formula: C10H22O

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Alcohol – Wikipedia,
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Ascrizzi, Roberta et al. published their research in Molecules in 2020 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Related Products of 106-21-8

Leek or garlic a chemical evaluation of elephant garlic volatiles was written by Ascrizzi, Roberta;Flamini, Guido. And the article was included in Molecules in 2020.Related Products of 106-21-8 The following contents are mentioned in the article:

“Aglione della Valdichiana” is listed among the Traditional Agronomic and Edible Products of Italy, as it is a typical product of the Chiana Valley (Tuscany, Italy). It is also known as “elephant garlic”, due to the dimension of its cloves, and, other than in the Italian Mediterranean area, its presence is also reported in North Africa and Southwest Asia. The current botanical classification identifies it as a leek variety (Allium ampeloprasum L.), although its appearance, except for its larger dimensions, resembles that of garlic. In the present study, the spontaneous volatile emission of whole and cut cloves of “Aglione della Valdichiana” (elephant garlic), garlic, and leek has been profiled by headspace solid phase micro-extraction The results have been subjected to statistical analyses (anal. of variance, hierarchical cluster, and principal component anal.) to assess whether the chem. profile confirmed the botanical proximity of elephant garlic and leek, rather than garlic. The phytochem. volatiles evaluation indicated a higher proximity of elephant garlic to garlic, rather than leek, at least for the Chiana Valley specimen analyzed in this study. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Related Products of 106-21-8).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Related Products of 106-21-8

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Munkuev, Aldar A. et al. published their research in Molecules in 2021 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.SDS of cas: 106-21-8

Novel Tdp1 inhibitors based on adamantane connected with monoterpene moieties via heterocyclic fragments was written by Munkuev, Aldar A.;Mozhaitsev, Evgenii S.;Chepanova, Arina A.;Suslov, Evgeniy V.;Korchagina, Dina V.;Zakharova, Olga D.;Ilina, Ekaterina S.;Dyrkheeva, Nadezhda S.;Zakharenko, Alexandra L.;Reynisson, Johannes;Volcho, Konstantin P.;Salakhutdinov, Nariman F.;Lavrik, Olga I.. And the article was included in Molecules in 2021.SDS of cas: 106-21-8 The following contents are mentioned in the article:

Tyrosyl-DNA phosphodiesterase 1 (Tdp1) is a promising target for anticancer therapy due to its ability to counter the effects topoisomerase 1 (Top1) poison, such as topotecan, thus, decreasing their efficacy. Compounds containing adamantane and monoterpenoid residues connected via 1,2,4-triazole or 1,3,4-thiadiazole linkers were synthesized and tested against Tdp1. All the derivatives exhibited inhibition at low micromolar or nanomolar concentrations with the most potent inhibitors having IC50 values in the 0.35-0.57 μM range. The cytotoxicity was determined in the HeLa, HCT-116 and SW837 cancer cell lines; moderate CC50 (μM) values were seen from the mid-teens to no effect at 100 μM. Furthermore, citral derivative 20c, α-pinene-derived compounds 20f, 20g and 25c, and the citronellic acid derivative 25b were found to have a sensitizing effect in conjunction with topotecan in the HeLa cervical cancer and colon adenocarcinoma HCT-116 cell lines. The ligands are predicted to bind in the catalytic pocket of Tdp1 and have favorable physicochem. properties for further development as a potential adjunct therapy with Top1 poisons. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8SDS of cas: 106-21-8).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.SDS of cas: 106-21-8

Referemce:
Alcohol – Wikipedia,
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Mohamed, K. Kasim et al. published their research in Journal of Chromatographic Science in 2022 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Formula: C10H22O

GC-MS and surface characteristics of polyvinyl siloxane-an in vitro analysis was written by Mohamed, K. Kasim;Banu, R. Fathima;Kumar, V. Anand;Sundaram, Lakshmi;Thyagarajan, S. P.. And the article was included in Journal of Chromatographic Science in 2022.Formula: C10H22O The following contents are mentioned in the article:

To assess the surface characteristics, composition and release of components of Polyvinyl siloxane (PVS) impression material and explore the use of the material other than for impressions. Forty samples of 0.5-mm thickness and 8-mm diameter PVS disks, with ew perforations, were prepared and divided into four groups. Group 1 in methanol was analyzed by GC-MS immediately and on 1st, 7th and 14th day. Group 2 and 3 placed in 10 mL of human saliva and in artificial nasal fluid, resp., were analyzed by GC-MS at 24 h. Group 4 was subjected to surface characteristics anal. by placing five PVS disks each in 1 mL of human saliva and 1 mL of artificial nasal fluid, resp. On Day 1, Dodecanoic acid, Me ester, Cyclononasiloxane, octadecamethyl, Cyclodecasiloxane and eicosamethyl (four peaks) were observed in Group 1. At 24 h, Group 2 had addnl. compounds of 2-Decene,7-methyl-(Z)-, 2-Undecene,8-methyl-(Z)- and Lauryl acetate. Group 3 showed release of 32 compounds, but their retention time was less. Surface characteristics on Day 14 revealed no noticeable changes. The study revealed that there was a lack of any adverse component release from PVS for a period of 2 wk based on GC-MS anal. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Formula: C10H22O).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Formula: C10H22O

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Nguyen, Manh Linh et al. published their research in Journal of Physical Chemistry B in 2021 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Safety of 3,7-Dimethyloctan-1-ol

The Role of the 1,2,3-Triazolyl Heterocycle in the Helical Columnar Assembly and Electric Field Response was written by Nguyen, Manh Linh;Byun, Jaeduk;Cho, Byoung-Ki. And the article was included in Journal of Physical Chemistry B in 2021.Safety of 3,7-Dimethyloctan-1-ol The following contents are mentioned in the article:

Here, we have proven the role of the 1,2,3-triazolyl group in the helical assembly and elec. field (E-field) response upon comparing liquid crystal analogs I and II (1 and 2, resp.) based on 1,2,3-triazolyl and 1,3,4-oxadiazolyl linkers, resp. An ordered helical column was only observed in 1, driven by the hydrogen-bonding interactions between the adjacent triazolyl nitrogen and hydrogen atoms. X-ray diffraction and energy simulations indicate that the helical column is a 112 helix and the helical axis does not coincide with the center of the mol. long axis. The key for the formation of the helical column is the tilted conformation of 1 originating from the steric repulsion between the triazolyl C-H and C-H of the aromatic core. Anal. of the dynamics in the simple hexagonal columnar phase revealed that the in-plane rotational motion of the triazolyl linker (1) is allowed, while the oxadiazolyl linker of 2 has limited conformational flexibility. A uniform alignment under an E-field only occurs in 1, demonstrating the requirement for conformational flexibility in the polar linker. This alignment enhances the elec. conductance of 1 by approx. two-fold. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Safety of 3,7-Dimethyloctan-1-ol).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Safety of 3,7-Dimethyloctan-1-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Ouedrhiri, Wessal et al. published their research in Environmental Science and Pollution Research in 2018 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Recommanded Product: 106-21-8

Antioxidant and antibacterial activities of Pelargonium asperum and Ormenis mixta essential oils and their synergistic antibacterial effect was written by Ouedrhiri, Wessal;Balouiri, Mounyr;Bouhdid, Samira;Harki, El Houssaine;Moja, Sandrine;Greche, Hassane. And the article was included in Environmental Science and Pollution Research in 2018.Recommanded Product: 106-21-8 The following contents are mentioned in the article:

In this work, the chem. composition, the antioxidant, and the antibacterial activities of two Moroccan essential oils less studied, extracted from Pelargonium asperum and Ormenis mixta, were investigated. According to the gas chromatog. coupled to mass spectrometry anal., citronellol (25.07%), citronellyl ester (10.52%), geraniol (10.46%), and buthyl anthranilate (5.93%) were found to be the major components of P. asperum, while O. mixta was mainly composed of D-germacrene (11.46%), 1,8-cineole (10.28%), and cis-Me isoeugenol (9.04%). Moreover, O. mixta essential oil exhibited an important antioxidant activity being significantly higher than that exhibited by P. asperum oil (P < 0.001). As regards the antimicrobial activity of both essential oils, the zones of growth inhibition and the min. inhibitory concentration values showed that P. asperum essential oil was more active than that of O. mixta. Thereafter, the impact of the binary combination of essential oils on their antimicrobial effect was investigated against Staphylococcus aureus using the fractional inhibitory concentration index calculation The results showed a promising synergistic antibacterial interaction between essential oils studied. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Recommanded Product: 106-21-8).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Recommanded Product: 106-21-8

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Zhang, Cun-zhi et al. published their research in Anhui Nongye Kexue in 2022 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Product Details of 106-21-8

Analysis of aroma components in fruit development period of “muscat” was written by Zhang, Cun-zhi;Liu, Jing;Zhang, Hong;Wei, Peng;Zhang, Hong-sheng;Cheng, Qian. And the article was included in Anhui Nongye Kexue in 2022.Product Details of 106-21-8 The following contents are mentioned in the article:

Headspace solid phase microextraction (HSPME) was used to extract the aroma components from six different development stages of grape, and the components were determined and analyzed by gas chromatog.-mass spectrometry (GC-MS) to reveal the change rule of aroma components and content in different development stages. The results showed that 60 kinds of aroma components were detected in the grape fruits of “Muscat”, and the aroma components and their contents varied greatly in different development stages of the fruit. Among them, the most changed linalool, the relative content increased rapidly from 3.24% in the late color transition period to 55.26% in the maturity period, followed by C13 alkanes, the relative content surged from 1.63% in the pre-color conversion to 18.84% in the late color conversion stage, an increase of 10.56 times, then rapidly decreased, and disappeared in the maturity period, which was neg. correlated with the change of linalool. Terpenoids were the main aroma of “Muscat” grapes, of which linalool was the most important component, and the pre-color transition-the late color transition was the synthesis period of the precursor substances of the aroma components. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Product Details of 106-21-8).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Product Details of 106-21-8

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Kim, Taegon et al. published their research in Nanoscale in 2019 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Application In Synthesis of 3,7-Dimethyloctan-1-ol

Visual detection of odorant geraniol enabled by integration of a human olfactory receptor into polydiacetylene/lipid nano-assembly was written by Kim, Taegon;Moon, Dongseok;Park, Jin Hyuk;Yang, Heehong;Cho, Seongyeon;Park, Tai Hyun;Ahn, Dong June. And the article was included in Nanoscale in 2019.Application In Synthesis of 3,7-Dimethyloctan-1-ol The following contents are mentioned in the article:

A new polydiacetylene lipid/human olfactory receptor nano-assembly was fabricated for the visual detection of an odorant for the first time. The assembly consisted of phospholipid-mixed polydiacetylenes (PDAs) and human olfactory receptors (hORs) in detergent micelles. To overcome the limitations of bioelectronic noses, hOR-embedded chromatic complexes (PDA/hORs) were developed, introducing PDAs that showed color and fluorescence transitions against various stimuli. The chromatic nanocomplexes reacted with target mols., showing a fluorescence intensity increase in a dose-dependent manner and target selectivity among various odorants. As a result, a color transition of the assembly from blue to purple occurred, allowing the visual detection of the odorant geraniol. Through CD (CD) spectroscopy and a tryptophan fluorescence quenching method, the structural and functional properties of the hORs embedded in the complexes were confirmed. Based on this first work, future array devices, integrating multiple nano-assemblies, can be substantiated and utilized in environmental assessment and anal. of food quality. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Application In Synthesis of 3,7-Dimethyloctan-1-ol).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Application In Synthesis of 3,7-Dimethyloctan-1-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts