Alcohols-buliding-blocks

Some low molecular weight alcohols of industrial importance are produced by the addition of water to alkenes. 141699-55-0, formula is C8H15NO3, Ethanol, isopropanol, 2-butanol, and tert-butanol are produced by this general method. Two implementations are employed, the direct and indirect methods. HPLC of Formula: 141699-55-0

Yan, Qi;Wang, Yujie;Zhang, Wei;Li, Yingxia research published 《 Novel azetidine-containing TZT-1027 analogues as antitumor agents》, the research content is summarized as follows. A conformational restriction strategy was used to design and synthesize nine TZT-1027 analogs. 3-Aryl-azetidine moiety was used to replace phenylethyl group of TZT-1027 at the C-terminus. These analogs exhibited moderate to excellent antiproliferative activities, and the most potent compound 1a showed IC50 values of 2.2 nM against A549 and 2.1 nM against HCT116 cell lines, resp. However, 1a could not achieve effective inhibition at all the dose levels in the A549 xenograft model (up to 5 mg/kg, injection, once a day), which is only 16%-35% inhibition at the end of the experiment

141699-55-0, Tert-butyl 3-hydroxyazetidine-1-carboxylate is a useful research compound. Its molecular formula is C8H15NO3 and its molecular weight is 173.21 g/mol. The purity is usually 95%.

Tert-butyl 3-hydroxyazetidine-1-carboxylate has been shown to be a good substrate for the preparation of N-protected amino alcohols and amines by the process of reductive amination. In this synthesis, tert-butyl azetidinium chloride is used as a catalyst in the reaction with sodium hydroxide. The tert-butyl group can be removed using ammonium hydroxide in the presence of a base such as triethylamine. This reaction can be performed on a large scale, making it useful in the manufacture of pharmaceuticals. The efficiency and solubility of this process make it suitable for use as an introduction to other processes involving N-protected amino alcohols or amines., HPLC of Formula: 141699-55-0

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. 141699-55-0, formula is C8H15NO3, Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Methanol, ethanol, and propanol are miscible in water. Butanol, with a four-carbon chain, is moderately soluble. Electric Literature of 141699-55-0

Yan, Hao;Li, Xincheng;Wang, Chunxiang;Wan, Boshun research published 《 Silver-catalyzed cyclization of nitrones with 2-azetine: a radical approach to 2,3-disubstituted quinolines》, the research content is summarized as follows. A silver-catalyzed intermol. tandem cyclization of nitrones with 2-azetine was developed for the synthesis of 2,3-disubstituted quinolines I (R = H, 8-MeO, 6-Cl, etc.; Ar = Ph, 4-FC₆H₄, 4-MeOC₆H₄, etc.) under mild conditions with good yields. This approach features a C-N bond cleavage of 2-azetine and an N-O bond cleavage of nitrones via a radical pathway. The results of this study provide a new reaction pattern for nitrones and may find applications in the synthesis of other heterocycles.

Electric Literature of 141699-55-0, Tert-butyl 3-hydroxyazetidine-1-carboxylate is a useful research compound. Its molecular formula is C8H15NO3 and its molecular weight is 173.21 g/mol. The purity is usually 95%.

Tert-butyl 3-hydroxyazetidine-1-carboxylate has been shown to be a good substrate for the preparation of N-protected amino alcohols and amines by the process of reductive amination. In this synthesis, tert-butyl azetidinium chloride is used as a catalyst in the reaction with sodium hydroxide. The tert-butyl group can be removed using ammonium hydroxide in the presence of a base such as triethylamine. This reaction can be performed on a large scale, making it useful in the manufacture of pharmaceuticals. The efficiency and solubility of this process make it suitable for use as an introduction to other processes involving N-protected amino alcohols or amines., 141699-55-0.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Synthetic Route of 72824-04-5, In chemistry, an alcohol is a type of organic compound that carries at least one hydroxyl functional group (−OH) bound to a saturated carbon atom. 72824-04-5, name is 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, An important class of alcohols, of which methanol and ethanol are the simplest examples, includes all compounds which conform to the general formula CnH2n+1OH.

Yamamoto, Yoshihiko;Kuroyanagi, Eisuke;Suzuki, Harufumi;Yasui, Takeshi research published 《 Catalyst-Free Csp-Csp³ Cross-Coupling of Bromodifluoroacetamides with 1-Iodoalkynes under Visible-Light Irradiation》, the research content is summarized as follows. Herein the cross-coupling of bromodifluoroacetamides with (iodoethynyl)arenes proceeds without recourse to any photocatalyst when exposed to visible light at room temperature to afford alkynyldifluoroacetamides in 62-83% yields (27 examples) is described. Several control experiments suggest that the reaction involves the homolysis of bromodifluoroacetamides and the coupling of the resultant difluoromethyl radical species with the 1-iodoalkynes via a radical chain process. Divergent transformations of the coupling products led to various organofluorine compounds, demonstrating the synthetic utility of the developed photo-coupling method.

72824-04-5, Allylboronic acid pinacol ester is a useful research compound. Its molecular formula is C9H17BO2 and its molecular weight is 168.04 g/mol. The purity is usually 95%.
Allylboronic acid pinacol ester is an allylation reagent that is used to produce aldehydes from ketones. It reacts with water, yielding the desired product and formaldehyde as a byproduct. The reaction proceeds through a sequence of steps, in which the boronate ester first reacts with water to form an allylboronate ion and hydrogen gas. This intermediate then reacts with potassium t-butoxide to produce the desired allyl alcohol and potassium borohydride. Finally, the palladium complex catalyst reduces the carbonyl group of the starting material, converting it into an aldehyde. Allylboronic acid pinacol ester is commercially available as a white solid, but can also be synthesized from 2-chloro-5-pinacolylborane (pinacol) in high yield using catalytic cross coupling reactions., Synthetic Route of 72824-04-5

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. 141699-55-0, formula is C8H15NO3, Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Methanol, ethanol, and propanol are miscible in water. Butanol, with a four-carbon chain, is moderately soluble. Quality Control of 141699-55-0

Yamaki, Susumu;Yamada, Hiroyoshi;Nagashima, Akira;Kondo, Mitsuhiro;Shimada, Yoshiaki;Kadono, Keitaro;Yoshihara, Kosei research published 《 Synthesis and structure activity relationships of carbamimidoylcarbamate derivatives as novel vascular adhesion protein-1 inhibitors》, the research content is summarized as follows. Vascular adhesion protein-1 (VAP-1) is a promising therapeutic target for the treatment of diabetic nephropathy. Here, the authors conducted structural optimization of the glycine amide derivative (I), which the authors previously reported as a novel VAP-1 inhibitor, to improve stability in dog and monkey plasma, and aqueous solubility By chem. modification of the right part in the glycine amide derivative, the authors identified the carbamimidoylcarbamate derivative, which showed stability in dog and monkey plasma while maintaining VAP-1 inhibitory activity. The authors also found that conversion of the pyrimidine ring in the derivative into saturated rings was effective for improving aqueous solubility This led to the identification of two moderate VAP-1 inhibitors with excellent aqueous solubility Further optimization led to the identification of 2-fluoro-3-{3-[(6-methylpyridin-3-yl)oxy]azetidin-1-yl}benzyl carbamimidoylcarbamate (II), which showed similar human VAP-1 inhibitory activity to I with improved aqueous solubility II showed more potent ex vivo efficacy than I, with rat plasma VAP-1 inhibitory activity of 92% at 1 h after oral administration at 0.3 mg/kg. In the pharmacokinetic study, II showed good oral bioavailability in rats, dogs, and monkeys, which may be due to its improved stability in dog and monkey plasma.

Quality Control of 141699-55-0, Tert-butyl 3-hydroxyazetidine-1-carboxylate is a useful research compound. Its molecular formula is C8H15NO3 and its molecular weight is 173.21 g/mol. The purity is usually 95%.

Tert-butyl 3-hydroxyazetidine-1-carboxylate has been shown to be a good substrate for the preparation of N-protected amino alcohols and amines by the process of reductive amination. In this synthesis, tert-butyl azetidinium chloride is used as a catalyst in the reaction with sodium hydroxide. The tert-butyl group can be removed using ammonium hydroxide in the presence of a base such as triethylamine. This reaction can be performed on a large scale, making it useful in the manufacture of pharmaceuticals. The efficiency and solubility of this process make it suitable for use as an introduction to other processes involving N-protected amino alcohols or amines., 141699-55-0.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

With respect to acute toxicity, simple alcohols have low acute toxicities. Doses of several milliliters are tolerated. 7748-36-9, formula is C3H6O2, For pentanols, hexanols, octanols and longer alcohols, LD50 range from 2–5 g/kg (rats, oral). Ethanol is less acutely toxic.All alcohols are mild skin irritants. Product Details of C3H6O2

Xue, Ting;Zhang, Zongnan;Zeng, Rong research published 《 Photoinduced Ligand-to-Metal Charge Transfer (LMCT) of Fe Alkoxide Enabled C-C Bond Cleavage and Amination of Unstrained Cyclic Alcohols》, the research content is summarized as follows. An alkoxy radical process for the C-C bond cleavage and functionalization of unstrained tertiary and secondary cyclic alcs. was reported. In the absence of a chlorine atom, the readily available iron catalysts [Fe(OBu-t)₃ or Fe(acac)₃/t-BuONa] facilitate alkoxy radical formation via the direct ligand-to-metal charge transfer of Fe alkoxide and further enable the ring opening and amination of cyclic alcs. The remote amino carbonyl compounds could be obtained with a broad scope in up to excellent yields under the mildly redox-neutral system. Light-driven electron transfer, alkoxy radical formation, and subsequent C-C bond cleavage via β-scission were the keys to the transformation.

Product Details of C3H6O2, Oxetan-3-ol is a useful research compound. Its molecular formula is C3H6O2 and its molecular weight is 74.08 g/mol. The purity is usually 95%.
Oxetan-3-ol is a synthetic hydroxy compound with the chemical formula C6H12O3. It is an organic solvent that can be used in reactions involving vinyl alcohol and oxetane, such as ring-opening polymerization and cationic polymerization. Oxetan-3-ol has also been shown to react with ethyl bromoacetate to form the corresponding oxetane, which can be used as a bioisostere for chloropropane, a potential replacement for chlorofluorocarbons., 7748-36-9.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Simple alcohols are found widely in nature. Ethanol is the most prominent because it is the product of fermentation, a major energy-producing pathway. 16545-68-9, formula is C3H6O, Other simple alcohols, chiefly fusel alcohols, are formed in only trace amounts. More complex alcohols however are pervasive, as manifested in sugars, some amino acids, and fatty acids. , HPLC of Formula: 16545-68-9

Xue, Lian;Shi, Da-Hua;Harjani, Jitendra R.;Huang, Fei;Beveridge, Julia G.;Dingjan, Tamir;Ban, Kung;Diab, Sarah;Duffy, Sandra;Lucantoni, Leonardo;Fletcher, Sabine;Chiu, Francis C. K.;Blundell, Scott;Ellis, Katherine;Ralph, Stuart A.;Wirjanata, Grennady;Teguh, Silvia;Noviyanti, Rintis;Chavchich, Marina;Creek, Darren;Price, Ric N.;Marfurt, Jutta;Charman, Susan A.;Cuellar, Matthew E.;Strasser, Jessica M.;Dahlin, Jayme L.;Walters, Michael A.;Edstein, Michael D.;Avery, Vicky M.;Baell, Jonathan B. research published 《 3,3′-Disubstituted 5,5′-Bi(1,2,4-triazine) Derivatives with Potent in Vitro and in Vivo Antimalarial Activity》, the research content is summarized as follows. A series of 3,3′-disubstituted 5,5′-bi(1,2,4-triazine) derivatives was synthesized and screened against the erythrocytic stage of Plasmodium falciparum 3D7 line. The most potent dimer, I, with an IC₅₀ (50% inhibitory concentration) of 0.008 μM, had high in vitro potency against P. falciparum lines resistant to chloroquine (W2, IC₅₀ = 0.0047 ± 0.0011 μM) and artemisinin (MRA1240, IC₅₀ = 0.0086 ± 0.0010 μM). Excellent ex vivo potency of I was shown against clin. field isolates of both P. falciparum (IC₅₀ = 0.022-0.034 μM) and Plasmodium vivax (IC₅₀ = 0.0093-0.031 μM) from the blood of outpatients with uncomplicated malaria. Despite I being cleared relatively rapidly in mice, it suppressed parasitemia in the Peters 4-day test, with a mean ED₅₀ value (50% ED) of 1.47 mg kg^-1 day^-1 following oral administration. The disubstituted triazine dimer I represents a new class of orally available antimalarial compounds of considerable interest for further development.

HPLC of Formula: 16545-68-9, Cyclopropanol is a cyclopropane in which a hydrogen atom is replaced by a hydroxy group. It is a member of cyclopropanes and an aliphatic alcohol.
Cyclopropanol is a useful research compound. Its molecular formula is C3H6O and its molecular weight is 58.08 g/mol. The purity is usually 95%.
Cyclopropanol is a cyclic organic compound that is synthesized from sodium hydroxide solution, nitrogen atoms, and carbonyl groups. Cyclopropanol has shown inhibitory effects on inflammatory bowel disease in rats. This drug also inhibits the production of hydrogen chloride and hydrochloric acid in the stomach, which can lead to ulcers. Cyclopropanol has been found to be effective against bowel diseases such as Crohn’s disease and ulcerative colitis. This drug has been shown to have strong antioxidant properties, which may be due to its ability to reduce hydroxyl radicals., 16545-68-9.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Simple alcohols are found widely in nature. Ethanol is the most prominent because it is the product of fermentation, a major energy-producing pathway. 527-07-1, formula is C6H11NaO7, Other simple alcohols, chiefly fusel alcohols, are formed in only trace amounts. More complex alcohols however are pervasive, as manifested in sugars, some amino acids, and fatty acids. , HPLC of Formula: 527-07-1

Xu, Yanqun;Yuan, Qiang;Li, Zemin;Shi, Caijun;Wu, Qihong;Huang, Yanlin research published 《 Correlation of interlayer properties and rheological behaviors of 3DPC with various printing time intervals》, the research content is summarized as follows. The weak interlayer of 3D printing cementitious materials (3DPC) remains a critical challenge for 3D printing technol., which can print fresh materials layer by layer based on a pre-defined computer model. In this paper, the effects of the printing time interval on rheol. behavior, shear bond strength, penetration resistance to chloride and CO2 of 3DPC interlayers were investigated, and the correlations among them were analyzed based on the gray relational anal.(GRA) method, a statistical method for measuring correlations between factors by their trends. The results showed that the carbonation resistance is the most sensitive to the printing time interval, followed by chloride penetration and shear bond strength. The rheol. behaviors of 3DPC had weaker correlation with the shear bond strength when comparing with the interlayer surface moisture. Addnl., the porosity was more related to the shear bond strength than the number of pores. Furthermore, a quant. relationship between shear bond strength and printing time interval was established.

HPLC of Formula: 527-07-1, Sodium Gluconate is the sodium salt of gluconic acid with chelating property. Sodium gluconate chelates and forms stable complexes with various ions, preventing them from engaging in chemical reactions.
Sodium gluconate is an organic sodium salt having D-gluconate as the counterion. It has a role as a chelator. It contains a D-gluconate.
D-Gluconic acid sodium salt is a glycol ether that is used as an injection solution. It has been shown to have antibacterial efficacy against wild-type strains of bacteria such as Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. The in vitro antimicrobial action of D-gluconic acid sodium salt was found to be due to its ability to inhibit bacterial growth by interfering with the synthesis of DNA. D-gluconic acid sodium salt also has been shown to have antihypertensive effects in rats through the inhibition of angiotensin II type 1 receptor (AT1) signaling pathway and erythrocyte proliferation. This drug also has been shown to bind benzalkonium chloride and x-ray diffraction data show that it is crystalline in nature. The analytical method for determining the concentration of D-gluconic acid sodium salt is by electrochemical impedance, 527-07-1.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

In general, the hydroxyl group makes alcohols polar. 24034-73-9, formula is C20H34O, Because of hydrogen bonding, alcohols tend to have higher boiling points than comparable hydrocarbons and ethers. Quality Control of 24034-73-9

Xu, Xiujuan;Lu, Ping;Shi, Qingzhao;Chen, Mengqi;Yang, Chunqiang;Qu, Zhan;Cui, Kai;Li, Mingzhe;He, Baojiang;Hu, Shaodong research published 《 Chemical analysis and sensory evaluation of main components in essential oil of cigar tobacco》, the research content is summarized as follows. In order to analyze the chem. components in the essential oil of cigar tobacco and to evaluate their effects, the essential oil of cigar tobacco was prepared by using subcritical extraction and mol. distillation technol. The enrichment effects of various components in the essential oil at different distillation temperatures were clarified. The main chem. components of the essential oil were analyzed by GC/MS, and the influences of mass fractions of various components in the essential oil on the sensory quality of cigarettes were further verified through sensory panel evaluation. The relationships between some aroma components and sensory evaluation indexes were studied via relevant anal. The results showed that at the distillation temperature of 60-80 °C, the mass fractions of nicotine, alkanes and long-chain aliphatic esters were reduced, and the aroma components with cigar styles were effectively enriched. The mass fractions of geranyl acetone, β-ionone, megastigmatrienone, dihydroactinidiolide, farnesyl acetone, phenylacetic acid, acetic acid, propionic acid, dihydro-β-ionone, n-hexanoic acid, 6-methyl-5-heptene-2-one, thujopsene and (E)-nerolidol in the essential oil were significantly pos. or extremely significantly pos. correlated with the quality evaluation indexes of cigarettes, including aroma, comprehensive taste, woody and honeysweet scents. Therefore, these compounds can be used as the main indexes for evaluating the quality of essential oil of cigar tobacco.

24034-73-9, Geranylgeraniol is a diterpenoid that is hexadeca-2,6,10,14-tetraene substituted by methyl groups at positions 3, 7, 11 and 15 and a hydroxy group at position 1. It has a role as a plant metabolite, a volatile oil component and an antileishmanial agent. It is a diterpenoid and a polyprenol.

Geranylgeraniol, a precursor to geranylgeranylpyrophosphate, is an intermediate in the mevalonate pathway. Geranylgeraniol has been shown to prevent bone re-absorption, inhibition of osteoclast formation, and kinase activation in vitro. When working with statins, Geranylgeraniol can reduce the toxicity without inhibiting the cholesterol-producing effects. Geranylgeraniol has been documented to counteract the effects of fluvastatin by inhibiting activation of caspase-1 and production of IL-1. Additionally Geranylgeraniol has been found to induce apoptosis in HL-60 cells.
, Quality Control of 24034-73-9

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Simple alcohols are found widely in nature. Ethanol is the most prominent because it is the product of fermentation, a major energy-producing pathway. 647-42-7, formula is C8H5F13O, Other simple alcohols, chiefly fusel alcohols, are formed in only trace amounts. More complex alcohols however are pervasive, as manifested in sugars, some amino acids, and fatty acids. , Computed Properties of 647-42-7

Xu, Wei;Wang, Wen;Hao, Lifen;Liu, Hongna;Hai, Fang;Wang, Xuechuan research published 《 Synthesis and properties of novel triazine-based fluorinated chain extender modified waterborne polyurethane hydrophobic films》, the research content is summarized as follows. A novel triazine-based fluorinated diol, CC-F, was synthesized from cyanuric chloride (CC), octafluoropentanol (OFP), and ethanolamine (MEA). Subsequently, a series of fluorinated waterborne polyurethanes (CC-FPUF-n, n expressed as mass percentages of CC-F in product formula) were synthesized using CC-F as the chain extender. The chem. structure of the product was verified using the Fourier transform IR (FTIR) spectroscopy and NMR spectroscopy techniques. The influence of the CC-F contents on the properties of the latex particles, surface properties, thermal stabilities, and mech. properties of CC-FPUF films was determined using the transmission electron microscopy (TEM), dynamic light scattering (DLS), XPS, SEM, at. force microscopy (AFM), water contact angle (WCA), thermogravimetric anal. (TGA), differential scanning calorimetry (DSC), and X-ray diffraction (XRD) techniques. Mech. tests were also conducted for the same. The results revealed that the hydrophobic and mech. properties of the CC-FPUF films were improved. Water contact angle and tensile strength values of the CC-FPUF-8 film were 125.8° and 36.63 MPa, resp., which were, resp., 34.1° and 24.47 MPa higher than those of the CC-FPUF-0 film. Thus, the embedding of CC-F into polyurethane mols. could significantly improve the hydrophobic and mech. properties of the waterborne polyurethane films. Therefore, these novel fluorinated waterborne polyurethanes can be potentially used for hydrophobic coatings in the future.

647-42-7, 3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctan-1-ol, also known as 1H,1H, 2H, 2H-Tridecafluoro-1-n-octanol , is a useful research compound. Its molecular formula is C8H5F13O and its molecular weight is 364.1 g/mol. The purity is usually 95%.

1H,1H, 2H, 2H-Tridecafluoro-1-n-octanol is a material used to improve nanotube composites. It is also used in the synthesis of a recyclable fluorous hydrazine carbothioate compound with NCS to catalyze the acetalization of aldehydes.

1H,1H,2H,2H-Tridecafluoro-1-n-octanol is a potent and selective halogenated hydrocarbon. It binds to DNA at the dinucleotide phosphate site, which is an important site for polymerase chain reaction (PCR) activation. 1HFN has been shown to be more effective than other halogenated hydrocarbons in vitro assays on rat liver microsomes. It has been used as an additive in wastewater treatment to remove organic contaminants and metal ions. In vivo studies have been carried out in CD-1 mice to determine the effects of 1HFN on the liver and kidneys; these studies showed no toxicological effects on these organs. 1HFN also has been shown to inhibit enzymes such as cytochrome P450 and monoamine oxidase B that are involved in drug metabolism and may lead to adverse reactions with drugs metabolized by these enzymes., Computed Properties of 647-42-7

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. 647-42-7, formula is C8H5F13O, Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Methanol, ethanol, and propanol are miscible in water. Butanol, with a four-carbon chain, is moderately soluble. Formula: C8H5F13O

Xu, Wei;Wang, Wen;Hao, Lifen;Zhao, Weijia;Liu, Hongna;Wang, Xuechuan research published 《 Effect of generation number on properties of fluoroalkyl-terminated hyperbranched polyurethane latexes and its films》, the research content is summarized as follows. The 1-3 generations of hyperbranched polyesters (HBPE-1/2/3) were synthesized from trimethylolpropane (TMP) and 2,2-dimethylol propionic acid (DMPA) by ”quasi-one-step method”. Then, isophorone diisocyanate (IPDI), polybutylene adipate (CMA-1044), DMPA and 1,4-butanediol (BDO) were utilized to prepare the urethane prepolymer (PU), which was reacted with HBPE to synthesize hyperbranched polyurethanes (HBPU). Finally, 1-3 generations of fluoroalkyl-end-capped hyperbranched polyurethanes (FHBPU) latexes were obtained by the reaction of perfluorohexyl ethanol (S 104) and HBPU as well as the self-emulsification process. Structure of the products, the properties of different FHBPU emulsions and its films were investigated by FTIR, ¹H NMR, TEM, DLS, TGA, XPS, XRD, SEM, AFM and static contact angle measuring instrument. Results showed that the particle size of FHBPU latexes increased gradually with the increase of generation number SEM and XRD results verified that an amount of the crystal particles was increased with the increase of generation number XPS and AFM demonstrated that degree of microphase separation and film roughness was increased with the increase of branching degree. Static water contact angles could attain 95.9°, 100.3°, and 107.0°, resp. on the 1-3 generations of FHBPU films, compared to that on PU (75.1°).

Formula: C8H5F13O, 3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctan-1-ol, also known as 1H,1H, 2H, 2H-Tridecafluoro-1-n-octanol , is a useful research compound. Its molecular formula is C8H5F13O and its molecular weight is 364.1 g/mol. The purity is usually 95%.

1H,1H, 2H, 2H-Tridecafluoro-1-n-octanol is a material used to improve nanotube composites. It is also used in the synthesis of a recyclable fluorous hydrazine carbothioate compound with NCS to catalyze the acetalization of aldehydes.

1H,1H,2H,2H-Tridecafluoro-1-n-octanol is a potent and selective halogenated hydrocarbon. It binds to DNA at the dinucleotide phosphate site, which is an important site for polymerase chain reaction (PCR) activation. 1HFN has been shown to be more effective than other halogenated hydrocarbons in vitro assays on rat liver microsomes. It has been used as an additive in wastewater treatment to remove organic contaminants and metal ions. In vivo studies have been carried out in CD-1 mice to determine the effects of 1HFN on the liver and kidneys; these studies showed no toxicological effects on these organs. 1HFN also has been shown to inhibit enzymes such as cytochrome P450 and monoamine oxidase B that are involved in drug metabolism and may lead to adverse reactions with drugs metabolized by these enzymes., 647-42-7.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts