Alcoli

<p>Tetrahydropyran-2-methanol is a hydrogenated, hydrated, triflic acid derivative that belongs to the group of organic compounds known as ethers. The presence of a hydroxyl group on one end and a chloride group on the other end provides tetrahydropyran-2-methanol with two reactive sites for reactions with metals. It has been shown to react with metal surfaces in order to form an adduct under acidic conditions that can be used as an ion exchange resin. Tetrahydropyran-2-methanol also reacts rapidly with hydrochloric acid to form tetrahydrothiophene and methanol. This reaction time can be sped up by heating the liquid at atmospheric pressure or by adding sulfuric acid. Tetrahydropyran-2-methanol is also capable of reacting with water in order to produce hydrogen gas and alcohol.</p>

<p>2-Thiopheneethanol tosylate (2TEtOS) is an antitubercular agent that belongs to the class of thiopheneethanol esters. It is a potent inhibitor of Mycobacterium tuberculosis and other bacteria by blocking the transfer reactions that are required for bacterial growth. The molecular structure of 2TEtOS consists of a thiophene ring with an allyl group attached to it and a chiral sulfur atom in the center. This molecule can be derivatized with various ligands, which enables the control experiments to be performed. 2TEtOS has been shown to have redox potentials and diffraction properties that are similar to those of borohydride reduction agents, suggesting that 2TEtOS may also act as a reducing agent.</p>

<p>Conjugated linoleic acid (CLA) is a fatty acid found in beef and dairy products. It is a conjugated form of linoleic acid, which means it has two or more double bonds in its chemical structure. CLA may help to regulate energy metabolism by inhibiting the activity of enzymes involved in fat and carbohydrate metabolism. CLA has also been shown to have inhibitory properties against polymerase chain reaction (PCR), an enzyme that copies DNA during cell division. CLA has also been shown to reduce the symptoms of bowel disease, including reducing inflammation and improving insulin sensitivity. CLA may suppress body weight gain and fat accumulation in humans, as well as reduce the development of type 2 diabetes mellitus. In addition, CLA may be effective against infectious diseases such as tuberculosis and HIV/AIDS because it can lower levels of pro-inflammatory cytokines like tumor necrosis factor-α (TNF-α)</p>

<p>Glycerol tristearate is a triglyceride, which is derived from the esterification of glycerol with stearic acid, a saturated fatty acid. This compound is typically sourced from natural fats and oils through a process involving the hydrogenation of vegetable oils, which facilitates its pure and controlled production.The mode of action of glycerol tristearate involves its function as an effective emulsifier. It stabilizes mixtures of water and oil by reducing interfacial tension, thus enabling the formation of stable emulsions. Its solid form at room temperature also contributes to its ability to enhance texture and stability in various formulations.Glycerol tristearate is widely used in diverse applications including the food industry, where it acts as a texturizer and stabilizer in products like margarine, chocolate, and confectionery. Additionally, it plays a significant role in the cosmetics and personal care sectors, where it improves the texture and stability of creams and lotions. Its properties make it a valuable ingredient for controlling crystallization and improving consistency across multiple industry settings.</p>

<p>Polyisoprenylated benzophenone from Garcinia indica; HAT inhibitor</p>

<p>Please enquire for more information about 6-Chloro-1,7-naphthyridin-4-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Chloro-4-hydroxybenzyl alcohol is an organic compound that has been shown to be soluble in aqueous alkali metal solutions, but insoluble in water. It is also insoluble in polymer solvents such as acetone and ethyl ether. 2-Chloro-4-hydroxybenzyl alcohol is a sugar alcohol with 3 hydroxyl groups. The molecule has a molecular weight of 150.17 g/mol, melting point of -123°C (-198°F), boiling point of 179°C (354°F), and refractive index of 1.5774 at 20°C (68°F). This chemical can be used in the synthesis of polyhydric alcohols such as glycerol or hexanol. 2-Chloro-4-hydroxybenzyl alcohol is not soluble in hydrochloric acid, benzene or chloroform, and does not react to form any es</p>

<p>Rac-1-anthracen-2-yl-ethanol is an apolar, injecting alcohol. It has two isomers. Rac-1-anthracen-2-yl-ethanol has a selectivity profile that is different from other compounds in its class, and it outperforms amine solvents in the separation of similar compounds. This compound's selectivity profile is due to interactions with the solvent and stationary phase that are unique to this compound. Rac-1-anthracen-2-yl-ethanol also has a low nature and low toxicity profile.</p>

<p>Fully reduced form of coenzyme Q10</p>

<p>2-(4-Methyl-2-phenyl-1-piperazinyl)-3-pyridinemethanol is an impurity in hexane that is generated during the reaction of pyridine with acetonitrile. The impurity is removed by crystallizing it from methanol. 2-(4-Methyl-2-phenyl-1-piperazinyl)-3-pyridinemethanol has a high efficiency, and can be used to synthesize hexamethyldisiloxane. This product can be used as a metal catalyst for reactions involving alkali metals or metal halides. It can also be used as an alcohol solvent, but not hydrogenated.</p>

<p>2,2,4-Trimethyl-1,2-dihydroquinoline is a chemical compound with the formula C8H10N2. It is a white solid that is insoluble in water but soluble in nonpolar solvents such as benzene, toluene and hexane. 2,2,4-Trimethyl-1,2-dihydroquinoline has been shown to induce liver lesions in rats at doses of 1.25 g/kg/day. It also reacts with hydrogen fluoride to form calcium stearate. This compound is also used as a precursor for the synthesis of diazonium salts and has been shown to be carcinogenic in animal studies.</p>

<p>Please enquire for more information about 4-Aminophenyl ethyl carbinol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Chlorophenyl)diphenylmethanol is an antifungal drug that blocks the function of a calcium ionophore in fungal cells. It has been shown to be effective against a variety of filamentous fungi, including Aspergillus fumigatus, Candida albicans, and Trichosporon cutaneum. This drug is used as a topical antifungal agent for treatment of skin infections caused by these fungi. 2-Chlorophenyl)diphenylmethanol has been shown to have anti-inflammatory properties in animal models of kidney fibrosis and cell binding. Clinical data suggests that it can be used for the prevention or treatment of stem cell transplantation complications such as graft versus host disease and leukemia.</p>

<p>Please enquire for more information about 4-[(4-Chlorophenyl)phenylmethyl]-1-piperazineethanol dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Campestanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>2-Acetamidophenol is an apoptotic agent that has been used as a hydroxyl radical scavenger in the treatment of oxidative injury. The drug has also been shown to possess anti-inflammatory properties. 2-Acetamidophenol is a stable complex with nitrite ion, which is formed during the redox cycle and may be responsible for the drug's antirheumatic activity. The drug does not react with p-hydroxybenzoic acid, which may be due to its protective effect on enzymes such as cytochrome P450 that are involved in the metabolism of drugs. 2-Acetamidophenol can be detected by analytical methods such as nmr spectra or gas chromatography under neutral pH conditions.</p>

<p>Intermediate in the synthesis of mirabegron</p>

<p>Stigmast-7-enol is a naturally occurring compound found in plants such as Oroxylum indicum and Carthamus tinctorius. It was first isolated from the plant Stigmasta crispa. The chemical composition of stigmast-7-enol includes a hydroxyl group, a carboxylic acid group, and an ester bond. It has been shown to have hypoglycemic effects in animal models. This compound is stable at acidic pH levels, but is unstable at physiological pH levels. Stigmast-7-enol also binds to the mitochondrial membrane potential and inhibits the synthesis of p-hydroxybenzoic acid in cells.</p>

<p>4-Aminophenethyl alcohol is a monosubstituted, basic compound that is used in the laboratory as a cell culture medium supplement to promote growth of fibroblasts. This compound has been shown to stimulate human intestinal cells and human peripheral blood mononuclear cells. 4-Aminophenethyl alcohol acts as a hydroxyl group donor, which may be due to its ability to form hydrogen ions when reacted with sodium hydroxide solution. The reaction of this compound with diazonium salt produces an intermediate, which can be hydrolyzed by the addition of sodium hydroxide solution. The resultant chloride ion reacts with the aminophenethyldihydroxylamine (APDA) moiety to produce APDCl. This product has been shown to increase the population growth rate of fibroblasts in culture by causing DNA synthesis and protein synthesis. Linear regression analysis revealed that there was no statistically significant difference between the control and experimental groups for either DNA</p>

<p>Pigment Yellow 138 is a polycarboxylic acid with the chemical formula C8H6Cl4O2. Pigment Yellow 138 has a molecular weight of 434.07 and can be used as a yellow pigment in paint, plastics, and textiles. Pigment Yellow 138 has an acidic pH and can be prepared by reacting phthalic anhydride with sodium hydroxide in aqueous solution to produce the sodium salt of pigment yellow 138. Pigment Yellow 138 is also soluble in hydroxide solutions, which makes it an excellent cross-linking agent for polymers. The color of pigments depends on the size of their particles; pigments with larger particle sizes are more opaque than those with smaller particle sizes.</p>

<p>2-[3-(S)-[3-(2-(7-Chloro-2-quinolinyl)ethenyl)phenyl]-3-hydroxypropyl]benzoic acid methyl ester is a synthetic compound that can be used as a reagent in the synthesis of polynucleotides and polypeptides. It can also be used as an inhibitor of ketoreductase, which is an enzyme involved in the synthesis of fatty acids and ketones. 2-[3-(S)-[3-(2-(7-Chloro-2-quinolinyl)ethenyl)phenyl]-3-hydroxypropyl]benzoic acid methyl ester has been shown to inhibit the growth of wild type and mutant strains of E. coli. The molecular weight of this compound is 439.</p>

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<p>Please enquire for more information about (Ala6,D-Trp8,L-alaninol15)-Galanin (1-15) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>7,9-Dimethoxycarbonyl-2-ethoxycarbonyl-1H-pyrrolo-[2,3-f]quinoline-4,5-dione is a chemical compound that is used as an intermediate for research chemicals. It has a CAS number of 80721-47-7 and is classified as a fine chemical with the Chemical Abstracts Service (CAS) classification code of 3272. This compound is a versatile building block that can be used in the synthesis of other compounds. 7,9-Dimethoxycarbonyl-2-ethoxycarbonyl-1H-pyrrolo-[2,3f]quinoline 4,5dione can be used to produce high quality products.</p>

<p>Please enquire for more information about Boc-Thionoleu-1-(6-nitro)benzotriazolide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Linoleic acid is a polyunsaturated fatty acid that is an important component of cell membranes. It has been shown to inhibit oxidative injury and improve mitochondrial functions. Linoleic acid also has a role in energy metabolism, as it is the precursor for biosynthesis of eicosanoids and arachidonic acid. The physiological effects of linoleic acid have been studied using a model system consisting of isolated rat adipose tissue and mitochondria. This model system has been used to investigate the inhibitory properties of linoleic acid on caproic acid-induced lipid peroxidation. Linoleic acid has also been shown to have anion radical scavenging activity when in the presence of iron. This compound can be analyzed using gas chromatography-mass spectrometry (GC-MS) based on its chemical composition, which consists mainly of linear 18-carbon chains with two double bonds at positions 9 and 12.</p>

<p>a-Zearalenol is a steroidal compound that has been shown to be effective in the treatment of autoimmune diseases. It has been found to have a matrix effect on the transcription of genes and can be used in wastewater treatment. Further, it has been shown to inhibit the activity of complex enzymes such as lysyl oxidase and prolyl hydroxylase. The hybridoma cell line was developed for the production of monoclonal antibodies against zearalenone, and an analytical method using LC-MS/MS with fluorescence detection for a-zearalenol was also developed.</p>

<p>3-Bromopyridin-4-ol is a pyrrole that can be used as a cancer therapy. It inhibits the growth of cancer cells by binding to the mkn-45 on the surface of the cell, which prevents it from binding to other proteins and initiating cell proliferation. 3-Bromopyridin-4-ol also inhibits 2-amino-4-hydroxypyridine aminations, which are reactions that produce compounds that promote cancer. This compound class has inhibitory activity against the growth of cancer cells in vitro and in vivo. 3-Bromopyridin-4-ol is an oxindole and amide with a hydroxy group on its side chain. It can be synthesized from 3-bromo-5 hydroxypyridine by reacting it with ammonia or methylamine. The synthesis of this compound can be achieved by reacting 2 chloroacetaldehyde with nitroethane in presence</p>

<p>Please enquire for more information about 4-Chlorophenyl-2-pyridinylmethanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,3,6,7,10,11-Triphenylenehexathiol is a drug that belongs to the class of disulfide bonds. It is used as a fluorescent probe in biochemical studies and has been shown to be an inhibitor of transcription-polymerase chain reaction (PCR) and protein synthesis. 2,3,6,7,10,11-Triphenylenehexathiol inhibits the activity of enzymes that maintain cellular homeostasis by binding with sulfur atoms in their active site. This drug also binds to nerve cells in the trigeminal nerve and may have anti-inflammatory properties.</p>

<p>6,7-Dihydro-5H-quinolin-8-one is a quinoline derivative that can be used to treat cancer. It is an inhibitor of topoisomerase II, which is an enzyme that catalyzes the formation of single stranded breaks in DNA and then reseals them. The inhibition of topoisomerase II leads to the accumulation of single strand breaks, which causes cell death. 6,7-Dihydro-5H-quinolin-8-one has been shown to have inhibitory activity against cancer cells in laboratory tests and also inhibits the growth of breast cancer cells in mice. This compound also has a number of other biological effects including being a ligand for some receptors and amine oxidases as well as having antihistamine properties.</p>

<p>6,6-Dimethyl-1-heptene-4-yn-3-ol is a chlorinating agent that is used in the production of epidermophyton. It also has antifungal properties and can be used as an antimycotic. 6,6-Dimethyl-1-heptene-4-yn-3-ol can be added to hydrochloric acid or magnesium chloride to form an acetylide. This agent has been shown to have selective chlorination activity at temperatures below 10°C. It is also capable of minimizing organometallic chloride catalysts and has been shown to reduce microsporum gypseum and microsporum titinium at pH 2.5.</p>

<p>5-Nitro-2-aminophenol is an aminophenol that has been shown to be a carcinogen in animal studies. It can cause allergic reactions and has been shown to have oxidative DNA damage, which can lead to cancer. 5-Nitro-2-aminophenol is used as a chemical intermediate in the preparation of other chemicals and pharmaceuticals. This chemical has been studied extensively for its analytical properties and is used as a reagent in chromatography. The coordination geometry of 5-nitro-2-aminophenol is octahedral, with nitro groups occupying one axial site each. The toxicity of this compound in animals has been studied extensively, including carcinogenic potential and mutagenicity studies, and it has been shown to inhibit the growth of cultured cells at high concentrations.</p>

<p>4-Chloro-6,7-dimethoxyquinoline (4C6DMQ) is a potent inhibitor of the growth of prostate cancer cells. 4C6DMQ is an analog of chloropropyl chloride, which inhibits the growth of epidermal growth factor receptor (EGFR). The binding site for 4C6DMQ on EGFR is the same as that for chloropropyl chloride. 4C6DMQ inhibits EGFR by preventing the activation of downstream signaling cascades, leading to a decrease in cell proliferation and tumor size. The IC50 values for 4C6DMQ are approximately 10 times higher than those for chloropropyl chloride. This drug has been shown to be more potent than other inhibitors of EGFR such as erlotinib and gefitinib.</p>

<p>1-O-Hexadecyl-sn-glycerol is a glycol ether that is used as a surfactant and emulsifier in cosmetic products. It has been shown to have minimal toxicity, and to not be carcinogenic or teratogenic. 1-O-Hexadecyl-sn-glycerol has been shown to increase the stability of proteins in rat liver microsomes, and it also prevents the hydrolysis of carbohydrates. The surface glycoprotein adsorbed by 1-O-Hexadecyl-sn-glycerol may play an important role in the binding of monoclonal antibodies. This compound affects cellular calcium levels, with high concentrations resulting in increased cytosolic calcium concentrations. Zirconium oxide can replace calcium ions in 1-O-Hexadecyl-sn-glycerol for this purpose, although this substitution reduces enzyme activity.</p>

<p>1,5-Decalindiol is a cyclic alicyclic compound that can be synthesized by the Diels-Alder reaction between 1,5-hexadiene and maleic anhydride. It contains two stereoisomers with different reactivity. One isomer reacts more rapidly than the other one. The termination of 1,5-decalindiol is calcitriol, which can be synthesized by reacting 1,5-decalindiol with naphthalene. The sequence of reactions for the synthesis of 1,5-decalindiol are analyzed in detail. Methoxy groups on the a ring play an important role in the reaction rate of this molecule.<br>1,5-Decalindiol also has an interaction with acetonitrile and a reaction product with dihydroxynaphthalenes.</p>

<p>2,2'-Biquinoline is a coordination compound that has been used as an analytical reagent in the determination of copper and nitrogen. It has been shown to be stable in a variety of matrices, including human serum and copper chloride. 2,2'-Biquinoline is also used as an antimicrobial agent against Gram-positive bacteria, including Staphylococcus aureus. The redox potentials of this compound are dependent on the number of nitrogen atoms present.</p>

<p>Product FB158451, cis, trans-2-Buten-1,4-diol, is a versatile chemical compound with the CAS number 110-64-5. It is used a key building block in various chemical synthesis processes, making it an essential component for researchers and industrial applications. Its versatile nature allows it to be employed in the production of polymers, resins, and specialty chemicals, making it a valuable asset for a wide range of applications.</p>

<p>Please enquire for more information about (aR)-a-[[[2-(4-Aminophenyl)ethyl]amino]methyl]-benzenemethanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>p-Xylene-α,α'-diol is a water-soluble polymer that can be prepared by the reaction of ethylene diamine with sodium citrate. The resulting product has a low molecular weight and high viscosity. The polymer is insoluble in water at pH values higher than 9.5 and soluble in acidic solutions. p-Xylene-α,α'-diol has been shown to exhibit good chemical stability and thermal expansion properties when exposed to temperatures of up to 300 °C. The polymer is soluble in organic solvents such as benzene, chloroform, acetone, ether, and carbon tetrachloride. The polymer has been shown to have transport properties for some drugs, such as ketoprofen and ibuprofen, with good kinetic data at various concentrations.</p>

<p>2,2,6,6-Tetramethyl-4-piperidinol 1-oxyl (TEMPO) is a reactive oxygen species that belongs to the group of nitroxide radicals. It can be used as a radical scavenger and has been shown to inhibit the production of pro-apoptotic proteins in human macrophages. TEMPO has also been shown to bind to DNA and prevent the binding of HIV viral protein gp120. TEMPO can be used as an inhibitor for glycol ethers in laboratory experiments. The most common use is as a water vapor scavenger during polymerization reactions in organic chemistry.</p>

<p>4-Fluoro-3-nitrobenzyl alcohol (4FNA) is a potent, orally bioavailable, and selective inhibitor of the tyrosine kinase AXL. 4FNA binds to the ATP binding site on AXL and blocks phosphorylation of its tyrosine kinase domain. This binding leads to a conformational change in the AXL protein that prevents it from interacting with downstream signaling molecules, inhibiting T cell activation.</p>

<p>D-Ala2,N-Me-Phe4,methionin(O)-ol5)-Enkephalin trifluoroacetate salt H-Tyr-D-Ala-Gly-N-Me-Phe-methionin(O)-ol trifluoroacetate salt is an analog of the endocannabinoid neurotransmitter, anandamide. It has been shown to be effective in the treatment of autoimmune diseases such as multiple sclerosis and inflammatory bowel disease. D-(3R)-3-[(1S,2R,3R,5R) -3-[2-(2,6 dichlorophenyl)ethenyl] -1H -indole]-1 -butanamine trifluoroacetate salt has been shown to inhibit the replication of a number of viruses including human immunodeficiency virus type 1 (HIV). This drug also inhibits the growth of organisms that are resistant</p>

<p>1,3-Bis(dimethylamino)-2-propanol is a polymeric compound that is soluble in water and organic solvents. It has been shown to have a viscosity of less than 2.0 centipoise (cP) at 20°C and pH 8.5. This compound also has a high solubility in buffers, carboxylates, and chloride ions. 1,3-Bis(dimethylamino)-2-propanol has been used as an additive for silicone surfactants and in the production of tetranuclear gold nanoparticles for use in chemiluminescence applications.</p>

<p>Naphthalene-1,8-diol is a compound that belongs to the class of polycyclic aromatic hydrocarbons. It has been shown to inhibit polymerase chain reactions (PCR) in a nuclear DNA template. Naphthalene-1,8-diol also inhibits the production of melanin and reduces the number of skin lesions in the wild-type strain of Galleria mellonella. Naphthalene-1,8-diol is an antioxidant compound that has been shown to protect against radiation and dermatitis. This molecule contains a hydroxyl group that can form hydrogen bonds with other molecules. This property may account for its anti-inflammatory effects.</p>

<p>6-Keto cholestanol is a chemical compound that is structurally similar to cholesterol. It has a phase transition temperature of -65°C, and the hydroxyl group on the side chain can be replaced with other functional groups to alter its properties. 6-Keto cholestanol has been shown to induce autophagy in cells by binding to mitochondria and increasing mitochondrial membrane potential. This compound also increases the level of fatty acid oxidation and decreases levels of glycerolipids in the cell, which may be due to its ability to bind fatty acids. 6-Keto cholestanol binds to the styryl dye, benzalkonium chloride, and inhibits its fluorescence emission. This compound also binds to adenine nucleotide, which may lead to decreased ATP production in cells.</p>

<p>2,3,6-Trimethylphenol is an industrial chemical that is produced by the acylation of 2,6-dimethylaniline with formaldehyde. The optimal reaction conditions for this process are at a temperature of 100°C and a pressure of 10 bar. This chemical has been shown to be an effective catalyst for the chlorination of hydrocarbons. Trimethylphenol is also used as a reagent in the preparation of other chemicals and is found in many products due to its low energy requirements. The logistic regression model has been used to assess the relationship between population growth and industrial preparation. It has been shown that there is a positive correlation between these two variables. 2,3,6-Trimethylphenol can also be found in polluted environments where it reacts with chloride ions to produce hydrogen chloride gas or methyl chloride gas. Redox potential values have been measured for this compound and it was found that the reduction potential is -0.07</p>

<p>Phenol,2,2'-sulfonylbis[3,4,6-trichloro] is a sulfate-containing compound that has been shown to stimulate the immune system and activate mitogen-activated protein kinases (MAPKs) in mosquitoes. The inclusion of this substance in vaccines may lead to increased immunity against various diseases. Phenol,2,2'-sulfonylbis[3,4,6-trichloro] has also been shown to reduce cancer cell proliferation by modulating antigen-presenting cells and inducing apoptosis in ovarian cancer cells. This substance can be used as a cost-effective alternative to dextran sulfate for generating pluripotent stem cells from adult cells and can also be used as a scalable process for generating pluripotent cells from human amniotic fluid.</p>

<p>(S)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthalene-2,2'-diol is a synthetic compound that has been prepared by a Diels-Alder reaction. It is used as an asymmetric synthesis catalyst for the production of optically active compounds. The ligands are catalysts for the reaction and can be easily replaced with different ligands to produce different products. This compound has been researched for its potential use in the production of pharmaceuticals and other chemicals.</p>