Alcohols

<p>The (+)-isomer of 6-methyl-1-octanol is a chiral, primary alcohol that has been synthesized and characterized. It is an analytical reagent for the determination of hydroxy groups on a molecule. The (+)-isomer is also used as a synthetic intermediate in the synthesis of other bioactive molecules.</p>

<p>4,5-Bis(2-cyanoethylthio)-1,3-dithiole-2-thione is a fluorescent compound that exists in two orientations, cis and trans. It has been used as a linker for the construction of new compounds with interesting properties. 4,5-Bis(2-cyanoethylthio)-1,3-dithiole-2-thione has been shown to be an effective ligand for palladium cross coupling reactions. This compound can also be used in supramolecular chemistry due to its ability to fluoresce brightly.</p>

<p>2-Bromo-5-(trifluoromethyl)benzyl alcohol is a fine chemical that is used as an intermediate in the synthesis of other chemicals. It can be used to synthesize novel organic compounds, such as pharmaceuticals and pesticides. This chemical has been shown to react with various other organic compounds, including amines, thiols, and carboxylic acids. 2-Bromo-5-(trifluoromethyl)benzyl alcohol is also known for its ability to form complexes with metals.</p>

<p>4-Methoxy propranolol is an intermediate in the synthesis of propranolol, a beta blocker.</p>

<p>L-Tyrosinol hydrochloride is a chiral molecule that is the hydrogenated form of L-tyrosine. It is an intermediate in the synthesis of L-dopa, which is used to treat Parkinson's disease. The enzymatic reaction that converts L-tyrosinol hydrochloride to L-dopa requires adenosine 5'-phosphosulfate as cofactor and histidine as a catalyst. The conversion of L-tyrosinol hydrochloride to L-dopa occurs with high yield and has been shown to be stereoselective. This synthetic pathway has been shown to have an activation energy of 53 kcal/mol and a reaction time of 30 minutes at room temperature.</p>

<p>The fluoroquinolone 5-Fluoro-2-methylphenol (5FM) is an inhibitor of angiotensin, an enzyme that is involved in the regulation of blood pressure and fluid balance. The structure of this compound was optimized to make it more potent and selective for angiotensin, while minimizing its adverse effects. This optimization was achieved using high throughput screening and x-ray crystallography. The fluorine atom in 5FM binds to aspartyl protease, which prevents the protease from breaking down proteins into smaller amino acid chains. This binding also inhibits the activity of other enzymes that are involved in protein synthesis, such as aspartyl proteases and salicylic acid esterases. 5FM has been shown to inhibit the growth of bacteria such as Staphylococcus aureus at concentrations that are not toxic to mammalian cells.</p>

<p>3-Chloro-4-(trifluoromethyl)benzyl alcohol is a versatile building block for synthesis of various chemical compounds. It is used as a reagent, reaction component, or building block in organic synthesis. It is also useful as a speciality chemical or research chemical. CAS No. 65735-71-9</p>

<p>Bis(8-quinolinolato)zinc (II) is a molecule that contains carboxylate groups. It has been shown to be processable and can be used in fabrication processes. Bis(8-quinolinolato)zinc (II) also exhibits optical properties. The metal ion in the molecule is able to form complexes with other metals, which may affect transport properties, ionization mass and morphology of the compound. It can also be used for magnetic resonance spectroscopy studies, as well as plasma mass spectrometry.</p>

<p>8-Fluoroquinoline is a quinoline derivative that has been shown to have in vitro anticancer activity against colon adenocarcinoma cells. It is a chiral molecule that can exist as two stereoisomers, (R)-8-fluoroquinoline and (S)-8-fluoroquinoline. These isomers may have different interactions with the tumorigenic cells, but both of them have anticancer activity. 8-Fluoroquinoline also interacts with cytochrome P450 enzymes, enhancing their ability to metabolize carcinogens.</p>

<p>4-Butoxy-1-butanol is a solvent that has been shown to be safe for use in humans. It is used to modify the chemical structure of d-glycero-d-galacto-heptose and can be used as a solvent. 4-Butoxy-1-butanol was found to be safe for primary cells and was able to normalize their metabolism and growth rate. This compound has also been shown to have diagnostic properties based on its ability to inhibit the production of camaldulensis leaves, which are known to produce naphthalene. The mechanism by which this compound inhibits camaldulensis leaf production is unknown, but it may involve an acceptor molecule or biochemical reactions.</p>

<p>3-(Aminomethyl)adamantan-1-ol HCl is a chemical substance that can be used as a reaction component, reagent, and useful scaffold in the synthesis of pharmaceuticals. It is also a speciality chemical with versatile building block and useful intermediate properties. 3-(Aminomethyl)adamantan-1-ol HCl has been shown to be an effective building block for complex compounds, such as those used in the synthesis of anti-inflammatory drugs.</p>

<p>Biotinyl-6-aminoquinoline is a synthetic chemical that has been shown to inhibit the growth of cancer cells in laboratory mice. It was synthesized to be a substrate for the enzyme quinolinate synthase, which is involved in the synthesis of nicotinic acid. Biotinyl-6-aminoquinoline is an analytical method that has been used in urinary samples from patients with bladder cancer as well as healthy individuals. The sequences of each individual were determined and analyzed using an algorithm that performs logistic regression, which can predict whether or not the patient has bladder cancer.</p>

<p>2,5,6-Triaminopyrimidin-4-ol sulphate is a fine chemical that is used as a reagent in the synthesis of other compounds. It can be used as a building block for research chemicals and speciality chemicals such as pesticides. This compound is also useful in the manufacture of pharmaceuticals and agrochemicals. 2,5,6-Triaminopyrimidin-4-ol sulphate has been shown to react with aniline derivatives to produce a variety of products including pyrrolidine and piperidine derivatives. This versatile compound can also be used as a scaffold in the synthesis of complex molecules.</p>

<p>Fmoc-L-threoninol is a conjugate of L-threoninol with a protecting group, Fmoc. It is synthesized by the solid-phase method on an activated resin and then cleaved from the resin to give the desired product. The linker used in this synthesis is succinic acid diacetate. This compound has been shown to have anti-inflammatory effects in human serum, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>2,4-Dihydroxyquinoline is a malonic acid derivative that is used as an antimicrobial agent. It is a diazonium salt that can be synthesized from 2-chloro-4-nitrobenzene and malonic acid. The reaction mechanism for this compound involves the formation of a diazo intermediate, which reacts with the amine to form a quinoline. This compound has been shown to have antibiotic properties and is able to inhibit the growth of bacteria such as Salmonella typhi, Mycobacterium tuberculosis, Escherichia coli, and Staphylococcus aureus. 2,4-Dihydroxyquinoline has also been shown to have anticancer activity in vitro on human liver cells (HepG2) and human hepg2 cells.</p>

<p>2,5-Dichlorobenzyl alcohol is a lacteous compound that is used as a herbicide. It inhibits the growth of plants by inhibiting the activity of enzymes that are involved in the biosynthesis of amino acids and fatty acids. 2,5-Dichlorobenzyl alcohol is also used to produce polychlorinated compounds and has significant effects on weed science. 2,5-Dichlorobenzyl alcohol may be used as a linker molecule in chemical reactions. This compound can be catalysed by dioxygenation to produce chlorobenzal or benzaldehyde.</p>

<p>2,4,6-Tribromo-3-methoxyphenol is a high quality reagent that is used as an intermediate in the production of many fine chemicals. It is also a useful building block for the synthesis of speciality chemicals and research chemicals. This chemical can be used as a versatile building block for reactions with other compounds. 2,4,6-Tribromo-3-methoxyphenol has CAS number 24967-79-1 and can be found at Chemical &amp; Laboratory Equipment.</p>

<p>Allopurinol is a drug that is used in the treatment of gout and other disorders caused by excessive production of uric acid. It functions as an inhibitor of xanthine oxidase, which is the enzyme responsible for converting hypoxanthine to xanthine, and xanthine to uric acid. Allopurinol blocks the conversion of these compounds, thereby reducing the formation of uric acid. Allopurinol has been shown to be effective for treating inflammatory bowel disease such as ulcerative colitis and Crohn's disease. This drug also inhibits nuclear DNA synthesis, antioxidant vitamins (e.g., vitamin E), and brain functions. Allopurinol has been shown to be effective in protecting neurons against oxidative injury that may lead to neurodegenerative diseases such as Parkinson's disease.</p>

<p>4-Methylresorcinol is a phenolic compound that has been shown to have a broad spectrum of antimicrobial activity. It is an inhibitor of 3-hydroxybenzoic acid, a key metabolic intermediate in the biosynthesis of aromatic amino acids and lignin. 4-Methylresorcinol inhibits the enzyme tyrosine ammonia lyase, which converts tyrosine to 3-hydroxybenzoic acid. The synthetic nature of 4-methylresorcinol makes it an attractive candidate for use as an antifungal agent, since it does not produce any byproducts in the human body. 4-Methylresorcinol also has antifungal activity against other organisms such as Candida albicans, Aspergillus niger, and Trichoderma viride.</p>

<p>N-Methyl-5-tetrazolethiol is a vitamin B6 (pyridoxine) analog that inhibits bacterial growth by competitively inhibiting enzymes involved in the synthesis of folate. It has been shown to be toxic for animals and humans at high doses, but the toxicity of this compound has not been studied extensively. N-Methyl-5-tetrazolethiol has been shown to inhibit the activity of enzymes such as methionine synthase, cytochrome C reductase, and nitroreductase in vitro. This drug is used as a treatment for infectious diseases such as malaria and toxoplasmosis. The mechanism of action of N-methyl tetrazolethiol is not known, but it is believed to be related to its ability to inhibit enzyme activity.</p>

<p>1,12-Dodecanediol is a polymeric matrix that has been shown to be effective in inhibiting the growth of microorganisms. The antimicrobial activity of 1,12-dodecanediol is primarily due to its ability to form hydrogen bonds. This polymer can be used as a film-forming polymer for hydrophobic and lipophilic compounds. It also has chemical properties that include an intramolecular hydrogen bond, which provides stabilization and protection from degradation by enzymes. This chemical compound also has the ability to bind with fatty acids and phosphodiesterase activity (which may account for its anti-inflammatory activities).</p>

<p>Glycerol tripalmitate is a triglyceride that is composed of three molecules of glycerol and one molecule of palmitic acid. It is used in the manufacture of sephadex g-100, a chromatographic material that separates proteins based on their size. Glycerol tripalmitate has been shown to have high chemical stability, which is important for its use as a pharmaceutical excipient. This substance also has a physiological function in the human body, including the production of lipids, such as fatty acids and triglycerides. Glycerol tripalmitate can be used to study phase transition temperature by using surface methodology. Carbonyl oxygens are present on the surface of this substance, which may have neurotrophic effects.</p>

<p>Cholesterol linoleate is a model system that is used to study the role of cholesterol in atherosclerosis. It consists of a cholesterol-based polymer and linoleic acid, which are chemically similar to the natural lipids found in human cells. In vitro studies have shown that this model system has an inhibitory effect on ATP binding cassette transporter A1 (ABCA1) and ABCG1. These proteins transport cholesterol from cellular membranes to other parts of the cell, where they are degraded by enzymes called lysosomes. Cholesterol linoleate also inhibits basic protein, an enzyme that breaks down cholesteryl, leading to reduced levels of cholesteryl esters in the atheromatous lesions. This model system has been shown to reduce disease activity in animals with atherosclerotic lesions.</p>

<p>2-(Aminooxy)ethanol is an organic compound that has the chemical formula CH3NOCH2CH2OH. It belongs to the group of cyclic ketones and is a colorless liquid with a boiling point of 78°C. This substance can be produced by dehydrogenation of ethylene oxide or by reaction of formamide with sodium hydroxide and hydrochloric acid. The product can also be prepared from 2-hydroxyethanol, which reacts with ethylene in presence of HCl. The reaction time for this process is around 1 hour at room temperature. The chemical formula for 2-(Aminooxy)ethanol is C4H11NO2O.</p>

<p>2-Chlorophenol is an organic compound that is used as a disinfectant and antiseptic. It has been shown to adsorb onto activated carbon and other organic matter in wastewater treatment facilities, where it is degraded by the intramolecular hydrogenation of 2-chlorophenol to 2-hydroxybenzoic acid. <br>This reaction can be catalyzed by sodium citrate, which acts as a proton donor. The kinetics of this transformation can be described using the pseudo-first order rate law. 2-Chlorophenol also regulates transcriptional activity through binding to DNA at specific sites. This binding can be detected using solid phase microextraction techniques on copper chloride or surfactant sodium dodecyl. The reaction mechanism for the conversion of 2-chlorophenol to 2-hydroxybenzoic acid involves intermolecular hydrogen bonding with a proton donor that leads to the oxidation of the substrate. The redox potential for this process</p>

<p>a-[2-(Methylamino)ethyl]benzyl alcohol is a zwitterion that forms an imine when reacted with piperazine. It has been shown to have antibacterial activity in subcritical water extraction and HPLC analysis. This compound also has a profile of impurities, including β-unsaturated aldehydes and pseudoephedrine.</p>

<p>(S)-(+)-1-Indanol is a substrate for the human liver alcohol dehydrogenase and can be used to study the enzyme. The molecule has two phenyl groups that are capable of forming hydrogen bonds with other molecules. The hydrogen bond is a relatively weak, noncovalent interaction between two polar molecules. It can be formed by the donation of a lone pair of electrons from one side of an oxygen atom in one molecule to a lone pair of electrons on another oxygen atom in another molecule. This type of bond is responsible for many important biological processes, including DNA replication and protein folding. The (S)-(+)-1-Indanol can also undergo carbonyl reduction, which is the conversion of an organic compound containing a carbonyl group into a corresponding hydrocarbon derivative containing hydroxyl groups. The (S)-(+)-1-Indanol contains both hydroxyl and carbonyl functionalities that make it suitable for this process. (S)-</p>

<p>4-Cyano-2-fluorobenzyl alcohol is a reagent that is used to produce chlorine and hydrochloric acid. It is also used industrially in the production of potassium chloride, a compound that is used in fertilizers, animal feed supplements, and water treatment. 4-Cyano-2-fluorobenzyl alcohol reacts with chloride ions to form hypochlorous acid (HOCl), which then reacts with water to form hydrogen chloride gas. The reaction with fluoride ions leads to the formation of hydrofluoric acid (HF).</p>

<p>3-Hydoxy-2-nitrobenzyl alcohol is a high quality reagent that can be used as a complex building block, useful scaffold, and versatile building block for the synthesis of speciality chemicals. It is also used as a reaction component in the preparation of 3-hydroxy-2-nitrobenzyl chloride, which is an intermediate for the production of various pharmaceuticals. This chemical has a CAS number of 34112-74-8 and is classified as a research chemical.</p>

<p>Epifriedelanol is a sesquiterpene lactone that belongs to the group of natural compounds. This molecule is produced by the plant B. dracunculifolia and has shown anti-inflammatory properties in vitro. Epifriedelanol has been shown to inhibit mitochondrial membrane potential and activity index, which are important for cancer cell growth and survival. Epifriedelanol also has anticancer effects on colorectal adenocarcinoma cells as well as skin cancer cells. It may also be used for urinary tract infections due to its inhibition of bacterial growth.</p>

<p>2-Aminophenol is a water soluble redox catalyst that is used in wastewater treatment. It has been shown to be a potent antimicrobial agent against bacteria, fungi, and viruses. 2-Aminophenol is active against the Gram-positive bacteria Staphylococcus aureus and Enterococcus faecalis. The mechanism of the reaction of 2-aminophenol with picolinic acid is believed to be due to intramolecular hydrogen bonding between nitrogen atoms (N) and amines (NH). The binding site for this reaction is not well understood, but it may involve an electrochemical mechanism such as constant pressure or electrochemical impedance spectroscopy. 2-Aminophenol also participates in electron transfer reactions involving NAD+/NADH or cytochrome c/cytochrome c oxidase.</p>

<p>Tilbroquinol is a coordination complex that contains a fatty acid. It is used in the treatment of bowel disease, infectious diseases, cancer and autoimmune diseases. Tilbroquinol has been shown to have broad-spectrum antimicrobial activity against bacteria such as Escherichia coli, Bacillus subtilis, Pseudomonas aeruginosa, Staphylococcus aureus and Salmonella typhimurium. It inhibits bacterial growth by inhibiting fatty acid synthesis through the inhibition of enzymes such as enoyl-acyl carrier protein reductase (ENR) and 3-hydroxyacyl-coenzyme A dehydrogenase (HAD). This drug also has anti-inflammatory properties because it is an antagonist of prostaglandin synthesis.</p>

<p>2-(4-Methylphenyl)ethanol is a chemical compound that is used as a solvent. It is also used in the synthesis of 2-hydroxyphenylacetic acid, an intermediate in the synthesis of 4-methylbenzoic acid and 4-methylphenol. The toxicologic properties of 2-(4-methylphenyl)ethanol are not well known. However, it has been shown to inhibit tyrosinase activity and stimulate melanogenesis in rats. The chemical structure of 2-(4-methylphenyl)ethanol consists of two functional groups: a phenyl group with a methyl substitution and an alcohol group. The molecular formula for this compound is C9H12O2, which indicates that it contains one carbon atom, nine hydrogen atoms, one oxygen atom, and two hydrogens. This compound has been studied by nuclear magnetic resonance spectroscopy (NMR).</p>

<p>Sumaresinolic acid is a naturally occurring triterpenoid compound, which is typically isolated from certain plant species, such as those belonging to the Sumac (Rhus) family. This compound is characterized by its complex molecular structure that endows it with various biochemical activities. Sumaresinolic acid acts primarily through anti-inflammatory and antioxidant pathways, influencing cellular signaling and modulating enzymatic activity related to inflammation and oxidative stress.</p>

<p>3-((2-Mercapto-1-methylpropyl)thio)-2-butanol is a high quality synthetic intermediate that can be used as a reagent, a building block for the synthesis of complex compounds, or as an intermediate for the production of speciality chemicals. 3-((2-Mercapto-1-methylpropyl)thio)-2-butanol is soluble in organic solvents and has a high boiling point. It is also useful as a reaction component in the synthesis of fine chemicals and research chemicals. 3-(2 Mercaptoethylthio) 2 butanol has CAS No. 54957-02-7, and may be found under various synonyms such as 1-(3 mercaptoethylthio) butane, 1-(3 mercaptoethylthiobutane), or 1-[3-(mercaptomethyl)propyl] thiobutane.</p>

<p>4-Bromo-2,6-difluorobenzyl alcohol (4BDFA) is a molecule that has been shown to be able to produce magnetic resonance images. It can be used in tumor diagnosis as well as in the imaging of tumors. 4BDFA is synthesized by coupling 2,6-difluoroaniline with bromoacetaldehyde diethyl acetal. The syntheses are carried out under phase transfer catalysis conditions and the reaction is monitored by thin layer chromatography.<br>The synthesis of 4BDFA starts with the preparation of 2,6-difluoroaniline via a Grignard reaction between aniline and magnesium metal. The Grignard reagent is then added to bromoacetaldehyde diethyl acetal in dichloromethane followed by addition of triethylamine dropwise to maintain pH neutrality. The product is then extracted from the organic solution using ethyl ether</p>

<p>2-Hydroxy-5-methoxybenzyl alcohol (2HMB) is a methide that is used as an inductor in the synthesis of Taxol. 2HMB has been shown to induce apoptosis in MCF-7 cells and to promote the hydration of oxacycles. It can also be used in cancer research as a kinetic probe for the hydration of oxacycles. 2HMB activates MCF-7 cells and induces apoptosis, which may be due to its nucleophilic properties.</p>

<p>1-Boc-amino-3,6,9-trioxaundecanyl-11-ol is a PEG polymer categorised as monofunctional (OH-PEG-X). Used as a linker, 1-boc-amino-3,6,9-trioxaundecanyl-11-ol is used to attached PEG to proteins, peptides, oligonucleotides, nanoparticles and small molecules via pegylation, a bioconjugation technique.</p>

<p>(6S)-5,6,7,8-Tetrahydro-6-[propyl[2-(2-thienyl)ethyl]amino]-1-naphthalenol is a potent and selective dopamine receptor agonist. It acts by binding to the dopamine receptors in the brain. This binding stimulates the release of dopamine and prevents it from being reabsorbed into the neurons, which in turn increases levels of extracellular dopamine in the synapse. (6S)-5,6,7,8-Tetrahydro-6-[propyl[2-(2-thienyl)ethyl]amino]-1-naphthalenol has been shown to have antidepressant effects in animal models of depression. It also has a long half life and can be administered as a transdermal patch for prolonged relief from depression symptoms.</p>

<p>4-Keto retinol is an analog of vitamin A, which is used in the treatment of various diseases. It has been shown to reduce the levels of PGE2 and increase the redox potential in cells. 4-Keto retinol has also been shown to increase locomotor activity and improve energy metabolism. The structural analysis of 4-keto retinol has revealed that it binds to DNA polymerase, inhibiting transcriptional activity. The pharmacokinetic properties of this drug have been studied in rats and mice, but not yet humans. This compound will most likely be administered orally or intravenously with a dosage range from 0.01 mg/kg to 10 mg/kg per day.</p>

<p>3-Nitrobenzyl alcohol is a low potency drug that is used for the treatment of cancer. It is a derivative of trifluoroacetic acid, which has been shown to have anti-tumor effects in animals. 3-Nitrobenzyl alcohol binds to the matrix on the surface of cells by hydrogen bonding and forms an intramolecular hydrogen bond with the nitrogen atom. This process leads to increased fluorescence intensity, which can be detected using matrix-assisted laser desorption ionization mass spectrometry (MALDI MS). The fatty acid group found in 3-nitrobenzyl alcohol increases its solubility in water and facilitates penetration into lipid bilayers. This compound exhibits cytotoxicity against monoclonal antibody-positive B cell lymphoma cells and may also have anti-inflammatory properties due to its inhibition of picolinic acid synthesis.</p>

<p>4-Bromo-2-(5-isoxazolyl)phenol is a fine chemical that is used as a building block in the synthesis of other chemicals. It is also useful as a reagent, speciality chemical, and intermediate to produce complex compounds. This compound has versatile uses as it can be used in reactions involving nucleophilic substitution, electrophilic substitution, and elimination. 4-Bromo-2-(5-isoxazolyl)phenol is also a useful scaffold for the synthesis of new molecules with biological activity.</p>

<p>Ferruginol is a natural compound that can be found in the bark of the plant Phellodendron amurense. It has significant cytotoxicity against k562 cells and dextran sulfate, which may be due to its ability to inhibit mitochondrial membrane potential and cause apoptosis. Ferruginol also has anti-inflammatory properties and can inhibit the proliferation of colorectal adenocarcinoma cells by inducing pro-apoptotic protein expression. This compound binds to basic structures such as proteins, nucleic acids, lipids, and carbohydrates. Ferruginol is also known to be a potent inhibitor of disease activity for coronary heart diseases and other diseases such as Crohn's disease.</p>

<p>2-Hydroxy-3-methoxybenzyl alcohol is a phenolic compound that belongs to the class of mandelonitrile. It is an envenomation agent that has been shown to have a molecular weight of 146, and is synthesized by reacting 2-hydroxy-4-methoxybenzaldehyde with formic acid. This drug also has been shown to have high binding affinity for the androgen receptor, which allows it to be used as an antihormone therapy. 2-Hydroxyl-3-methoxybenzyl alcohol binds to hormone receptors in cells and prevents them from binding with the hormones needed for transcription. The hydroxyl group on this molecule allows it to act as an acceptor for other molecules in reactions involving formylation and hydroxylation reactions.</p>

<p>2-[2-(2-t-Boc-aminoethoxy)ethoxy]ethanol is a versatile chemical building block that can be used to synthesize a variety of compounds. It has been shown to be useful as a reaction component in the synthesis of pharmaceuticals and agrochemicals. The compound is also used as an intermediate for the preparation of other compounds. 2-[2-(2-t-Boc-aminoethoxy)ethoxy]ethanol is soluble in organic solvents, such as chloroform, ethanol, or acetone. It has a CAS number of 139115-92-7 and is relatively easy to purify by recrystallization from methanol.</p>

<p>Please enquire for more information about 5-Methyl-4,5-dihydro-1,2,4-triazino[5,6-b]indole-3-thione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromo-2-nitroethanol is a chemical reagent that has the hydroxyl group. It is a site specific biocide, which is used to kill bacteria. 2-Bromo-2-nitroethanol has bactericidal activity against gram negative and gram positive bacteria. It can be used as a preservative in food and pharmaceutical products. This chemical is also effective for killing bacteria in water and wastewater treatment plants. 2-Bromo-2-nitroethanol is applied to surfaces by spraying or dipping, or it can be added to water at concentrations of 0.5 ppm or higher. 2-Bromo-2-nitroethanol can also be used to treat textiles, paper, leather, and rubber products by dipping or spraying these materials with the chemical solution containing 2% concentration of 2-bromo-2 nitroethanol in an aqueous solution of sodium hydroxide (0.5</p>

<p>Please enquire for more information about 4-(1H-Imidazol-2-yl)phenol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Benzyl-4-piperidyl)methanol is a linker molecule that can be used to connect a variety of heterocycles with the ability to modulate their biological activities. This molecule has been shown to be a potent inhibitor of 5-HT receptor activity and has been used in molecular modeling studies. 1-Benzyl-4-piperidyl)methanol also has the potential for use as an environmental pollutant, which may be due to its reactivity with naphthalene compounds. The modifications that are possible on this molecule include introducing substituents on the benzene ring or amide groups, which can provide potent inhibitory activity.</p>

<p>Cetearyl alcohol is a type of fatty alcohol, which is derived from natural sources like coconut oil or palm kernel oil. It is a combination of cetyl and stearyl alcohols. This compound functions primarily through its emulsifying properties, allowing oil and water to mix effectively and form stable emulsions. It does this by reducing surface tension, thus facilitating the blending of disparate ingredients.</p>

<p>6-Benzyloxy-1-hexanol is a linker compound that has been used in the synthesis of galnac and trifluoromethylated compounds. This substance can be synthesized by a solid-phase synthetic method using a fluorine-containing reagent as an additive. The enzyme catalyzed reaction can be carried out using control agents to regulate the reaction rate. 6-Benzyloxy-1-hexanol has been used as a chiral building block for the synthesis of vitamin D3 and other polycyclic aromatic hydrocarbons.</p>

<p>1,2-Distearoyl-sn-glycerol (DAG) is a lipid molecule that is found in the cell membrane and can be used as an antimicrobial agent. DAG has been shown to inhibit the growth of bacteria by binding to their fatty acid chains. It also has been shown to bind to the receptor P2Y6, which is involved in mediating inflammatory responses, and inhibits its activity. This drug may be useful for treating diseases such as atherosclerosis and diabetes mellitus type 2.</p>

<p>Propranolol hydrochloride is a prodrug that is converted to the active form, (S)-propranolol, by deesterification in vivo. Propranolol hydrochloride has been used for more than 50 years as a beta-blocker for the treatment of hypertension and angina pectoris. It is also used to treat other cardiovascular diseases such as arrhythmias and myocardial infarction. Propranolol hydrochloride inhibits the activity of human estrogen receptor (ER) and blocks the synthesis of proteins that are necessary for tumor growth. This drug has been shown to be effective against metastable polymorphs in urine samples and can be used as an analytical method to differentiate enantiomers.</p>

<p>Please enquire for more information about 17α-Estradiol 17-valerate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Phloroglucinol is a group P2 compound that has been shown to have significant cytotoxicity. It binds to the response element of phloroglucinol-induced chronic cough in vitro and in vivo, and inhibits the synthesis of DNA. Phloroglucinol is a dinucleotide phosphate that reacts with hydrogen bonding interactions. The chemical biology of phloroglucinol includes its ability to cause synchronous fluorescence at high concentrations. Phloroglucinol also possesses sodium citrate-dependent intermolecular hydrogen bonding properties.</p>

<p>2-Methoxy-5-nitrophenol (2MNOP) is a compound that has been shown to inhibit the growth of bacteria in nutrient solutions by reducing the activity of glutamate pyruvate transaminase and pyridoxine hydrochloride. 2MNOP is a potent inhibitor of bacterial enzyme activities, such as neutral ph, hydrochloric acid, nitro, and toxicity studies. It is not active against eukaryotic cells or plants. The uptake of 2MNOP is enhanced by the presence of diamine tetraacetic acid and ethylene diamine. 2MNOP has also been shown to be effective against multi-walled carbon nanotubes.</p>

<p>2,4,5-Trimethylbenzyl alcohol (2,4,5-TMB) is an organic solvent that has been used as a photocatalyst. It has been shown to be an efficient and selective radical oxidation catalyst for the conversion of toluene to benzaldehyde. 2,4,5-TMB can also be used in UV irradiation as a sensitizer for the production of oxiranes from ethylene oxide and oxygen. 2,4,5-TMB is soluble in many common solvents such as ethers and chlorinated hydrocarbons. The reaction product is not known with certainty because it has not been isolated. However, it is thought that it may form radical anion radicals when irradiated with UV light or other forms of radiation.</p>

<p>2-Bromo-4-methoxybenzyl alcohol is a fine chemical that can be used as a versatile building block, intermediate, or reaction component in research. It is also a useful building block for the synthesis of complex compounds. 2-Bromo-4-methoxybenzyl alcohol has been shown to be a reagent with high quality and can be used as a speciality chemical. This compound has been shown to react with ammonia to form an amide bond, which has led to the development of several new drugs.</p>

<p>3-Bromo-2-methoxybenzyl alcohol is a reaction component that is used in the synthesis of a number of chemical compounds. It has been shown to be a useful scaffold, with versatile building blocks and intermediates. 3-Bromo-2-methoxybenzyl alcohol is an intermediate for the synthesis of complex compounds such as antihypertensive drugs, anti-inflammatory agents, and immunosuppressant drugs. This compound also has a variety of uses in research including as a reagent for the determination of enzyme activity and as an analytical reference standard.</p>

<p>2-(4-Nitrophenoxy)ethanol (NPEO) is a water soluble, synthetic compound that has been shown to have anti-tumor properties. NPEO was found to be toxic to tumor cells in vitro and inhibits the growth of tumor cells in vivo. NPEO also inhibits the synthesis of DNA and RNA, which are important for cell division. This inhibitory effect may lead to the death of cancer cells by interfering with their ability to grow and divide.</p>

<p>5-Hexen-2-ol is a constituent of various natural products such as the racemosum and macrocyclic lactones. It has been found to have a broad spectrum of biological activities, including antibacterial, antifungal, antiparasitic and antimalarial activity. 5-Hexen-2-ol has also been used in the synthesis of various macrocyclic lactones and macrolactones. This compound has been found to inhibit penicillium growth by competitive inhibition of ergosterol biosynthesis.</p>

<p>DL-Phenylethanolamine is a hydroxy amine that is used in the synthesis of other chemicals. It is obtained by reacting phenylacetic acid with hydroxylamine. DL-Phenylethanolamine is an intermediate in the synthesis of the anti-inflammatory drug Indomethacin. This molecule contains a asymmetric carbon atom, which can be distinguished using infrared spectroscopy. The uptake of DL-phenylethanolamine into cells can be measured by detecting the release of amines from lysosomes and mitochondria. In addition, this molecule has conformational properties that can be detected by NMR spectroscopy, making it useful for detection sensitivity and identification purposes.</p>

<p>3-Phenethylphenol is a hydrophobic, sterically-interacting compound that binds to molybdenum. It has been shown to inhibit the growth of fungi such as Poria and Coriolus. 3-Phenethylphenol also has functionalities such as peroxide, acetonitrile, and nature. This compound is not soluble in water and must be dissolved in solvents such as acetonitrile or polyvinyl acetate before use. 3-Phenethylphenol has been shown to have chromatographic properties, allowing it to be used as an adsorbent for the separation of organic compounds.</p>

<p>(1-Methylpiperidin-2-yl)methanol is a gaseous organic acid that belongs to the piperazine class of compounds. It is used as an intermediate in the synthesis of various pharmaceuticals, including antipsychotics and antidepressants. (1-Methylpiperidin-2-yl)methanol has been shown to be an agonist of ganglion cells and can be used for the treatment of glaucoma. This compound also has shown to have anti-inflammatory properties, which may be due to its ability to inhibit nitric oxide production. Furthermore, (1-methylpiperidin-2-yl)methanol has been shown to inhibit 13c nuclear magnetic resonance spectroscopy with epoxides and hydroxyl groups. The reaction product is a crystalline solid with a molecular formula of C6H14O3N2, which corresponds to the molecular formula of 2-(dimethylam</p>

<p>2-Oxo-1,2,3,4-tetrahydroquinoline-4-carboxylic acid is a carboxylic acid that is an intermediate in the chemical synthesis of 2H and 3H tetrahydroquinolines. It can be synthesized by the oxidation of 2-(N,N-dimethylamino)benzaldehyde with hydrogen peroxide in methanol. The compound has been used to label animals for use in mass spectrometry studies and as a reactant in electron and nuclear magnetic resonance (NMR) spectroscopy experiments. In addition, 2-oxo-1,2,3,4-tetrahydroquinoline-4-carboxylic acid has been used to study equilibrium and reversible reactions as well as to identify the abundances of different spectral peaks. 2-Oxo-1,2,3,4-tetrahydroquinoline-4</p>

<p>Phenol red is a pH indicator that finds broad applications from chemistry to microbiology. Colour varies from yellow at pH&lt;6.8 (lmax 443nm) through to light red/pink at 6.8&lt;pH&lt;8.2 (lmax 570 nm) to vivid purple/red at pH&gt;8.2. It is widely used in cell culture to monitor pH and for colorimetric titration. For example, phenol red can be used to quantify Br- content in sea or fresh water. It is added to VTM as pH indicator, at the concentration of 10mg/ml, maintaining a pink colour at neutral pH.</p>

<p>Linolenic acid is a polyunsaturated fatty acid that belongs to the omega-6 family. It has been shown to have apoptosis-inducing effects in various experimental models and has anti-oxidant properties. Linolenic acid also protects against UV radiation and skin cancer. In addition, linolenic acid may be beneficial for eye disorders such as dry eye syndrome and age-related macular degeneration. Clinical studies have shown that linolenic acid may help with weight loss, improve body mass index, and reduce inflammation.</p>

<p>4-tert-Butylbenzyl alcohol is a chemical compound that binds to the acetyltransferase enzyme and blocks the conversion of acetate to acetyl-CoA. It is used as an inhibitor in biochemical research, where it is commonly used in control experiments. 4-tert-Butylbenzyl alcohol has a binding constant of 10 M, which is much higher than other inhibitors such as ethylene diamine (K = 3 x 10 M) and hydroxymethyl furfural (K = 1 x 10 M). This compound has been shown to inhibit wild type viruses by binding with the active site on their surface. The reaction mechanism for 4-tert-butylbenzyl alcohol involves forming an intermediate with chloride ions, which then reacts with ethylene diamine to form ethyl formate. The non-nucleoside inhibitors are thought to bind at the same site as nucleoside analogues, which inhibits reverse transcriptase activity</p>

<p>2-Amino-8-hydroxyquinoline is a molecule that has been shown to have optical properties. 2-Amino-8-hydroxyquinoline has also been shown to be reactive in vitro and inhibit the growth of cancer cells. It is thought that this inhibition may be due to its ability to bind to the active site of DNA polymerase, preventing DNA replication. 2-Amino-8-hydroxyquinoline has also been shown in vitro studies and vivo studies to have potent inhibition activity against human serum albumin (HSA). The molecules that are used as linkers to attach 2-amino 8 hydroxyquinoline to other molecules are thermodynamically stable. The isomers of 2 amino 8 hydroxyquinoline have also been studied by X-ray crystallography and nuclear magnetic resonance spectroscopy, which provides information about the structure of the molecule. Finally, 2 amino 8 hydroxyquinoline has been found to be an odorant</p>

<p>Please enquire for more information about 5-(Indol-3-ylmethyl)-4-(4-methoxyphenyl)-1,2,4-triazole-3-thiol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Laquinimod is an immunomodulator drug that inhibits the activity of the immune system. It binds to toll-like receptor 7, which is a protein on the surface of certain cells that responds to infection and inflammation. Laquinimod has been shown to inhibit neurodegeneration in vitro, which may be due to its ability to bind with neuronal death receptors and block the inflammatory response. Laquinimod also inhibits bowel disease by reducing inflammation and controlling immunity in the intestinal tract. Laquinimod has been shown to have long-term efficacy when administered at physiological levels. This drug is chemically stable, even after exposure to light.</p>

<p>2-[2-[2-(2-Hydroxyethoxy)ethoxy]ethoxy]-1-(p-toluenesulfonyl)-ethanol is a PEG polymer categorised as monofunctional (OH-PEG-X). Used as a linker, 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]-1-(p-toluenesulfonyl)-ethanol is used to attached PEG to proteins, peptides, oligonucleotides, nanoparticles and small molecules via pegylation, a bioconjugation technique.</p>

<p>2,6-Dimethoxybenzyl alcohol is a synthetic compound that is a peroxidase substrate. It is used as an alternative for papaverine in the synthesis of penicillin and cephalosporin antibiotics. 2,6-Dimethoxybenzyl alcohol reacts with Mn2+ ions to form hydronium and hydrogen peroxide. This reaction has been shown to be more efficient than the decomposition of hydrogen peroxide by catalases or superoxide dismutases. 2,6-Dimethoxybenzyl alcohol also forms a reactive congener with erythrocytes and plasma proteins that can cause vasoconstriction in the blood vessels. The dimethoxybenzyl group (DMB) is a monosubstituted phenol group that binds to the active site of enzymes such as cytochrome P450s and glutathione reductase.</p>

<p>1-(3-Methylphenyl)ethanol is an organic compound that has a hydroxyl group, homochiral carbonyl group, and aromatic hydrocarbon. It is a product of the catalysed reaction between a hydroxyl compound and an alkyne molecule. The reaction mechanism begins with the formation of an imine intermediate. This intermediate then undergoes a double displacement to form the desired product and regenerate the catalyst. 1-(3-Methylphenyl)ethanol can be used as a building block for other organic compounds, such as epoxides or esters.</p>

<p>Emax (230 nm) = 3113</p>

<p>Folin-Ciocalteu's phenol reagent is a chemical used in analytical chemistry. It is a mixture of sodium carbonate and tannins that reacts with caffeic acids to form a red product. This reaction is used as an indicator for the presence of phenolic compounds, such as tannins. Folin-Ciocalteu's phenol reagent is also used in pharmaceutical dosage forms, where it can be found in lipid peroxide tablets or suppositories. It can also be used to measure the antioxidant activity of plant extracts. The hydrochloric acid present in the reagent reversibly inhibits this radical scavenging activity.</p>

<p>4-(1-Adamantyl)-2-nitrophenol is a versatile building block that can be used to construct complex compounds. It is a research chemical that can be used as a reagent, as well as in the synthesis of pharmaceuticals and other chemicals. 4-(1-Adamantyl)-2-nitrophenol is soluble in water and ethanol, and has an odorless and colorless appearance. This chemical can be found under the CAS number 32599-84-1.</p>

<p>Gestadienol is a synthetic, reconstituted drug that is used to treat congestive heart failure. Gestadienol is produced by reacting hydrochloric acid with isopropyl palmitate and diluent. The reaction yield of this process can be increased by implanting the drug into animal tissue for a period of time before extraction. Gestadienol binds to glucuronidated compounds in the blood, which may be due to its chemical similarity to estradiol. This binding prevents the glucuronidated compound from being excreted in urine and increases their concentration in the bloodstream. Gestadienol has been shown to increase postnatal development in rats, which may be due to its ability to bind progesterone receptors on cells and inhibit progesterone-mediated effects.</p>

<p>2-Amino-4-cyano-phenol is a compound that has been shown to have antitubercular activity. It modulates the activity of cromakalim, which is a drug used for the treatment of tuberculosis. 2-Amino-4-cyano-phenol is also an antibacterial agent and has been shown to activate bacterial DNA replication and protein synthesis. The mechanism of action of this compound is thought to be due in part to its ability to bind with the ribosomes on the outside surface of cells and inhibit their function. 2-Amino-4-cyano-phenol has also been shown to have structural similarities with phenylephrine, which inhibits bacterial growth by binding to DNA gyrase, thereby preventing transcription and replication.</p>

<p>2-(2,5-Dimethylphenyl)ethanol is a reagent that reacts with an electrophile to form an alkenylated product. It is used in the synthesis of 2-methylbenzaldehyde and other aromatic hydrocarbons. 2-(2,5-Dimethylphenyl)ethanol reacts with an alkyne to form a substituted ethyl group. This reaction is called alkenylation. The active species of this reagent are the electrophilic carbocations generated by its reaction with the alkene.</p>

<p>3-Hydroxyphenylmethylcarbinol is a phenolic compound that has been shown to increase the uptake of iron by cells. It has been shown to induce apoptotic signaling in cancer cells and to be cytotoxic. 3-Hydroxyphenylmethylcarbinol is synthesized from 2-hydroxyphenylacetic acid, which is found in many natural sources such as plants and animals. This compound can be extracted from hexane or other organic solvents. 3-Hydroxyphenylmethylcarbinol has two isomers: 3HPMC and 3HPMC-O-β-D-glucopyranoside. The latter form has a greater affinity for iron than the former.</p>

<p>3,4-Methylenedioxyphenethyl alcohol (MDPA) is a model compound that is used to study the mechanism of action and synthesis of aniracetam. It has been shown to be an antagonist of pentylenetetrazole, a convulsant drug. MDPA was also found to have anticonvulsant properties in mice. It was found that this compound had no effect on the inhibition of movement when administered at doses up to 100 mg/kg. This compound is an analog of liriodenine, which has been shown to have anti-inflammatory properties. 3,4-Methylenedioxyphenethyl alcohol is not active in the central nervous system due to its stereoselectivity; this means it can only bind to one stereoisomer within the brain and does not cross the blood-brain barrier.</p>

<p>2,5-Dimethylphenylmethyl carbinol is a reagent that is used in the synthesis of aromatic hydrocarbons and alkenylated products. It reacts with an electron-deficient alkyl compound to form an alkenylated product. 2,5-Dimethylphenylmethyl carbinol is highly selective for electron-deficient alkyl compounds. The reaction rate of 2,5-dimethylphenylmethyl carbinol can be increased by increasing the temperature or adding a base catalyst, such as sodium methoxide or potassium tert-butoxide.</p>

<p>Halquinol, a mixture of 5,7-dichloro-8-quinolinol, 5-chloro-8-quinolinol, 7-chloro-8-quinolinol and 8-hydroxyquinoline, is an important intermediate in organic synthesis. It has been used as a reagent in the synthesis of a variety of complex compounds. Halquinol has also been used as a building block for the synthesis of many other chemical products. The CAS number for halquinol is 806769-4.</p>

<p>Isohexanol is a chemical cross-linking agent that reacts with amines to form amide bonds. It is used in the synthesis of polyvinylpyrrolidone, which is an important component of pharmaceutical preparations. Isohexanol has been shown to react with glycol ethers to form ether adducts and has been used as a kinetic study reagent. The chemical reactions of isohexanol depend on its pH level, which can range from acidic (pH 2) to neutral (pH 7). At lower pH ranges, isohexanol will undergo side-chain cleavage to form methyl myristate, which is a fatty acid. Higher pH levels result in the formation of methyl ethyl and other volatile products.</p>