Amines

<p>Please enquire for more information about 5-({[2-(4-Chlorophenyl)-1,3-oxazol-4-yl]methyl}thio)-1,3,4-thiadiazol-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The compound is a stereoselective amine. The molecule has two diastereomers, one of which is the (1R,2S) configuration and the other of which is the (1S,2R) configuration. The compound is an efficient method for preparing fatty acid esters with aromatic hydrocarbons.<br>The chemical structure of the molecule provides a cavity that can be used to bind with ethyl bromoacetate. This cavity has been shown in x-ray crystal structures to be able to bind with ethyl bromoacetate and provide an efficient method for preparing fatty acid esters with aromatic hydrocarbons.</p>

<p>2-Methyltryptamine is a tryptamine derivative that binds to the 5-HT2 receptors in the brain and blocks the action of serotonin. It has been proposed as a possible treatment for human immunodeficiency, but more research is needed to determine its efficacy. 2-Methyltryptamine acts as an agonist at 5-HT2 receptors and can be used in plate tests to detect histones deacetylase activity.</p>

<p>Please enquire for more information about [2-(1,2,6-Trimethyl-1H-indol-3-yl)ethyl]amine hydrochloride 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 N-[2-(4-Benzylpiperazin-1-yl)-2-oxoethyl]-N-methylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>9-(Benzylamino)-1,2,3,4-tetrahydroacridin-1-ol maleate is a cholinergic drug that is used for the treatment of inflammatory diseases. It inhibits phosphodiesterase activity and has been shown to be effective in clinical studies against a number of inflammatory diseases. This drug also has anti-inflammatory properties and can be used to treat acute inflammation. 9-(Benzylamino)-1,2,3,4-tetrahydroacridin-1-ol maleate is also conjugated with fatty acids and this formation helps to increase its bioavailability.</p>

<p>Please enquire for more information about 6-Bromo-1,2,3,4-tetrahydronaphthalen-2-ylamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(4-Aminophenoxy)acetamide is a chemical compound that belongs to the class of acetamides. It is used in the production of polyester fibers and dyes. 2-(4-Aminophenoxy)acetamide is a colorless, crystalline solid that has not been identified in nature.</p>

<p>Please enquire for more information about 5-Amino-2-(trifluoromethyl)isonicotinic acid 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 2-(4-fluorophenyl)-n-methylethanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Amino-1-methyl-5-nitrosouracil is a neutral form of the molecule that has both protonated and unprotonated forms. It is a bidentate ligand that can bind to a metal ion. The nitrogen atom in the molecule is an important part of its structure, as it contains two nitro groups and one amino group. 6-Amino-1-methyl-5-nitrosouracil has been used in techniques such as spectroscopies and dinitroso analysis. The neutral form of the molecule can be converted into its ionic form by adding either chlorine or nitrate ions to it, which causes the nitrogen atoms to be more electronegative. This conversion changes the nature of the compound, making it more acidic. Dehydration also occurs when water molecules are removed from 6-amino 1 methyl 5 nitrosourea, which causes a change in shape and shifts its properties to</p>

<p>2-Chloro-3,4-dimethoxyphenethylamine is an intermediate in the synthesis of zepines. It can be synthesized by reduction of borohydride with 2-chloro-1,2,3,4-tetrahydrobenzaldehyde.</p>

<p>3-Amino-4-methoxypyridine is a molecule that has been shown to have anesthetic activity. It has been shown to inhibit the uptake of glycogen by glioblastoma cells and decrease the rate of glycogen synthesis in these cells. 3-Amino-4-methoxypyridine also inhibits the production of ATP in cardiac muscle cells, which may be due to its ability to inhibit glycogen synthase kinase-3 (GSK3) and glycogen synthase. This drug also inhibits cancer cell growth by inhibiting protein synthesis, as well as inflammatory disease progression by inhibiting NFκB activation and cytokine production. 3-Amino-4-methoxypyridine can be synthesized from aminopyridines such as isonicotinic acid or nicotinic acid, which are oxidized with hydrogen peroxide and sodium nitrite in the presence of a base catalyst.</p>

<p>O-(Tert-butyldimethylsilyl)hydroxylamine is a stereospecific, oxidized, insoluble, tautomeric hydroxamic acid. It is used as a reagent in organic synthesis to form lactams by reaction with hexamethylenetetramine. The compound can be prepared by treatment of hydroxylamine with diacetate in the presence of aluminium chloride. The product is an orange liquid that crystallizes from water, but is not soluble in most organic solvents.</p>

<p>5-(Aminomethyl)-2-furoic acid hydrochloride is a molecule that belongs to the group of carboxylates. It has a molecular weight of 191.2 g/mol and a chemical formula of CHNO. The structure of 5-(aminomethyl)-2-furoic acid hydrochloride is similar to that of hexamethylenetetramine, a common organic compound with the formula (CH)N(H)CH. 5-(Aminomethyl)-2-furoic acid hydrochloride can be used as an acceptor in hydrogen chloride gas generation reactions, which are used in the synthesis of some pharmaceutical drugs and other organic compounds. The molecule also has potential use in telomerase research because it is structurally similar to natural telomeres. In addition, this molecule has been shown to have anti-inflammatory properties due to its ability to inhibit prostaglandin synthesis.</p>

<p>3-Methoxybenzene-1,2-diamine is a chloride surfactant that is cationic at low concentrations. It is most commonly used as a cross-linking agent in polymers and also has anti-inflammation properties. 3-Methoxybenzene-1,2-diamine is an osmotic agent that binds to water molecules, which prevents the loss of water from cells and increases cell volume. This chemical also has been shown to be an antagonist of 5Ht4 receptors and can be used for the treatment of inflammatory diseases such as asthma. 3-Methoxybenzene-1,2-diamine has been shown to have low toxicity in rats when consumed in dietary concentrations.</p>

<p>Please enquire for more information about 2-Amino-5-nitroindan hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-1-Z-1,2-diaminoethane·HCl is a stable isotope of N-1-Z-1,2-diaminoethane. It is used for the analysis of plant tissue to quantify the amount of leaves or other plant parts that are present in a sample. This compound can be used to monitor changes in the level of leaves or other plant parts over time and to measure recovery rates after harvest. N-1-Z-1,2-diaminoethane·HCl is labeled with deuterium (D) in order to be detected by liquid chromatography–mass spectrometry (LC–MS). The quantification of N-1-Z-1,2-diaminoethane·HCl can be monitored using multiple reaction monitoring (MRM). The use of this stable isotope overcomes many problems associated with traditional methods, such as environmental variability and tissue degradation.</p>

<p>Ammonium carbonate is an inorganic salt that consists of ammonium ion and carbonate ion. It is a white crystalline solid with a molecular weight of about 166.4 g/mol. Ammonium carbonate is soluble in water, alcohol, acetone, and other organic solvents. It has been used as a buffer solution for pH adjustment and as a source of ammonium ions in analytical chemistry. Ammonium carbonate can be formed by the reaction of sodium carbonate with ammonia gas or liquid ammonia, or the reaction of sodium bicarbonate with ammonia gas or liquid ammonia. The thermal expansion coefficient of ammonium carbonate is higher than those of sodium salts such as sodium chloride and potassium chloride. Electrochemical impedance spectroscopy (EIS) measurements have shown that the reactivity between ammonium carbonate and plasma mass spectrometry is high due to its high values on the electric spectrum graph at low frequencies (1 kHz).</p>

<p>Please enquire for more information about N-2,3-Dihydro-1H-inden-2-yl-N-propylamine 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 4-chloro-5-fluoropyrimidin-2-amine 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 E-3-(Tributylstannyl)-2-propen-1-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

(2R)-1-[2-[(3-Hydroxytricyclo[3.3.1.1(3,7)]dec-1-yl)amino]acetyl]-2-pyrrolidinecarbonitrile is a drug that belongs to the class of DPP-IV inhibitors and is used for the treatment of type 2 diabetes mellitus. It has been shown to be effective in reducing postprandial blood glucose levels in patients with type 2 diabetes mellitus. The mechanism of action of this drug is not fully understood, but it may have an effect on insulin release from pancreatic beta cells and/or inhibition of gastric emptying or intestinal absorption of glucose. This drug has been shown to reduce tubulointerstitial injury in diabetic rats and can be used as a combination therapy for type 2 diabetes mellitus. There are no known clinically relevant interactions between (2R)-1-[2-[(3-Hydroxytricyclo

<p>(1R,2R)-1-Amino-2-benzyloxycyclopentane is achiral. It is a synthetic chemical that has been used as an initiator for polymerization of amines and hexafluoroisopropanol. The synthesis of this compound can be achieved through a chiral technique known as interfacial polymerization. (1R,2R)-1-Amino-2-benzyloxycyclopentane is an initiator for the production of polymers with alternating helical chains. This process relies on the presence of achiral molecules to initiate the polymerization process.</p>

<p>2-(2-Aminoethoxy)ethanol (2-AE) is a natural compound that has been synthesized from ethanol and 2-aminoethanol. It has been shown to react with sodium carbonate to form stable complexes that are resistant to hydrolysis by amines. The stability of the complex is attributed to the formation of an intermolecular hydrogen bond between the hydroxyl group on the 2-AE molecule and the carboxylate group on the sodium carbonate molecule. 2-AE reacts with benzalkonium chloride, a quaternary ammonium salt, in water vapor to produce an alcohol and a fatty acid, which is then hydrolyzed by glycol ethers into glycolates. This mechanism is similar to that of other reactions involving quaternary ammonium salts, such as those in fatty acids or glycol ethers.</p>

<p>Please enquire for more information about 4-Amino-3-(trifluoromethoxy)benzoic acid 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 1-Benzyl-4-phenylamino-4-(methoxymethyl)piperidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Phenylhydroxylamine is a chemical compound that is used in wastewater treatment. It is a hydrophobic compound that has been shown to irreversibly inhibit the nitrite reductase enzyme, which is responsible for converting nitrite ions into nitrate ions. This reaction mechanism was studied using in vitro assays with picolinic acid and nitrobenzene. N-Phenylhydroxylamine binds to the active site of the enzyme and blocks access by the substrate, preventing it from being converted into its product. The reaction can be reversed by adding hydrogen fluoride, which displaces the N-phenylhydroxylamine molecule from its binding site. N-Phenylhydroxylamine also binds to nitrogen atoms and participates in transfer reactions with other molecules, making it reactive and capable of reacting with other compounds. The sample preparation process should include separating N-phenylhydroxylamine from water samples after extraction because it will react with</p>

<p>Please enquire for more information about 1-(Fmoc-amino)-4,9-dioxa-12-dodecanamine·HCl 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 (2-{2-[2-(2-Aminoethyl)-4,5-dimethoxybenzyl]-4,5-dimethoxyphenyl}ethyl)amine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

2-(4-Aminophenylthio)acetic acid is an analytical reagent that is used for the determination of nitrite ion. It reacts with nitrous acid to form a red-colored dye. 2-(4-Aminophenylthio)acetic acid has been shown to be an effective anhydrase inhibitor, which can be used in analytical chemistry as a method for determining the concentration of nitrate ion. This compound also has a constant value of 1.5, which can be used to calculate the concentration of nitric acid in hydrochloric acid by using the following equation: 2 NaOH + HCl → NaCl + 2 H2O 1.5 (aq) + 4H+(aq) → 6H2O(l) 6H2O(l) ÷ 1.5 (mol/L) = 3 mol/L 3 mol/L ÷ 0.037 (mol/g) =

<p>N,N,N',N'-Tetramethyl-1,3-diaminopropane is a chemical compound that is used as a cross-linking agent. It reacts with fatty acids and hydroxyl groups in the presence of sodium citrate to form cross-links between molecules. This reaction is useful for modifying the transport properties of fat cells. N,N,N',N'-Tetramethyl-1,3-diaminopropane can also be used as a reactive chemical in the synthesis of other compounds such as selenium compounds.</p>

<p>Cis-4-Methylcyclohexylamine is a cyclic amine that is found in the form of its decarboxylated derivative, 4-methylcyclohexanamine, which is used as an inhibitor for various enzymes. The methyl group on the cyclohexane ring is responsible for the compound's activity. Magnetic resonance spectroscopy has shown that cis-4-Methylcyclohexylamine binds to the active site of carbonyl reductase and inhibits its enzymatic activity, thereby blocking a step in the citric acid cycle. Cis-4-Methylcyclohexylamine has also been shown to have anti-inflammatory effects by inhibiting protein kinase C (PKC) and NFkB activation.</p>

<p>Please enquire for more information about 1-(2-Aminopyrimidin-5-yl)ethanone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(Dimethylamino)ethyl methacrylate is a monomer that belongs to the class of water-soluble acrylic monomers. It is used as a polymerization initiator and in the preparation of hydrogels, which are materials with high water content. 2-(Dimethylamino)ethyl methacrylate copolymers have shown inhibitory properties against bacterial growth, including Staphylococcus aureus and Pseudomonas aeruginosa. The antimicrobial activity of these copolymers may be due to their acidic nature or their ability to form acid complexes with metal ions. Other biological properties include cytotoxicity and significant inhibition of cell proliferation. 2-(Dimethylamino)ethyl methacrylate polymerizes readily at low temperatures, making it useful for sample preparation techniques such as thin layer chromatography (TLC).</p>

<p>Please enquire for more information about Ethyl 3-{[(1E)-(dimethylamino)methylene]amino}-5-methoxy-1-methyl-1H-indole-2-carboxylate 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 1-(RS)-2-(Dibutylamino)-2-[2,7-dichloro-9-(4-chlorobenxylidene)]-9H-fluoren- 4-yl]ethanol - E/Z mixture including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,3-Diaminotoluene is a compound that can be synthesized through the reaction of 2,4-diaminotoluene and picric acid. It has been used as a fluorescent probe for palladium complexes and has been shown to have efficient fluorescence properties in chromatographic applications. 2,3-Diaminotoluene has also been found to be an effective anti-bacterial agent against Gram-positive bacteria such as Staphylococcus aureus and Enterococcus faecalis. This compound has also been shown to have antitumour activity against leukemia cells. The synthesis of 2,3-diaminotoluene involves the reaction of amines with formaldehyde followed by dehydration.</p>

<p>Please enquire for more information about 2-Amino-1-(2,3-dihydro-benzofuran-5-yl)-ethanol 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 Methyl 3-amino-5-fluoro-1-methyl-1H-indole-2-carboxylate 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 4-Benzyloxy-3-methoxy-N-methylphenethylamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(4-Bromobenzyl)methylamine hydrochloride is a reagent that is used for the analysis of carboxylic acids. It has been used in a number of studies to analyze cellular metabolism and energy metabolism. This reagent has also been used to study the functional groups of organic acids, as well as their reactivity. (4-Bromobenzyl)methylamine hydrochloride can be used in liquid chromatography or electrospray ionization methods to analyze samples using mass spectrometry.</p>

<p>N-Nitrosodicyclohexylamine (NDCA) is a chemical that is used as a corrosion inhibitor. The stability of NDCA in the environment has been studied extensively and found to be resistant to many conditions including heat, light, and pH. NDCA is absorbed by the skin or ingested and has been shown to cause genotoxic effects in human lymphocytes. The genotoxic potential of NDCA has also been demonstrated in V79 cells. NDCA reacts with amines to form an intermediate that spontaneously decomposes into nitrosamines, which are carcinogenic. This reaction mechanism was confirmed using analytical methods such as gas chromatography-mass spectrometry (GC-MS).</p>

<p>Please enquire for more information about N,N'-bis-Fmoc-diaminoacetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Hydroxy-4-amino-butyric acid is a synthetase that catalyzes the formation of 3-hydroxy-4 amino butyric acid from 3-hydroxy butyric acid and ammonia. This reaction occurs in the presence of chloride ions, ethyl bromoacetate and butyric acid. The isolated yield of this reaction is 47%. The product can be converted to 3-amino butyric acid by dehydrating it with hydrochloric acid. 3-Hydroxy-4 amino butyric acid has been shown to have anticancer properties in vitro. It also has been shown to have antiinflammatory properties, which may be due to its ability to inhibit the production of prostaglandin E2, an inflammatory mediator.</p>

<p>Please enquire for more information about 1,4-Piperidinedicarboxylic acid, 4-aMino-, 1-(1,1-diMethylethyl) 4-ethyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(2S,3S)-5-[2-(Dimethylamino)ethyl]-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4-one hydrochloride is a racemic mixture of two enantiomers. It is a prodrug that is hydrolyzed to its active form, diltiazem. The drug has been shown to be effective in the treatment of hypertension and angina pectoris. (2S,3S)-5-[2-(Dimethylamino)ethyl]-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4-one hydrochloride has been shown to inhibit the activity of the enzyme phosphodiesterase which breaks down cyclic AMP. This inhibition results in an increase in levels of</p>

<p>Please enquire for more information about (1-Methyl-1H-indazol-3-yl)methanamine 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 5-(3-Methylphenyl)-1,3,4-oxadiazol-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N,N'-Bis(salicylidene)ethylenediamine is a catalyst that belongs to the group of transition metal complexes. It is used in hydrogenation reactions in the presence of a palladium-based catalyst. The coordination geometry is octahedral with two bridging ethylene diamine ligands and one terminal ethylene diamine ligand. The complex has been shown to catalyze the reaction between aryl chlorides and alkynes as well as between alkenes and sulfur dioxide to produce corresponding nitriles. N,N'-Bis(salicylidene)ethylenediamine has also been shown to be active in polymerization reactions and can be used as an effective chiral catalyst for polymer compositions.</p>