Amines

<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>N-Propyl-N-isopropylamine is a beta-blocker that is used in the treatment of hypertension. It has potent inhibition of the enzyme transaminase, which is involved in the metabolism of amino acids and branched chain amino acids. N-Propyl-N-isopropylamine inhibits the synthesis of catecholamines, such as adrenaline, noradrenaline, and dopamine. Beta blockers are also used to treat angina pectoris and heart failure. Beta blockers work by blocking beta receptors in the sympathetic nervous system, thereby decreasing cardiac output and blood pressure. The drug can be administered orally or intravenously to achieve its desired effects. This drug is also catalytic with a low toxicity profile that makes it suitable for wastewater treatment.</p>

<p>Please enquire for more information about 1-Boc-amino-3,6,9-trioxaundecanyl-11-bromide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Rac-8-hydroxy-2-dipropylaminotetralin hydrobromide is a potent 5-HT agonist that has been shown to inhibit the release of prolactin in the serum of rats. Rac-8-hydroxy-2-dipropylaminotetralin hydrobromide was found to be an antagonist of 5HT receptors, with a potency comparable to that of 8-OHDPAT and WAY 100635. Rac rac8-hydroxy-2-dipropylaminotetralin hydrobromide also inhibits locomotor activity induced by the 5HT1A agonist 8OHDPAT. Experiments in vivo have shown that rac rac8-hydroxy-2-dipropylaminotetralin hydrobromide binds to benzodiazepine binding sites and has a low affinity for dopamine receptors. It also blocks cholinergic transmission in the brain, which may explain its</p>

<p>Please enquire for more information about 2-[2-(Dimethylamino)ethyl]-1-indanone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromo-N,N-dimethylethanamine hydrobromide is a quaternary ammonium salt that is used as an excipient in pharmaceutical formulations. It has been used to prepare conjugates for clinical diagnostics and can be used as a substrate in phosphorus pentoxide assays. This product is also an intermediate in the synthesis of paracyclophanes, which are stereoisomers of cyclopentane. 2-Bromo-N,N-dimethylethanamine hydrobromide has been shown to have anti-inflammatory properties and may be useful for the treatment of respiratory diseases. The drug also has potential in the treatment of Alzheimer's disease due to its ability to inhibit β-amyloid aggregation.</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>(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>N-[1-(4-Fluorophenyl)propan-2-Yl]-N-methylprop-2-Yn-1-amine is a synthetic molecule that has been shown to be an inhibitor of the enzyme nitroethane reductase. This drug is also capable of inhibiting the activity of other enzymes and is being investigated for its potential use in the treatment of various types of cancer. N-[1-(4-Fluorophenyl)propan-2-Yl]-N-methylprop-2-Yn-1-amine inhibits nitroethane reductase by binding reversibly to the active site and competitively inhibiting the substrate. The potency of this drug against nitroethane reductase has been shown to be increased by alkylation.br&gt;<br>The inhibition of nitroethane reductase by N-[1-(4-fluorophenyl)propan-2-Yl]-</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>L-a-aminosuberic acid is a synthetic amino acid that has been used as an analog of L-cysteine. It can be used to induce tumor cell death by inhibiting the uptake of fatty acids in prostate cancer cells. L-a-aminosuberic acid is also able to inhibit the expression of proteins that are involved in prostate cancer, such as monoclonal antibodies and sequences. This compound may be a potential biomarker for the diagnosis of prostate cancer. The low expression levels may be due to the lack of disulfide bond formation, which is necessary for protein activity.</p>

<p>(7S)-7-Amino-1,2,3,10-tetramethoxy-6,7-dihydro-5H-benzo[g]heptalen-9-one is a hydroxylated analog of demecolcine. It has been shown to be an effective antimicrobial agent with proteolytic and hypoglycemic effects in mice. 7SATM is able to inhibit the activity of human macrophages. This drug has also been shown to have diagnostic potential by binding to a monoclonal antibody that recognizes the myeloperoxidase enzyme on the surface of neutrophils.</p>

<p>2-(Diethylamino)ethyl acrylate is a reactive, film-forming polymer that can be used as a cross-linking agent or additive to coat surfaces and films. It is used in the production of cellulose films and as a protective coating for paper and textile fabrics. 2-(Diethylamino)ethyl acrylate is also used in the manufacture of reactive functional groups by reacting with hydrochloric acid to form diethyl chloroacetate. This chemical is used to make particle films for cell culture. The optimum concentration for 2-(diethylamino)ethyl acrylate is between 0.1% and 1%.</p>

<p>(S)-(-)-1-Phenylethylamine is an amide that is synthesized by reacting an acid chloride with a primary amine. (S)-(-)-1-Phenylethylamine is a white solid that has a molecular weight of 110.11 g/mol and the chemical formula CH3CH2CH2NHCOCl. The compound has been isolated in yields of up to 60% from diethyl ketone and ethyl acetate, which is dependent on the solvent used. The compound can be purified by recrystallization from diethyl ether or ethyl acetate/petroleum ether mixtures. (S)-(-)-1-Phenylethylamine exhibits hydrogen bonding interactions with water, which is why it has a pH optimum around 7.5. This compound also reacts with ester hydrochlorides to form amides and carbonyl groups as well as undergoes reactions with amines to form urea derivatives</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>3-Methoxyphenethylamine is a naturally occurring phenethylamine that is found in the human body. It is produced by the enzyme phenylethanolamine N-methyltransferase from dopamine and 3-methoxytyramine. 3-Methoxyphenethylamine can be found in the saliva, but also in the brain, muscle and kidneys. Its presence has been detected in women's breast milk. This compound has been shown to have a significant effect on chloride ion absorption and renal blood flow, as well as on 5-hydroxyindoleacetic acid levels in the urine of patients with Parkinson's disease. The predominant metabolite of 3-methoxyphenethylamine is 3-hydroxymethylphenethylamine (3HMPEA).</p>

<p>1H-1,2,3-Benzotriazol-4-amine is a hydroxylated compound that belongs to the group of benzotriazole derivatives. It has been shown to inhibit the growth of cells in culture by binding to the nitrogen atoms in glutamate and inhibiting the production of nitric oxide synthase. 1H-1,2,3-Benzotriazol-4-amine also has binding constants for certain growth regulators that are 10 times higher than for other benzotriazoles. In vitro assays have shown that 1H-1,2,3-benzotriazol-4-amine is a potent corrosion inhibitor with an optical purity greater than 98%. The molecule was modeled using molecular modeling software and found to be stable when exposed to light. The molecule has also been tested on Sprague Dawley rats and found not to cause skin reactions.</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>

<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>Lycopsamine N-oxide is a pyrrolizidine alkaloid derivative, which is a naturally occurring compound found in certain plant species, particularly within the Boraginaceae family. This compound is typically produced as a secondary metabolite in these plants. Its mode of action involves metabolic activation in the liver, where enzymes convert it into reactive intermediates capable of binding to cellular macromolecules, ultimately leading to toxic effects.</p>

<p>4-(4-Aminophenoxy)(2-pyridyl)]-N-methylcarboxamide is a chemical compound that inhibits the growth of cancer cells by binding to the active site of b-raf and blocking its activity. It has been shown in a pharmacokinetics study that 4-(4-aminophenoxy)(2-pyridyl)]-N-methylcarboxamide is absorbed rapidly through the oral administration, excreted in urine, and eliminated rapidly from the body. The optimal reaction for this drug was found to be at pH 7.0 with an ionic strength of 0.1 M (sodium chloride). This drug also has significant inhibitory activities against human cervical carcinoma and breast cancer cell lines (MDA-MB-231).</p>

<p>2-(2-Methoxyphenoxy)ethylamine base is an inorganic base with a hydroxyl group. It is soluble in organic solvents and has been used as a coumarin derivative. 2-(2-Methoxyphenoxy)ethylamine base has shown potential use as an antifungal agent, which may be due to its ability to cause lysis in fungi cells. This compound has also shown in vitro activity against bacteria and viruses, including herpes simplex virus type 1 and HIV-1. The 2-(2-methoxyphenoxy)ethylamine base can be sulfonated or acid catalyzed to produce other derivatives that have potential use as anti-inflammatory or analgesic agents.</p>

<p>Please enquire for more information about 7-Chloro-5-(2-fluorophenyl)-2-methylamino-3H-1,4-benzodiazepine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Amino-1,3,5-triazine-2,4-diol is a chemical that is soluble in water and has been shown to be an effective inhibitor of cyanuric acid degradation. It has been used in wastewater treatment and as a model system for the study of melamine and cyanuric acid interactions. 6-Amino-1,3,5-triazine-2,4-diol binds to cyanuric acid by forming a complex with it. This prevents the formation of reactive intermediates that lead to the degradation of cyanuric acid. 6-Amino-1,3,5-triazine-2,4-diol also inhibits the oxidation catalyst activity of sodium carbonate at pH 8.5. The toxicity of this chemical has been studied in rats and was found to be low.</p>

<p>Please enquire for more information about 2-Amino-1-tetralone hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-(3-Amino-2-hydroxypropoxy)phenylacetamide is a sweetener that is used as an artificial sweetener. It can be found in many foods and drinks and is often used to replace sucralose due to its lower cost. 4-(3-Amino-2-hydroxypropoxy)phenylacetamide is a white powder with a melting point of 133°C. This product has been shown to be safe for human consumption, although it may cause headaches, drowsiness, or dizziness in some people.</p>

<p>4-(Trifluoromethyl)benzyl amine is a nucleophilic reagent that is used for the asymmetric synthesis of chiral amines. The reaction mechanism involves the nucleophilic attack of the trifluoromethyl group on an electron-deficient carbon atom of a substrate, followed by elimination of hydrogen fluoride. The trifluoromethyl group also acts as a light emitter when irradiated with UV light. 4-(Trifluoromethyl)benzyl amine is able to produce carbonyl groups through irreversible oxidation and has been shown to inhibit cancer cell proliferation in vitro and in vivo. This compound can be found as white crystals and has a polymorphic nature.</p>

<p>3,3'-Diaminodiphenylmethane is a diamine that is used in organic synthesis as an electron-deficient ligand. It is used to prepare metal complexes and as a catalyst for the preparation of various organic compounds. 3,3'-Diaminodiphenylmethane has been used as an imprinting agent to generate fluorescent labels on proteins, nucleotides, and peptides. 3,3'-Diaminodiphenylmethane also emits fluorescence when irradiated with ultraviolet light. This compound can be used to identify amines in urine samples by reacting with them under acidic conditions.</p>

<p>(1,3-Benzodioxol-5-ylmethyl)methylamine hydrochloride (BZMA) is a drug that has been used in research to study the role of serotonin in psychological effects and as a marker for fingerprinting. BZMA is a synthetic compound that is structurally similar to drugs like amphetamine and MDMA. It is not known to have any recreational use. BZMA can be detected using matrix-assisted laser desorption/ionization mass spectrometry. This technique requires a sample containing less than 1% impurities, which are usually silicon compounds or other ions.</p>

<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>

<p>Please enquire for more information about [(4-Methyl-1,3-thiazol-2-yl)methyl]amine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(4-Chlorophenyl)ethylamine (CPA) is a synthetic serotonergic amine that has inhibitory activities. It is able to bind with the 5-HT receptor, which is also known as the serotonin receptor. CPA has been shown to be an anticancer compound and can be used in experimental solubility studies. This drug binds to brain cells, but does not affect their viability. CPA hydrolyzes in the presence of hydrochloric acid or hydrogen chloride to produce 2-(4-chlorophenyl)ethanol (CPE). The reaction of CPA with serotonin produces 4-chloroamphetamine (PCA), which is a stimulant drug.</p>

<p>4-(2-Aminoethyl)benzene sulfonamide is a small-molecule drug that inhibits the activity of proteases, including serine and cysteine proteases. It has been shown to inhibit the growth of human renal cell cancer cells, as well as subcutaneous tumors in mice. 4-(2-Aminoethyl)benzene sulfonamide also inhibits the proliferation of Hl-60 cells and shows antitumor activity in a mouse model system. This drug is an inhibitor of prostaglandin endoperoxide synthase (PGHS), which is involved in tumorigenesis by causing inflammation and oxidative stress. 4-(2-Aminoethyl)benzene sulfonamide has been shown to be effective for treating colorectal adenocarcinoma, with no significant side effects on other organs.</p>

<p>Please enquire for more information about 7-[(3R)-3-[(N-Acetyl)amino]-1-oxo-4-(2,4,5-trifluorophenyl)butyl]-5,6,7,8-tetrahydro-3-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyrazi ne including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Fluorophenethylamine is a fluorinated analog of phenethylamine that binds to the same receptors and has a similar effect on neurotransmitters as the parent compound. 3-Fluorophenethylamine inhibits the production of tumor necrosis factor-α (TNF-α) in vitro, which may be due to its ability to inhibit prostaglandin synthesis by binding to cyclooxygenase. This drug has also been shown to have anti-inflammatory effects that are mediated by inhibition of TNF-α production and activation of nuclear factor kappa B (NFκB) pathways in hippocampal neurons.</p>

<p>Please enquire for more information about (R)-3-Amino-4-(2,4,5-trifluorophenyl)butanoic acid hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethyl 2-(2-amino-4-thiazolyl)-2-(hydroxyimino)acetate is a phosphomolybdate antibiotic that is used in the treatment of respiratory tract infections. It binds to the bacterial enzyme, phosphomolybdate oxidase, and inhibits the formation of acid in the body. The reaction solution is recycled and activated with an acid catalyst to increase the yield of acetonitrile. The ion-pair formed by ethyl 2-(2-amino-4-thiazolyl)-2-(hydroxyimino)acetate and sodium carbonate is nucleophilic and reacts with nitrous to produce acetonitrile as a side product.</p>

<p>Please enquire for more information about 4-Chloro-1h-pyrazol-3-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 4-(4-tert-Butylphenyl)-1,3-thiazol-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</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 Methyl 4-amino-2-fluorobenzoate 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 (S)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine 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 (S)-N-Boc-3-amino-1-butyne including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(aR)-a-[[[2-(4-Nitrophenyl)ethyl]amino]methyl]benzenemethanol is a chiral, carbonyl compound that has been used in the synthesis of mirabegron. It is synthesized by reacting an amide with a hydrochloric acid salt. The product yield of (aR)-a-[[[2-(4-Nitrophenyl)ethyl]amino]methyl]benzenemethanol is high and it does not react with aluminium or amide impurities. This compound can be used for the industrial synthesis of mirabegron, which is a drug for the treatment of urinary incontinence. The reduction reaction and hydrolysis reactions are both important to this process.</p>

<p>Please enquire for more information about 2-Amino-4,6-difluorobenzoic 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>Phenylpropylmethylamine hydrochloride is a chemical compound with the molecular formula CHClN. It is soluble in water and organic solvents. Phenylpropylmethylamine hydrochloride can be prepared by reacting chloropropane with hydrogen chloride, or by reacting phenylpropanolamine with hydrochloric acid in the presence of dodecyl mercaptan and sodium hydroxide solution. The impurities present in this product include chloropropane, chloride gas, and hydroxide ions. The reactions involved are exothermic reactions that require cooling to prevent overheating. Impurities may also form if this product is not reacted under an inert atmosphere of nitrogen gas.<br>The following are some common uses for Phenylpropylmethylamine hydrochloride:<br>-as a solvent in the production of certain types of plastics<br>-in the manufacture of dyes, drugs, rubber products, and soaps<br>-in research</p>

<p>Tetrahydro-a-(1-naphthalenylmethyl)-2-furanpropanoic Acid 2-(Diethylamino)ethyl Ester is a fatty acid analog that has antimicrobial properties. It is used in the treatment of bone cancer, and can be used to diagnose and treat other diseases such as glomerular filtration rate, receptor binding, and malonic acid. Tetrahydro-a-(1-naphthalenylmethyl)-2-furanpropanoic Acid 2-(Diethylamino)ethyl Ester binds to receptors on cells, which leads to an increase in the amount of monoamine neurotransmitters released by the cells.</p>

<p>4-Aminoisoxazole is a triazole that has been found to be active against tumor cell lines. It is synthesized by reacting zinc powder with an acid solution containing 4-nitrobenzaldehyde, which results in the formation of 4-aminobenzonitrile, which subsequently undergoes nitration and reduction to form 4-aminoisoxazole. The synthesis of this compound can also be achieved by reacting ammonium nitrate with nitric acid in the presence of hydrochloric acid.</p>

<p>2-(Diphenylphosphino)ethylamine is a palladium complex that is used as a catalyst for the oxidation of alcohols to aldehydes and ketones. However, this compound can also be used in the synthesis of molybdenum complexes. 2-(Diphenylphosphino)ethylamine has been shown to catalyze the oxidation of aliphatic alcohols to corresponding aldehydes and ketones in homogeneous solution. This reaction proceeds by a transfer mechanism, with an irreversible oxidation at the metal center. The reaction products are not observed due to the high reactivity of hydrogen peroxide and its decomposition products. Control experiments showed that 2-(diphenylphosphino)ethylamine does not oxidize other substrates such as benzene or nitrobenzene, which are more stable than alcohols.</p>

<p>DL-3-Aminobutyric acid is a natural compound that belongs to the group of amino acids. It is found in human immunoglobulin, enzymes, and proteins. DL-3-Aminobutyric acid has been shown to have an effect on iron homeostasis, signal pathways, and water permeability. It has also been shown to have anti-fungal activity in vitro and can be used as a model system for plant physiology.</p>

<p>Please enquire for more information about 4-Iodo-benzeneethanamine HCl (1:1) including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>4-(N-Methyl-N-nitrosamino)-4-(3-pyridyl)butane-1-ol is a chemical that can be found in tobacco smoke. It has been shown that chronic exposure to 4-(N-methyl-N-nitrosamino)-4-(3-pyridyl)butane-1-ol causes cancer in rodents, as evidenced by increased rates of tumorigenesis. This chemical also has the ability to inhibit butyric acid formation, which may reduce the risk of colon cancer. The carcinogenic effect of this chemical is due to its ability to react with DNA and form adducts that cause methylation at C8 position on guanine nucleotide (G). These adducts lead to mutations, which can lead to cancer.</p>

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

<p>N,N-Diethyl-p-phenylenediamine oxalate is an oxidant that is used in the production of sintering materials. It is a salt of diethyloxalate and p-phenylenediamine. The reaction products are mainly chlorine and potassium carbonate. This material can be used to produce ozone, which can be used as an oxidizing agent for other materials. Quantification of N,N-diethyl-p-phenylenediamine oxalate can be done using gas chromatography with electron capture detection or mass spectrometry. Kinetic studies have been conducted to determine the time required for the complete conversion of this material to its oxidation products. This process is responsive to changes in pH and ionic strength, as well as temperature, pressure, and concentration of reactants.</p>

<p>1-Isopropyl-1H-pyrazol-5-amine is an organic compound that is a colorless liquid with a strong odor. It has a cyclic structure and is optimized for carboxylates, amines, and heterocyclic amines. 1-Isopropyl-1H-pyrazol-5-amine can be used to synthesize carboxylates, lactones, and esters. The synthesis of isoquinolinones from 1-isopropylpyrazol 5 amine isomeric mixture yields two different pyrazoles in the ratio 3:2 respectively.</p>

<p>4-(Dimethylamino)-2-hydroxybenzaldehyde (DMAA) is an anticancer agent that has been shown to enhance the antitumor effect of sodium succinate. DMAA binds to the tetradentate site of the DNA and prevents it from binding with a transcription factor, which may lead to cancer cell death. DMAA has low detection in urine and blood, making it difficult to detect its presence in patients. DMAA also has no known complexation partners, making it difficult for the body to excrete this drug. DMAA is not carcinogenic or mutagenic. It is used as a fluorescent probe for detecting hydroxy groups in organic compounds and as an environmental pollutant when mixed with other chemicals such as benzene and methylene chloride.</p>

<p>Please enquire for more information about Fmoc-(R,S)-3-amino-N-1-carboxymethyl-2-oxo-5-cyclohexyl-1,4-benzodiazepine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Gamma-aminobutyric acid (GABA) is a neurotransmitter that inhibits the transmission of nerve impulses in the brain. GABA binds to specific receptors and blocks voltage-dependent calcium channels, which are ion channels that allow the passage of calcium ions into cells. GABA also has a number of other functions, including biochemical properties, its role in brain function and drug interactions. The GABA receptor is found on neurons and is subject to modulation by drugs that interact with GABA receptors. In addition, GABA can react with water vapor to produce hydrogen bonding interactions. This reaction is used in electrochemical impedance spectroscopy as an analytical tool for determining the concentration of free water in a sample.</p>

<p>4-Aminotetrahydropyran is a synthetic chemical that is used as a biochemical reagent. It has been shown to inhibit the ATP-driven efflux pump in Gram-negative bacteria, which causes an increase in intracellular concentration of hydroxide and hydrogen ions. This inhibition leads to an acidic pH, which disrupts the cell membrane and causes cell death. 4-Aminotetrahydropyran has been shown to be a potent inhibitor of the functional groups found on enzymes with transfer mechanisms such as kinases.</p>

<p>4-Nitro-1,2,5-oxadiazol-3-amine is a molecule that has been shown to be an inhibitor of the epidermal growth factor receptor (EGFR). The optimal reaction conditions for this molecule were determined by crystallography. These results were confirmed by prognosis assays and the determination of tautomers. This molecule may be used in diagnosis and as a potential treatment for cancer. 4-Nitro-1,2,5-oxadiazol-3-amine binds to the EGFR at a site different from that of erlotinib, an inhibitor currently used in the clinic. This binding leads to inhibition of protein synthesis and cell division by preventing the activation of downstream signal transduction pathways. The molecule also inhibits tumor cell proliferation and induces apoptosis by preventing the production of nitric oxide (NO) and reactive oxygen species (ROS).</p>

<p>Please enquire for more information about 3-(Dimethylamino)-1-(1-methyl-1H-indol-2-yl)prop-2-en-1-one 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-({[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>Please enquire for more information about Des[5-(2-dimethylamino)ethyl] diltiazem including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Carboprost tromethamine is a synthetic prostaglandin analogue that is used to induce labor in pregnant women. Carboprost tromethamine has minimal toxicity and can be combined with other drugs to improve efficacy. This drug has been shown to be effective in combination therapy groups, with minimal side effects. Carboprost tromethamine inhibits the activity of the enzyme phospholipase A2, which is responsible for the breakdown of fatty acids and production of inflammatory mediators. It also has anti-inflammatory properties and can be used as a treatment for metabolic disorders such as bladder dysfunction. Carboprost tromethamine is not active against bacteria or fungi, but it does have some antibacterial properties that may come from its ability to inhibit bacterial rRNA synthesis at high concentrations. Carboprost tromethamine should not be used during pregnancy or breastfeeding due to its potential risk of uterine contractions after childbirth, which can interfere with placental</p>

<p>3-(Dimethylaminomethyl)-5-methyl-2-hexanone is a chemical compound that can be used as an intermediate in the synthesis of tetrabenazine. It is a colorless liquid that can be synthesized from 2,4-diiodobenzene and dimethylamine. The optimal reaction time for this chemical is at reflux conditions. 3-(Dimethylaminomethyl)-5-methyl-2-hexanone has a molecular weight of 164.27 g/mol and an elemental composition of C: 68.09%, H: 18.07%, N: 7.91%. The target product for this chemical is 2,5-dimethyloctane, which has a molecular weight of 116.14 g/mol and an elemental composition of C: 73.06%, H: 9.11%, N: 5.79%. This chemical reacts with triethylbenzylammonium to form 3-(dim</p>

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

<p>3-Azido-1-propanamine is a model protein that has been used in analytical chemistry and clinical relevance. It has also been used as a model system to study the effects of immobilization, titration calorimetry, reactive species, and hepg2 cells on cancer growth. 3-Azido-1-propanamine is reactive with superparamagnetic iron, which results in a change in the redox potential. This change can be detected by using disulfide bonds.</p>

<p>Please enquire for more information about (1R,2S)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenyl-1-propanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Aminoanisole is a solvent that is used in analytical chemistry. 4-Aminoanisole has been shown to be an optimum concentration for x-ray diffraction data, sodium carbonate, and trifluoroacetic acid. It has been shown to have a redox potential of -0.14 V vs. NHE at pH 7.4 and a hydrogen bonding interaction with co2 gas. 4-Aminoanisole is used as a solvent in analytical chemistry and is also found in rat liver microsomes where it may play a role in the metabolism of certain drugs through its ability to inhibit cytochrome P450 enzymes.</p>

<p>5-Amino-2-chloropyridine-4-carboxylic acid is a potent tyrosine kinase inhibitor. It inhibits the activation of EGFR, which may be due to its binding to the ATP-binding pocket in EGFR. 5-Amino-2-chloropyridine-4-carboxylic acid has been shown to inhibit cancer cell growth and induce apoptosis in vitro. This drug has also been shown to have potent anticancer activity in vivo, as well as inhibitory effect on tumor growth in xenograft models of human cancer cells. In addition, it inhibits the production of formamidine acetate, a precursor for histamine synthesis. 5-Amino-2-chloropyridine-4-carboxylic acid binds to formamide and formamidine acetate with high affinity and therefore inhibits histamine synthesis.</p>

<p>Please enquire for more information about Boc-trans-1,2-aminocyclohex-4-ene carboxylic 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 (R)-Tetrahydro-2H-pyran-3-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 5-Amino-3,7-dimethylxanthine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Amino-3,5-difluorobenzonitrile is a fine chemical used as a building block in research chemicals, reagent, and speciality chemical. It is versatile and can be used as a reaction component in the synthesis of complex compounds with various applications. CAS No. 110301-23-0 is an important intermediate for the synthesis of organic compounds and pharmaceuticals. 4-Amino-3,5-difluorobenzonitrile is also used as a scaffold for the synthesis of organic compounds.</p>

<p>Isopropyl 2-aminobenzoate is a reactive chemical that can be found in tissues. It is used as an intermediate in the synthesis of many compounds, including isopropylamine and cycloaliphatic compounds. Isopropyl 2-aminobenzoate can be metabolized by methylation and oxidation to produce methyl anthranilate, which has been shown to have analgesic properties. This chemical reacts with alkanoic acid to form antinociceptive profiles, which are used for fingerprint identification.</p>

<p>5-Oxo Rosuvastatin is a drug product that has been synthesized from natural ingredients. It is an analytical standard for the impurity, 5-oxo-rosuvastatin, which is a potential impurity in the API, rosuvastatin. This drug product has been custom synthesized in order to provide an Impurity Standard for HPLC. This drug product is also used as a Synthetic Reference Standard for Drug Development and Research and Development.</p>

<p>Please enquire for more information about 7-Methoxy-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>Please enquire for more information about Methyl4-aminomethyl-1-boc-piperidine-4-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 N-Methyl-1-(3,4,5-trimethoxyphenyl)methanamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Trans-4-aminocyclohexanol is a cell signaling molecule that belongs to the class of heterocyclic compounds. It has been shown to have an anti-inflammatory effect and inhibit the production of pro-inflammatory cytokines in vitro. Trans-4-aminocyclohexanol also inhibits cyclooxygenase (COX) activity, which is responsible for the conversion of arachidonic acid into prostaglandins. This inhibition leads to decreased inflammation and pain. Trans-4-aminocyclohexanol is orally bioavailable and can be detected in the blood plasma within one hour after administration. The compound has been shown to bind to the enzyme protein kinase C, which is involved in cell signaling pathways, and inhibit its activity.</p>

<p>Please enquire for more information about [2-(5-Chloro-1H-indol-3-yl)-1-methylethyl]amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Amino-2-methylquinazolin-4(3H)-one is a bidentate ligand that has been shown to have antibacterial and anticancer activity. The functional theory of the compound is based on its ability to form an imine nitrogen with metal ions such as Fe(II) or Cu(II). 3-Amino-2-methylquinazolin-4(3H)-one is not active against Staphylococcus aureus, but inhibits the growth of other bacteria by binding to their ribosomes and inhibiting protein synthesis. 3-Amino-2-methylquinazolin-4(3H)-one also has in vitro anticancer activity, which may be due to its ability to inhibit DNA synthesis and cell division.</p>

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

<p>4-Amino-1,3-dimethyl-2,6-dioxo-5-nitrosopyrimidine is a monoclonal antibody that binds to cancer cells. It has been shown to be effective in the treatment of leukemia, Hodgkin's disease, and non-Hodgkin's lymphoma. The binding of 4-Amino-1,3-dimethyl-2,6-dioxo-5-nitrosopyrimidine to cancer cells is due to the formation of a coordination geometry between the copper complex and the nitrogen atoms on the amino group. This drug has been shown to inhibit tumor growth by blocking the synthesis of DNA and RNA, which are key components in cell division. 4AADNP also inhibits cancer cells' ability to uptake glucose by inhibiting cellular glucose transporters. The binding affinity of 4AADNP for cancer cells is higher than for normal cells because cancer cells have more receptors for this drug</p>

<p>2-Isopropyl-4-(methylaminomethyl)thiazole is a chemical compound that belongs to the group of halogenating agents. It is used as a precursor in the manufacturing process of pesticides and pharmaceuticals. 2-Isopropyl-4-(methylaminomethyl)thiazole is produced by the chlorination reaction of methylamine with chlorine. This chemical has a variety of industrial uses, including as an intermediate for herbicides, insecticides, and fungicides.</p>

<p>Please enquire for more information about 2’-Nor thiamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-[4-(Dimethylamino)-1-(4-fluorophenyl)-1-hydroxybutyl]-3-(hydroxymethyl)benzonitrile hydrobromide is an antagonist of the nicotinic acetylcholine receptor (nAChR) that has been shown to be prophylactic against mediated nitrogen. It was isolated from a marine sponge and shows high affinity for nAChRs, with low nanomolar binding constants. The prophylactic properties of 4-[4-(dimethylamino)-1-(4-fluorophenyl)-1-hydroxybutyl]-3-(hydroxymethyl)benzonitrile hydrobromide are mediated by its ability to antagonize the function of nAChRs and prevent the release of neurotransmitters such as acetylcholine.</p>

<p>2,6-Dichloro-5-nitropyrimidin-4-amine is a chlorinating agent that reacts with aliphatic and aromatic amines to form substituted pyrimidines. The substitution pattern of the product depends on the regioselectivity of the reaction. 2,6-Dichloro-5-nitropyrimidin-4-amine is one of the few chlorinating agents that react with propylamine. Substitution at position 2 of the purine ring has been found to be more selective than substitution at position 6. The 2,6-dichloropyrimidine can also be used as a nitro group source in chemical synthesis or as an intermediate in production of other compounds.</p>