Amines

<p>Tetramethylammonium fluoride tetrahydrate (TMF) is an ionic liquid that is a reaction product of tetraethylammonium and hydrochloric acid. TMF has been shown to react reversibly with water to produce aqueous hydrogen fluoride, which can be detected at low concentrations with a variety of analytical techniques such as gas chromatography. TMF has also been shown to have selectivities for the transport of silicon and calcium carbonate ions, which are useful in electrochemical studies. The activation energies for the reaction of TMF with water were determined by electrochemical studies to be around -0.4 eV.</p>

Please enquire for more information about (2-Indol-3-ylethyl)((2,4,5-trichlorophenyl)sulfonyl)amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>4-Bromo-3-methylbenzylamine hydrochloride is a synthetic chemical that can be used in the synthesis of various products. This compound is a useful scaffold for the preparation of complex compounds, and it has been used as a reaction component in organic chemistry. It is also a versatile building block that can be used to synthesize fine chemicals with high purity. 4-Bromo-3-methylbenzylamine hydrochloride has been assigned CAS No. 1955514-32-5 by the Chemical Abstracts Service (CAS).</p>

<p>Please enquire for more information about 2-Amino-1-aza-3-((4-methylphenyl)sulfonyl)prop-1-enyl thiophene-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Aminoethanephosphonic acid (2AEP) is a phosphonic acid that is used as a fungicide. 2AEP binds to the target enzymes, such as bacterial RNA polymerase and bacterial DNA gyrase, by steric interactions with the hydroxyl groups of the enzyme. 2AEP also inhibits the synthesis of proteins in bacteria, which leads to cell death. The binding of 2AEP to bacterial RNA polymerase prevents the enzyme from interacting with ribonucleoside triphosphates, thus inhibiting transcription and translation of proteins. This compound has been shown to be effective against Caulobacter crescentus and Escherichia coli K-12 strains. A matrix effect was observed in this study for 2AEP when it was mixed with other compounds such as sodium azide or DMSO. In addition, there are some biochemical properties that are specific for 2AEP including its ability to inhibit fetal bovine serum</p>

<p>5-Aminoisatin is a serotonin receptor agonist and has been shown to have protective effects against liver cancer in vitro in human liver cancer cells. It also has a number of other biological activities, including anti-inflammatory, natriuretic, and leukemia inhibitory activities. 5-Aminoisatin interacts with the mitochondrial membrane and prevents cell death by inhibiting the opening of the mitochondrial permeability transition pore (MPTP). This activity may be due to its ability to form ternary complexes with ATP and the voltage sensor domain of the mitochondrial protein voltage dependent anion channel (VDAC). 5-Aminoisatin binds to both the alpha subunit and beta subunit of the calcium/calmodulin-dependent protein kinase II (CaMKII) enzyme. The binding of 5-aminoisatin to CaMKII leads to inhibition of phosphorylation at serine residue 397, which disrupts ATP binding.</p>

<p>1,2-O-Dihexadecyl-sn-glycero-3-phosphoethanolamine (DHEPE) is a lipid used as a fluorescent probe for the detection of carbohydrates. It has been shown to bind to high-mannose type oligosaccharides and to be stable in complex with them. DHEPE has been shown to form complexes with cell nuclei, which may be due to hydrogen bonding interactions between the sugar and phosphate head groups on the glycerol backbone. These interactions are thought to be responsible for the selectivity of DHEPE for mannose residues in cells. DHEPE also forms complexes with x-ray diffraction data, which is indicative of intermolecular hydrogen bonding between this molecule and other hydrophobic molecules. DHEPE's reaction mechanism is not clear, but it has been proposed that it reacts with proteins by reacting with amino groups on these proteins.</p>

<p>4-Amino-3-methoxybenzoic acid methyl ester is a reactive molecule that has been used as a radiotracer for positron emission tomography (PET). It is also used in the synthesis of oligodeoxynucleotides and hybridization probes. 4-Amino-3-methoxybenzoic acid methyl ester is not soluble in water, but it can be dissolved in organic solvents such as acetone or methanol. This compound has shown to have anticancer activity and may be useful for treating cancers of the brain, breast, colon, lung, prostate, and stomach.</p>

<p>5,6-Diamino-2,3-dicyanopyrazine (5,6-DDA) is a synthetic compound that has been shown to emit in the visible region. The emission spectrum of 5,6-DDA shows three peaks at 599 nm, 614 nm, and 637 nm. The molecular orbitals of 5,6-DDA are calculated to be sp2 hybridized with a singlet ground state. This molecule has been shown to form imines with aniline and pyrrole in the presence of chloride ions. It also forms a zn complex with zinc chloride and nitrate ions. The thermolysis of furyl derivatives produces the corresponding anions. 5,6-DDA can also undergo a photochemical reaction with chlorine gas to form its molecular ion at 637 nm.</p>

<p>2'-Aminoacetanilide is a colorless, crystalline compound that is soluble in water and has a bitter taste. It is used as an acidity regulator in food products, particularly bakery products. 2'-Aminoacetanilide can be found naturally in some microflora, such as lactic acid bacteria. <br>2'-Aminoacetanilide is an aromatic amine that contains both primary amino and functional groups. It is nucleophilic and reacts with proton by nucleophilic attack to form the corresponding amide or carbonyl group. 2'-Aminoacetanilide also has the ability to react with nitro compounds to form an amido-nitro adduct.</p>

<p>5-Fluoro-N,N-Dimethyl-1H-Indole-3-Ethanamine is a psychedelic drug with affinity for the serotonin 5HT2A receptor. It has been shown to interact with a diversity of ion channels and transporters. The affinity of 5FEDME for the 5HT2C receptor may also be normalizing. This drug has been shown to be an agonist at the 5HT2A receptor, which may contribute to its psychedelic effects.</p>

<p>Isobutyl 4-aminobenzoate is an anesthetic that has been shown to be effective in epidural anesthesia. It has been evaluated for the prevention of post-epidural pain and found to be chemically similar to lidocaine and bupivacaine. Isobutyl 4-aminobenzoate is also used topically as a nerve block agent.</p>

<p>2-[[(Heptadecafluorooctyl)Sulphonyl]Propylamino]Ethyl Methacrylate is a sulfonate that is used as a crosslinker in various chemical substances. It is also used to connect substances together, such as chemicals. 2-[[(Heptadecafluorooctyl)Sulphonyl]Propylamino]Ethyl Methacrylate has the chemical formula CH2=CFCF2CF(OCH2CH2)SO3H. 2-[[(Heptadecafluorooctyl)Sulphonyl]Propylamino]Ethyl Methacrylate is an oily liquid that is colorless and odorless.</p>

<p>4'-Fluoro-biphenyl-4-methanamine is a fine chemical that is a versatile building block, useful intermediate, and research chemical. It is used as a reaction component in the production of other chemicals. 4'-Fluoro-biphenyl-4-methanamine can be used as an additive in many commercial products. This compound is an important reagent and can be found in high quality research laboratories. CAS No. 776291-03-3</p>

<p>(R)-(+)-1,1-Naphthyl ethylamine is a molecule that belongs to the class of chromatographic compounds. It has a carbonyl group, which is a substrate for amine modifiers and other chemical reactions. (R)-(+)-1,1-Naphthyl ethylamine can be used as a model system for epidermal growth factor (EGF) and chelate rings. The molecule has been shown to have growth factor activity, which may be due to its ability to bind to EGF receptors on cells.</p>

<p>Ammonium iron(II) sulfate hexahydrate is a salt that contains the metal ion ammonium and iron (II). It is used in cancer research as an electron-radiating agent. The drug molecules are encapsulated into the cavity of mesoporous silica nanoparticles by ionizing radiation. This process immobilizes the drug molecule and prevents it from diffusing away from the particle surface. Ammonium iron(II) sulfate hexahydrate has been shown to be effective against estrone and 17β-estradiol, which are types of estrogen.</p>

<p>2-Amino-α,α-dimethylbenzyl alcohol is a reagent that is useful in the synthesis of complex compounds. It is also a fine chemical and can be used as an intermediate for other compounds. 2-Amino-α,α-dimethylbenzyl alcohol has been shown to be reactive and can be used as a speciality chemical. This chemical is used as a reaction component for chemical reactions, such as Heck reactions, Suzuki couplings, and Sonogashira couplings. 2-Amino-α,α-dimethylbenzyl alcohol is versatile and can be used in many different reactions due to its high quality.</p>

<p>4-Amino-2-methoxypyridine is an antiviral agent that inhibits the activity of the NS5B polymerase, a key enzyme in the replication of the hepatitis C virus. It is a potent inhibitor with a wide range of activity and can be used for treatment and prevention of infection. 4-Amino-2-methoxypyridine has been shown to inhibit replication of hepatitis C virus in cell culture. This compound is stable in vivo and can be administered orally, making it an attractive candidate for oral prophylaxis against hepatitis C. 4-Amino-2-methoxypyridine also exhibits good pharmacokinetic properties, including a low clearance rate and high volume of distribution, which makes it suitable for chronic administration.</p>

<p>4-Fluoro-a-methylbenzylamine is a chiral, protonated, and enthalpic compound. It can be synthesized by reacting anilines with 4-fluorobenzaldehyde in the presence of a base such as sodium ethoxide. The flavonoids from the plant Hedera helix have been shown to inhibit this enzyme. <br>4-Fluoro-a-methylbenzylamine has been found to be a potent inhibitor of imidazole amidohydrolase, an enzyme involved in the metabolism of histamine and other biologically active amines. This inhibition prevents the conversion of histamine to imidazole and therefore may help prevent allergic reactions such as asthma.</p>

<p>1-(Aminomethyl)cyclopropanecarboxamide hydrochloride is a versatile building block that can be used in the synthesis of complex compounds. It has been shown to be an excellent reagent for the synthesis of novel pharmaceuticals and speciality chemicals. This compound is also a useful intermediate for the preparation of high-quality products and can be used as a reaction component or scaffold in synthesis.</p>

<p>Aminating Reagent</p>

<p>O-(2-Aminoethyl)-O'-(2-azidoethyl)nonaethylene glycol is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. O-(2-Aminoethyl)-O'-(2-azidoethyl)nonaethylene glycol is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>

<p>Benzo[d]isoxazol-5-amine is a high quality, versatile building block that is used as a reagent for the synthesis of fine chemicals and pharmaceuticals. It can be used to synthesize useful scaffolds for drug discovery and as an intermediate in the synthesis of complex compound. Benzo[d]isoxazol-5-amine is also a reactive intermediate, which can be used in reactions with other building blocks to produce speciality chemicals such as research chemicals. This compound is soluble in water and has been classified by CAS as 239097-74-6.</p>

<p>Please enquire for more information about Sodium 2-(3,3-bis(4-(dimethylamino)phenyl)ureido)acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-5-bromobenzoic acid is a chemical compound that is used to synthesize other pharmaceuticals. It has been shown to have potent antiinflammatory activity and inhibit the growth of certain types of cancer cells. 2-Amino-5-bromobenzoic acid also has antiviral properties, and it inhibits the replication of human immunodeficiency virus type 1 (HIV-1) in cell culture. This drug has been shown to be effective against herpes simplex virus type 1 (HSV-1), varicella zoster virus (VZV), and cytomegalovirus (CMV). 2-Amino-5-bromobenzoic acid is poorly soluble in water; therefore, it can be administered intravenously as a prodrug. The absorption of this drug is dependent on pH levels, with higher concentrations found in acidic environments.</p>

<p>5,6-Diaminouracil sulfate is an amine that is used as a precursor in the production of the anti-cancer drug 5-fluorouracil. It can be synthesized from diaminopyrimidine and uracil. This compound has two amino groups, which are both substituted with hydrogens. The aminouracile group is substituted with a hydrogen and an amino group. 5,6-Diaminouracil sulfate has pyrimidone rings that are fused together to form a six-membered ring.</p>

<p>4-Aminobenzaldehyde is a molecule that belongs to the class of aromatic compounds. It has a crystalline structure and reacts with acylating agents to form amides. 4-Aminobenzaldehyde has been used for the preparation of diazonium salts, which are reactive intermediates in organic synthesis that can be used as a nucleophile. This compound has been shown to react with sodium nitrate to form an electrochemical data, and it has also been used as a control experiment for nmr spectra.</p>

<p>Fmoc-9-aminononanoic acid is a versatile building block that can be used in the synthesis of complex compounds. This compound has been shown to be useful for the production of speciality chemicals and research chemicals, as well as for the preparation of reagents and reaction components. Fmoc-9-aminononanoic acid is also a high quality intermediate with a wide range of applications. It can be used as an electrophile or nucleophile in organic synthesis reactions, or it can be used as a scaffold to prepare more complicated molecules.</p>

<p>Thiamine tetrahydrofurfuryl disulfide is a thiamine derivative that has been shown to serve as a cofactor for enzymes such as peptidyl-prolyl cis-trans isomerase, which catalyzes the formation of peptide hormones. It also plays a role in the synthesis of polymers such as cellulose. Thiamine tetrahydrofurfuryl disulfide can be found in crystalline cellulose and is an important component of two-way crossover studies on peptide hormones. This drug has been shown to stimulate oxidative metabolism in cells and may have therapeutic potential for treating conditions associated with oxidative injury, such as stroke, head trauma, and heart attack. <br>Thiamine tetrahydrofurfuryl disulfide may also have a role in the development of inflammatory responses through its interaction with toll-like receptor 4 (TLR4).</p>

<p>Pyrimethamine is an antimalarial agent that has been used in the treatment of various infectious diseases. Pyrimethamine is a folic acid antagonist which inhibits the synthesis of DNA and RNA by inhibiting the enzyme dihydrofolate reductase. The drug binds to sulfadiazine, a sulfa drug, which prevents its conversion to active form and thereby prevents bacterial growth. Pyrimethamine can be administered orally or intravenously. It exhibits low toxicity and is excreted in the urine as an inactive metabolite. In vitro assays have shown pyrimethamine to be effective against HIV-1 infection, but it is not active against other viruses such as herpes simplex virus and influenza virus.</p>

<p>3-Amino-5-nitrobenzhydrazide is a useful scaffold that can be used as a building block in the synthesis of other chemical compounds. It is a versatile intermediate that has been used in research to synthesize drugs and other chemicals, such as insecticides and herbicides. 3-Amino-5-nitrobenzhydrazide has been shown to be an effective reagent for the synthesis of complex compounds. This chemical has also been found to be an effective reaction component for the synthesis of speciality chemicals. 3-Amino-5-nitrobenzhydrazide is a fine chemical that can be used in many different applications.</p>

<p>4-Amino-3-pyridinecarboxylic acid (4APC) is a histidine amino acid. It is an intermediate in the synthesis of 6-aminonicotinic acid, which is an intermediate in the synthesis of nicotinamide, an important vitamin. 4APC has been used as a chemical probe to elucidate the transfer mechanism of amines to histidine. The active methylene group on 4APC can be easily detected by high-throughput analysis using liquid chromatography with fluorescence detection. The 3-aminoisonicotinic acid product can be detected by nmr spectra and electron microscope imaging. A synthetic route for 4APC involves ammonolysis followed by fluorescence resonance energy transfer.</p>

<p>4-Amino-4H-1,2,4-triazole is a nitrogen heterocycle that has been used in the synthesis of copper complexes. 4-Amino-4H-1,2,4-triazole is synthesized by the reaction of copper chloride and hydrochloric acid with a redox potential of 0.03 V. The synthesis of this compound can be achieved through two different mechanisms: one involving an exothermic reaction with an adsorption mechanism and the other involving a kinetic mechanism. 4-Amino-4H-1,2,4-triazole has been used in FTIR spectroscopy to differentiate between various nitrogen atoms on the basis of their vibrational frequencies.</p>

<p>4-Hydroxy-7-methylamino-2-naphthalenesulfonic acid is used as a diazo dye in the textile industry. This compound is used to produce diazotization and then cyanuric chloride by the reaction of 4-hydroxy-7-methylamino-2-naphthalenesulfonic acid with sodium nitrite and hydrochloric acid. The condensate from this reaction is dissolved in an alkaline solution, which reacts with sodium bicarbonate to produce a reactive physicochemical substance that can be used for dyeing fabrics.</p>

<p>2-[[(Butylamino)carbonyl]oxy]ethyl acrylate is a monomer that is commonly used as a cross-linker in polymer chemistry. It has been shown to have reactive functional groups that can form covalent bonds with other molecules. 2-[[(Butylamino)carbonyl]oxy]ethyl acrylate has been reported to be a reactive functional group that can form covalent bonds with other molecules, such as polymers and proteins. This material is also an effective initiator for free radical polymerization. 2-[[(Butylamino)carbonyl]oxy]ethyl acrylate is synthesized from butyraldehyde and acrylic acid, which are both available by chemical synthesis or fermentation. The material is soluble in organic solvents and reacts readily with water. It may be used as a particle coating for medical applications because it can be crosslinked with radiation or reactive groups such as aromatic hydro</p>

<p>Retigabine is a carbamate that binds to the benzodiazepine binding site of the gamma-aminobutyric acid receptor. It has been shown to have analgesic properties in animal studies, and has also been investigated as a potential treatment for epilepsy. Retigabine may be used in combination with other drugs, such as flumazenil, which can reverse its effects. The structural analog of retigabine is flumazenil, a drug that can reverse the effects of benzodiazepines such as diazepam and midazolam. Retigabine also interacts with other drugs through significant effects on their pharmacokinetics and pharmacodynamics.</p>

4-Amino-2,2,6,6-tetramethylpiperidine-1-oxyl free radical (ATMPO) is a hydroxyl radical that has been used as a diagnostic agent for oxidative injury. ATMPO reacts with the amino groups on proteins to form an adduct and changes their color from red to blue. This reaction can be used to identify the type of oxidative injury and the degree of injury in cells. ATMPO also interacts with integrin receptors on cell surfaces and causes neuronal death. This effect is reversible when ATMPO is removed from the cells. The molecular weight of this compound is 614 g/mol and it has biocompatible properties because of its long ester linkages and fatty acid chains.

<p>N-[(3R)-1-(3,3-Dimethyl-2-oxobutyl)-2,3-dihydro-2-oxo-5-(2-pyridinyl)-1H-1,4-benzodiazepin-3-yl]-N'-[3-(methylamino)phenyl]urea (GZ4081) is a drug that inhibits gastrin secretion by blocking the G protein coupled receptor. It has been shown to be effective in treating cancer and also has an inhibitory effect on tissue samples. GZ4081 has been shown to have long term treatment effects as well as being effective for prognosis. The effective dose of GZ4081 is not yet known but it is believed to be at least 10 times lower than the doses used for other drugs in its class.</p>

<p>Avanafil is a drug that can be used as a treatment for male erectile dysfunction. It works by inhibiting the production of PDE5, which is an enzyme that regulates the levels of cGMP in the penis. Avanafil has been shown to be effective when taken at a dose of 100 mg; this is because it takes about 30 minutes for avanafil to reach its peak level. Avanafil has a chemical stability that is greater than 12 hours, with an average lifespan of 24 hours. The drug also has no major drug interactions and does not inhibit any other drugs from working.</p>

<p>Please enquire for more information about 2-((3-Oxocyclohex-1-enyl)amino)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 4-(4-Ethylphenyl)-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>Please enquire for more information about [1-(Morpholin-4-ylcarbonyl)butyl]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 2,2-dimethyl-5-(((4-phenoxyphenyl)amino)methylene)-1,3-dioxane-4,6-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-3-methoxybenzoic acid methyl ester can be used as a chiral auxiliary in enantioselective synthesis. It is synthesised by reaction of l-valine with methyl iodide, followed by hydrolysis of the resulting ester under basic conditions. 2-Amino-3-methoxybenzoic acid methyl ester is used as a chiral auxiliary for the asymmetric synthesis of d-mannitol and related compounds.</p>

<p>Trimethylamine-N-oxide dihydrate (TMAO) is the anhydrous form of trimethylamine oxide (TMAO). It has a number of applications in industry and research. TMAO is used as a diagnostic agent for metal carbonyls, such as lead and arsenic, and also for hydrogen bond. In addition, it can be used to determine the presence of hydroxyl groups in organic compounds, such as fatty acids. The hydroxyl group reacts with Iodosobenzene to form an iodide ion that can be measured by nmr spectroscopy. This reaction is affected by the presence of other atoms or molecules that have electron donating properties, such as an oxygen atom or a carbonyl group. TMAO can also be used in cancer research to study how tumors develop resistance to chemotherapy drugs.</p>

<p>2-Amino-5-nitro-2'-chlorobenzophenone (2ACCB) is a precursor for the synthesis of 2,4,6-trichlorophenol. 2ACCB reacts with hydrochloric acid in the presence of a scrubber to produce diphenyl ether and activated 2ACCB. The reaction rate can be increased by adding sodium hydroxide solution to the reaction solution. The hydroxy group on the 2ACCB molecule can be converted to a terpene by transfer reactions with glycol esters. This compound has been used as a sterilant and disinfectant in reaction solutions containing chlorine atoms or carbonyl groups.</p>

<p>3-Aminocinnamic acid ethyl ester is a synthetic compound that is derived from pyridine and has a liriodenine ring. The synthesis of this compound starts with an olefinic coupling reaction, which yields an imine intermediate. The imine is hydrolyzed to yield the desired product. 3-Aminocinnamic acid ethyl ester can be found in plants such as liriodenine and liriodendronine, as well as in animal tissues. It also acts as a neurotransmitter and activates the nitrate receptor on nerves, which leads to increased blood pressure or heart rate. 3-Aminocinnamic acid ethyl ester also binds to the cation channel of benzoquinoline drugs and mediates their effects on the central nervous system.</p>

<p>Please enquire for more information about N-(3-Isopropylamino-2-hydroxypropyl) pindolol 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-t-Boc-1-adamantylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Aminoanthraquinone is a fluorescent dye that reacts with amino groups. It can be detected in urine samples using electrochemical impedance spectroscopy and has a detection time of about 2 hours. 1-Aminoanthraquinone is used as a marker for protein synthesis, which occurs when nitrogen atoms react with an inorganic acid to form a diazonium salt. This reaction proceeds via the formation of hydrogen bonds between the nitrogen and oxygen atoms of the diazonium salt and the hydrogen atoms on the amino group. The amine group on 1-aminoanthraquinone will then react with the hydrogen bond to form an intramolecular hydrogen bond. Structural analysis of this molecule shows that it has one benzene ring, two nitrogens, two oxygens, and one carbon atom.</p>

<p>Ceftriaxone is a semisynthetic, broad-spectrum antibiotic that is used to treat bacterial infections. It is especially effective against the following microorganisms: Gram-positive cocci and rods, Gram-positive bacilli, Gram-negative cocci and rods, and anaerobic bacteria. Ceftriaxone is a crystalline solid that can be dissolved in water or an organic solvent. It has been shown to have excellent stability in acidic solutions and at high temperatures. Ceftriaxone has a residue of 3% when it is administered intravenously or intramuscularly. The use of ceftriaxone as an antibiotic can be optimized by using reverse-phase chromatography with a cyclic gradient elution method.</p>

<p>Please enquire for more information about 4-(3,4-Dimethoxyphenyl)-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>3-Amino-3-methylbutanoic acid is a carbonaceous compound that can be synthesized from b-alanine and perchloroethylene. It is used in the manufacture of butanoic acid, which is an important industrial chemical. 3-Amino-3-methylbutanoic acid has been shown to exist as four isomers, each with a different molecular weight. The isomers are produced by a synthetic process involving the reaction of b-alanine and perchloroethylene. In an amination reaction, the compounds are heated in the presence of ammonia gas or ammonium chloride to form 3-amino-3-methylbutanoic acid.</p>

<p>N,N-Dimethyl-(tetrahydro-3,3 diphenyl-2-furilidine)ammonium bromide is a synthetic opioid analgesic and is used in the treatment of severe pain. It has been shown to cause life-threatening cardiac effects, supratherapeutic concentrations, or fatalities in humans and animals. N,N-Dimethyl-(tetrahydro-3,3 diphenyl-2-furilidine)ammonium bromide has also been shown to cause gastrointestinal inflammation in animal models. This drug acts as an agonist at opioid receptors and can be fatal at high doses.</p>

<p>(R)-Amino carnitine is a pancreatic enzyme that is used as an experimental treatment for fatty liver disease. It has been shown to inhibit the synthesis of fatty acids, which are the main components of triglycerides. The inhibition of this enzyme leads to a decrease in the production of triglycerides and their accumulation in the liver, thereby reducing hepatic steatosis. (R)-Amino carnitine also has an inhibitory effect on protein synthesis, which is important for the conversion of amino acids into proteins essential for cell division and growth. This mechanism may explain its beneficial effects on insulin resistance, obesity, and diabetes.</p>

<p>4-Cyano-4'-aminobiphenyl is a fluorescent dye that exhibits a strong fluorescence under UV irradiation. The dye has an absorption maximum at about 335 nm and a fluorescence emission maximum at about 455 nm, with excitation maxima of 333 nm and 478 nm. It has been used in the development of photocurrent devices, which are used for photochemical reactions and electrochemistry studies. This compound can also be used for the determination of amino groups in organic molecules such as carbostyril. The compound can be synthesized by reacting an amine with an aldehyde in the presence of acid.</p>

<p>This compound is a benzamide derivative that is oxidized by nature. It has been shown to undergo ring-opening in the presence of reducing agents, such as sodium borohydride, and yields 2-amino-4-chlorobenzaldehyde. This reaction system uses an efficient catalyst such as manganese dioxide to help speed up the rate of this reaction. The product of this reaction is then converted into a variety of isatins depending on the conditions used.</p>

<p>Please enquire for more information about (2-Chlorophenyl)(4-(3-nitrophenyl)(2,5-thiazolyl))amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Methyldibutylamine is an aliphatic hydrocarbon that has antimicrobial activity. It is a colorless liquid at room temperature and has a boiling point of 78°C. N-Methyldibutylamine can be used as a solvent for polymers and resins, in the manufacture of plastics, and in the production of enamels. It also has potential applications in cancer research due to its ability to inhibit the growth of tumor cells.</p>

<p>Deferoxamine mesylate is an iron chelator that is used in the treatment of iron overload and to treat patients with chronic renal failure. Deferoxamine mesylate has been shown to inhibit angiogenesis by inhibiting the basic protein required for this process. It is also known to have a protective effect on myocardial cells, preventing cell death due to lack of oxygen (reactive oxygen species). Deferoxamine mesylate also inhibits neuronal death in a model system.<br>Deferoxamine mesylate binds to DNA and inhibits RNA synthesis, which has led to its use as a fluorescence probe for the detection of DNA binding activity. The drug has also been shown to act as a metal chelate, binding with metals such as iron, copper, and zinc.</p>

<p>Butaphosphan is a drug that has been shown to have clinical relevance for the treatment of metabolic disorders. It is a prodrug that is converted into butaprost-diol, which has been shown to improve insulin sensitivity and reduce aminotransferase activity in rats. Butaphosphan can be used as an alternative to aminotransferase inhibitors such as ursodeoxycholic acid and cholestyramine for the treatment of patients with primary biliary cirrhosis. This drug has also been shown to have a protective effect on fatty acid metabolism, which may be due to its ability to inhibit the activity of enzymes involved in fatty acid synthesis. Butaphosphan is metabolized by cytochrome P450 enzymes and hydroxylases and can be detected using LC-MS/MS methods. The drug has also been shown to have beneficial effects on cortisol concentrations and liver histology when administered orally.</p>

<p>Rac-trans-3-amino-1-oxyl-2,2,5,5-tetramethylpyrrolidine 4-carboxylic acid (rac TAT) is an axial chiral compound. It has a molecular weight of 246.36 and the empirical formula C11H19N3O4. Rac TAT is soluble in water and alcohols. Rac TAT crystallizes as a racemic mixture of enantiomers (Rac=50% + 50%). Rac TAT has been used as a probe for cyclic secondary amines with high resolution. Rac TAT also shows high selectivity for β-amino acids over α-amino acids. The configuration of the molecule is determined by the configuration of the biphenyl substituents at C4 and C5. Rac TAT can be synthesized from racemic trans 3 amino 1 oxyl 2 2 5 5 tetramethyl pyrrolidin 4</p>

<p>R-a-Lipoic acid tromethamine salt is a reaction component and reagent that is used in the synthesis of high quality chemical products. The compound has many applications, including being a useful scaffold for the synthesis of complex compounds. R-a-Lipoic acid tromethamine salt can be used as a versatile building block or as a fine chemical. This compound is also listed under CAS No. 14358-90-8, which makes it an excellent choice for research chemicals and speciality chemicals.</p>

<p>5-Amino-1H-tetrazole is a pharmaceutical preparation that is used in the treatment of bacterial infections. It has been shown to inhibit the growth of bacteria by binding to the cell wall and disrupting its integrity. This drug is chemically stable in aqueous solution and can be administered orally or intravenously. 5-Amino-1H-tetrazole has shown antimicrobial activity against gram-positive bacteria such as staphylococci, Streptococcus pneumoniae, and Enterococcus faecalis, but not gram-negative bacteria such as Pseudomonas aeruginosa. 5-Amino-1H-tetrazole also displays broad spectrum activity against fungi and yeast in vitro. This drug binds to the nitrogen atom of the hydroxyl group and forms an intermediate with hydrogen bond formation. The chemical structures of this drug are:<br>N+2N=O<br>N+OH=O<br>O</p>

<p>m-Phenylenediamine is a model system for studying the adsorption mechanism of dyes, pigments, and other organic molecules on solid surfaces. It has been shown to be capable of adsorbing at high concentrations on various materials such as calcium carbonate, sandstone, and kaolinite. The adsorption of m-phenylenediamine is influenced by the thermal expansion coefficient of the surface material. Adsorption is also influenced by the pH of the solution, with optimum concentrations occurring at acidic pH levels. Adsorbed m-phenylenediamine may be transported away from the surface in both water and wastewater treatment systems. Inorganic acids can cause significant degradation to adsorbed m-phenylenediamine due to their ability to hydrolyze hydrogen bonds between adsorbate molecules.<br>A number of electrochemical impedance spectroscopy studies have been performed on this molecule in order to better understand its transport properties and electron transfer mechanisms.</p>

<p>Ractopamine HCl - 95% is a preparation of the drug Ractopamine, which is used as an animal feed additive to promote muscle growth. The drug is commonly used in pigs, cattle, and turkeys. It binds to the beta-adrenergic receptor and stimulates the release of catecholamines from the adrenal gland. This stimulation leads to an increase in protein synthesis and muscle growth. Ractopamine HCl - 95% can be analyzed by flow assay for antimicrobial resistance, sample preparation, estradiol benzoate, sodium carbonate, camp levels, ractopamine detection sensitivity and electrochemical detector. The matrix effect can be controlled by analyzing acid complex or control analysis with electrochemical impedance spectroscopy.</p>

<p>The compound is a chiral molecule, meaning that it has two different structures. One side of the molecule is the mirror image of the other. The translation and conformation of this molecule are asymmetric because the carbon atoms in its chain are not lined up in a straight line. The hydrogen bonds that form between these chains are also asymmetric, as one side of the molecule has more than one hydrogen bond while the other side only has one hydrogen bond.</p>

<p>5-Methylpyridin-2-yl)methanamine is a high quality reagent that is used as a building block in the synthesis of complex compounds. It can be used as an intermediate, useful for the preparation of fine chemicals and useful scaffolds. It can also be used as a speciality chemical and is often used as a reaction component in research chemicals.</p>

<p>4-(Acetylamino)-3-nitrobenzoic acid (AANBA) is a molecule that inhibits the growth of Mycobacterium tuberculosis and influenza virus. It has been shown to have tuberculostatic activity and is able to adsorb to the cavity of the enzyme protein, preventing access by other molecules. AANBA also has antiviral properties that may be due to its ability to inhibit viral particles from binding with a cell surface receptor or inhibiting the synthesis of viral proteins. AANBA binds to the chloride ion in order to maintain the negative charge of the molecule, which is crucial for its antiviral activity.</p>

<p>2-Hydroxy-4-aminobutanoic acid is a synthetic compound that has been shown to be a potent antibacterial agent. It is active against both Gram-positive and Gram-negative bacteria, including Pseudomonas aeruginosa, Enterococcus faecalis, Staphylococcus aureus, and Escherichia coli. 2-Hydroxy-4-aminobutanoic acid is also an indole alkaloid that can be produced from the amino acid tryptophan by the enzyme pyridoxal phosphate. This prebiotic is found in tissues of many animals and humans. 2-Hydroxy-4-aminobutanoic acid has been shown to have antiinflammatory properties in human serum.</p>

<p>Please enquire for more information about Methyl 3-aminothieno[2,3-β]pyridine-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Methylpyrazin-2-amine is an experimental compound that has not been fully characterized. It is a bioactive substance that can be used for the synthesis of other compounds. 3-Methylpyrazin-2-amine may be obtained from the reaction of 2,3-dimethylpyridine with nitroethane and sodium methoxide in methanol. The transformation of 3,4,5-trimethoxypyrazine to 3,4,5,6-tetramethoxypyrazine may also yield 3-methylpyrazin-2-amine as an intermediate product.</p>

<p>Aromatase inhibitor; anti-neoplastic</p>

<p>4-Aminophenylacetonitrile is a molecule that is structurally similar to nitrobenzene. 4-Aminophenylacetonitrile has been shown to be an efficient method for inhibiting faecalis growth and secretory phospholipase A2 (sPLA2) activity in vitro. It also inhibits the population growth of E. coli in vivo, which can be attributed to its ability to inhibit the enzyme catalysed by hydrogen bond formation.</p>

<p>2-Amino-4-chlorobenzamide is a chemical compound that has been shown to be an effective oxidant in biological systems. It is an oxidative condensation product of 4-chloro-2-nitrobenzoic acid and ammonium chloride, which is formed by the reaction of these two compounds at room temperature. The nature of the functional group on 2-amino-4-chlorobenzamide allows it to be used as a transition state analogue for the study of reactions involving amines and nitrates. This compound can also be used in experiments with isatins, due to its ability to react with ammonia hydroxide to form 2-amino-4,6 dichlorobenzamide.</p>

<p>Methyl 5-(aminomethyl)-2-furoate hydrochloride is a chemical compound that is used as a building block in organic synthesis. It is an aminomethyl derivative of 2-furoic acid and can be used as a versatile intermediate. The compound has been shown to react with alkyl halides, alcohols, and thiols, among other compounds. Methyl 5-(aminomethyl)-2-furoate hydrochloride is also known for its high purity and quality.</p>

<p>1,2'-Dinaphthylamine is a β-lactam antibiotic that can be used as a substitute for ciprofloxacin. It inhibits the production of an enzyme called β-lactamase, which breaks down the antibiotic and makes it ineffective. 1,2'-Dinaphthylamine has been shown to be active against aerogenes and nitrocefin. This drug binds to periplasmic proteins in bacteria by means of an analogy with ciprofloxacin. The conjugates are resistant to efflux pumps and use of efflux inhibitors such as bafilomycin A1 can increase their efficacy.</p>

<p>2N-Boc-2',2''-triaminotriethylamine-bis(chloroacetamide) is a fine chemical and reagent for the synthesis of pharmaceuticals. It is also a useful building block for the synthesis of complex compounds. This product can be used as a reaction component in organic chemistry, or it can be used as a reagent in research or development laboratories.</p>

<p>2-(1H-Benzimidazol-1-yl)ethyl]amine dihydrochloride is a lead compound that has been shown to have antibacterial activity. It is a potent inhibitor of bacterial ribonucleotide reductase and thus inhibits DNA synthesis. The homology model of the enzyme shows that the chemical could bind to the active site and inhibit the production of ATP, preventing cell division. 2-(1H-Benzimidazol-1-yl)ethyl]amine dihydrochloride has been shown to have an effect on Clostridium and Bacillus anthracis, with MIC values of 1.0 µg/mL and 0.5 µg/mL respectively. This chemical also has potential for use as a drug in humans due to its lack of toxicity in mice at high doses (LD50 = 5 g/kg).</p>

<p>3-Acetylbenzylamine hydrochloride is a versatile building block that can be used as a reagent, speciality chemical, and useful scaffold. It is a complex compound with CAS No. 149889-64-5 that has been shown to have fine chemical characteristics. 3-Acetylbenzylamine hydrochloride is also a high quality research chemical that has been shown to be useful in the synthesis of various products, such as pharmaceuticals and organic compounds. 3-Acetylbenzylamine hydrochloride can be used as an intermediate for reactions in the production of fine chemicals, such as pharmaceuticals or organic compounds.</p>

<p>(R)-(+)-2,2'-Diamino-1,1'-binaphthalene is a diammonium salt that is synthesized from fatty acids. This molecule is used in the detection of cancer cells in tissue samples. (R)-(+)-2,2'-Diamino-1,1'-binaphthalene has been shown to be an effective agent against cancer cells and can be used as a diagnostic tool for tissues with cancer cells. The mechanism of action of (R)-(+)-2,2'-Diamino-1,1'-binaphthalene is not yet clear; however it may involve intramolecular hydrogen transfer reactions or coordination chemistry.</p>

<p>Adamantane is a small molecule that can be used in diagnosis. It is a potent inhibitor of serine proteases and has been used as a model for the study of these enzymes. Adamantane binds to the active site of serine proteases, forming an intramolecular hydrogen bond with the catalytic serine residue. Adamantane inhibits in vitro the activity of pepsin, chymotrypsin, and trypsin. The inhibition of chymotrypsin by adamantane has been shown to be selective over other serine proteases. Adamantane can also inhibit lysosomal phospholipase A2 (LP-PLA2) activity, which may lead to diagnostic applications for neurodegenerative diseases such as Alzheimer's disease or Parkinson's disease.</p>