Amines

<p>Applications (2S,3R,4E)-3-Benzoyl-2-tert-butyloxycarbonylamino-4-octadecen-1,3-diol (cas# 299172-59-1) is a compound useful in organic synthesis.<br>References Kinjo, Y., et al.: Chem. Biol., 15, 654 (2008),<br></p>

<p>Applications: 2-Amino-7,8-dihydro-7,7-dimethyl-4-propyl-5(6H)quinazolinone (cas# 331966-05-3) is a compound useful in organic synthesis.<br></p>

<p>Applications 2-(2-Benzyloxyphenoxy)ethylamine (cas# 72955-81-8) is a compound useful in organic synthesis.<br></p>

<p>Applications 2-(3-Aminopropylamino)ethanol is the hydroxy analogue of WR-1065 (A576820), a metabolite of Amifostine (A576810). Amifostine is an organic thiophosphate that has the ability to protect a broad range of tissues from cytotoxicity (e.g. from chemotherapeutic agents) without inducing an antitumour response. 2-(3-Aminopropylamino)ethanol is also used as an nucleophilic tag in the detection of human butyrylcholinesterase adducts.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Antonadou, D., et al.: Int. J. Rad. Oncol. Biol. Phys., 52, 739 (2002); Kemp, G., et al.: J. Clin. Oncol., 14, 2101 (1996)<br></p>

<p>Applications (±)-trans-1,2-Diaminocyclohexane is a reagent used in the thyroid receptor agonists for treatment of androgenetic alopecia.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Li, J. J., et al.: Bioorg. Med. Chem. Lett., 20, 306 (2010)<br></p>

<p>Applications pentan-2-amine hydrochloride (cas# 76716-21-7) is a useful research chemical.<br></p>

<p>Applications (1S,3R,4S)-Ethyl 4-Amino-3-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate Oxalate has been used as a reactant for the preparation of oxadiazole compounds containing cyclohexanediamine moiety.<br></p>

<p>Applications Used in the preparation of (R)-Sulforaphane (S699105).<br></p>

<p>Applications 17-Amino-10-oxo-3,6,12,15-tetraoxa-9-azaheptadecanoic Acid is used for preparation of glutamic acid-containing acylating reagents for selective acylation of amino group(s) in peptides or proteins.<br>References Christensen, C., et al.: PCT Int. Appl. (2010), WO 2010084169 A2 20100729.<br></p>

<p>Stability Temperature Sensitive<br>Applications A reagent which releases Nitric Oxide into aqueous solutions at controlled rates for in vitro studies.<br></p>

<p>Applications Ethyl 3-Aminocrotonate is used as a reagent to synthesize Nitrendipine (N490150), a calcium channel antagonist that is used to treat patients with hypertension. Ethyl 3-Aminocrotonate is also used as a reagent to synthesize (S)-Felodipine (F232370), a calcium entry blocker that has antihypertensive properties.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Bailey, D., et al.: Clin. Invest. Med., 12, 357 (1989); Bean, B.: Proc. Nat. Acad. Sci., 81, 6388 (1984); Kwon, K., et al.: Tetrahedron, 67, 10222 (2011); Leenen, F. &amp; Holiwell, D.: Am. J. Cardio., 69, 639 (1992); Meyer, H., et al.: Arz. Forsch., 33, 1528 (1983); Stoepel, K., et al.: Arz. Forsch., 31, 2056 (1980)<br></p>

<p>Applications ethyl 2-(methylamino)-2-oxoacetate (cas# 18522-95-7) is a useful research chemical.<br></p>

<p>Applications Lonidamine<br></p>

<p>Applications N1-(3,4-Dichlorophenyl)-1,3-propanediamine is a compound being used in the synthesis of novel amide-based biaryl complexes which can act as allosteric binding site antagonists of NR1A/NR2B NMDA receptors.<br>References Mosley, C.A., et al.: Bioorg. Med. Chem. Lett., 17, 6463-6480 (2009)<br></p>

<p>Applications 2-Aminobenzylcyanide is a useful reagent for organic synthesis and other chemical processes. It is used in the synthesis of triazolopyridines as a selective JAK1 inhibitors.<br>References Menet, C. J., et al.: J. Med. Chem., 57, 9323 (2014)<br></p>

<p>Applications N-[[4-(Phenylmethoxy)phenyl]methyl]-2-[(3-thienylcarbonyl)amino]-4-thiazoleacetamide is derived from ethyl 2-amino-4-thiaxolacetate (E899330) which is used in the synthesis of various pharmaceutical and biologically active compounds including inhibitors and antibiotics.<br>References Inamoto, Y., et al.: J. Antibiot., 41, 828 (1988)<br></p>

<p>Applications Dimethylamine (40% aq.) is a compound often used in industry as a precursor to Nitrosodimethylamine (N525625), a potent carcinogen that is produced during disinfection of wastewater effluent, and is also present in trace amounts in food and polluted air. Dimethylamine is also present in human urine and can be indicative of certain disorders.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Gereke, A. &amp; Sedlak, D.: Env. Sci. Tech., 37, 1331 (2003); Mitch, W., et al.: Env. Eng. Sci., 20, 389 (2003); Tsikas, D., et al.: J. Chromatogr. B, 851, 229 (2007)<br></p>

<p>Applications 2-amino-2-cyclopropylpropan-1-ol (cas# 1184403-67-5) is a useful research chemical.<br></p>

<p>Applications 5-Aminopentanenitrile Hydrochloride is a useful research chemical.<br></p>

<p>Applications 3-Amino-2-hydroxybenzonitrile<br></p>

<p>Applications 3-[(2-Hydroxyethyl)Amino]Propanoic Acid (cas# 5458-99-1) is a useful research chemical.<br></p>

<p>Applications 2-(methylamino)octanoic acid (cas# 101080-67-5) is a useful research chemical.<br></p>

<p>Impurity Vildagliptin Impurity<br>Applications 1-Amino-3-nitroadamantane has potential application in co-catalyst for transition metal reactions and maybe a useful intermediate for the synthesis of Vildagliptin (V305000), an antidiabetic drug that inhibits dipeptidyl peptidase 4 (DPP-4). Vildagliptin exhibits antioxidant properties and may be an apoptotic compound against pancreatic cancer cells.<br>References Amritha, C., et al.: JCDR 9, FC14 (2015); Ahren, B., et al.: J. Clin. Endocrinol. Metab., 89, 2078 (2004), Ahren, B., et al.: Diabetes Care, 27, 2874 (2004), Barlocco, D., et al.: Curr. Opin. Invest. Drugs, 5, 1094 (2004)<br></p>

<p>Applications Z-3-(Tributylstannyl)-2-propen-1-amine (cas# 146829-37-0) is a compound useful in organic synthesis.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>Applications Ammonium Hydroxide is in numerous household cleaning agents.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Lokshin, E.P., et al.: Russ. J. App. Chem., 86, 450 (2013); Alghamdi, A.A., et al.: J. Material. Chem. A. Mater. Energy. Sustain., 1, 5165 (2013);<br></p>

<p>Stability Light Sensitive<br>Applications (E,E)-5-[4-(Diethylamino)phenyl]penta-2,4-dienal is used in polymerization process.<br>References Innocenzi, P., et al.: J. Mater Chem., 15, 3821 (2005), Cai, Y., et al.: Polymer, 2006, 47, 6560 (2006),<br></p>

<p>Applications 3-(N,N-Dimethylamino)phenylboronic Acid (cas# 178752-79-9) is a compound useful in organic synthesis.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>Applications N-[3-(4-Aminophenyl)propyl]-N,N-dimethylamine<br></p>

<p>Applications A compound used in anti-corrosive coating material for the prevention of corrosion in metals.<br>References Weng, C. et al.: Chem. Mat., 22, 2075 (2011);<br></p>

<p>Applications [4-[3-[[(Methylamino)methylene]amino]phenyl]-2-thiazolyl] Guanidine is a guanidino heterocyclic phenylamidines with pharmaceutical properties.<br>References Bietti, G., et al.: Eur. Pat. Appl. (1983), EP 89730 A2 19830928<br></p>

<p>Applications Tetrabutylammonium Azide (cas# 993-22-6) is a useful research chemical.<br></p>

<p>Applications Ammonium Carbonate Carbamate is used in the study of amino acids and has important implications in biochemical studies.<br>References Nanping, W. et al.: J. Phys. Chem., 99, 359 (1995);<br></p>

<p>Applications Ethyl 5-amino-1-benzofuran-2-carboxylate is used as an synthetic intermediate in the preparation of indolebutylpiperazines, a class of dual 5-HT1A receptor agonists and serotonin reuptake inhibitors. Ethyl 5-amino-1-benzofuran-2-carboxylate was also used as a potential radiolabelled analog for melanoma imaging and targeted radiotherapy.<br>References Chezal, J.M., et al.: J. Medn. Chem., 51, 3133 (2008); Heinrich, T., et al.: J. Medn. Chem., 47, 4684 (2004);<br></p>

<p>Applications Tetramethylammonium Tetrafluoroborate (cas# 661-36-9) is a useful research chemical.<br></p>

<p>Impurity Potassium Clavulanate EP Impurity K<br>Applications tert-Octylamine (Potassium Clavulanate EP Impurity K) is used in the synthesis of aminomethyltetracycline dericatives as novel antibacterial agents. Also used in the preparation of carbonyl or sulfonylpyrrolidine containing uracil derivatives which have potent effect in the inhibitoon of deoxyuridine triphosphatase inhibitors.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Clark, R. et al.: J. Med. Chem., 56, 8112 (2013); Miyakoshi, H. et al.: J. Med. Chem., 55, 2960 (2012);<br></p>

<p>Stability Volatile<br>Applications 2-Furfurylamine is used in the synthesis of 2-Amino-N-(2-furylmethyl)propanamide, as a novel alanylglycine equivalent synthesized by bacilysin synthetase.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Mah, R., et al.: Appl. Microbiol., 15, 866 (1967), Faber, K., et al.: Pure Appl. Chem., 69, 1613 (1997), Marahiel, M., et al.: Chem. Biol. 4, 561 (1997),<br></p>

<p>Applications Ethyl 4-[[(methylphenylamino)methylene]amino]benzoate<br></p>

<p>Ammonium benzenesulfonate is a glycol ester that belongs to the class of ammonium salts. It is used as a synergist for the synthesis of sodium salts, which are used in analytical methods. Ammonium benzenesulfonate has been shown to have an effect on autoimmune diseases by inhibiting the production of inflammatory cytokines, such as TNF-α and IL-6, in human serum. This compound also has been shown to have a synergistic effect when combined with monoethyl ethers and sodium salts. The mechanism of this reaction is not well understood but it may be due to intramolecular hydrogen transfer or air entrainment.</p>

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

<p>Tetrahydropyran-3-ylamine is a potent and selective inhibitor of dipeptidyl peptidase IV (DPP-IV), an enzyme that plays an important role in the metabolism of proteins. Tetrahydropyran-3-ylamine is used for the treatment of type 2 diabetes and other metabolic disorders. This compound has been shown to inhibit DPP-IV activity in human plasma and in vitro, with IC50 values of 0.6 μM and 0.2 μM respectively. Tetrahydropyran-3-ylamine also inhibits the production of amyloid β peptides, which are associated with Alzheimer's disease. Tetrahydropyran-3-ylamine is orally active and stable at acidic pH levels, making it suitable for oral administration. It has a high degree of crystallinity, with the crystalline substance being thermally stable up to 200°C. Tetrahydropyr</p>

<p>Please enquire for more information about tert-Butyl 3-(cyclopropylamino)azetidine-1-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(1,3-Benzodioxol-5-yl)ethanamine is a psychostimulant drug that is structurally related to amphetamine. It has been shown to increase the hatchability of eggs and also to have supersensitivity effects on embryos. The hatchability was increased by pretreatment with 1-(1,3-benzodioxol-5-yl)ethanamine before being incubated with d-amphetamine. The supersensitivity effects were demonstrated by experiments in which the hatchability of eggs was enhanced when they were incubated with various concentrations of this drug. 1-(1,3-Benzodioxol-5-yl)ethanamine has not been shown to have any effect on motility or vocalization in organisms.</p>

<p>5-[3-Methoxy-4-(4-methoxy-benzyloxy)-benzyl]-pyrimidine-2,4-diamine is a monoclonal antibody that blocks the signal of CTLA-4, a receptor on T cells. It has been shown to be effective in inhibiting skin cancer and primary breast cancers. This drug also has immunomodulatory effects and can be used to treat autoimmune diseases. 5-[3-Methoxy-4-(4-methoxy-benzyloxy)-benzyl]-pyrimidine-2,4-diamine binds to ctla-4 with high affinity and specificity, preventing the interaction of ctla-4 with its ligands such as CD80 (B7.1) and CD86 (B7.2). This prevents the activation of T cells by antigen presenting cells and suppresses the immune response.</p>

<p>Fmoc-trans-4-(aminomethyl)cyclohexane-1-carboxylic acid is a synthetic amino acid that has been shown in vitro to inhibit the growth of prostate cancer cells. It is an analog of butyric acid, a naturally occurring fatty acid. Fmoc-trans-4-(aminomethyl)cyclohexane-1-carboxylic acid has been synthesized by solid phase methods and labeled with radiotracers such as indium 111 or technetium 99m. The use of Fmoc-trans-4-(aminomethyl)cyclohexane-1-carboxylic acid in vivo is limited by its short circulating half life, rapid metabolism, and high toxicity.</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>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>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>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>3,4-Methylenedioxy amphetamine hydrochloride is an enantiomer of methylenedioxyamphetamine. It is a synthetic molecule that has been used as a drug and chemical intermediate. 3,4-MDA has not been detected in any natural products. 3,4-MDA is not soluble in water but is soluble in most organic solvents and oils. 3,4-MDA can be made into a non-polymeric form by adding acid to the molecule. The impurities are typically related to the solvent used during synthesis and include unreacted starting materials, side products from chemical reactions, and traces of other chemicals such as acetyl derivatives or polymers. 3,4-MDA can be assayed using high performance liquid chromatography (HPLC) with fluorescent detection; however, due to the impurities present in this substance it may be difficult to obtain a reliable result. There are two polymorphs for 3,4-MDA:</p>

<p>2-(Benzyloxy)-1-ethanamine is a radionuclide that has been shown to have potent antitumor activity. It is an imidazopyridine that binds to the 5-HT2C receptor and blocks serotonin from binding to it. This leads to an increase in dopamine levels, which is associated with the therapeutic effects of this drug. The 2-(Benzyloxy)-1-ethanamine molecule has two isomers, with different pharmacological properties: 2-(benzyloxy)ethylamine and 2-(benzyloxy)propylamine. Both molecules are ligands that bind to metal ions and can be used as pharmaceutical formulations. They are also used as modifiers in drug molecules.</p>

<p>Methyl aminomethanimidothioate hydroiodide (MAI) is a nitro-substituted methylated analogue of the natural amino acid methionine. It has been shown to inhibit creatine kinase, which is an enzyme that regulates the conversion of energy from ATP to creatinine. MAI also inhibits adenosine receptors and can be used as an anti-inflammatory agent. It has been shown to suppress inflammatory diseases, such as arthritis and cancer, by inhibiting the production of inflammatory cytokines. MAI has been shown to be effective against viruses such as HIV and herpes simplex virus type 1 (HSV-1).</p>

<p>4-(Aminomethyl)benzoate hydrochloride is a peroxidase-like enzyme that has been shown to inhibit cancer cell proliferation in vitro and in vivo. This enzyme inhibits HDACs, which are enzymes that regulate the expression of genes by removing acetyl groups from histones. 4-(Aminomethyl)benzoate hydrochloride has been shown to have anti-cancer properties and may be used for the prevention and treatment of colon cancer. 4-(Aminomethyl)benzoate hydrochloride also has anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis.</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>Please enquire for more information about N-alpha-Boc-Ngamma-Azido-L-2,4-diaminobutyric acid cyclohexylamine salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(4-Aminophenyl)boronic acid pinacol ester is a semiconducting material that can be used in thin film devices. It has been shown to be a good candidate for transistor and device applications due to its high yield, low cost, and high stability. This compound can also be used to modify the structure of other compounds through substitution reactions. (4-Aminophenyl)boronic acid pinacol ester has been synthesized from inexpensive starting materials, such as triphenylamine and amines.</p>

<p>Please enquire for more information about 3-(4'-Methoxy-3'-sulfonamidophenyl)-2-propylamine, hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Amino-3-bromoisoquinoline is an isocyanide that reacts with nucleophilic heteroatoms such as the amino group. It also reacts with bromine to form a bromopyridine. The nitrile group of 4-amino-3-bromoisoquinoline can be reduced with sodium borohydride to produce 4-aminoquinoline. This compound has shown potential for use in chemotherapy and treating bacterial infections.</p>

<p>N-Methylphenethylamine (NMPEA) is a chemical substance that is found in many natural compounds. It can be synthesized by reacting phenethylamine with trifluoroacetic acid and reacts with ionization sources to produce ions detectable in mass spectrometry. NMPEA has been detected in human urine samples and has been shown to have significant interactions with the hepg2 cell line. The uptake of NMPEA into cells is facilitated by amines, which are abundant in heart tissue.</p>

<p>Triethanolamine hydrochloride, widely known as TEA-HCl, is a buffer used in biochemistry to maintain a stable pH in the range of 7.3 to 8.3 during processes like protein extraction and purification. They are also used in enzyme assays.</p>

<p>N-Methyl-5H-dibenzo[a,d]cycloheptene-5-propylamine hydrochloride (NMBPD) is a drug with anti-inflammatory properties that belongs to the class of tricyclic antidepressants. It has been shown to have synergistic effects with synthetic matrix in vitro. This drug also has receptor activity and can be used to treat infectious diseases such as HIV and tuberculosis. NMBPD is excreted in the urine, which can lead to kidney fibrosis. The drug is metabolized by α1-acid glycoprotein, which may be related to its potential adverse effects on the liver and kidneys. The analytical method for quantification of NMBPD includes gas chromatography with mass spectrometry detection (GC/MS).</p>

<p>O,O'-Bis(3-aminopropyl)polyethylene glycol is a PEG polymer categorised as homobifunctional PEG (X-PEG X). Used as a linker, O,O'-bis(3-aminopropyl)polyethylene glycol is used to attached PEG to proteins, peptides, oligonucleotides, nanoparticles and small molecules via pegylation, a bioconjugation technique.</p>

<p>3-Pyridazinemethanamine is an amide that binds to the vasopressin V2 receptor. It is a selective agonist of the vasopressin V2 receptor and has a high affinity for this receptor. 3-Pyridazinemethanamine has been shown to be a functional antagonist at the vasopressin V1A receptors, which may be due to its chemical structure. 3-Pyridazinemethanamine is not metabolized by cytochrome P450 and does not inhibit other cytochrome P450 enzymes, making it an attractive drug candidate for use in humans.</p>

<p>Please enquire for more information about tert-Butyl 4-(aminomethyl)-4-methylpiperidine-1-carboxylate 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>N-(2-Aminoethyl)piperazine (NAPE) is a chemical compound that can be used as an environmentally friendly catalyst for the degradation of ethylene diamine and other amines. NAPE has been shown to be stable under alkaline conditions, and its fluorescence probe has been used to monitor the progress of the reaction. This compound is a coordination complex with nitrogen atoms at the corners of a square and two amines at opposite corners of the square. The amine groups are coordinated to metal ions in a geometry that is determined by the atomic number of the metal ion. Disulfide bonds form between two cysteine residues on adjacent chains. Glycol ethers can also form disulfide bonds with NAPE, forming glycol ether-NAPE complexes. Antibodies have been shown to bind to glycol ether-NAPE complexes, suggesting that these complexes may play a role in antibody response, although experimental solubility data have not yet confirmed this</p>

<p>Please enquire for more information about tert-Butyl 6-(aminomethyl)-1,4-oxazepane-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 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>Please enquire for more information about Fmoc-S-trityl-D-penicillamine 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-(Dimethylaminocarbonyl)ethylboronic acid, pinacol ester 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-(N-Boc-aminomethyl)azetidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(4-(Aminomethyl)phenyl)pyridin-1-ium chloride is a chemical compound that belongs to the class of pyridines and has pinpoint as its molecular weight. It is an ionic liquid that can be used in analytical methods, such as liquid chromatography and ionization techniques, for the identification of unsaturated fatty acids. This compound can be analyzed by gas chromatography with either electron capture detection or chemical ionization. The GC separation column used for this analysis would have to be a phase column with an unsaturated fatty acid stationary phase. GC-EID and GC-CI are two common ionization techniques that could be used in conjunction with this analytical method. The lower limit of detection for this technique is about 0.1 ppm, which makes it a sensitive analytical tool for use in food production and quality control laboratories. The yield of 1-(4-(Aminomethyl)phenyl)pyridin-1-</p>

<p>1-Amino-2,4-imidazolidinedione-13C3 is an antibiotic that belongs to the group of nitrofurans. It is used for the treatment of infections caused by bacteria that are resistant to other antibiotics. The LC-MS/MS analysis showed that 1-aminohydantoin was formed as a degradation product of chloramphenicol and that this metabolite had been detected in urine samples from patients treated with chloramphenicol. Nitrofuran is also a possible degradation product. A reaction monitoring experiment using ionization monitoring and monitoring on the precursor ion at m/z 287 confirmed the presence of 1-aminohydantoin in a sample containing both chloramphenicol and nitrofuran. Quantification was performed using calibration curves obtained from pure standards.</p>

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<p>Please enquire for more information about [(1-Benzyl-1H-pyrazol-4-yl)methyl]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 2,3-Dihydro-1-(3-hydroxypropyl)-5-[(2R)-2-[[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl]amino]propyl]-1H-indole-7-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>