Amines

<p>Applications 2-(Acetylamino)-N-(phenylmethyl)propanamide, has shown to have anticonvulsant activity in vitro. Likely an impurity in the medication Lacosamide, (L098500).<br>References Martinez, J C. et al: MATCH, Vol. 67, issue 3, P: 745-758 (2012);<br></p>

<p>Applications Methoxylamine is a methoxime derivative used as internal standard for Prostaglandin assays by gas chromatography-mass spectrometry.<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 Herold, D.A. et al.: Prostaglandins, 33, 599 (1987);<br></p>

<p>Applications Tris(2-​aminoethyl)​amine is a tetradentate chelating ligand and forms stable complexes with transition metals.<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 Xu, C., et al.: J. Mater. Chem. A, 3, 16229-16234 (2015); Sietzen, M., et al.: Organometallics, 34, 1118-1128 (2015);<br></p>

<p>Applications N-Nitrosodipropylamine is a a N-nitrosamine derivative. The mutagenic activities of the carcinogenic N-nitrosamines were studied on both S. typhimurium TA100 and TA98, revealing moslty mutagenic activities on TA100 with few exceptions on TA98 (1). Water contaminant (2). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.<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 1. Yahagi, T. et al.: Mutat. Res. Fund. Mol. Mech. Mut. 1977. Apr:48(2) p121-1292. Mestankova, H. et al.: Water Res. 2016 Apr 15;93:110-20<br></p>

<p>Applications 9-(2-Chloro-ethyl)-9H-purin-6-ylamine (cas# 19255-48-2) is a compound useful in organic synthesis.<br></p>

<p>Stability Hygroscopic<br>Applications Neamine is normally found as a core structure of aminoglycoside antibiotics. It is used in the synthesis of disaccharide neamine derivatives as antibacterial agents.<br>References Kawaguchi, H., et al.: J. Antibiot., 25, 695 (1972), Fourmy, D., et al.: Science, 274, 1367 (1996), Riguet, E., et al.: J. Med. Chem., 47, 4806 (2004)<br></p>

<p>Applications Alkylated Diphenylamines are a derivative of aniline, a common chemical reagent. Good antioxidant agent.<br></p>

<p>Stability Unstable in Aqueous Solution<br>Applications 4-Amino-1-butanol is used in the synthesis of NSAIDs with anti-inflammatory properties. Also used in the synthesis of polyamine transport ligands with specificity against human cancers allowing easy access to specific cancer cells.<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 Majumder, J. et al.: Langmuir, 29, 10254 (2013); Muth, A. et al.: J. Med. Chem., 56, 5819 (2013)<br></p>

<p>Applications N-[(4-chlorophenyl)methyl]cyclopentanamine is a useful reagent for the preparation of γ-​lactams.<br>References Fujii, T., et al.: Tetrahedron Letters, 61, 152276 (2020)<br></p>

<p>Applications 3,5-Tolylenediamine, is a building block<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 Diethylammonium Dihydrogen Phosphate (cas# 68109-72-8) is a compound useful in organic synthesis.<br></p>

<p>Applications 2-(Diphenylmethoxy)-N-ethylamine (cas# 17349-94-9) is a compound useful in organic synthesis.<br></p>

<p>Applications 1-Amino-2-propanol is a reagent used in the synthesis of protein kinase CK2 inhibitors used in the treatment of neoplasia and other infective diseases.<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 Pagano, M. et al.: J. Med. Chem., 47, 6239 (2004);<br></p>

<p>Stability Hygroscopic<br>Applications N-​Ethyl-​α-​methyl-​3-​(trifluoromethyl)​-benzeneethanamine hydrochloride has been used in case studies for the study of impulsivity, motor skills, and anxiogenic effects in the neuroscience community.<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 Whitney, K.N., et al.: Exp. Clin. Psychopharm., 21, 345-54 (2013); Arrant, A.E., et al.: Neuropharmacology, 65, 213-22 (2013)<br></p>

<p>Applications 2-(7-Amino-2-oxo-2H-chromen-4-yl)acetic acid (cas# 85157-21-7) is a useful research chemical.<br></p>

<p>Applications 1-Phenyl-2-butanamine (cas# 30543-88-5) is a useful research chemical.<br></p>

<p>Stability Hygroscopic<br>Applications Benzyltrimethylammonium chloride (cas# 56-93-9) is a useful research chemical.<br></p>

<p>Applications 3-Aminobiphenyl<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 Bis(4-tert-butylphenyl)amine could be a useful reagent for synthesizing efficient luminogens with AIE features that permit imaging the brain through an intact skull.<br>References Qin, W., et al.: Adv. Mater. (Weinheim, Germany), 32, 2000364 (2020)<br></p>

<p>Applications Didecylamine is a nitrogen containing organic building blocks. It is also shown to be used as a substrate for the growth of gram-negative Pseudomonas sp bacteria obtained from the activated sludge.<br>References Ginkel, C., et al.: Biodegradation, 19, 129, (2008);<br></p>

<p>Applications 1,3,5-Tris(4-aminophenyl)benzene (cas# 118727-34-7) is a useful reagent for catalytic asymmetric synthesis of chiral covalent compounds.<br>References Wang, J., et al.: J. Am. Chem. Soc., 142, 16915 (2020)<br></p>

<p>Applications Aromatic amines likely to have high carcinogenic potency. QSARs of aromatic amines.<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 Franke, R., et al.: Carcinogenesis, 22, 1561 (2001), Benigni, R., et al.: Chem. Rev., 105, 1767 (2005), Benigni, R., et al.: Environ. Mol. Mutagen., 50, 152 (2009),<br></p>

<p>Applications Hydroxylamine Hydrochloride acts as a mild reducing agent in various organic and inorganic chemical reactions.<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 Shahjamali, M. et al.: Adv. Func. Mat., 22, 849 (2012); Macakova, K. et al.: Food Chem., 135, 2584 (2012);<br></p>

<p>Applications Has a DNA binding effect.<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 Mikata, Y., et al.: Chem. Pharm. Bull., 48, 477 (2000),<br></p>

<p>Applications 2-​[(2-​Hydroxyethyl)​octadecylamino]​ethyl ester octadecanoic acid is used as a modifier to Polymer films of LDPE and ethylene-​vinyl acetate copolymers (EVA) to enhance antifog properties.<br>References Irusta, L., et al.: J. Appl. Polym. Sci., 111, 2299-2307 (2009);<br></p>

<p>Applications 4-Aminobenzamide (cas# 2835-68-9) is a useful research chemical.<br></p>

<p>Stability Stable at RT<br>Applications An intermediate used for the sythesis of xanthine derivatives.<br>References Daly, J.W., et al.: J. Med. Chem., 28, 487 (1985), Erickson, R.H., et al.: J. Med. Chem., 34, 3405 (1991),<br></p>

<p>Stability Hygroscopic<br>Applications Ammonium oxalate is used as an analytical reagent and general reducing agent. It is commonly employed in soil chemical analysis to extract iron and aluminum from poorly-crystal line minerals.<br>References Seyed, D., et al.: J. Photo. Chem., 394, 112486 (2020); Blanchard, F., et al.: Cryst. Growth Des., 18, 4593-4601 (2018)<br></p>

<p>Stability Hygroscopic<br>Applications N,N,N'-Trimethyl-1,3-propanediamine is a reactant that as a ligand, racemizes aromatic alcohols completely in the prescence of a ruthenium-based racemization catalyst.<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 Riermeier, T.H., et. al.: Tetrahedron Lett., 46, 3403 (2005)<br></p>

<p>Applications Octylamine is used as a reactant in the synthesis of 2H-indazoles and 1H-indazolones which are used as myeloperoxidase(MPO) inhibitor.<br> E0<br>References Roth, A., et al.: Bioorg. Med. Chem., 22, 6422 (2014);<br></p>

<p>Applications 2-(Aminooxy)ethanol<br></p>

<p>Applications N,N-Dimethyldodecylamine is used as a reagent in the synthesis of epoxy quaternary ammonium salt surfactants which exhibit potential antibacterial activity.<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 Liu, Y., et al.: J. Disper. Sci. Technol., 35, 1460 (2014)<br></p>

<p>Applications 1,5-Dimethylhexylamine is an aliphatic secondary amine which shows leucine aminotransferase inhibition. 1,5-Dimethylhexylamine is used in the preparation of glycosyl β-amino acids with antitubercular activity.<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 Raunio, R. et al.: Acta Chem. Scand., 27, 985 (1973); Tripathi, R.P. et al.: Eur. J. Med. Chem., 37, 773 (2002);<br></p>

<p>Applications N-Iodoacetyltyramine is used in iodine-125 labelling of various molecules for chemical analysis.<br>References Lin, C. et al.: Anal. Biochem., 179, 389 (1989);<br></p>

<p>Applications A reagent used for the synthesis of hydroxylamines and hydroxyamates.<br>References Magin, D.F., et al.: J. Chromatogr., 178, 219 (1979), Safavy, A., et al.: Bioconjug. Chem., 13, 327 (2002),<br></p>

<p>Stability Hygroscopic<br>Applications Bis(tributylammonium) Pyrophosphate is an phosphorylating reagent used in the synthesis of phosphorylated deoxynucleosides.<br>References Santner, T. et al.: Bioorg. Med. Chem, 20, 2416 (2012); Sun, D. et al.: ChemMedChem, 4, 1649 (2009)<br></p>

<p>Stability Hygroscopic<br>Applications N-(2-Chloroethyl)-1,2-ethanediamine Dihydrochloride is an analog of 2-(2-Aminoethylamino)ethanol (A608990); a reagent used in the synthesis of various pharmacologically active compounds and functional groups. Also used in the synthesis of antitumor anthracene-diones and antitumor DNA intercalators. More recently used in the synthesis of ionic liquids with various thermal, dielectric and catalytic 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 Bair, K. et al.: J. Med. Chem., 33, 2385 (1990); Krapcho, A. et al.: J. Med. Chem., 37, 828 (1994); Karadag, A. et al.: J. Mol. Liq., 177, 369 (2013)<br></p>

<p>Impurity Phenylephrine USP Related Compound D<br>Applications (αR)-3-Hydroxy-α-[[methyl(phenylmethyl)amino]methyl]-benzenemethanol (Phenylephrine USP Related Compound D) is a derivative of (R)-Phenylephrine (P320640, HCl salt) which is an α-Adrenergic agonist.<br>References Warren, M.R., et al.: J. Pharmacol. Exp. Ther., 86, 284 (1946); Gaglia, C.A., et al.: Anal. Profiles Drug Subs., 3, 483 (1974)<br></p>

<p>Stability Hygroscopic<br>Applications 4-(2-Aminoethyl)benzene-1,2-diol has been studied for its role in Parkinson's disease.<br>References Segura-Aguilar, J.: Neural Regeneration Research, 12, 897 (2017)<br></p>

<p>Applications Aromatic amines likely to have high carcinogenic potency. QSARs of aromatic amines.<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 Franke, R., et al.: Carcinogenesis, 22, 1561 (2001), Benigni, R., et al.: Chem. Rev., 105, 1767 (2005), Benigni, R., et al.: Environ. Mol. Mutagen., 50, 152 (2009),<br></p>

<p>Applications Tert-butyl 4-Aminobutanoate Hydrochloride is used as a substance in the prevention of drug-induced memory impairement by immunopharmacotherapy.<br>References Treweek, J. B., et al.: J. Med. Chem., 51, 6866 (2008)<br></p>

<p>Stability Hygroscopic<br>Applications Diethanolamine similar to triethanolamine (T775580) is used as a surfactant. It also has the potential to be a corrosion inhibitor by means of chemisorption.<br>References Bhajiwala, H.M et al.: Bull. Electrochem., 17, 441 (2001); Yu, J. et al.: Thin. Solid. Films., 379, 7 (2000);<br></p>

<p>Stability Hygroscopic<br>Applications N-[4-[(4-Hydroxyphenyl)amino]phenyl]acetamide is used in the synthesis of lithographic plates.<br></p>

<p>Applications N,N-Dimethyldecylamine is a useful synthetic intermediate. It can be used to prepare emodin (E523000) quaternary ammonium salt derivatives as potential anticancer agents It is also a reactant used to synthesize Benzyldecyldimethylammonium chloride (B234550), a biocide.<br>References Wang, W., et al.: Eur. J. Med. Chem., 56, 320 (2012); Qiu, B., et al.: Zhongguo Yaowu Huaxue Zazhi, 20, 353 (2010); Shao, J., et al.: Eur. J. Med. Chem., 56, 308 (2012); Lee, M., et al.: Appl. Micro. Biotech., 87, 1109 (2010)<br></p>

<p>Applications 3-Amino-4-hydroxybenzenesulfonamide is a reagent used to synthesize antagonists for somatostatin receptor subtype 5 (SST5R). It also has utility in dye applications.<br>References Martin, R. E., et al.: J. Med. Chem 50, 6291 (2007); Sokolowska-Gajda, J. et al.: Dyes Pigm. 30, 1 (1996)<br></p>

<p>Applications N-Methyl-N-nitroso-1-hexadecanamine is a compound found in a wide range of cosmetic products and cleaning emulsions.<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 Kamp, E.. et al.: Food. Chem. Toxicol., 29, 203 (1991); Lalljie, S. P. D., et al.: Adv. Mass. Spec., 14, 33790 (1998); Abidi, S.L., et al.: J. Chroma., 324, 209 (1985);<br></p>

<p>Applications 1,3-Diaminopropane is a common chemical reagent, used in the synthesis of 7-methoxytacrine-adamantylamine heterodimers as cholinesterase inhibitors applied in the treatment of Alzheimer’s disease. Also used in the synthesis of thrombosis 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 Spilovska, K. et al.: Molecules, 18, 2397 (2013); Smith, S. et al.: Blood, 120, 5103 (2012);<br></p>

<p>Applications Ethylamine Solution is used as a reagent in the synthesis of a series of hexadentate ligands as potential antibacterial agents. Also used as a reagent in the synthesis of tetrahydrothiazolopyridine derivatives as potent smoothened antagonists.<br>References Zhang, M., et al.: Chem. Biol. Drug Des., 84, 659 (2014); Ma, H., et al.: Eur. J. Med. Chem., 89, 721 (2015)<br></p>