Amines

<p>5-FAM SE, a single-isomer green fluorophore, labels peptides, proteins, nucleotides.</p>

<p>6-TAMRA (6-Carboxytetramethylrhodamine) serves as a popular fluorophore for the creation of bioconjugates, particularly in the synthesis of fluorescent</p>

<p>5(6)-CFDA: cell-permeable, esterase-responsive viability probe; fluoresces upon activation, indicating enzymatic activity and membrane integrity.</p>

<p>Applications 1,3,5-Benzenetriamine could have cosmetic applications. It could be used for colouring hair with nitrile-containing dyes.<br>References Suenger, G., et al.: PCT Int. Appl. (2005), WO 2005120445 A2<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 Ethanolamine is used in the preparation of various pharmaceutical compounds and inhibitors. Substituted carboxamides are synthesized using Ethanolamine that show potent antitumor activity. Also used in the synthesis of aminoquinolones which display anti-plasmodial 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 Lombardo, L. et al.: J. Med. Chem., 47, 6658 (2004); Egan, T.: J. Med. Chem., 43, 283 (2000);<br></p>

<p>Applications Aminobutanol is used in the preparation of CDK 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 Wang, J. et al.: Chin. J. Chem., 31, 1181 (2013); Tahghighi, A. et al.: J. Enz. Inhib. Med. Chem., 28, 843 (2013);<br></p>

<p>Applications 3-[(4-Bromophenyl)(methyl)amino]propanoic acid (cas# 231278-20-9) is a quinazoline derivative and an aryl iodide. 3-[(4-Bromophenyl)(methyl)amino]propanoic acid has also been used in the design, synthesis and biological evaluation of quinazoline-phosphoramidate mustard conjugates as anticancer drugs.<br>References Zhang, Y.; et al.: Bioorg. Med. Chem. Lett., 27, 1584 (2017); Lin, S.; Eur. J. Med. Chem., 127, 442 (2017).<br></p>

<p>Applications An intermediate for the synthesis of antitumor drugs used in chemotherapy<br>References Foster, A.B., et al.: J. Med. Chem., 24, 1399 (1981), Sorsa, M., et al.: Mutat. Res. Genet. Toxicol., 204, 465 (1988),<br></p>