Building Blocks

<p>Applications (S)-2-((S)-2-Amino-4-methylpentanamido)-4-methylpentanoic acid (cas# 3303-31-9) is a useful research chemical.<br></p>

<p>Applications An intermediate in the production of many biological inhibitors.<br>References Lambertucci, C., et al.: Bioorg. Med. Chem., 17, 2812 (2009), Lebsack, A., et al.: Bioorg. Med. Chem. Lett., 19, 40 (2009), Griffith, D., et al.: J. Med. Chem., 52, 234 (2009),<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 1,1,3,3-Tetaramethylguanidine is used as a strong, non-nucleophilic base for alkylations in organic synthesis. 1,1,3,3-Tetramethylguanidine is an efficient and selective catalyst for the benzoylation of alcohols.<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 Kim, S. et al.: Bull. Chem. Soc., 5, 205 (1984); Ishikawa, T. et al.: Sunthesis, 2006, 737 (2006);<br></p>

<p>Applications N-3-(Sulfopropyl)-3-methoxy-5-methylaniline is used as a reagent for the evaluation of basic property and long-term stability of reagents for enzymically assaying triglyceride, cholesterol and uric acid.<br>References Yamaguchi, T., Iryo to Kensa Kiki-Shiyaku., 3, 591-597 (2007).<br></p>

<p>Applications Thioacetamide is a carcinogen, a hepatotoxicant. Thioacetamide induces acute chronic liver injury through the activation of protein synthesis of RNA, DNA, and gamma-glutamyl transpeptitase. Thioacetamide has been used in the synthesis of [email protected] nano-array core-shell structure.<br>References Akhtar, T., Sheikh, N.: Toxin Reviews, 32, 43 (2013); Yuan, A., et. al.: Adv. Mater. Res., 652, 683 (2013)<br></p>

<p>Applications Tryptophol is a metabolite formed in the liver after disulfiram treatment that induces sleep in humans. It is also a secondary product of alcoholic fermentation.<br>References Cornford, E.M., et al.: J Clin Invest, 63, 1241-1248 (1979)<br></p>

<p>Applications 1-Amino-imidazolidine-2,4-dione (cas# 6301-02-6) is a useful research chemical.<br></p>

<p>Applications Fatty acid ester with glycerol chlorohydrins shows mutagenic activity.<br>References Janis, R., et al.: J. Food Lipids, 13, 199 (2006), Seefelder, W. et. al.: Food Additiv. Contamin., 1, 10 (2007)<br></p>

<p>Applications 2-(2-Aminoethylamino)ethanol is a reagent used in the synthesis of various pharmacologically active compounds and functional groups. Its 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>Applications 2-Aminoethyl Diphenylborinate is a transient receptor potential (TRP) activator for TRPV1, TRPV2, and TRPV3 (1). 2-Aminoethyl Diphenylborinate inhibits TRPC6 and TRPM8. 2-Aminoethyl Diphenylborinate may potentially be used as a therapeutic agent for pain management and treatment for diseases caused by hypersensitivity and temperature misregulation.<br>References (1) Hu, H.Z., et. al.: J. Biol. Chem., 279, 35741 (2004)<br></p>

<p>Applications A powerful complexing agent. A potent acid sphingomyelinase inhibitor.<br>References Marathe, S., et al.: J. Biol. Chem., 273, 4081 (1998), Lang, P., et al.: Nat. Med., 13, 164 (2007), Nara, F., et al.: J. Antibiot., 52, 525 (1999), Szajnman, S., et al.: Bioorg. Med. Chem. Lett., 15, 4685 (2005),<br></p>