Building Blocks

<p>Applications Ethyl 4-Bromobutanoate is a building block which has been used as a reactant for the preparation of firefly luciferase inhibitor-conjugated peptide derivatives.<br>References Poutiainen, P.K., et. al.: Bioconjugate Chem., 25, 4 (2014)<br></p>

<p>Applications 2-Ethoxybenzoic Acid is a component of dental cement. Low concentrations of 2-Ethoxybenzoic Acid in combination with Eugenol (E938640), gives a stabilizing effect to liposomes to lower damages to cells.<br>References Fujisawa, S., et al.: J. Dent. Res., 82, 43(2003); Brauer, G.M., et al.: J. Dent. Res., 62, 366 (1983); Brauer, G.M., et al.: J. Dent. Res., 63, 137 (1984); Fujisawa, S., et al.: J. Biomed. Mater. Res., 21, 89 (1987)<br></p>

<p>Applications A sulfonate ester as potential genotoxic impurity in drug substances. It may exert genotoxic effects in bacterial and mammalian cell systems.<br>References Eder, E., et al.: Xenobiotica, 12, 831 (1982), Li, W., et al.: J. Chromatogr., 1046, 297 (2004), Glowienke, S., et al.: Mutat. Res., 581, 23 (2005), Colon, I., et al.: J. Pharm. Biomed. Anal., 39, 477 (2005),<br></p>

<p>Applications cis-Linalool Oxide is a derivative of Linalool (L465950), which is a terpene alcohol common in various flowers and spice plants. cis-Linalool Oxide has been employed to assess the effect of vine on the glycosylated flavour procurers in grapes.<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 Baratta, M. T., et al.: J Essent Oil Res 10, 618 (1998); Bureau, S. M., et al.: J. Agric. Food Chem. 48, 1290 (2000)<br></p>

<p>Applications trans-Linalool Oxide is a derivative of Linalool (L465950), which is a terpene alcohol common in various flowers and spice plants. trans-Linalool Oxide is also an isomer of cis-Linalool Oxide, which has been employed to assess the effect of vine on the glycosylated flavour procurers in grapes.<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 Baratta, M. T., et al.: J Essent Oil Res 10, 618 (1998); Bureau, S. M., et al.: J. Agric. Food Chem. 48, 1290 (2000)<br></p>

<p>Applications cis-2,6-Lupetidine, is used in elimination reactions, and also as a reactant for corrosion inhibitors for iron in HCl. It can also be used as a catalyst for the preparation of aliphatic 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 Pyun, S., et al.: J. Org. Chem., 73(23), 9451 (2008); Rea BR, B., et al.: J. Org. Chem. Chem., 67 (15), 5232 (2002); Arimitsu, K., et al.: J. Mater. Chem., 14, 336 (2004);<br></p>

<p>Applications Dynamin Inhibitor I, Dynasore is an inhibitor of Dynamin I and Dynamin II.<br></p>

<p>Applications 1-(4-Hydroxyisoxazole)-carboxylic Acid (cas# 178316-77-3) is a compound useful in organic synthesis.<br></p>

<p>Applications 5-Hydroxyindole is a hydroxylated indole used as a building block in the preparation of various pharmaceutical compounds such as indole based neurochemicals. 5-Hydroxyindole is a metabolite of Tryptophan (T894800). 5-Hydroxyindole displayed weak inhibitory activity on human melanoma tyrosinase. 5-Hydroxyindole also showed inhibition of serotonin transport by blood platelets.<br>References Yamazaki, Y. et al.: Zeitsch. Naturforsch. C: J. Biosci., 65, 49 (2010); Kay, W.W. et al.: Gen. Pharmacol., 8, 201 (1977); Ghebregzabher, M. et al.: J. Chrom. Biomed. Appl., 222, 191 (1981);<br></p>

<p>Applications D-Xylonic Acid Calcium Salt Hydrate is a compound useful in organic synthesis.<br></p>

<p>Applications 4-(4-Diethylaminostyryl)-1-methylpyridinium iodide is a fluorescent cationic styryl probe for mitochondrial staining. It is used in the functional live cell fluorescence imaging for pulmonary neuroepithelial body microenvironments.<br></p>

<p>Applications 2-Hydroxytetrahydrofuran (cas# 5371-52-8) is a compound useful in organic synthesis.<br></p>

<p>Applications 2,5-Xylidine, is a Vanillin derivative, used as as potential inhibitors of FtsZ. These compounds were also assayed for antibacterial activity against Escherichia coli, Pseudomonas aeruginosa, etc.<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 Sun, J., et al.: Med. Chem. Res. (2013);<br></p>

<p>Applications 3-Hydroxyindole is a mutation product of toluene-4-monooxygenase (T4MO), that gets spontaneously converted to indigo. Used in the preparation of indolyl-oxadiazoles with anticonvulsant activity.<br>References Rajak, H. et al.: Int. J. Pharm. Sci. Nanotech., 2, 661 (2009); McClay, K. et al.: Appl. Environ. Microbiol., 71, 5476 (2005); Berry, A. et al.: J. Ind. Microbiol. Biotech., 28, 127 (2002)<br></p>

<p>Applications Xylenesulfonic Acid is a hydrotrope used to solubilise hydrophobic compounds and in aqueous solutions as well is in the study of liposome systems.<br>References Friberg, S.E. et al.: J. Disp. Sci. Technol., 19, 19 (1998); Odeh, F. et al.: J. Disp. Sci. Technol., 27, 665 (2006);<br></p>

<p>Applications 2-Hydroxyisobutyric Acid is used as a reagent in the preparation of fully functionalized tetronic acids. Also used in the synthesis of bioisosteres of trimethadione, N-derivative-1,2,3-oxathiazolidine-4-one-2,2-dioxides from α-hydroxyamides which display anticonvulsant activity.<br>References Prousis, K., et al.: Tetrahedron, 71, 8637 (2015); Pastore, V., et al.: Bioorgan. Med. Chem., 21, 841 (2013);<br></p>

<p>Applications: Intermediate in the preparation of Propantheline Bromide.<br></p>

<p>Applications 3-Hydroxynaphthalene-2,7-disulfonic Acid Disodium Salt, is used in analytical studies for detecting organic explosives and propellants by fast liquid chromatography quadrupole time-of-flight mass spectrometry.<br>References DeTata, D., et al.: Forensic Sci, Int., 233, 63 (2013); Mathis, J., et al.: J. Chromatogr. A., 988, 107 (2003)<br></p>

<p>Applications 8-Hydroxy-2(1H)-quinolinone is a substituted quinolinone derivative used in the preparation of pharmaceutical compounds.<br>References Li, F. et al.: J. Proteome. Res., 12, 1369 (2013)<br></p>