Building Blocks

Applications Ethyl Diazoacetate is used in the synthesis of Arteludovicinolide A as well as pyrimidoazepine analogs as seritonin 5-HT2A/C receptor ligands for treatment of obesity. This compound contains solvent for added stability.
E0
References Yang, H. et al.: Eur. J. Med. Chem., 63, 558 (2013); Kreuzer, A. et al.: Org. Lett., 15, 3420 (2013);

Applications Ethyl phenylacetate is one of the odour active components in a variety of foods such as mango (Mangifera indica L. cv. Corazon), guava wine, and soypaste.
References Pino, J.: Int. J. Food Sci. Tech., 47, 1944 (2012); Pino, J. & Queris, O.: J. Agr. Food Chem., 59, 4885 (2011); Zhang, Y., et al.: Molecules, 15, 3421 (2010)

Applications 2,2’-Thiodiethanol is a reagent used in the synthesis of water soluble gold-N-heterocyclic carbene complexes for catalytic homogenous acid.
References Ibrahim, H. et al.: Adv. Synth. Catal., 357 ,3893 (2015);

Applications 2-Ethyl-4-methyl-1-pentanol is a volatile chemical that can be used to diagnose ratoon stunting disease in Sugar cane.
References Berna, A. Z., et al.: Pro. of the Conf. of the Austr. Soc. of Sugar Cane Tech., 37th, 150-157 (2015)

Stability Moisture Sensitive
Applications Ethyl Trifluoroacetate is an intermediate used in the synthesis of various pharmaceutically active molecules and agricultural products. Ethyl Trifluoroacetate is also useful for the preparation of trifluoroacylated compounds.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References HugenBerg, V., J. Fluorine. Chem., 131, 942 (2010); Belyakova, Z.V., et al.: Russ. J. Gen. Chem., 79, 2634 (2009); Wu, J.L., et al.: Jingxi. Huagong. Zhongjianti., 40, 64 (2010);

Applications Mono and dibasic phosphate esters are anionic surfactants which have the main feature of the stability in alkaline conditions over other surfactants. They have a wide range of properties including outstanding wetting, emulsification, lubrication, coupling activity and detergency.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Ramirez, F., et al.: Tetrahedron, 35, 1581 (1979);

Applications Monobenzyl Malonate is a useful synthetic intermediate. It was used to synthesize constrained cyclic agonists of the cholecystokinin CCK-B receptor. It was also used to prepare aspartate transcarbamoylase inhibitors.
References Blommaert, A., et al.: J. Med. Chem., 40, 647 (1997); Coudray, L., et al.: Bioorg. Med. Chem., 17, 7680 (2009)

Applications A powerful complexing agent. A potent acid sphingomyelinase inhibitor.
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),

Applications 2'-Nitroacetophenone (cas# 577-59-3) is a compound useful in organic synthesis.

Applications 3'-Nitroacetophenone is used as a reactant in the synthesis of fluorine based aminothiazoles with antimicrobial activity.
References Singh, K., Sharma, P.K.: Int. J. Pharmacy Phamaceut. Sci., 6, 429 (2014)

Stability Hygroscopic
Applications N,N,N',N'-Tetramethyl-p-phenylenediamine dihydrochloride (cas# 637-01-4) is a useful compound for membrane-tethering cytochrome c to study its impact on cell death in yeast.
References Toth, A., et al.: Cell Death Dis., 11, 722 (2020)

Applications 2-(2-Nitrophenyl)malondialdehyde (cas# 53868-44-3) is a useful research chemical.

Applications N-Nitrosohexamethylenimine is a carcinogen.
References Goodall, C. M., et al.: Toxicology, 33, 251 (1984); Lijinsky, W., et al.: J. Cancer Res. Clin. Oncol., 108, 46 (1984); Goodall, C. M., et al.: JNCI, J. Natl Cancer Inst., 73, 1215 (1984)

Applications 2-Nitrosopyridine is a useful reactant in organic synthesis.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Li, Xing, et al.: J. of Org. Chem., 84(7), 4402-4412 (2019);Zhang, Jingchuan, et al.: Chem. - A Euro. J., 24(17), 4289-4293 (2018)

Applications A Sulfamethoxazole metabolite.
References Gill, H., et al.: Br. J. Clin. Pharmacol., 42, 347 (1996), Winter, H., et al.: Clin. Pharmacol. Ther., 76, 579 (2004), Vyas, P., et al.: Biochem. Pharmacol., 70, 275 (2005), Vyas, P., et al.: Drug Metab. Dispos., 34, 16 (2006),