Étalons relatives au phénol

Applications A common enironmental pollutant showing weak estrogenic effects. Has been shown to cause harm to the male reproductive system of vertebrates in particular among aquatic species where gonadal intersex, altered sex ratios, and reduced gonad size has been observed. 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 Nakano, S., et al.: J. Health Sci., 48, 83 (2002), Nishio, E., et al.: Biosci., Biotechnol., Biochem., 69, 1226 (2005), Barber, L., et al.: Aquatic Toxicol., 82, 36 (2007), Vajda, A., et al.: Environ. Sci. Technol., 42, 3407 (2008),

Applications p-Cresol Glucuronide-d7, is the labeled analogue of p-Cresol Glucuronide (C782005), which is a metabolite of o-Cresol (C781910). References Goerge, G., et al.: Xenobiotica, 17, 1293 (1987),

Applications 2,3,3',4,4',5-Hexachlorobiphenyl-2',6,6'-d3 (CAS# 1219798-44-3) is a useful isotopically labelled compound. It has been used for wearable monitoring devices to detect environment chemical exposure. References O’Connell, S., & Anderson, K.: U.S. Pat. Appl. Publ. (2016), US 20160209298 A1

Applications 4-(3’,6’-Dimethyl-3’-heptyl)phenol Monoethoxylate (cas# 1119449-37-4) is a compound useful in organic synthesis.

Applications Labelled Bisphenol F, a bisphenol derivative with antioxidant activities. Bisphenol F has been reported to exhibit estrogen agonistic properties. References Higashihara, N. et al.: Arch. Toxicol., 81, 825 (2007); Kanai, H. et al.: Int. J. Cancer, 93, 20 (2001); Pospisil, J. et al.: Kinet. Mech. Polyreacti.Int. Symp. Macromol. Chem. Prepr.,5, 383 (1969);