Toxicology

<p>Applications 1,2-Cyclohexanedicarboxylic Acid Mono 4-Methyloctan-1-ol Ester is a possible metabolite of the di(isononyl)cyclohexane-1,2-dicarboxylate (DINCH) monoester (MINCH).<br>References Koch, H., et al.: Arch. Toxicol., 87, 799 (2013)<br></p>

<p>Stability Hygroscopic<br>Applications Sulfosate is a non-selective systemic herbicide used primarily for weed control.<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 Martin-Duvall, T., et al.: Proc. Calif. Weed Sci. Soc., 54, No pp given (2000); (Trouslard, B.: Phytoma, 429, 47 (1991); Yarborough, D. &amp; Hess, T.: Proc. Northeastern Weed Sci. Soc., 54, 6 (2000)<br></p>

<p>Applications s-Triazine-1,3,5-triethanol (cas# 4719-04-4) is a compound useful in organic synthesis.<br></p>

<p>Applications Labelled Octopamine (O239750). A biogenic amine that is the phenol analog of Noradrenaline. It is a neurosecretory product found in several vertebrates and invertebrates. Adrenergic.<br>References Pisano, et al.: Biochim. Biophys. Acta., 43, 566 (1960), Breen, C.A., et al.: Nature, 303, 716 (1983)<br></p>

<p>Applications Pyribambenz-Propyl is used in methods and formulations for preventing downward migration of agricultural materials.<br>References Essig, Kenneth J., et al.:PCT Int. Appl., (2020);<br></p>

<p>Applications Coumatetralyl is used as an anticoagulant rodenticide. Coumatetralyl is widely used to control rodent populations.<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 Jones, A., et al.: Bull Environ. Contain Toxicol., 56, 8 (1996), Brakes, C., et al.: J. Appl. Ecol., 42, 118 (2005), Giraudoux, P., et al.: Environ. Res., 102, 291 (2006),<br></p>

<p>Applications Diclosulam is used as a broadleaf herbicide that is used to control weeds in soybean and peanut crops. Diclosulam is applied either preplant or preemergence in order to maintain maximum control of weed growth.<br>References Grichar, W., et al.: Crop Protect., 23, 1145 (2004); Lancaster, S., et al.: Proc. Am. Peanut Res. Ed. Soc., No vol. given, No pp. given, (2006); Sheppard, B., et al.: Proc. South. Weed Sci. Soc., 50, 161 (1997)<br></p>

<p>Applications Used as a broad range pesticide against insects, fungi, vegetation and bacteria. It has become a common environmental contaminant and probable human carcinogen.<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 Gulcan, H., et al.: Chem. Res. Toxicol., 21, 1503 (2008), Toropov, A., et al.: Bioorg. Med. Chem., 16, 5999 (2008), Franco, A., et al.: Envir. Toxicol. Chem., 28, 2018 (2009), Jensen, S., et al.: J. Agric. Food Chem., 57, 5872 (2009),<br></p>

<p>Applications Tianeptine Sodium Salt is a tricyclic compound with psychostimulant, anti-ulcer and anti-emetic properties. Antidepressant.<br>References Malen, C., et al.: Experientia, 28, 811 (1972),<br></p>

<p>Applications Labelled trichloroethylene metabolite<br>References Werner, M., et al.: Chem. Res. Toxicol., 9, 41 (1996), Bruning, T., et al.: Toxicol. Sci., 41, 157 (1998), Newman, D., et al.: Drug Metab. Disposition, 35, 43 (2007),<br></p>

<p>Applications Methyclothiazid, is derivative of Hydrochlorothiazide (H714560), which is a diuretic used in the hospital or for personal use to promote excess fluid associated with congestive heart failure. It is also used as an antihypertensive.<br>References Piala, J.J., et al.: J. Pharmacol. Exp. Ther., 134, 273 (1961), Deppeler, H.P., et al.: Anal. Profiles Drug Subs., 10, 405 (1981),<br></p>

<p>Applications Broflanilide is a pesticide for controlling animals and microbial pests such as unwanted insects. Broflanilide is a prominent insecticide because of it’s effective against pests with resistance to cyclodienes and fipronil. Broflanilide is metabolized to desmethyl-broflanilide that acts as a noncompetitive resistant-to-dieldrin (RDL) γ-aminobutyric acid (GABA) receptor antagonist.<br>References An, X., et al.: J. Sep. Sci., 41, 4515 (2018); Zhao, P., et al.: Nongyao Kexue Yu Guanli, 36, 23 (2015); Jeanmart, S., et al.: Bioorg. Med. Chem., 24, 317 (2016); Nakao, T., et al.: Bioorg. Med. Chem., 24, 372 (2016)<br></p>

<p>Applications A new antitumor derivative of Vinblastine; a dimeric Vinca alkaloid for cancer therapy.<br>References Chakravarty, et al.: J. Med. Chem., 26(5), 638 (1983), Christensson., et al.: Eu.r J. Biochem., 194, 755 (1990), Mayer, et al.: J. Med. Chem., 34, 3029 (1991), Yu, H., et al.: Clin. Biochem., 27, 75 (1994)<br></p>

<p>Applications Harpagoside is an iridoid glycoside along with with Harpagide (H105270), the potential to be strong anti-inflammatory agents providing the bulk of the observed effects from their plant origins.<br>References Zhang, L. et al.: Bioorg Med. Chem., 19, 4882 (2011); Wen, B. et al.: J. Ethnopharm., 147, 503 (2013);<br></p>

<p>Applications Androsterone glucuronide (ADT-G) is one of the major circulating C19-steroid metabolites in humans. Exaggerated Androsterone (A637535) metabolism is observed in hyper-androgenic as well as in some normo-androgenic women with acne and androsterone glucuronide could be a marker in differentiating acne and hirsutism in hyperandrogenic women.<br>References Thompson, D.L. et al.: Clin. Endocrinol., 32, 283 (1990); Stener-Victorin, E. et al.: J. Clin. Endocrinol. Metab., 95, 810 (2010);<br></p>

<p>Applications Dicamba is a herbicide. Dicamba functions by increasing plant growth rate. At sufficient concentrations, the plant outgrows its nutrient supplies and dies. Dicamba has been approved by the EPA for use on genetically modified soybeans and cotton.Environmental toxin on US EPA Toxic Release Inventory list (TRI) list.<br>References Oehler, D.D., et al.: J. Agric. Food Chem., 28, 685 (1980); Griffin, J., et al.: Weed Techno., 27, 696 (2013); Chem. and Eng. News, Nov. 14, 2016, p. 17<br></p>

<p>Applications Antitussive. Chain between 6 and 17 units of ethylene glycol with the major product containing 10 units.<br>References Scholtissek, C., et al.: Antiviral Res., 38, 213 (1998), McGovern, S., et al.: J. Med. Chem., 45, 1712 (2002), Regenthal, R., et al.: Hum. Exp. Toxicol., 21, 343 (2002),<br></p>