Composés deutérés

Applications Dimethyl phthalate-3,4,5,6-d4

Applications n-Pentyl 4-Hydroxybenzoate-2,3,5,6-d4 (CAS# 1219798-66-9) is a useful isotopically labeled research compound.

Applications Isotope labelled Methanol (M276585), which is a common chemical reagent in organic synthesis participating in a variety of reactions. Used to prepare novel triazole-polyphenol hybrid compounds as FabG4 (Rv0242c) enzyme inhibitors for the treatment of Mycobacterium Tuberculosis (1). Also used in the synthesis of prodelphinidin B1/B2/B4 which display antitumor activities against prostate cancer cells.Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.
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 1. Banerjee, D. et al.: Org. Biomol. Chem. 2014 Jan 7;12(1):73-85.

Applications Labelled Indole (I577320). Can be used in perfumes and in the synthesis of tryptophan.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

Applications 1,3,5-Tribromobenzene-d3 (CAS# 52921-77-4) is a useful isotopically labeled research compound.

Applications Regorafenib-d3 is the isotope labelled analog of Regorafenib (R143000); a compound that inhibits PDGFR tyrosine kinase with IC50=83nM and is useful for the treatment of inflammation. Also an anti-proliferative agent.
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 Leuner, C., et al.: Eur. J. Pharm. Biopharm., 50, 47 (2000)

Applications A labelled thioxanthone derivative useful as photoinitiators.
References le Fur, Y., et al.: J. Agric. Food Chem., 47, 2860 (1999), Sanz, M., et al.: Food Chem., 84, 133 (2004), Herent, M., et al.: J. Pharm. Biomed. Anal., 43, 886 (2007),

Applications Labelled analogue of Acrolein 2,4-Dinitrophenylhydrazone, a dinitrophenylhydrazone (DNPH) derivative of an aliphatic alldehyde found in mainstream cigarette smoke.
References Delgado, B. et al.: J. Liq. Chrom. Rel. Technol., 31, 361 (2008); Miller, J.H. et al.: J. Chrom. Sci., 48, 12 (2010);

Applications 4-tert-Butylphenol-D9 is the labelled analogue of 4-tert-Butylphenol (B694105). 4-tert-Butylphenol is a reactant in the preparation of (2-bromocyclopent-2-en-1-yl)phenols.
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 Speck, K., et. al.: Org. Lett., 17, 1982 (2015)

Applications The toxicity of halogenated benzoic acids was found to be directly related to the compound's hydrophobicity. Toxicity and quantitative structure-activity relationships of benzoic acids to Pseudokirchneriella subcapitata. This is the labelled analog.
References Moore, D., et al.: Environ. Toxicol. Chem., 16, 794 (1997), Zhao, Y., et al.: Sci. Total Environ., 216, 205 (1998), Fiorentino, A., et al.: J. Agric.Food Chem., 51, 1005 (2003),

Applications Labelled Sulfanilic acid (S689095). Sulfanilic acid is a toxic metabolite of Tartrazine (T007700). Used as Ehrlich’s reagent, for detecting of nitrites. Antibacterial.
References Collins, T., et al.: Food Chem. Toxic., 28, 821 (1990), Levine, W., et al.: Drug Metab. Rev., 23, 235 (1991), Sasaki, Y., et al.: Mutat. .Res., 519, 103 (2002),

Applications Bezafibrate-d4 (cas# 1189452-53-6) is a compound useful in organic synthesis.

Applications Nonanal-d18, is the labeled analogue of Nonanal (N649330), a component of essential oils. Nonanal possesses a strong fruity odor. Essential oils have varying effects from antibacterial activity to hypolipidemic activity.
References Zorrilla-Fontanesi, Yet al.: Plant. Phys., 159, 851 (2012): Taherkhani, M. et al.: Asian. J. Chem., 24, 1461 (2012); Ahmadvand, H. et al.: Iran. J. Pharm. Res., 11, 1219 (2012);

Applications Maleic-2,3-d2 Acid is an isotope labelled compound of Maleic Acid (M124302). Maleic Acid is a reagent used in the preparation of TiO2/carbon nanotube composites.
References Le, L. et al.: ChemMedChem., 8, 289 (2013); Yao, Y. et al.: Env. Sci. Tech., 42, 4952 (2008)l

Applications Carbetamide-D5 is the labelled analogue of Carbetamide (C178028). Carbetamide is used in the determination of pesticides.
References Jia, W., et al.: Journal of Chromatogr. A., 1395, 160-166 (2015)

Applications A labelled metabolite of Malachite Green in seafood products. A labelled triphenylmethane dye with fungicidal and limited antiseptic activity. The term Malachine green applies to the oxalate as well as the chloride. Harmful if swallowed. Avoid release to the environment.
References Carter, S.G., et al.: J. Biochem. Biophys. Methods, 7, 7 (1982), Saikan, S., et al.: J. Chem. Phys., 79, 4154 (1983), Clemmensen, S., et al.: Arch. Toxicol., 56, 43 (1984),

Applications Labelled Dimethomorph (D460530). Agricultural fungicide.
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 Lu, X., et al.: Phytopathol., 100, 1162 (2010), Schafer, R., et al.: Environ. Sci. Technol., 45, 1665 (2011),

Applications Labelled Diflufenican (D445640). (Pre and post emergence foliar absorbed herbicide for winter weed control in cereal crops; carotenoid biosynthesis inhibitor.
References Conte, E., et al.: J. Agric. Food Chem., 46, 4766 (1998),

Applications A labelled form of Fenoxycarb (F248870), a carbamate insect growth regulator by preventing immature insects from reaching maturity by mimicking juvenile hormone. Used as a standard for Pesticide detection. Fenoxycarb is also used in cannabis testing kits as a component of pesticide mixes (P698235).
References El-Saeid, M.H., et al.: J. Chem., 10, (2013); Coors, A., et al.: Environ. Toxicol. Chem., 31, 1239 (2012);

Applications Simazine-d10 is the isotope labelled analog of Simazine (S465900); a selective pre-emergence herbicide.
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 Bailey, G.W., et al.: Residue Rev., 10, 97 (1965); Chun, O., et al.: Food Chem. Toxicol., 41, 1063 (2003); Berrada, H., et al.: Food Control., 21, 36 (2010)