Compuestos deuterados

Applications Norfloxacin-d5 is deuterium labeled Norfloxacin (N681000), a synthetic fluoroquinolone and an antibacterial agent. Norfloxacin can be used to treat urinary tract infections.
References Koga, H., et al.: J. Med. Chem., 23, 1358 (1980), Hirai, K., et al.: Antimicrob. Agents Chemother., 19, 188 (1981), Holmes, B., et al.: Drugs, 30, 482 (1985),

Applications Has a mutagenic potency
References Cash, G., et al.: Mutat. Res., 491, 31 (2001), Cash, G., et al.: Environ. Toxicol. Chem., 21, 2095 (2002), Glende, C., et al.: Mutat. Res., 515, 15 (2002),

Applications Isotope labelled Oxamyl is a pesticide used in the treatment and protection of crops from parasites and insects.
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 Villatte, F. et al.: Pest. Biochem. Phys., 67, 95 (2000); Zapata, A. et al.: Pankey, J. et al.: Weed. Tech., 18, 698 (2004);

Applications Diethanolamine similar to triethanolamine (T775580) is used as a surfactant. It also has the potential to be a corrosion inhibitor by means of chemisorption. This is the labelled analog.
References Bhajiwala, H.M et al.: Bull. Electrochem., 17, 441 (2001); Yu, J. et al.: Thin. Solid. Films., 379, 7 (2000);

Applications Dodecane-d26, is the labeled analogue of Dodecane (D494625), which is used in the synthesis of triblock polymers that deliver nanoparticles to the oil/water interface and degrade non-tocxc non-aqueous liquids.
References Saleh, N. et al.: Nano. Lett., 2489, 5 (2005); Scarso, A. et al.: J. Am. Chem. Soc., 126, 13512 (2004);

Applications Pentadecafluorooctanoic Acid-13C is an isotopomeric compound of Pentadecafluorooctanoic Acid (P268100). Pentadecafluorooctanoic Acid is used to produce fluoropolymers. It also exhibits a long half-life in human blood and interferes with the binding between liver-fatty acid binding protein and fatty acids.
References Biegel, L. B., et al.: Toxicol. Sci 60, 44 (2001); Luebker, D. J., et al.: Toxicology 176, 175 (2002); Butenhoff, J., et al.: Toxicol. Sci 60, 44 (2002)

Applications Labelled Glycolic Acid (G645600). Constituent of sugar cane juice.
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 Smyth, H.F., et al.: J. Ind. Hyg. Toxicol., 23, 259 (1941),

Applications A labelled analog of a naturally occurring purine derivative.
References Wetmore, D., et al.: J. Biol. Chem., 285, 30516 (2010), Jung, Y., et al.: J. Agric. Food Chem., 58, 10458 (2010), Cao, H., et al.: J. Biol. Chem., 285, 28044 (2010),

Applications Hexanoic-5,5-d2 Acid (CAS# 55320-68-8) is a useful isotopically labeled research compound.

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 Ethyl Acetate-13C2 can be used in the synthesis of carbon-13-labeled 5-(diethylphosphono)-2-pentanone ethylene ketal, a reagent for the synthesis of multi carbon-13-labeled steroids.Environmental contaminants; 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 Degraw, J., et al.: J. Lable Compd Radiopharma, 19, 945 (1982);

Stability Hygroscopic
Applications Labelled rac 3-Hydroxybutyric Acid (H833020). Optically active 3-hydroxybutyric acids are key intermediates of the biosynthesis and metabolism of fatty acids and exist widely in biological systems.
References Freeman, J., et al.: Pediatrics, 102, 1358 (1998), Thio, L., et al.: Neurology, 54, 325 (2000), Rho, J., et al.: Epilepsia, 43, 358 (2002),

Applications 2-Benzothiazolethiol-d4 (cas# 1346598-64-8) is a compound useful 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

Applications Labelled O,O-Diethyl Dithiophosphate (D444265). Used in the synthesis of novel phosphorothioates and phosphorodithioates as cholinesterase inhibitor.
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 Millard, C., et al.: J. Neurochem., 64, 1909 (1995), Nicolet, Y., et al.: J. Biol. Chem., 278, 41141 (2003), Casida, J., et al.: Chem. Res. Toxicol., 17, 983 (2004),

Applications Bis(2-butoxyethyl) 2-Hydroxyethyl-d4 Phosphate Triester is a labeled form of Bis(2-butoxyethyl) 2-Hydroxyethyl Phosphate Triester (B415190), which is a metabolite of Tris(2-butyloxyethyl)phosphate (T875030), an organophosphate, that is used in the preparation of flame retardant, such as viscose fiber.
References Wang, Y., et al.: Fangzhi Xuebao, 33, 16 (2012); Xiaoshan, L. et al.: Aquatic Toxicology, 114, 173 (2012);

Applications A labelled metabolite of Di-n-pentyl phthalate (DPP), used mainly as a plasticizer in nitrocellulose.
References Schmid, P., et al.: Xenobiotica, 1985, 15, 251 (1985), Nativelle, C., et al.: Food Chem. Toxicol., 37, 905 (1999), Howdeshell, K., et al.: Toxicol. Sci., 105, 153 (2008),

Applications n-Pentacosane-d52 (CAS# 121578-13-0) is a useful isotopically labeled research compound.

Applications n-Triacontane-d62 is the labeled compound of Triacontane (CAS #: 638-68-6). Triacontane releases selective material in thermally degradable capsule. It also, increases charge carrier mobility and molecular packing of a solution sheared Diketopyrrolopyrrole-based donor-acceptor copolymer by Alkyl side chain modification.
References Shkolnikov, V., et al.; PCT Int. Appl., (2018); Hambsch, M., et al.: Journal of Materials Chemistry C: Materials for Optical and Electronic Devices, 7, 3665-3674, (2019);

Applications Sodium Acetate-d3, is the labeled analogue of Sodium Acetate, the sodium salt of acetic acid, with a wide range of uses. Sodium Acetate is used in the textile industry to neutralize sulfuric acid waste streams, and as a photoresist while using aniline dyes. Sodium Acetate may be added to foods as a seasoning.
References Clayden, j., et al.: Org. Chem., 1st ed. (2001);