Composti deuterati

Applications N-Acetylethylene Urea-d4 (cas# 1189701-94-7) is a compound useful in organic synthesis.

Applications 5-Hydroxy-7-methoxy-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-one-d3 is an intermediate for the synthesis of Alternariol Monomethyl Ether-d3 (A575771), labelled methyl este analog fo Alternariol. An alternaria mycotoxin and genotoxin, found in common edible crops. It inhibits the activity of various DNA-topoisomerases, increasing the rate of DNA strand breaks.
References Asam, S., et al.: J. Agric. Food Chem., 57, 5152 (2009); Fehr, M., et al.: Mol. Nut. Food Res., 53, 441 (2009); Tiemann, U., et al.: Toxicol. Lett., 186, 139 (2009)

Applications Sodium Methanethiolate-13C, is the labeled analogue of Sodium Methanethiolate (S644805), used as a nucleophile in organic synthesis. Sodium methanethiolate is also being used as a reagent to synthesize thiol-based suberoylanilide hydroxamic acid (SAHA) analogues, compounds that act as potent histone deacetylase inhibitors.
References Bergman, A. & Wachtmeister, Chemosphere, 7, 949 (1978); Suzuki, T.,et al.: Bioorg. Med. Chem. Lett., 14, 3313 (2004)

Applications The formation of p-Cresol-(methyl-13C) via phenol methylation at higher temperature from the deactivation of basic catalyst.
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 Borodina, I. B., et al.: Russ. J. Phys. Chem., 80, 892-898 (2006)

Applications 2-Chloroethanol is used in the preparation of TTFTT (tetrathiafulvalene-2,3,6,7-tetrathiolate) and important building block in TTF syntheis. In addition, it is used in the synthesis of vinyltriazoles. This is the labeled analog.
Dangerous Goods Info This compound is forbidden to ship by air under IATA regulations.
References Svenstrup, N. et al.: Synthesis, 8, 809 (1994); Thibault, R. et al.: J. Am. Chem. Soc., 128, 12084 (2006);

Applications Trixylyl Phosphate-d10 is a deuterated form of Trixylyl Phosphate (T891900), which is used commercially as hydraulic fluids, flame retardants, and plasticizers. Trixylyl Phosphate inhibits the human ether-a-go-go-related gene (hERG) channel, which is a voltage-gated potassium (K+) channel involved in the repolarization of the cardiac action potential.
References Chigwada, G., et al.: Polym. Degrad. Stab. 89, 85 (2005); Xia, M., et al.: Toxicol Appl Pharmacol 252, 250 (2011)

Applications A labelled isotope of a toxic volatile hydrazine found in rocket fuel systems.
References Oanasyuk, A.G. et al.: Vis. Nat. Tekh. Univ. KhPI, 13, 59 (2010);

Applications N-Methyl-d3-N-nitroso-p-toluenesulfonamide is the labeled version of Diazald; Diazomethane precursor.
References Takizawa, et al.: J. Pharm. Soc. Jpn., 70, 490 (1950)

Applications Glycolic Acid-13C Sodium Salt is the isotope labelled analog of Glycolic Acid Sodium Salt; a compound that increases the glycolate oxidase activity in the liver when fed to rats. It also increases the lactate dehydrogenase activity in the liver and kidney. This compound is suitable for lactate dehydrogenase (LDH) related research.
References Murthy M.S.R., et al.: Ann. Nutr. Metab., 27, 355 (1983)

Hydrazine sulfate-15N2 is a trimethylsilylated hydrazine sulfate. It is used as an intermediate for the synthesis of N-trimethylsilylhydrazines and other trimethylsilylhydrazines. The compound can also be used to prepare glutamine as it reacts with dl-glutamine to form hydroxylamine, which then reacts with hydrogen sulfide to form glutathione. Hydrazine sulfate-15N2 is mainly used as a catalyst in the production of nitric acid from ammonia and oxygen gas.

Dideuterosulfuric acid is a protonated molecule that is found in the tropone class of organic compounds. It has been shown to have optical properties similar to those of ferrocene, which is why it is often used as a replacement for this compound. Dideuterosulfuric acid has been studied extensively using a kinetic method with the goal of determining its mechanism and rate constants. Hydroxyl groups are found on the molecule's trifluoroacetic acid side chains, which may contribute to its reactivity with chloride ions and nitrogen atoms. Electrophotographic measurements show that hydrogen bonding occurs between molecules in dilute solutions.