Composés deutérés
Les composés deutérés sont des molécules organiques dans lesquelles un ou plusieurs atomes d'hydrogène sont remplacés par du deutérium, un isotope stable de l'hydrogène. Ces composés sont essentiels dans divers domaines scientifiques, notamment la spectroscopie RMN, la spectrométrie de masse et les études cinétiques d'isotopes. Les composés deutérés améliorent la clarté et la précision des signaux dans les analyses en réduisant le bruit de fond et en offrant des perspectives uniques sur les mécanismes réactionnels et les structures moléculaires. Chez CymitQuimica, vous trouverez une large gamme de composés deutérés spécialement conçus pour soutenir vos recherches en chimie analytique et en études moléculaires.
4232 produits trouvés pour "Composés deutérés"
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2,4,6-Tribromophenol-1,2,3,4,5,6-13C6
CAS :Formule :C6H3Br3OCouleur et forme :NeatMasse moléculaire :336.76Sodium Methanethiolate-13C
CAS :Produit contrôlé<p>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.<br>References Bergman, A. & Wachtmeister, Chemosphere, 7, 949 (1978); Suzuki, T.,et al.: Bioorg. Med. Chem. Lett., 14, 3313 (2004)<br></p>Formule :CH3NaSDegré de pureté :>90%Couleur et forme :NeatMasse moléculaire :71.0825-Hydroxy-7-methoxy-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-one-d3
CAS :Produit contrôlé<p>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.<br>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)<br></p>Formule :C11D3H9O5Couleur et forme :NeatMasse moléculaire :227.228N-Acetylethylene Urea-d4
CAS :Produit contrôlé<p>Applications N-Acetylethylene Urea-d4 (cas# 1189701-94-7) is a compound useful in organic synthesis.<br></p>Formule :C5H4H4N2O2Couleur et forme :NeatMasse moléculaire :132.15N,N-(Dimethyl-d6)hydrazine Hydrochloride
CAS :Produit contrôlé<p>Applications A labelled isotope of a toxic volatile hydrazine found in rocket fuel systems.<br>References Oanasyuk, A.G. et al.: Vis. Nat. Tekh. Univ. KhPI, 13, 59 (2010);<br></p>Formule :C2H3D6ClN2Couleur et forme :NeatMasse moléculaire :102.60Glycolic Acid-13C Sodium Salt
CAS :Produit contrôlé<p>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.<br>References Murthy M.S.R., et al.: Ann. Nutr. Metab., 27, 355 (1983)<br></p>Formule :CCH3NaO3Couleur et forme :NeatMasse moléculaire :99.0262-Chloroethanol-1,1,2,2-d4
CAS :Produit contrôlé<p>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.<br>Dangerous Goods Info This compound is forbidden to ship by air under IATA regulations.<br>References Svenstrup, N. et al.: Synthesis, 8, 809 (1994); Thibault, R. et al.: J. Am. Chem. Soc., 128, 12084 (2006);<br></p>Formule :C22H4ClOHCouleur et forme :Colourless OilMasse moléculaire :84.54Trixylyl Phosphate-d10
CAS :Produit contrôlé<p>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.<br>References Chigwada, G., et al.: Polym. Degrad. Stab. 89, 85 (2005); Xia, M., et al.: Toxicol Appl Pharmacol 252, 250 (2011)<br></p>Formule :C20D10H9O4PCouleur et forme :NeatMasse moléculaire :364.4Diazald-d3
CAS :<p>Applications N-Methyl-d3-N-nitroso-p-toluenesulfonamide is the labeled version of Diazald; Diazomethane precursor.<br>References Takizawa, et al.: J. Pharm. Soc. Jpn., 70, 490 (1950)<br></p>Formule :C8D3H7N2O3SCouleur et forme :Pale Yellow to Light Yellow SolidMasse moléculaire :217.06004p-Cresol-(methyl-13C)
CAS :Produit contrôlé<p>Applications The formation of p-Cresol-(methyl-13C) via phenol methylation at higher temperature from the deactivation of basic catalyst.<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 Borodina, I. B., et al.: Russ. J. Phys. Chem., 80, 892-898 (2006)<br></p>Formule :CC6H8OCouleur et forme :NeatMasse moléculaire :109.13Hydrazine sulfate-15N2
CAS :Produit contrôlé<p>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.</p>Formule :H4N2·H2O4SDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :132.11 g/molRef: 3D-FH166902
Produit arrêtéDideuterosulfuric acid
CAS :Produit contrôlé<p>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.</p>Formule :D2SO4Degré de pureté :Min. 95%Masse moléculaire :100.09 g/mol
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