Toluene-d8
Toluene-d8 structure
|
Common Name | Toluene-d8 | ||
|---|---|---|---|---|
| CAS Number | 2037-26-5 | Molecular Weight | 100.188 | |
| Density | 0.9±0.1 g/cm3 | Boiling Point | 110.6±3.0 °C at 760 mmHg | |
| Molecular Formula | C7D8 | Melting Point | -84ºC | |
| MSDS | Chinese USA | Flash Point | 4.4±0.0 °C | |
| Symbol |
GHS02, GHS07, GHS08, GHS09 |
Signal Word | Danger | |
|
Position-Specific Isotope Analysis of Xanthines: A (13)C Nuclear Magnetic Resonance Method to Determine the (13)C Intramolecular Composition at Natural Abundance.
Anal. Chem. 87 , 6600-6, (2015) The natural xanthines caffeine, theobromine, and theophylline are of major commercial importance as flavor constituents in coffee, cocoa, tea, and a number of other beverages. However, their exploitation for authenticity, a requirement in these commodities th... |
|
|
The ionization mechanisms in direct and dopant-assisted atmospheric pressure photoionization and atmospheric pressure laser ionization.
J. Am. Soc. Mass Spectrom. 25(11) , 1870-81, (2014) A novel, gas-tight API interface for gas chromatography-mass spectrometry was used to study the ionization mechanism in direct and dopant-assisted atmospheric pressure photoionization (APPI) and atmospheric pressure laser ionization (APLI). Eight analytes (et... |
|
|
Differentiation of South American crack and domestic (US) crack cocaine via headspace-gas chromatography/mass spectrometry.
Drug Test. Anal. 7(3) , 241-6, (2015) South American 'crack' cocaine, produced directly from coca leaf, can be distinguished from US domestically produced crack on the basis of occluded solvent profiles. In addition, analysis of domestically produced crack indicates the solvents that were used fo... |
|
|
On the nature of the transition state characterizing gated molecular encapsulations.
Molecules 19(9) , 14292-303, (2014) Gated molecular encapsulations, with baskets of type 1, are postulated to occur by the mechanism in which solvent molecule penetrates the inner space of 1, through one of its apertures, while the residing guest simultaneously departs the cavity. In the transi... |
|
|
Ionization of EPA contaminants in direct and dopant-assisted atmospheric pressure photoionization and atmospheric pressure laser ionization.
J. Am. Soc. Mass Spectrom. 26 , 1036-45, (2015) Seventy-seven EPA priority environmental pollutants were analyzed using gas chromatography-mass spectrometry (GC-MS) equipped with an optimized atmospheric pressure photoionization (APPI) and an atmospheric pressure laser ionization (APLI) interface with and ... |
|
|
Syntheses, structures, and (1)H, (13)C{(1)H} and (119)Sn{(1)H} NMR chemical shifts of a family of trimethyltin alkoxide, amide, halide and cyclopentadienyl compounds.
Dalton Trans. 44 , 16156-63, (2015) The synthesis and full characterization, including Nuclear Magnetic Resonance (NMR) data ((1)H, (13)C{(1)H} and (119)Sn{(1)H}), for a series of Me3SnX (X = O-2,6-(t)Bu2C6H3 (), (Me3Sn)N(2,6-(i)Pr2C6H3) (), NH-2,4,6-(t)Bu3C6H2 (), N(SiMe3)2 (), NEt2, C5Me5 (),... |
|
|
Inherent organic compounds in biochar--Their content, composition and potential toxic effects.
J. Environ. Manage. 156 , 150-7, (2015) Pyrolysis liquids consist of thermal degradation products of biomass in various stages of its decomposition. Therefore, if biochar gets affected by re-condensed pyrolysis liquids it is likely to contain a huge variety of organic compounds. In this study the c... |
|
|
Synthesis of deuterium-labelled isotopomer of deferasirox.
J. Labelled Comp. Radiopharm. 58 , 163-5, (2015) A d4 -labeled isotopomer of deferasirox was synthesized as internal standard for use in a LC/mass spectroscopy (MS)/MS method developed for the simultaneous quantitative determination of deferasirox in human serum. d4 -deferasirox was synthesized from d8 -tol... |
|
|
Fourier transform NMR in liquids at high pressure. III. Spin-lattice relaxation in toluene-d8. Wilbur DJ and Jonas J.
J. Chem. Phys. 62(7) , 2800-2807, (1975)
|
|
|
Formation of deuterium atoms in the pyrolysis of toluene-d8 behind shock waves. Kinetics of the reaction C7D8+ H ? C7D7H + D Rao VS and Skinner GB.
J. Phys. Chem. 88(94) , 4362-4365, (1984)
|