Acetonitrile-d3 structure
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Common Name | Acetonitrile-d3 | ||
|---|---|---|---|---|
| CAS Number | 2206-26-0 | Molecular Weight | 44.070 | |
| Density | 0.7±0.1 g/cm3 | Boiling Point | 63.5±3.0 °C at 760 mmHg | |
| Molecular Formula | C2D3N | Melting Point | -46ºC | |
| MSDS | Chinese USA | Flash Point | 5.6±0.0 °C | |
| Symbol |
GHS02, GHS07 |
Signal Word | Danger | |
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Development of a purity control strategy for pemetrexed disodium and validation of associated analytical methodology.
J. Pharm. Biomed. Anal. 105 , 46-54, (2015) Stability-indicating reversed phase HPLC methods have been developed and validated for the determination of 13 potential process and degradation impurities in pemetrexed disodium drug substance (DS) and pemetrexed for injection drug product (DP). This paper d... |
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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 (),... |
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HPLC-SPE-NMR hyphenation in natural products research: optimization of analysis of Croton membranaceus extract.
Magn. Reson. Chem. 43(9) , 771-5, (2005) The HPLC-SPE-NMR technique was used for the analysis of a root-bark extract of Croton membranaceus. The components of the extract were separated on an analytical-size reversed-phase HPLC column, the chromatographic peaks were trapped on SPE (solid-phase extra... |
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Organic deuterium compounds: XVI. Synthesis of α-deuterated alkyl nitriles. Leitch LC.
Can. J. Chem. 35(4) , 345-347, (1957)
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Pressure dependencies of rotational, translational, and viscous friction coefficients in water-d2, acetonitrile-d3, acetonitrile, chloroform, and benzene. Wakai C and Nakahara M.
J. Chem. Phys. 100(11) , 8347-8358, (1994)
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Dynamics of a wetting liquid in nanopores: An optical Kerr effect study of the dynamics of acetonitrile confined in sol-gel glasses. Loughnane BJ, et al.
J. Chem. Phys. 111(11) , 5116-5123, (1999)
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The lowest triplet state of 1, 3, 5-hexatrienes: Quantum chemical force field calculations and experimental resonance Raman spectra. Negri F, et al.
J. Chem. Phys. 90(11) , 5944-5963, (1989)
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Proton polarizability caused by collective proton motion in intramolecular chains formed by two and three hydrogen bonds. Implications for charge conduction in bacteriorhodopsin. Brzezinski B, et al.
J. Phys. Chem. 91(11) , 3077-3080, (1987)
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Acetonitrile-d3 as a probe of Lewis and Broensted acidity of zeolites. Pelmenschikov AG, et al.
J. Phys. Chem. 97(42) , 11071-11074, (1993)
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Magnetic Resonance Studies of Anisotropic Molecular Rotation in Liquid Acetonitrile-d3. Bopp TT.
J. Chem. Phys. 47(9) , 3621-3626, (1967)
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