推荐产品
等級
ACS reagent
analytical standard
for NMR spectroscopy
品質等級
蒸汽壓力
11.66 psi ( 20 °C)
化驗
≥99.5% (GC)
形狀
liquid
自燃溫度
842 °F
折射率
n20/D 1.358 (lit.)
n20/D 1.359
bp
26-28 °C (lit.)
mp
−99 °C (lit.)
密度
0.648 g/mL at 25 °C (lit.)
應用
environmental
格式
neat
儲存溫度
2-8°C
SMILES 字串
C[Si](C)(C)C
InChI
1S/C4H12Si/c1-5(2,3)4/h1-4H3
InChI 密鑰
CZDYPVPMEAXLPK-UHFFFAOYSA-N
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一般說明
四甲基硅烷已被国际纯粹与应用化学联合会(IUPAC)推荐为所有核素的通用参考品。它通常用作核磁共振(NMR)的参考标准品,用于测量质子的化学位移,TMS在氯仿、甲醇和二甲基亚砜等溶剂中的1H化学位移的温度依赖性已进行了研究。
應用
四甲基硅烷可用作定量NMR(qNMR)法定量分析药用植物提取物和草药产品的内标物。它也可用作FT-IR光谱法和质子核磁共振(1H NMR)技术研究过氧化物化学系统中等规聚丙烯交联反应的内标物。
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Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 65(3-4), 787-791 (2006-03-15)
The decomposition of trimethylsilane and tetramethylsilane has been investigated for the first time, using hot wire (catalytic) at various temperatures. Trimethylsilane is catalytic-dissociated in these species SiH(2), CH(3)SiH, CH(3), CH(2)Si. Time of flight mass spectroscopy signal of these species are
Physics in medicine and biology, 48(21), 3555-3564 (2003-12-05)
First measurements with a prototype ionization chamber are described to be applied in online monitoring of modulated fields in radiation therapy. The liquids isooctane, isononane (TMP) and tetramethylsilane (TMS) are used in a high purity grade in order to realize
Magnetic resonance in chemistry : MRC, 45 Suppl 1, S174-S186 (2007-12-25)
Computations for chemical shifts of molecular organic compounds using the gauge-including projector augmented wave method and the NMR-CASTEP code are reviewed. The methods are briefly introduced, and some general aspects involving the sources of uncertainty in the results are explored.
Journal of magnetic resonance (San Diego, Calif. : 1997), 163(2), 325-331 (2003-08-14)
The chemical shift of TMS is commonly assumed to be zero. However, it varies by over 1 ppm for 1H and 4 ppm for 13C and shows a correlation with the physical properties of the solvent. Using the commonly accepted
ChemMedChem, 9(6), 1176-1187 (2014-05-23)
A series of methoxy- and fluorine-substituted [salophene]platinum(II) complexes (salophene=N,N'-bis(salicylidene)-1,2-phenylenediamine) were synthesized and characterized by (1) H NMR spectroscopy and mass spectrometry. The structure was confirmed on the example of [5-OCH3 -salophene]platinum(II) (4-Pt) by crystal structure analysis. The cytotoxicity of all
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