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蒸汽密度
2 (vs air)
蒸汽壓力
14.39 psi ( 55 °C)
184 mmHg ( 20 °C)
3.67 psi ( 20 °C)
同位素純度
≥99.9 atom % D
化驗
≥99% (CP)
包含
1 % (v/v) TMS
expl. lim.
13.2 %
包裝
pk of 10 × 1 mL
雜質
≤0.0500% water
water
折射率
n20/D 1.355 (lit.)
bp
55.5 °C (lit.)
mp
−93.8 °C (lit.)
密度
0.872 g/mL at 25 °C (lit.)
質量偏移
M+6
SMILES 字串
[2H]C([2H])([2H])C(=O)C([2H])([2H])[2H]
InChI
1S/C3H6O/c1-3(2)4/h1-2H3/i1D3,2D3
InChI 密鑰
CSCPPACGZOOCGX-WFGJKAKNSA-N
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一般說明
Acetone-d6 is is a deuterated NMR solvent containing 1% (v/v) TMS (tetramethylsilane). It is useful in NMR-based research and analyses. Its Infrared and Raman spectra have been analyzed. Pyrolysis and photolysis of acetone-d6 and methane mixtures have been investigated as a function of temperature. It has been reported to be prepared by reacting heavy water with propyne-d4.
應用
Acetone-d6 may be used as an internal standard to detect aldehydes and acetone in water by headspace-solid-phase microextraction and gas chromatography-mass spectrometry.
訊號詞
Danger
危險聲明
危險分類
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
標靶器官
Central nervous system
安全危害
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 1
閃點（°F）
-2.2 °F - closed cup
閃點（°C）
-19 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves
The Pyrolysis and Photolysis of Acetone-d6 in the Presence of Methane.
McNesby JR and Gordon AS.
Journal of the American Chemical Society, 76(16), 4196-4198 (1954)
Hyun-Ji Kim et al.
Journal of separation science, 34(6), 693-699 (2011-02-15)
We describe a simple and automatic method to determine nine aldehydes and acetone simultaneously in water. This method is based on derivatization with 2,2,2-trifluoroethylhydrazine (TFEH) and consecutive headspace-solid-phase microextraction and gas chromatography-mass spectrometry. Acetone-d(6) was used as the internal standard.
Vibrational spectra and assignment of acetone, ααα acetone-d3 and acetone-d6.
Dellepiane G and Overend J.
Spectrochimica Acta Part A: Molecular Spectroscopy, 22(4), 593-614 (1966)
Neue Synthese von Aceton-d6.
Hunziker H, et al.
Helvetica Chimica Acta, 45(1), 59-62 (1962)
Ofentse Mazimba et al.
Bioorganic & medicinal chemistry, 22(23), 6564-6569 (2014-12-03)
A series of 3-nitrochalcones have been synthesized enroute towards fused ring pyrazolones and isoxazolones. Base catalyzed condensation of the chalcones with ethylacetoacetate yielded cyclohexenones in good yields (74-76%). The treatment of cyclohexenones with hydrazine hydrate or hydroxylamine chloride in the
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