推荐产品
方案
99%
表单
liquid
expl. lim.
0.34-6.3 %
折射率
n20/D 1.388 (lit.)
沸点
94-95 °C (lit.)
mp
−92 °C (lit.)
溶解性
water: soluble 8.21 g/L at 20 °C
密度
0.805 g/mL at 25 °C (lit.)
SMILES字符串
CC(C)C(C)=O
InChI
1S/C5H10O/c1-4(2)5(3)6/h4H,1-3H3
InChI key
SYBYTAAJFKOIEJ-UHFFFAOYSA-N
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一般描述
3-Methyl-2-butanone (Methyl isopropyl ketone, MIPK, isopropyl methyl ketone), an aliphatic ketone, is a volatile organic compound. Photodegradation of MIPK in gas-phase has been reported. Asymmetric hydrogenation of MIPK with high enantioselectivity in the presence of Rh-PennPhos (rhodium-P,P′-1,2-phenylenebis(endo-2,5-dialkyl-7-phosphabicyclo[2.2.1]heptane) complex has been reported.
应用
3-Methyl-2-butanone may be used to prepare (R)-3-methyl-2-butanol via asymmetric hydrogenation in the presence of a wool-Pd complex.
警示用语：
Danger
危险声明
危险分类
Flam. Liq. 2
储存分类代码
3 - Flammable liquids
WGK
WGK 1
闪点(°F)
26.6 °F - closed cup
闪点(°C)
-3 °C - closed cup
法规信息
危险化学品
Photocatalytic destruction of VOCs in the gas-phase using titanium dioxide.
Alberici RM and Jardim WF.
Applied Catalysis. B, Environmental, 14(1), 55-68 (1997)
Highly enantioselective hydrogenation of simple ketones catalyzed by a Rh-PennPhos complex.
Jiang Q, et al.
Angewandte Chemie (International Edition in English), 37(8), 1100-1103 (1998)
Sami Sajjadifar et al.
Molecules (Basel, Switzerland), 15(4), 2491-2498 (2010-04-30)
Methyl indolenines (4a-c) and(5a-c) were prepared in high yield by a Fischer indole synthesis reaction of o,m-tolylhydrazine hydrochlorides (1a-b) with isopropyl methyl ketone (2) and 2-methylcyclohexanone (3) in acetic acid at room temperature. o,p- Nitrophenylhydrazines (1c-d) were reacted with 2-methylcyclohexanone
Catalytic behavior of a Wool-Pd complex in asymmetric hydrogenation of diacetone alcohol and 3-methyl-2-butanone.
Yin MO, et al.
J. Mol. Catal. A: Chem., 147(1), 89-92 (1999)
E M Gagan et al.
Archives of environmental contamination and toxicology, 52(3), 283-293 (2007-01-27)
Frequently the toxicity of an organic chemical mixture is close to dose-additive, even when the agents are thought to induce toxicity at different molecular sites of action. These findings appear to conflict with the hypothesis that a strictly dose-additive combined
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