추천 제품
분석
99%
형태
liquid
expl. lim.
0.34-6.3 %
refractive index
n20/D 1.388 (lit.)
bp
94-95 °C (lit.)
mp
−92 °C (lit.)
solubility
water: soluble 8.21 g/L at 20 °C
density
0.805 g/mL at 25 °C (lit.)
SMILES string
CC(C)C(C)=O
InChI
1S/C5H10O/c1-4(2)5(3)6/h4H,1-3H3
InChI key
SYBYTAAJFKOIEJ-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
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.
애플리케이션
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.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point (°F)
26.6 °F - closed cup
Flash Point (°C)
-3 °C - closed cup
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Photocatalytic destruction of VOCs in the gas-phase using titanium dioxide.
Applied Catalysis. B, Environmental, 14(1), 55-68 (1997)
Catalytic behavior of a Wool-Pd complex in asymmetric hydrogenation of diacetone alcohol and 3-methyl-2-butanone.
J. Mol. Catal. A: Chem., 147(1), 89-92 (1999)
Highly enantioselective hydrogenation of simple ketones catalyzed by a Rh-PennPhos complex.
Angewandte Chemie (International Edition in English), 37(8), 1100-1103 (1998)
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
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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