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Merck
CN

L2009

Sigma-Aldrich

乙酰丙酸

98%

别名:

4-氧代戊酸, 4-酮正戊酸

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About This Item

线性分子式:
CH3COCH2CH2COOH
CAS号:
分子量:
116.12
Beilstein:
506796
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

蒸汽压

1 mmHg ( 102 °C)

质量水平

方案

98%

沸点

245-246 °C (lit.)

mp

30-33 °C (lit.)

密度

1.134 g/mL at 25 °C (lit.)

SMILES字符串

CC(=O)CCC(O)=O

InChI

1S/C5H8O3/c1-4(6)2-3-5(7)8/h2-3H2,1H3,(H,7,8)

InChI key

JOOXCMJARBKPKM-UHFFFAOYSA-N

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应用

乙酰丙酸是合成有用中间体如 γ-丙内酯、乙酰丙酸乙酯、戊酸和 2-甲基四氢呋喃的前提。 乙酰丙酸的衍生化和酯化产生了潜在的生物燃料。

它还可用于:
  • 合成 5-羟甲基糠醛和糠醛的催化复合物的制备。
  • 一种商品香料——油石的合成。
  • 吡咯烷酮衍生物通过还原胺化。
  • 分枝杆菌阿拉伯半乳聚糖的全合成。

象形图

CorrosionExclamation mark

警示用语:

Danger

危险声明

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1

储存分类代码

13 - Non Combustible Solids

WGK

WGK 2

闪点(°F)

208.4 °F - closed cup

闪点(°C)

98 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Diego Garcés et al.
ChemSusChem, 12(4), 924-934 (2018-12-15)
Homogeneous (HCl) and heterogeneous catalysts (various zeolites) were combined to enhance the upgrading of glucose into two different platform molecules: 5-hydroxymethylfurfural (HMF) and levulinic acid (LA). β-Zeolite was the most active material for the glucose isomerization to fructose, improving also
Selective and Efficient Iridium Catalyst for the Reductive Amination of Levulinic Acid into Pyrrolidones.
Wang S, et al.
ChemSusChem, 10(21), 4150-4154 (2017)
Nam H Phan et al.
Anti-cancer agents in medicinal chemistry, 18(9), 1349-1355 (2017-11-28)
The aim of this study was to develop and compare polymeric micelles of fucoidan, a sulfated polysaccharide, and hydrophobic drugs such as paclitaxel and curcumin. Paclitaxel and curcumin are both known for their medicinal properties, including anticancer efficacy. However, their
Synthesis of a New Type Perfume Fraistone [J].
Heping L, et al.
Fine Chemicals / ????, 6 (1998)
Vapor Phase Catalytic Transfer Hydrogenation (CTH) of Levulinic Acid to ?-Valerolactone Over Copper Supported Catalysts Using Formic Acid as Hydrogen Source.
Lomate S, et al.
Catalysis Letters, 148(1), 348-358 (2018)

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