245925
4-戊烯酸
97%
别名:
3-乙烯基丙酸, 烯丙基乙酸
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线性分子式:
CH2=CHCH2CH2COOH
化学文摘社编号:
分子量:
100.12
EC Number:
209-732-7
Beilstein/REAXYS Number:
1633696
MDL number:
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
Assay:
97%
Form:
liquid
产品名称
4-戊烯酸, 97%
InChI key
HVAMZGADVCBITI-UHFFFAOYSA-N
InChI
1S/C5H8O2/c1-2-3-4-5(6)7/h2H,1,3-4H2,(H,6,7)
SMILES string
OC(=O)CCC=C
vapor density
>1 (vs air)
assay
97%
form
liquid
refractive index
n20/D 1.428 (lit.)
bp
83-84 °C/12 mmHg (lit.)
mp
−22.5 °C (lit.)
density
0.981 g/mL at 25 °C (lit.)
functional group
allyl
carboxylic acid
storage temp.
2-8°C
Quality Level
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Application
用 4-戊烯酸（烯丙基乳酸）抑制大鼠心脏线粒体的脂肪酸氧化 。
General description
4-戊烯酸（烯丙基乳酸）磺化生成相应的 γ-内酯 。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
192.2 °F - closed cup
flash_point_c
89 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Rec. Trav. Chim., 111, 478-478 (1992)
Selina Schimka et al.
The Journal of chemical physics, 147(3), 031101-031101 (2017-07-25)
Here we report on a light triggered remote control of microgel size in the presence of photosensitive surfactant. The hydrophobic tail of the cationic surfactant contains azobenzene group that undergoes a reversible photo-isomerization reaction from a trans- to a cis-state
On the rate-determining step of fatty acid oxidation in heart. Inhibition of fatty acid oxidation by 4-pentenoic acid.
J C Fong et al.
The Journal of biological chemistry, 253(19), 6917-6922 (1978-10-10)
K Kassahun et al.
Drug metabolism and disposition: the biological fate of chemicals, 21(6), 1098-1106 (1993-11-01)
The terminal olefin metabolite of valproic acid (VPA), 4-ene VPA, is an analog of the experimental hepatotoxin 4-pentenoic acid and is believed to play a role in the hepatotoxicity of VPA. The formation of glutathione and N-acetylcysteine conjugates of the
Daniel C Whitehead et al.
Journal of the American Chemical Society, 132(10), 3298-3300 (2010-02-23)
A reagent controlled organocatalytic enantioselective chlorolactonization reaction has been developed. Several 4-aryl pentenoic acids were cyclized in the presence of 0.1 equiv of (DHQD)(2)PHAL, employing various N-chlorinated hydantoins as the terminal chlorenium source. Ten examples are presented with selectivities ranging
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