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About This Item
Linear Formula:
CH2=CHCH2CH2COOH
CAS Number:
Molecular Weight:
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
vapor density
>1 (vs air)
Quality Level
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
SMILES string
OC(=O)CCC=C
InChI
1S/C5H8O2/c1-2-3-4-5(6)7/h2H,1,3-4H2,(H,6,7)
InChI key
HVAMZGADVCBITI-UHFFFAOYSA-N
General description
The sulfonation of 4-pentenoic acid (Allylacetic acid) yields the corresponding γ-lactone.
Application
4-Pentenoic acid (Allylacetic acid) was used to inhibit fatty acid oxidation in rat heart mitochondria.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class
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
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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)
Rec. Trav. Chim., 111, 478-478 (1992)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 245925-5G | 04061825849775 |
| 245925-25G | 04061825849768 |

