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About This Item
Linear Formula:
C5H9CH2CO2H
CAS Number:
Molecular Weight:
128.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
214-368-7
MDL number:
InChI key
YVHAIVPPUIZFBA-UHFFFAOYSA-N
InChI
1S/C7H12O2/c8-7(9)5-6-3-1-2-4-6/h6H,1-5H2,(H,8,9)
SMILES string
OC(=O)CC1CCCC1
assay
97%
form
liquid
refractive index
n20/D 1.453 (lit.)
bp
133-134 °C/23 mmHg (lit.)
density
1.022 g/mL at 25 °C (lit.)
Application
Cyclopentylacetic acid has been used in a study to examine the butylation efficiency of free carboxylic acids.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
228.2 °F - closed cup
flash_point_c
109 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Cristhian C Chávez-Arias et al.
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Vascular wilt caused by Fusarium oxysporum is the most limiting disease that affects cape gooseberry (Physalis peruviana L.) crops in Colombia. The use of synthetic elicitors for vascular wilt management is still scarce in Andean fruit species. The objective of
Christian Hallmann et al.
Journal of chromatography. A, 1198-1199, 14-20 (2008-06-06)
The conversion efficiency of alkanoic, alkenoic, branched, alicyclic, aromatic, keto-substituted, and dioic carboxylic acids to their corresponding butyl esters was compared under different reaction conditions (time, temperature, catalyst). We show that boron trifluoride is generally a more efficient catalyst than
Gas Phase Oxidation of Campholenic Aldehyde and Solution Phase Reactivity of its Epoxide Derivative.
William C Thomas et al.
The journal of physical chemistry. A, 121(1), 168-180 (2016-12-13)
The rate constant for the OH reaction with campholenic aldehyde (CA) was measured using the flow tube-chemical ionization mass spectrometry method with a relative rate kinetics technique and was found to be (6.54 ± 0.52) × 10
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