125490
Cyclopentylacetic acid
97%
Synonym(s):
Cyclopentaneacetic acid
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About This Item
Linear Formula:
C5H9CH2CO2H
CAS Number:
Molecular Weight:
128.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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.)
SMILES string
OC(=O)CC1CCCC1
InChI
1S/C7H12O2/c8-7(9)5-6-3-1-2-4-6/h6H,1-5H2,(H,8,9)
InChI key
YVHAIVPPUIZFBA-UHFFFAOYSA-N
Application
Cyclopentylacetic acid has been used in a study to examine the butylation efficiency of free carboxylic acids.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
228.2 °F - closed cup
Flash Point(C)
109 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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
Cristhian C Chávez-Arias et al.
Plants (Basel, Switzerland), 9(2) (2020-02-07)
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
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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