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C104507

Sigma-Aldrich

Cyclohexaneacetic acid

≥99%

Synonym(s):

Cyclohexylacetic acid

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About This Item

Linear Formula:
C6H11CH2CO2H
CAS Number:
5292-21-7
Molecular Weight:
142.20
Beilstein:
2041326
EC Number:
226-132-0
MDL number:
MFCD00001518
UNSPSC Code:
12352100
PubChem Substance ID:
24892314
NACRES:
NA.22

Quality Level

100

Assay

≥99%

form

solid

refractive index

n20/D 1.463 (lit.)

bp

242-244 °C (lit.)

mp

28-32 °C (lit.)

density

1.007 g/mL at 25 °C (lit.)

SMILES string

OC(=O)CC1CCCCC1

InChI

1S/C8H14O2/c9-8(10)6-7-4-2-1-3-5-7/h7H,1-6H2,(H,9,10)

InChI key

LJOODBDWMQKMFB-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Hiroaki Iwaki et al.
Current microbiology, 57(2), 107-110 (2008-04-09)
Six cyclohexylacetic acid-degrading strains were isolated from soil samples in Japan and identified as members of the genera Cupriavidus (strain KUA-1), Rhodococcus, and Dietzia by 16S rRNA gene sequence analysis. For the first time members of these genera were shown
J E Tulliez et al.
Lipids, 16(12), 888-892 (1981-12-01)
Among the urinary metabolites of dodecylcyclohexane or cyclohexylacetic acid, the glycine conjugate of 1-hydroxy-cyclohexylacetic acid was identified and its origin studied, using cyclohexylacetic acid as the starting molecule, as it results from beta-oxidation of cyclohexyldodecanoic acid produced by terminal oxidation
Rabea Schlüter et al.
Applied microbiology and biotechnology, 103(10), 4137-4151 (2019-04-04)
The cycloalkanes, comprising up to 45% of the hydrocarbon fraction, occur in crude oil or refined oil products (e.g., gasoline) mainly as alkylated cyclohexane derivatives and have been increasingly found in environmental samples of soil and water. Furthermore, short-chain alkylated
H J Ougham et al.
Journal of bacteriology, 150(3), 1172-1182 (1982-06-01)
A strain of Arthrobacter was isolated by enrichment culture with cyclohexaneacetate as the sole source of carbon and grew with a doubling time of 4.2 h. In addition to growing with cyclohexaneacetate, the organism also grew with cyclohexanebutyrate at concentrations
Dean M Quesnel et al.
Chemosphere, 84(4), 504-511 (2011-04-05)
Naphthenic acids (NAs) are a major contributor to toxicity in tailings waste generated from bitumen production in the Athabasca Oil Sands region. While investigations have shown that bacteria can biodegrade NAs and reduce tailings toxicity, the potential of algae to
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