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About This Item
Linear Formula:
C6H11CO2H
CAS Number:
Molecular Weight:
128.17
EC Number:
202-711-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
970529
MDL number:
grade
purum
assay
≥97.0% (GC)
refractive index
n20/D 1.461 (lit.)
bp
232-233 °C (lit.)
mp
29-31 °C (lit.)
density
1.033 g/mL at 25 °C (lit.)
SMILES string
OC(=O)C1CCCCC1
InChI
1S/C7H12O2/c8-7(9)6-4-2-1-3-5-6/h6H,1-5H2,(H,8,9)
InChI key
NZNMSOFKMUBTKW-UHFFFAOYSA-N
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - STOT RE 2
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Janice C Paslawski et al.
Biodegradation, 20(1), 125-133 (2008-07-18)
Naphthenic acids are a complex mixture of organic compounds which naturally occur in crude oil. Low molecular weight components of the naphthenic acids are known to be toxic in aquatic environments and there is a need to better understand the
A M Svardal et al.
Molecular and cellular biochemistry, 65(2), 107-115 (1985-01-01)
The conversion of cyclohexanecarboxylic acid to hippuric acid in subcellular fractions from guinea pig liver was studied using a gas chromatographic-mass spectrometric method employing selected ion monitoring. Comparison of the activities of the cyclohexanecarboxylic acid to hippuric acid converting system
S M Patton et al.
Biochemistry, 39(25), 7595-7604 (2000-06-20)
The side chain of the antifungal polyketide ansatrienin A produced by Streptomyces collinus contains a cyclohexanecarboxylic acid (CHC) derived moiety. This CHC in the coenzyme A activated form (CHC-CoA) is derived from shikimic acid via a pathway in which the
P Wang et al.
Journal of bacteriology, 178(23), 6873-6881 (1996-12-01)
We report the cloning of the gene encoding the 1-cyclohexenylcarbonyl coenzyme A reductase (ChcA) of Streptomyces collinus, an enzyme putatively involved in the final reduction step in the formation of the cyclohexyl moiety of ansatrienin from shikimic acid. The cloned
A M Svardal et al.
Molecular and cellular biochemistry, 67(2), 171-179 (1985-07-01)
The ability to convert cyclohexanecarboxylic acid to hippuric acid has been studied in liver from guinea pigs, rabbits, rats and mice using a gas chromatographic - mass spectrometric method employing selected ion monitoring. Guinea pig liver showed the highest activity
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