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101834

Sigma-Aldrich

Cyclohexanecarboxylic acid

98%

Sinónimos:

Hexahydrobenzoic acid

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About This Item

Fórmula lineal:
C6H11CO2H
Número de CAS:
98-89-5
Peso molecular:
128.17
Beilstein/REAXYS Number:
970529
EC Number:
202-711-3
MDL number:
MFCD00001461
UNSPSC Code:
12352100
PubChem Substance ID:
24846554
NACRES:
NA.22

assay

98%

form

solid

refractive index

n20/D 1.461 (lit.)

bp

232-233 °C (lit.)

mp

29-31 °C (lit.)

solubility

H2O: soluble 0.201g in 100g at 15 °C
organic solvents: soluble

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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Application

Cyclohexanecarboxylic acid was used in a study to determine complex binding constants of the three native cyclodextrins with seven cyclohexane derivatives.

Biochem/physiol Actions

Cyclohexanecarboxylic acid undergoes microbial degradation by a strain of Antherobacter to form para-hydroxybenzoic acid. Cyclohexanecarboxylic acid undergoes aromatization and converts to Hippuric acid in rat liver extracts in vitro. Cyclohexanecarboxylic acid is the starting reagent for the synthesis of polyketide-type antibiotics, Phoslactomycins.

Preparation Note

0.201g of cyclohexanecarboxylic acid dissolves in 100g water at 15°C.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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3-Cyclohexene-1-carboxylic acid 97%

Sigma-Aldrich

453757

3-Cyclohexene-1-carboxylic acid

A Gadre et al.
Journal of pharmaceutical sciences, 86(2), 236-243 (1997-02-01)
Complex binding constants of the three native cyclodextrins with seven cyclohexane derivatives (all possessing the carboxylic acid group) and with the series C6H5(CH2)nCOOH (n = 0 to 4) were measured in aqueous solution at 25 degrees C by potentiometry and
Biosynthesis of phoslactomycins: cyclohexanecarboxylic acid as the starter unit.
Sekiyama Y, et al.
Tetrahedron, 59(38), 7465-7471 (2003)
The microbial degradation of cyclohexanecarboxylic acid: a pathway involving aromatization to form p-hydroxybenzoic acid.
Blakley ER.
Canadian Journal of Microbiology, 20(10), 1297-1306 (1974)
Aromatization of cyclohexanecarboxylic acid.
B M Babior et al.
The Journal of biological chemistry, 241(16), 3643-3651 (1966-08-25)
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
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