W353108

Sigma-Aldrich

Cyclohexanecarboxylic acid

≥98%, FG

Synonym(s):
Hexahydrobenzoic acid
Linear Formula:
C6H11CO2H
CAS Number:
Molecular Weight:
128.17
FEMA Number:
3531
Beilstein/REAXYS Number:
970529
EC Number:
Council of Europe no.:
11911
MDL number:
PubChem Substance ID:
Flavis number:
8.060
NACRES:
NA.21

Quality Level

biological source

synthetic

grade

FG
Kosher

reg. compliance

EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 110

assay

≥98%

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.)

Documentation

see Safety & Documentation for available documents

Featured Industry

Flavors and Fragrances

Organoleptic

fruity; acidic

food allergen

no known allergens

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Cyclohexanecarboxylic acid occurs naturally in the leaves of Ormosia henryi Prain. It is also one of the aromatic volatile compounds found in the secretion of tail glands of red deer.

Packaging

100 g in glass bottle
1 kg in glass bottle

Other Notes

Download our Flavors and Fragrances Catalog to view our entire product line.

Subscribe to our Newsletter to keep up to date on our latest Flavors and Fragrances offerings.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Target Organs

Respiratory system

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

NONH for all modes of transport

WGK Germany

WGK 2

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

A new sexual signal in rutting male red deer: Age related chemical scent constituents in the belly black spot.
Martin J, et al.
Mammalian Biology-Zeitschrift fur Saugetierkunde, 79(6), 362-368 (2014)
GC-MS Analysis of Chemical Constituents of the Volatile Oil from Leaves of Ormosia henryi Prain.
Jiexiong NBZWF & Mi T.
Guangdong Forestry Science and Technology, 2, 012-012 (2012)
Christo Christov et al.
ChemMedChem, 6(1), 131-140 (2010-12-07)
2-(3,5-Dichlorophenylcarbamoyl)cyclohexanecarboxylic acid (1) is a potent and selective positive allosteric modulator of metabotropic glutamate receptor subtype 4 (mGluR4). The activity of 1 was reported to reside in the cis diastereomer with equal potency between its enantiomeric forms (Niswender et al., Mol. Pharmacol....
P G Egland et al.
Journal of bacteriology, 177(22), 6545-6551 (1995-11-01)
The first step of anaerobic benzoate degradation is the formation of benzoyl-coenzyme A by benzoate-coenzyme A ligase. This enzyme, purified from Rhodopseudomonas palustris, is maximally active with 5 microM benzoate. To study the molecular basis for this reaction, the benzoate-coenzyme...
Housna Mouttaki et al.
Environmental microbiology, 10(12), 3265-3274 (2008-08-19)
In methanogenic environments, the main fate of benzoate is its oxidization to acetate, H(2) and CO(2) by syntrophic associations of hydrogen-producing benzoate degraders and hydrogen-using methanogens. Here, we report the use of benzoate as an electron acceptor. Pure cultures of...

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service

Social Media

LinkedIn icon
Twitter icon
Facebook Icon
Instagram Icon

MilliporeSigma

Research. Development. Production.

We are a leading supplier to the global Life Science industry with solutions and services for research, biotechnology development and production, and pharmaceutical drug therapy development and production.

© 2021 Merck KGaA, Darmstadt, Germany and/or its affiliates. All Rights Reserved.

Reproduction of any materials from the site is strictly forbidden without permission.