Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

28972

Sigma-Aldrich

Cyclohexanecarboxaldehyde

technical, ≥90% (GC)

Synonym(s):

Hexahydrobenzaldehyde

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H11CHO
CAS Number:
Molecular Weight:
112.17
Beilstein/REAXYS Number:
878306
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

grade

technical

Quality Level

assay

≥90% (GC)

refractive index

n20/D 1.452 (lit.)
n20/D 1.452

bp

161-163 °C (lit.)

density

0.926 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

O=CC1CCCCC1

InChI

1S/C7H12O/c8-6-7-4-2-1-3-5-7/h6-7H,1-5H2

InChI key

KVFDZFBHBWTVID-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Caution

may become turbid on storage

replaced by

Product No.
Description
Pricing

pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

105.8 °F - closed cup

flash_point_c

41 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

[Mn(tmc)(O2)]+: a side-on peroxido manganese(III) complex bearing a non-heme ligand.
Mi Sook Seo et al.
Angewandte Chemie (International ed. in English), 46(3), 377-380 (2006-11-30)
Differential inactivation of DNA polymerases alpha and beta by aldehyde compounds.
K Suzuki et al.
Biochemical and biophysical research communications, 100(4), 1626-1633 (1981-06-01)
Ashfaq Ahmad et al.
Drug design, development and therapy, 14, 2165-2178 (2020-07-02)
The current study was designed to synthesize derivatives of succinimide and compare their biological potency in anticholinesterase, alpha-glucosidase inhibition, and antioxidant assays. In this research, two succinimide derivatives including (S)-1-(2,5-dioxo-1-phenylpyrrolidin-3-yl) cyclohexanecarbaldehyde (Compound 1) and (R)-2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)-2-phenylpropanal (Compound 2) were synthesized using

Questions

Reviews

No rating value

Active Filters

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