Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

C104655

Sigma-Aldrich

Cyclohexylamine

ReagentPlus®, 99%

Synonym(s):

Aminocyclohexane

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C6H11NH2
CAS Number:
108-91-8
Molecular Weight:
99.17
Beilstein:
471175
EC Number:
203-629-0
MDL number:
MFCD00001486
UNSPSC Code:
12352100
PubChem Substance ID:
24891956

vapor density

3.42 (vs air)

vapor pressure

10 mmHg ( 22 °C)
23 mmHg ( 37.7 °C)

product line

ReagentPlus®

Assay

99%

form

liquid

autoignition temp.

559 °F

refractive index

n20/D 1.459 (lit.)

bp

134 °C (lit.)

mp

−17 °C (lit.)

density

0.867 g/mL at 25 °C (lit.)

SMILES string

NC1CCCCC1

InChI

1S/C6H13N/c7-6-4-2-1-3-5-6/h6H,1-5,7H2

InChI key

PAFZNILMFXTMIY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 3 - Repr. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

80.6 °F - closed cup

Flash Point(C)

27 °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’.

Already Own This Product?

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

Visit the Document Library

Jang Sen Chang et al.
Environmental pollution (Barking, Essex : 1987), 259, 113867-113867 (2020-01-04)
This study aimed to evaluate the impacts of morphological-controlled ZnO nanoarchitectures on aerobic microbial communities during real wastewater treatment in an aerobic-photocatalytic system. Results showed that the antibacterial properties of ZnO nanoarchitectures were significantly more overwhelming than their photocatalytic properties.
Ala'a F Eftaiha et al.
Physical chemistry chemical physics : PCCP, 22(3), 1306-1312 (2019-12-19)
A comparative model for the chemisorption of CO2 was explored via three representative reaction pathways: carboxylation of cyclohexanone, carbonation of cyclohexanol, and carbamation of cyclohexylamine. The model substrates were activated using 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, an amidine superbase). For each of these
Fengyuan Tang et al.
Cancer research, 74(14), 3779-3789 (2014-05-30)
New therapeutic targets are needed that circumvent inherent therapeutic resistance of glioblastoma multiforme (GBM). Here, we report such a candidate target in the uncharacterized adaptor protein hMOB3, which we show is upregulated in GBM. In a search for its biochemical
Kenta Kanosue et al.
Physical chemistry chemical physics : PCCP, 17(45), 30659-30669 (2015-11-03)
The structure and optical properties of a newly synthesized imide compound (DHNHPI) that forms intramolecular double hydrogen bonds (intra-HBs) were investigated. This compound exhibits intense absorption at 372 nm (ε = 5091 cm(-1) M(-1)) and strong emission at 427 nm
Aditya Kapil Valiveti et al.
Chemico-biological interactions, 237, 125-132 (2015-06-14)
A series of mono pyridinium oximes linked with arenylacetamides as side chains were synthesized and their in vitro reactivation potential was evaluated against human acetylcholinesterase (hAChE) inhibited by organophosphorus inhibitors (OP) such as sarin, VX and tabun. The reactivation data
View All Related Papers

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