Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

240648

Sigma-Aldrich

Cyclohexylamine

ReagentPlus®, ≥99.9%

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:
24854426
NACRES:
NA.22

vapor density

3.42 (vs air)

Quality Level

200

vapor pressure

10 mmHg ( 22 °C)
23 mmHg ( 37.7 °C)

product line

ReagentPlus®

Assay

≥99.9%

form

liquid

autoignition temp.

559 °F

refractive index

n20/D 1.459 (lit.)

bp

134 °C (lit.)

mp

−17 °C (lit.)

solubility

organic solvents: miscible
water: miscible

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

Related Categories

General description

The fourier transform infrared spectroscopy, thermogravimetric analysis and temperature-programmed desorption of cyclohexylamine was studied.

Application

Cyclohexylamine was used in the synthesis of pendant-armed dialdehydes.

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBK6514
STBK3436
STBK2871
STBK0826
STBJ7038

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Slide 1 of 3

1 of 3

2-Chloroethyl isocyanate low HCl, 97%

Sigma-Aldrich

538337

2-Chloroethyl isocyanate

Aniline ACS reagent, ≥99.5%

Sigma-Aldrich

242284

Aniline

Cyclohexene analytical standard, ≥99.5% (GC)

Supelco

44028

Cyclohexene

Hui-Qing Chen et al.
Dalton transactions (Cambridge, England : 2003), 43(22), 8486-8492 (2014-04-23)
Two novel pendant-armed dialdehydes (1a and 1b) were prepared by a one-step reaction between 5-chloro-3-(chloromethyl)-2-hydroxybenzaldehyde/5-methyl-3-(chloromethyl)-2-hydroxybenzaldehyde and cyclohexylamine involving two nucleophilic substitutions, and they were used to react with 1,3-propanediamine to prepare Schiff-base macrocyclic complexes in the presence of ZnX2 salts
Kenia Salazar-Díaz et al.
iScience, 24(11), 103260-103260 (2021-11-13)
Spermidine (Spd) is a nitrogen sink and signaling molecule that plays pivotal roles in eukaryotic cell growth and must be finetuned to meet various energy demands. In eukaryotes, target of rapamycin (TOR) is a central nutrient sensor, especially N, and
Jyrki Viidanoja
Journal of chromatography. A, 1480, 106-111 (2016-12-21)
A new liquid chromatography-electrospray ionization-tandem Mass Spectrometry (LC-ESI-MS/MS) method was developed for the determination of more than 20 C1-C6 alkyl and alkanolamines in aqueous matrices. The method employs Hydrophilic Interaction Liquid Chromatography Multiple Reaction Monitoring (HILIC-MRM) with a ZIC-pHILIC column
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
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