240648

Sigma-Aldrich

Cyclohexylamine

ReagentPlus®, ≥99.9%

Synonym(s):
Aminocyclohexane
Linear Formula:
C6H11NH2
CAS Number:
Molecular Weight:
99.17
Beilstein/REAXYS Number:
471175
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

vapor density

3.42 (vs air)

vapor pressure

10 mmHg ( 22 °C)
23 mmHg ( 37.7 °C)

product line

ReagentPlus®

assay

≥99.9%

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

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.

Packaging

5, 100 mL in glass bottle

Legal Information

ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

Signal Word

Danger

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

UN 2357 3(8) / PGII

WGK Germany

WGK 1

Flash Point(F)

80.6 °F - closed cup

Flash Point(C)

27 °C - closed cup

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...
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...
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...

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.