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240648

Sigma-Aldrich

Cyclohexylamine

ReagentPlus®, ≥99.9%

Sinónimos:

Aminocyclohexane

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About This Item

Fórmula lineal:
C6H11NH2
Número de CAS:
108-91-8
Peso molecular:
99.17
Beilstein/REAXYS Number:
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)

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

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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

signalword

Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

80.6 °F - closed cup

flash_point_c

27 °C - closed cup

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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
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