240648
Cyclohexylamine
ReagentPlus®, ≥99.9%
Sinónimos:
Aminocyclohexane
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Fórmula lineal:
C6H11NH2
Número CAS:
Peso molecular:
99.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-629-0
Beilstein/REAXYS Number:
471175
MDL number:
Assay:
≥99.9%
Form:
liquid
Servicio técnico
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Permítanos ayudarlevapor 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
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
Clase de almacenamiento
3 - Flammable liquids
wgk
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
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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
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
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