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101842

Sigma-Aldrich

Cyclohexanemethylamine

98%

Synonym(s):

(Aminomethyl)cyclohexane, Hexahydrobenzylamine

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$158.00
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$322.00

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5 G
$59.37
25 G
$158.00
100 G
$322.00

About This Item

Linear Formula:
C6H11CH2NH2
CAS Number:
3218-02-8
Molecular Weight:
113.20
Beilstein/REAXYS Number:
635751
EC Number:
221-741-8
MDL number:
MFCD00001520
UNSPSC Code:
12352100
PubChem Substance ID:
24846555
NACRES:
NA.22

$59.37

List Price$62.50Save 5%
Web-Only Promotion

Available to ship onApril 29, 2025Details

Request a Bulk Order

Quality Level

100

assay

98%

refractive index

n20/D 1.462 (lit.)

bp

159-161 °C (lit.)

density

0.87 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

NCC1CCCCC1

InChI

1S/C7H15N/c8-6-7-4-2-1-3-5-7/h7H,1-6,8H2

InChI key

AVKNGPAMCBSNSO-UHFFFAOYSA-N

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Application

Cyclohexanemethylamine was used in the synthesis of Schiff′s base ligand, 4-methyl-2,6-bis(cyclohexylmethyliminomethyl)-phenol, which forms hexanuclear zinc(II) complexes[1]. Cyclohexanemethylamine was used during the synthesis of 1-acyl-4 cycloalkyl/arylsemicarbazides and 1-acyl-5-benzyloxy/hydroxyl carbamoylcarbazides from the nonsteroidal anti-inflammatory drugs[2].

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

hcodes

H226,H314

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

118.4 °F - closed cup

flash_point_c

48 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
SHBD1588V
S26989
15731CN
00109PG
00106AU

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Synthesis, characterization and fluorescence properties of hexanuclear zinc (II) complexes.
Roy P, et al.
Polyhedron, 28(6), 1133-1137 (2009)
I Perković et al.
European journal of medicinal chemistry, 51, 227-238 (2012-03-13)
The novel 1-acyl-4-cycloalkyl/arylsemicarbazides (5a-y) and 1-acyl-5-benzyloxy/hydroxycarbamoylcarbazides (8a-f) derived from the nonsteroidal anti-inflammatory drugs ibuprofen, fenoprofen and reduced ketoprofen were prepared, fully chemically characterized and evaluated for their cytostatic, antiviral and antioxidant activities. Compounds 5 and 8 consist of a region

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