Basic information Safety Supplier Related

(Aminomethyl)cyclohexane

Basic information Safety Supplier Related

(Aminomethyl)cyclohexane Basic information

Product Name:
(Aminomethyl)cyclohexane
Synonyms:
  • cyclohexanemethanamine
  • Cyclohexylmethanamine
  • RARECHEM AL BW 0122
  • HEXAHYDROBENZYLAMINE
  • CYCLOHEXANEMETHYLAMINE
  • AMINOMETHYLCYCLOHEXANE
  • Cyclohexanemethylamine,97%
  • Cyclohexylmethylamine, Hexahydrobenzylamine
CAS:
3218-02-8
MF:
C7H15N
MW:
113.2
EINECS:
221-741-8
Product Categories:
  • Pharmaceutical Intermediates
  • API intermediates
  • Amines and Anilines
  • 1
Mol File:
3218-02-8.mol
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(Aminomethyl)cyclohexane Chemical Properties

Melting point:
-8°C
Boiling point:
159-161 °C (lit.)
Density 
0.87 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.462(lit.)
Flash point:
110 °F
storage temp. 
2-8°C, protect from light
form 
Liquid
pka
10.42±0.29(Predicted)
color 
Clear colorless to slightly yellow
Water Solubility 
Slightly soluble in water.
Sensitive 
Air Sensitive
BRN 
635751
InChI
InChI=1S/C7H15N/c8-6-7-4-2-1-3-5-7/h7H,1-6,8H2
InChIKey
AVKNGPAMCBSNSO-UHFFFAOYSA-N
SMILES
C1(CN)CCCCC1
CAS DataBase Reference
3218-02-8(CAS DataBase Reference)
NIST Chemistry Reference
c-C6H11CH2NH2(3218-02-8)
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Safety Information

Hazard Codes 
C
Risk Statements 
10-34
Safety Statements 
16-26-36/37/39-45
RIDADR 
UN 2734 8/PG 2
WGK Germany 
3
RTECS 
GV6128000
HazardClass 
8
PackingGroup 
II
HS Code 
29213099
Storage Class
3 - Flammable liquids
Hazard Classifications
Flam. Liq. 3
Skin Corr. 1B

MSDS

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(Aminomethyl)cyclohexane Usage And Synthesis

Chemical Properties

Clear colorless to slightly yellow liquid

Uses

Cyclohexanemethylamine was used in the synthesis of Schiff′s base ligand, 4-methyl-2,6-bis(cyclohexylmethyliminomethyl)-phenol, which forms hexanuclear zinc(II) complexes. 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.

Synthesis Reference(s)

Tetrahedron Letters, 18, p. 2737, 1977 DOI: 10.1016/S0040-4039(01)83059-8
Synthesis, p. 441, 1981 DOI: 10.1055/s-1981-29473

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