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(+/-)-trans-1,2-Diaminocyclohexane

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(+/-)-trans-1,2-Diaminocyclohexane Basic information

Product Name:
(+/-)-trans-1,2-Diaminocyclohexane
Synonyms:
  • TIMTEC-BB SBB007639
  • (+/-)-TRANS-1,2-CYCLOHEXANEDIAMINE
  • TRANS-1,2-CYCLOHEXANEDIAMINE
  • 1,2-Cyclohexanediamine, trans-
  • trans-1,2-Cyclohexaneiamine
  • Cyclohexanediamine
  • Trans-(L)-1,2-Diaminecyclohexane
  • trans-1,2-Diaminocyclohexane(Racemic)
CAS:
1121-22-8
MF:
C6H14N2
MW:
114.19
EINECS:
601-163-6
Product Categories:
  • bc0001
Mol File:
1121-22-8.mol
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(+/-)-trans-1,2-Diaminocyclohexane Chemical Properties

Melting point:
14-15 °C(lit.)
Boiling point:
79-81 °C15 mm Hg(lit.)
Density 
0.951 g/mL at 25 °C(lit.)
vapor pressure 
0.4 mm Hg ( 20 °C)
refractive index 
n20/D 1.489(lit.)
Flash point:
156 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Liquid
pka
9.94(at 20℃)
color 
Clear colorless to light yellow
Water Solubility 
Soluble
Sensitive 
Air Sensitive
BRN 
506142
InChIKey
SSJXIUAHEKJCMH-WDSKDSINSA-N
CAS DataBase Reference
1121-22-8(CAS DataBase Reference)
NIST Chemistry Reference
trans-1,2-Cyclohexanediamine(1121-22-8)
EPA Substance Registry System
1,2-Cyclohexanediamine, (1R,2R)-rel- (1121-22-8)
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-36/37/39-45
RIDADR 
UN 2735 8/PG 2
WGK Germany 
3
10-34
TSCA 
Yes
HazardClass 
8
PackingGroup 
II
HS Code 
29213000

MSDS

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(+/-)-trans-1,2-Diaminocyclohexane Usage And Synthesis

Chemical Properties

clear colorless to light yellow liquid

Uses

(^+)-trans-1,2-Diaminocyclohexane is employed in the synthesis of macrocyclic [3+3] hexa Schiff base. It also plays an important role in the preparation of multidentate ligands, chiral auxiliaries and chiral stationary phases. Further, it is used to prepare [2+2] macrocyclization by reacting with aliphatic dialdehydes. In addition to this, it acts as a chiral ligand, which finds application in asymmetric catalysis.

Uses

(±)-trans-1,2-Diaminocyclohexane was used in the synthesis of macrocyclic [3+3] hexa Schiff base. It was also employed in the synthesis of multidentate ligands, chiral auxiliaries and chiral stationary phases.

General Description

(±)-trans-1,2-Diaminocyclohexane was condensed with aliphatic dialdehydes to form [3+3] or [2+2] macrocyclization products.

Purification Methods

Purify and store the diamine as for the cis-isomer above as it is a strong base and becomes yellow on storage. [Beilstein 13 IV 1.]

(+/-)-trans-1,2-Diaminocyclohexane Preparation Products And Raw materials

Preparation Products

(+/-)-trans-1,2-DiaminocyclohexaneSupplier

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