(±)-trans-1,2-Diaminocyclohexane CAS 1121-22-8 Purity ≥98.0% High Purity

Short Description:

Chemical Name: (±)-trans-1,2-Diaminocyclohexane

CAS: 1121-22-8

Appearance: Colorless or Yellowish Liquid

Purity: ≥98.0%

High Quality, Commercial Production

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Product Detail

Product Tags

Description:

Manufacturer Supply with High Purity and Stable Quality
Chemical Name: (±)-trans-1,2-Diaminocyclohexane
CAS: 1121-22-8
High Quality, Commercial Production

Chemical Properties:

Chemical Name	(±)-trans-1,2-Diaminocyclohexane
Synonyms	trans-1,2-Diaminocyclohexane; trans-1,2-Cyclohexanediamine
CAS Number	1121-22-8
CAT Number	RF-CC281
Stock Status	In Stock, Production Scale Up to Tons
Molecular Formula	C6H14N2
Molecular Weight	114.19
Melting Point	14.0-15.0℃ (lit.)
Boiling Point	79.0-81.0℃/15 mmHg (lit.)
Density	0.951 g/mL at 25℃ (lit.)
Refractive Index	n20/D 1.489 (lit.)
Solubility	Soluble in Water
Sensitivity	Air Sensitive, Hygroscopic
Shipping Condition	Shipped Under Ambient Temperature
Brand	Ruifu Chemical

Specifications:

Item	Specifications
Appearance	Colorless or Yellowish Liquid
Purity	≥98.0% (GC)
Water	≤1.00%
Total Impurities	≤2.00%
Test Standard	Enterprise Standard
Usage	Chiral Compounds; Pharmaceutical Intermediates

Package & Storage:

Package: Bottle, 25kg/Barrel, or according to customer's requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.

Advantages:

FAQ:

Application:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of (±)-trans-1,2-Diaminocyclohexane (CAS: 1121-22-8) with high quality.

(±)-trans-1,2-Diaminocyclohexane (CAS: 1121-22-8) is an organic compound with the formula C6H10(NH2)2. This diamine is a building block for C2-symmetric ligands that are useful in asymmetric catalysis. (±)-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.