• Chemical Name 2,6-DIMETHYLCYCLOHEXYLAMINE
  • CAS No. 6850-63-1
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Chinese Manufacturer supply 2,6-DIMETHYLCYCLOHEXYLAMINE 6850-63-1 in stock with high standard

  • Molecular Formula: C8H17N
  • Molecular Weight: 127.23
  • Vapor Pressure: 2.4mmHg at 25°C 
  • Boiling Point: 160.3°C at 760 mmHg 
  • Flash Point: 30°C 
  • PSA: 26.02000 
  • Density: 0.826g/cm3 
  • LogP: 2.47010 

2,6-DIMETHYLCYCLOHEXYLAMINE(Cas 6850-63-1) Usage

General Description

2,6-Dimethylcyclohexylamine is a chemical compound with the molecular formula C8H17N. It is an amine derivative, specifically a cyclohexylamine, and is composed of a cyclohexane ring with two methyl groups and an amine functional group. 2,6-DIMETHYLCYCLOHEXYLAMINE is used in various industrial applications, including as an intermediate in the manufacturing of pharmaceuticals and dyes. It is also used as a corrosion inhibitor in metalworking fluids and as a chemical intermediate in the production of rubber chemicals and surfactants. 2,6-Dimethylcyclohexylamine can be a hazardous material if not handled or stored properly, and exposure to it can cause irritation to the skin, eyes, and respiratory system.

InChI:InChI=1/C8H17N/c1-6-4-3-5-7(2)8(6)9/h6-8H,3-5,9H2,1-2H3

6850-63-1 Relevant articles

SULPHONYL UREA DERIVATIVES AS NLRP3 INFLAMMASOME MODULATORS

-

Paragraph 01072, (2019/07/13)

The present disclosure relates to compou...

Highly selective amination of o-and p-alkyl phenols over Pd/Al 2O3-BaO

Ma, Jianchao,Wang, Huabang,Sun, Meng,Yang, Fan,Wu, Zhiwei,Wang, Donghua,Chen, Ligong

experimental part, p. 387 - 392 (2012/05/04)

A series of Pd-based catalysts were prep...

N-substituted diphosphinoamines: Toward rational ligand design for the efficient tetramerization of ethylene

Kuhlmann, Sven,Blann, Kevin,Bollmann, Annette,Dixon, John T.,Killian, Esna,Maumela, Munaka C.,Maumela, Hulisani,Morgan, David H.,Pretorius, Marie,Taccardi, Nicola,Wasserscheid, Peter

, p. 279 - 284 (2007/10/03)

Bis(diphenylphosphino)amine (PNP) ligand...

Stereochemistry of hydrodenitrogenation: The mechanism of elimination of the amino group from cyclohexylamines over sulfided Ni-Mo/γ-Al2O3 catalysts

Prins,Ranade,Rota,Ranade

, p. 389 - 399 (2007/10/03)

HDS and HDN are among the most significa...

6850-63-1 Process route

cis,cis-2,6-dimethylcyclohexylamine
24213-44-3

cis,cis-2,6-dimethylcyclohexylamine

1,3-dimethylcyclohexane
638-04-0,2207-03-6,69685-67-2,69685-68-3,129939-72-6,129939-73-7,591-21-9

1,3-dimethylcyclohexane

1,3-dimethylcyclohexene
2808-76-6

1,3-dimethylcyclohexene

trans,trans-2,6-dimethylcyclohexylamine
24213-42-1

trans,trans-2,6-dimethylcyclohexylamine

cis,trans-2,6-dimethylcyclohexylamine
6850-63-1,24213-42-1,24213-44-3,24217-12-7,88824-88-8

cis,trans-2,6-dimethylcyclohexylamine

Conditions
Conditions Yield
With hydrogen; sulfided Ni-Mo; at 295 ℃; under 37503 Torr; Further Variations:; Temperatures; Product distribution;
N-(2,6-dimethylcyclohexylidene)hydroxylamine
19187-65-6,25457-21-0,60221-25-2

N-(2,6-dimethylcyclohexylidene)hydroxylamine

dl-cis,trans-2,6-dimethylcyclohexylamine
24213-42-1,24213-44-3,24217-12-7,88824-88-8,6850-63-1

dl-cis,trans-2,6-dimethylcyclohexylamine

Conditions
Conditions Yield
With hydrogen; In methanol; for 12h; under 2585.81 Torr;
64%

6850-63-1 Upstream products

  • 7647-01-0
    7647-01-0

    hydrogenchloride

  • 19187-65-6
    19187-65-6

    N-(2,6-dimethylcyclohexylidene)hydroxylamine

  • 64-19-7
    64-19-7

    acetic acid

  • 64-17-5
    64-17-5

    ethanol

6850-63-1 Downstream products

  • 87-62-7
    87-62-7

    2,6-dimethylaniline

  • 42846-29-7
    42846-29-7

    trans,trans-2,6-dimethylcyclohexanol

  • 24213-43-2
    24213-43-2

    (+/-)-2-benzamino-1r .3t -dimethyl-cyclohexane

  • 6850-63-1
    6850-63-1

    (+)-2r ,6t -dimethyl-cyclohexylamine