N-METHYL DICYCLOHEXYLAMINE

PRODUCT IDENTIFICATION

CAS NO. 7560-83-0

N-METHYL DICYCLOHEXYLAMINE

EINECS NO. 231-453-4
FORMULA (C6H11)2NCH3
MOL WT. 195.34
H.S. CODE  

TOXICITY

 
SYNONYMS Methyl Dicyclohexylamine; N-Cyclohexyl-N-methyl-cyclohexanamine;
N,N-Dicyclohexylmethylamine; Dicyclohexylmethylamine; N-Ciclohexil-N-metilciclohexilamina; N-Cyclohexyl-N-méthylcyclohexylamine;

DERIVATION

 

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE clear to yellow liquid
MELTING POINT  
BOILING POINT

265 C

SPECIFIC GRAVITY

0.912

SOLUBILITY IN WATER  
pH  
VAPOR DENSITY  
AUTOIGNITION

 

NFPA RATINGS  

REFRACTIVE INDEX

 

FLASH POINT

110 C

STABILITY Stable under ordinary conditions.

GENERAL DESCRIPTION & APPLICATIONS

Cyclohexane is the six-membered alicyclic hydrocarbon consisting of six carbon atoms linked to each other to form a ring, with each carbon atom bearing two hydrogen atoms, C6H12. A cyclic compound is an organic compound that contains one or more closed rings of carbon atoms. The term alicyclic refers to cyclic compound that behaves chemically like aliphatic compounds (open-chain), which means the exclusion of carbocyclic compounds of aromatic rings with an array of ��-electrons characteristic. Cyclohexane is a colorless, highly flammable, mobile liquid with a pungent odor. It is insoluble in water and soluble in alcohol, ether, and almost organic solvents. Cyclohexane is a non-corrosive and quick volatilize liquid and sublimes between -5 to 5 C. Cyclohexane can exist in a number of  interconvertible three-dimensional conformations, the two simplest being are the chair and boat conformation and others include the half-chair and twist-chair conformation. Cyclohexane can cause irritation to the eyes and mucous membranes in workers. Repeated and prolonged contact with skin may cause dermatitis. The substance has not been shown to cause the hematologic changes associated with exposure to benzene. Cyclohexane occurs naturally in crude oils. Some cyclohexane is recovered from petroleum streams by fractionation. The bulky commercial  production of cyclohexane is based on hydrogenation of benzene in closed system. Cyclohexane consumption is linked almost entirely to nylon production. Nylon is further processed into fibers for applications in carpeting, automobile tire cord, clothing, and other growing industrial fields. Cyclohexane is used as a solvent, oil extractant, paint and varnish remover, dry cleaning material, and in solid fuels. It has been used as a insecticide itself. Cyclohexane is used as a chemical intermediate to produce target molecules. Natural compounds of one to five alicyclic rings with great variety and complexity are found particularly in steroids and terpenes. Cyclohexane structure, six membered-ring, is one of the major skeleton in nature. Cyclohexane derivatives can be used for the synthesis of pharmaceuticals, dyes, herbicides, plant growth regulator, plasticizers, rubber chemicals, cycloamines and other organic compounds.

Dicyclohexylamine or a derivative thereof, is used as an additive for prevention of CO2, corrosion in steam pipelines and boilers. It is used as an intermediate for the production of antioxidants and vulcanization accelerator. It is used as a catalyst for flexible polyurethane foams.

SALES SPECIFICATION

APPEARANCE

clear to yellow liquid
PURITY

99.0% min

FREE AMINE

0.1% max

WATER

0.5% max

TRANSPORTATION
PACKING 180kgs in drum
HAZARD CLASS 8 (Packing Group: II)
UN NO. 2922
OTHER INFORMATION
Hazard Symbols: C, Risk Phrases: 22-34, Safety Phrases: 26-36/37/39-45