Dicyclohexylamine Chemical Properties

Melting point:

-2 °C

Boiling point:

256 °C

Density 

0.912 g/mL at 20 °C(lit.)

vapor density 

6 (vs air)

vapor pressure 

12 mm Hg ( 37.7 °C)

refractive index 

n20/D 1.4842(lit.)

Flash point:

205 °F

storage temp. 

Store below +30°C.

solubility 

organic solvents: soluble

form 

Crystalline Powder

pka

10.4(at 25℃)

color 

White to off-white

Odor

amine odor

PH

11 (1g/l, H2O, 20℃)

explosive limit

0.8-4.6%(V)

Water Solubility 

1 g/L (20 ºC)

FreezingPoint 

-2℃

Sensitive 

Air Sensitive

Merck 

14,3095

BRN 

605923

Stability:

Stable. Incompatible with strong acids, strong oxidizing agents.

InChIKey

XBPCUCUWBYBCDP-UHFFFAOYSA-N

LogP

2.724 at 25℃

CAS DataBase Reference

101-83-7(CAS DataBase Reference)

NIST Chemistry Reference

Cyclohexanamine, N-cyclohexyl-(101-83-7)

EPA Substance Registry System

Dicyclohexylamine (101-83-7)

Safety Information

Hazard Codes 

C,N

Risk Statements 

22-34-50/53-24/25

Safety Statements 

26-36/37/39-45-60-61

RIDADR 

UN 2565 8/PG 3

WGK Germany 

2

RTECS 

HY4025000

F 

8-9-23

Autoignition Temperature

240 °C

TSCA 

Yes

HazardClass 

8

PackingGroup 

III

HS Code 

29213000

Hazardous Substances Data

101-83-7(Hazardous Substances Data)

MSDS

• Language:English Provider:ACROS
• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

Dicyclohexylamine Usage And Synthesis

Description

Dicyclohexylamine is a combustible, colorlessliquid with a faint amine odor. Molecular weight=181.36;Boiling point=256℃; Flash point $99℃. HazardIdentification (based on NFPA-704 M Rating System): Health3, Flammability 1, Reactivity 0. Slightly soluble in water.

Chemical Properties

Dicyclohexylamine is a combustible, colorless liquid with a faint amine odor.

Chemical Properties

Dicyclohexylamine is strongly basic with reactive amine groups which readily form TV-substituted derivatives. It also forms salts with inorganic and organic acids. Dicyclohexylamine will also form crystalline hydrates and alcoholates.

Uses

Dicyclohexylamine is manufactured by reacting equimolar quantities of cyclohexanone and cyclohexylamine or cyclohexanone and ammonia. It is used as a solvent and in organic syntheses. It is reportedly used as a chemical intermediate for the synthesis of corrosion inhibitors, rubber vulcanization accelerators, textiles, and varnishes.

Uses

Dicyclohexylamine (DCHA) is an aliphatic amine. As an intermediate, it can be used in a broad range of applications in different industries.
Dicyclohexylamine is used as a vulcanization accelerator.
In lubricants and cutting fluids it does function as a corrosion inhibitor. Here it should be mentioned that Dicyclohexylamine does not form Nitrosamines when being used.

Reagent for preparation of crystalline amino acid derivative salts.
Dicyclohexylamine was used to constitute ionic liquid matrices for bacterial analysis in matrix assisted laser desorption/ionisation mass spectrometry.
It was used to develop a new palladium catalyst for Suzuki coupling reaction of aryl bromides with boronic acids.
It was used as extractant in determination of gold(III) by dispersive liquid-liquid microextraction and electrothermal atomic absorption spectrometry.

Uses

Industrial solvent; corrosion inhibitor.

Definition

ChEBI: Dicyclohexylamine is a primary aliphatic amine.

Production Methods

Several methods are employed for the manufacture of dicyclohexylamine. It can be manufactured by hydrogenation of equimolar amounts of cyclohexanone and cyclohexylamine. Alternatively, dicyclohexylamine can be prepared by vapor phase catalytic hydrogenation of aniline at elevated temperature and pressure. Fractionation of the crude reaction product yields cyclohexylamine, unreacted aniline, and a high boiling residue comprised of N-phenylcyclohexylamine and dicyclohexylamine (Windholz et al 1983).

General Description

A colorless liquid with a faint fishlike odor. Less dense than water. May be toxic by ingestion. Severely irritates skin, eyes and mucous membranes. Used to make paints, varnishes and detergents.

Air & Water Reactions

Slightly soluble in water. May be sensitive to air.

Reactivity Profile

DCHA reacts with oxidizing agents. Forms crystalline salts with many N-protected amino acids . Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.

Health Hazard

TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Health Hazard

Dicyclohexylamine is a strong irritant to skin and mucous membranes. Direct skin contact with the liquid or vapor should be avoided. Its systemic effects in man include nausea and vomiting, anxiety, restlessness and drowsiness. Individuals repeatedly exposed to this chemical may develop sensitivity to it (HSDB 1988).

Fire Hazard

Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.

Flammability and Explosibility

Non flammable

Industrial uses

Dicyclohexylamine is a widely used chemical intermediate. It can be used to absorb acidic gases, to preserve rubber latex, to plasticize casein, and to neutralize plant and insect poisons. Metal complexes of dicyclohexylamine are catalysts used in the paint, varnish, and ink industries. Dicyclohexylamine salts of fatty acids and sulfuric acid have soap and detergent properties used in the printing and textile industries. One of the most important uses of dicyclohexylamine is as a vapor phase corrosion inhibitor. It is used to protect packaged or stored ferrous metals from atmospheric corrosion (Schweizer et al 1978).

Safety Profile

Poison by ingestion and subcutaneous routes. Corrosive. A severe skin and eye irritant. Questionable carcinogen with experimental tumorigenic data. Human mutation data reported. Combustible when exposed to heat or flame; can react with oxidizing materials. To fight fue, use alcohol foam, CO2, dry chemical. When heated to decomposition it emits toxic fumes of NOx. See also CYCLOHEXYLAMINE.

Potential Exposure

Dicyclohexylamine salts of fatty acids and sulfuric acid have soap and detergent properties useful to the printing and textile industries. Metal complexes of DI-CHA are used as catalysts in the paint, varnish, the ink industries. Several vapor-phase corrosion inhibitors are solid DI-CHA derivatives. These compounds are slightly volatile at normal temperatures and are used to protect packaged or stored ferrous metals from atmospheric corrosion. Dicyclohexylamine is also used for a number of other purposes: plasticizers, insecticidal formulations; antioxidant in lubricating oils, fuels, and rubber; and as an extractant. Incompatibilities: Contact with strong oxidizers can cause fire and explosion hazard

First aid

Skin Contact: Flood all areas of body thathave contacted the substance with water. Do not wait toremove contaminated clothing; do it under the water stream.Use soap to help assure removal. Isolate contaminatedclothing when removed to prevent contact by others.Eye Contact: Remove any contact lenses at once. Flusheyes well with copious quantities of water or normal salinefor at lest 20-30 min. Seek medical attention.

Metabolism

The extensive use of cyclamates as artificial sweeteners a number of years ago led to extensive study on the metabolism and carcinogenicity of cyclohexylamine, a metabolic product of cyclamate. However, there is little such information available concerning dicyclohexylamine. Filov (1968) investigated the metabolism of cyclohexylamine and dicyclohexylamine. Both amines were readily absorbed from the gastro-intestinal tract. In addition, they rapidly entered the bloodstream following inhalation and penetrated intact skin. In rats, it was determined that 26-44% of dicyclohexylamine present in the stomach was eliminated unchanged, mostly in the urine. The clearance rate of the amines was also quite high, particularly for dicyclohexylamine.

storage

(1) Color Code—White: Corrosive or ContactHazard; Store separately in a corrosion-resistant location.(2) Color Code—Blue: Health Hazard/Poison: Store in asecure poison location. Prior to working with Di-Cha youshould be trained on its proper handling and storage. Storein tightly closed containers in a refrigerator away from oxidizers. Where possible, automatically pump liquid fromdrums or other storage containers to process containers.Protection from air is recommended for long-term storage.

Shipping

UN2565 Dicyclohexylamine, Hazard class: 8; Labels: 8-Corrosive material

Incompatibilities

Dicyclohexylamine salts of fatty acids and sulfuric acid have soap and detergent properties useful to the printing and textile industries. Metal complexes of DI-CHA are used as catalysts in the paint, varnish, the ink industries. Several vapor-phase corrosion inhibitors are solid DI-CHA derivatives. These compounds are slightly volatile at normal temperatures and are used to protect packaged or stored ferrous metals from atmospheric corrosion. Dicyclohexylamine is also used for a number of other purposes: plasticizers, insecticidal formulations; antioxidant in lubricating oils, fuels, and rubber; and as an extractant. Incompatibilities: Contact with strong oxidizers can cause fire and explosion hazard

Waste Disposal

Incineration; incinerator equipped with a scrubber or thermal unit to reduce nitrogen oxides emissions.

Dicyclohexylamine(101-83-7)Related Product Information

• Dicyclohexylamine
• Dicyclohexylammonium nitrite
• N,N-Dicyclohexylmethylamine
• N-ETHYLDICYCLOHEXYLAMINE
• N-Benzyloxycarbonyl-O-tert-butyl-L-tyrosine dicyclohexylamine salt
• N-ALPHA-Z-N-EPSILON-BOC-L-LYSINE DICYCLOHEXYLAMINE SALT
• N-ALPHA-(TERT-BUTYLOXYCARBONYL)-D-CYCLOHEXYLALANINE DICYCLOHEXYLAMINE,BOC-D-CHA-OH DCHA
• BOC-D-3-THIENYLALANINE DCHA SALT,BOC-D-3-THIENYLALANINE-DCHA,BOC-D-ALA(3-THIENYL)-OH DCHA
• N-ALPHA-(TERT-BUTYLOXYCARBONYL)-D-CYCLOHEXYLGLYCINE DICYCLOHEXYLAMINE,BOC-D-CHG-OH DCHA
• N-ALPHA-TERT-BUTYLOXYCARBONYL-L-ASPARTIC ACID BETA-TERT-BUTYL ESTER DICYCLOHEXYLAMINE
• BOC-HIS(BOC)-OH DCHA
• BOC-D-ALLYLGLYCINE-DCHA,BOC-D-ALLYLGLYCINE DCHA SALT,BOC-D-ALGLY-OH DCHA
• N-ALPHA-TERT-BUTYLOXYCARBONYL-L-NORLEUCINE DICYCLOHEXYLAMINE
• N-ALPHA-Z-NIN-BOC-L-TRYPTOPHAN DICYCLOHEXYLAMINE SALT
• BOC-D-CYCLOPROPYLALANINE-DCHA
• Cyclohexylamine
• BOC-HYP(BZL)-OH
• N-[(1-[1,1-biphenyl]-4-ylisopropyloxycarbonyl]glycine, compound with N-dicyclohexylamine (1:1)