Diamylamine

Diamylamine Structure
CAS No.
2050-92-2
Chemical Name:
Diamylamine
Synonyms
DIAMYLAMINE;Dipentylamin;Dipentanamine;DIPENTYLAMINE;amine,dipentyl;DI-N-AMYLAMINE;Di-2-amylamine;Twopentyl aMine;N,N-Diamylamine;Diamylamine >
CBNumber:
CB8306575
Molecular Formula:
C10H23N
Molecular Weight:
157.3
MOL File:
2050-92-2.mol
Modify Date:
2023/11/28 16:31:44

Diamylamine Properties

Melting point -44°C
Boiling point 202-203 °C(lit.)
Density 0.767 g/mL at 25 °C
vapor density 5.42 (vs air)
vapor pressure 0.3 mm Hg ( 20 °C)
refractive index n20/D 1.4258(lit.)
Flash point 157 °F
form clear liquid
pka 11.25±0.19(Predicted)
color Colorless to Light yellow to Light orange
Specific Gravity 0.775 (25/4℃)
Water Solubility Slightly soluble (0.1-1 g/100 mL)
BRN 906746
Dielectric constant 2.5
Stability Stable, but air-sensitive. Flammable. Incompatible with oxidizing agents.
CAS DataBase Reference 2050-92-2(CAS DataBase Reference)
NIST Chemistry Reference 1-Pentanamine, N-pentyl-(2050-92-2)
EPA Substance Registry System Diamylamine (2050-92-2)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS09,GHS02,GHS05,GHS06
Signal word  Danger
Hazard statements  H226-H301+H311-H301+H311+H331-H314-H400
Precautionary statements  P261-P273-P280-P301+P310-P305+P351+P338-P310-P210-P233-P240-P241+P242+P243-P260-P264-P270-P301+P330+P331+P310-P303+P361+P353+P310+P363-P304+P340+P310-P305+P351+P338+P310-P370+P378-P403+P235-P405-P501
Hazard Codes  T,N,C
Risk Statements  23/24/25-34-37/38-24-22-50/53
Safety Statements  26-27-36/37/39-45-61-60
RIDADR  UN 2841 3/PG 3
WGK Germany  3
RTECS  RZ9100000
HS Code  2921.19.6190
HazardClass  3.2
PackingGroup  III
NFPA 704
2
3 0

Diamylamine price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) D0286 Diamylamine (mixture) min. 97.0 %(total of isomer) 2050-92-2 25ML ₹2200 2022-05-26 Buy
TCI Chemicals (India) D0286 Diamylamine (mixture) min. 97.0 %(total of isomer) 2050-92-2 500ML ₹5100 2022-05-26 Buy
TCI Chemicals (India) D0129 Diamylamine min. 98.0 % 2050-92-2 25ML ₹5300 2022-05-26 Buy
Product number Packaging Price Buy
D0286 25ML ₹2200 Buy
D0286 500ML ₹5100 Buy
D0129 25ML ₹5300 Buy

Diamylamine Chemical Properties,Uses,Production

Chemical Properties

Diamylamine is a relatively strong base and forms salts with acids. Its vapors can form explosive mixtures with air.

Uses

Di-n-amylamine is manufactured from amyl chloride and ammonia. It is used in organic syntheses and as a solvent, rubber accelerator, flotation reagent, and corrosion inhibitor.

Production Methods

Diamylamine is manufactured by the same processes as n-amylamine by reaction of amyl chloride with ammonia and then separated from the amylenes and amyl alcohol by steam distillation (Hawley 1977). It also can be synthesized by amination of alkyl halides at high temperature and pressure (Schweizer et al 1978). The commercial product may be a mixture of amyl isomers (HSDB 1989).

General Description

A clear colorless liquid with an ammonia-like odor. Very slightly soluble in water. Density 6.40 lb / gal (less than water) Vapors heavier than air. Flash point 152°F. Difficult to ignite. Moderately toxic. Contact with liquid may cause a chemical burn. Vapors may irritate respiratory tract. Used in the manufacture of rubber, resins, and dyes.

Air & Water Reactions

Flammable. Sensitive to air and heat. Slightly soluble in water.

Reactivity Profile

Diamylamine neutralizes acids to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated in combination with strong reducing agents, such as hydrides.

Health Hazard

Diamylamine is a strong eye, skin, and respiratory irritant owing to its basicity (HSDB 1989). Vapor exposure results in irritation of the nose and throat with distressed breathing and coughing. Prolonged exposure may lead to pulmonary edema. Direct skin contact can cause secondary burns.

Fire Hazard

HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion and poison hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

Industrial uses

Diamylamine is less widely used than n-amylamine with only 20 tons being manufactured in the U.S. in 1976. Its most widespread use is as a corrosion inhibitor and rubber accelerator (Hawley 1977). It is also useful as a solvent for oils, resins, and some cellulose esters. Introduction of the amyl group imparts oil solubility to otherwise oil-insoluble substances. Diamylamine also is used in flotation reagents, dyestuffs and as a cockroach repellent (HSDB 1989).

Safety Profile

Poison by inhalation, ingestion, and skin contact. A severe skin irritant. See also AMINES. Flammable liquid when exposed to heat or flame; can react with oxidizing materials. To fight fire, use alcohol foam, foam, CO2, dry chemical. When heated to decomposition it emits toxic fumes of NOx.

Metabolism

In contrast to n-amylamine, little information is available on diamylamine metabolism, particularly with respect to its suitability as a substrate for the amine oxidases. Generally, the rate of oxidation of secondary amines by monoamine oxidase is slower than that of primary amines (Beard and Noe 1981). In agreement, Yamada et al (1965) demonstrated that crystalline amine oxidase prepared from Aspergillus niger oxidized diamylamine very slowly with respect to n-amylamine.
As with other secondary aliphatic amines, the propensity of diamylamine to form nitrosamines is of interest. It has been shown that treatment of diamylamine with nitrous acid in dilute aqueous solution gave optimum nitrosamine formation between pH 1 and 3, corresponding to stomach conditions (Sander et al 1968). When rats were fed a diet supplemented with sodium nitrite and secondary amines of low basicity, synthesis of nitrosamines in the stomach was observed. Malignant tumors arising through formation of nitrosamines in the stomach was demonstrated only when nitrite was present in the stomach concomitantly with secondary amines which readily formed carcinogenic nitrosamines.

Diamylamine Preparation Products And Raw materials

Global( 102)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
Career Henan Chemica Co +86-0371-86658258 +8613203830695 China 30253 58 Inquiry
Hefei TNJ Chemical Industry Co.,Ltd. 0551-65418671 China 34571 58 Inquiry
Hebei Guanlang Biotechnology Co., Ltd. +86-19930503259 +86-19930503259 China 18435 58 Inquiry
PT CHEM GROUP LIMITED +86-85511178 +86-85511178 China 35451 58 Inquiry
SUZHOU SENFEIDA CHEMICAL CO.,LTD +86-0512-83500002 +8615195660023 China 23053 58 Inquiry
LEAPCHEM CO., LTD. +86-852-30606658 China 43348 58 Inquiry
Aladdin Scientific +1-+1(833)-552-7181 United States 52927 58 Inquiry
ABCR GmbH & CO. KG 49 721 95061 0 Germany 6846 75 Inquiry
1-Pentanamine,N-pentyl- amine,dipentyl diamylamine(melanged’isomeres) diamylamine(mixedisomers) DIAMYLAMINE, TECH N,N-Diamylamine Dipentylamine,99% DipentylaMine, Mixture of isoMers 99% Twopentyl aMine diamylamine(non-specificname) diamylamines(mixedisomers) di-n-amylamine(dipentylamine) Dipentanamine Dipentylamin dipentylamine(mixedisomers) N,N-Dipentylamine DIAMYLAMINE (MIXTURE) N-Pentyl-1-aminopentan n-pentyl-1-pentanamin pentanamine,N-pentyl- Pentylamine, pentyl- pentyl-pentylamin N-Pentyl-1-pentanamine pentylpentylamine DI-N-PENTYLAMINE DI-N-AMYLAMINE DIPENTYLAMINE DIAMYLAMINE Dipentylamine, mixture of isomers DIPENTYLAMINE, 99%, MIXTURE OF ISOMERS Di-2-amylamine Diamylamine > Diamylamine (mixture)> Diquafosol Impurity 19 2050-92-2 2050922 CH3CH242NH C5H112NH C10H24N AMINE Organic Building Blocks Nitrogen Compounds Building Blocks Amines C9 to C10 Amines C9 to C10 Nitrogen Compounds