143-16-8

  • Product Name:Dihexylamine
  • Molecular Formula:C12H27 N
  • Molecular Weight:185.353
Inquiry

Product Details

Detail

  • Cas No: 143-16-8
  • Molecular Formula: C12H27 N
  • Appearance: colorless Clear liquid
  • Purity: 99%
Product Name Dihexylamine
Alias Bis(1-hexyl)amine; di-Normal-hexylamine; N,N-Dihexylamine; N-Hexyl-1-hexanamine; N-Hexylhexanamine
English
Molecular formula

C12H27N

Molecular weight 185.35
CAS No 143-16-8
EINECS
Specification Assay(GC)98%    
Appearance traits
Use For solvent, pharmaceutical industry, organic synthesis intermediates.
Package 160kg/drum
Other product information

Properties: 

Appearance:Colourless liquid,

Melting point:3 °C

Boiling point:193.5°C

Density:0.795 g/ml at 25 °C

Vapor density:6.4 (vs air)

Refractive index:N20/D 1.432

Flash(ing) point:203 °F

Water soluble properties:Miscible with water.

Factory supply Dihexylamine 143-16-8 (Di-n-hexylamine)  with low price

  • Molecular Formula:C12H27 N
  • Molecular Weight:185.353
  • Appearance/Colour:colorless Clear liquid 
  • Vapor Pressure:0.463mmHg at 25°C 
  • Melting Point:3 °C 
  • Refractive Index:n20/D 1.432(lit.)  
  • Boiling Point:193.5 °C at 760 mmHg 
  • PKA:pK1:11.0(+1) (25°C) 
  • Flash Point:95 °C 
  • PSA:12.03000 
  • Density:0.795 g/mL at 25 °C(lit.) 
  • LogP:4.12750 

DI-N-HEXYLAMINE(Cas 143-16-8) Usage

Air & Water Reactions

DI-N-HEXYLAMINE may be sensitive to prolonged exposure to air. Insoluble in water.

Reactivity Profile

DI-N-HEXYLAMINE 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

ACUTE/CHRONIC HAZARDS: DI-N-HEXYLAMINE is readily absorbed through the skin.

Fire Hazard

DI-N-HEXYLAMINE is combustible.

Safety Profile

poison by ingestion, skin contact, and intravenous routes. A skin exposed to heat or flame; can react with oxidizing materials. To fight fire, use CO2, dry chemical. When heated to decomposition it emits toxic fumes of NOx. See also AMINES.

General Description

Clear colorless liquid.

InChI:InChI=1/C12H27N/c1-3-5-7-9-11-13-12-10-8-6-4-2/h13H,3-12H2,1-2H3/p+1

Since its inception, the company has continuously expanded its business varieties and fields, to realize the business pattern with the expansion upstream and downstream as well as the complementary of internal and foreign trade. Based on technological innovation and guided by market orientation, we will accelerate the main business strategy, optimize supply chain elements, and build business flow, logistics flow, information flow, and capital flow in one mode, laying a solid foundation for supplying more high-quality and efficient services to a wider range of customers.

143-16-8 Relevant articles

Hydroaminomethylation of olefins using a rhodium carbene catalyst

Seayad, Abdul Majeed,Selvakumar, Kumaravel,Ahmed, Moballigh,Beller, Matthias

, p. 1679 - 1683 (2003)

Hydroaminomethylation of terminal as wel...

CO2-tuned highly selective reduction of formamides to the corresponding methylamines

Chao, Jianbin,Guo, Zhiqiang,Pang, Tengfei,Wei, Xuehong,Xi, Chanjuan,Yan, Leilei

supporting information, p. 7534 - 7538 (2021/10/12)

We herein describe an efficient, CO2-tun...

Highly Selective Hydrogenative Conversion of Nitriles into Tertiary, Secondary, and Primary Amines under Flow Reaction Conditions

Furugen, Chikara,Ito, Naoya,Jiang, Jing,Park, Kwihwan,Sajiki, Hironao,Shimizu, Eisho,Yamada, Tsuyoshi

, (2021/12/13)

Flow reaction methods have been develope...

Amination of aliphatic alcohols with urea catalyzed by ruthenium complexes: effect of supporting ligands

Dindar, Sara,Nemati Kharat, Ali

, (2020/09/02)

In the present study, ruthenium-catalyze...

One-pot reductive amination of carboxylic acids: a sustainable method for primary amine synthesis

Coeck, Robin,De Vos, Dirk E.

supporting information, p. 5105 - 5114 (2020/08/25)

The reductive amination of carboxylic ac...

143-16-8 Process route

hexan-1-amine
111-26-2

hexan-1-amine

Dipentylimine
65870-64-6

Dipentylimine

1-Pentyl-1-hexylamine
41495-45-8

1-Pentyl-1-hexylamine

dihexylamine
143-16-8

dihexylamine

Di-n-amylamine
2050-92-2

Di-n-amylamine

Conditions
Conditions Yield
With hydrogen; nickel; In cyclohexane; at 90 ℃; under 12000.9 Torr; Product distribution; Kinetics; Mechanism;
 
1-hexylpiperidine
7335-01-5

1-hexylpiperidine

piperidine
110-89-4

piperidine

1-pentylpiperidine
10324-58-0

1-pentylpiperidine

1-Pentyl-1-hexylamine
41495-45-8

1-Pentyl-1-hexylamine

dihexylamine
143-16-8

dihexylamine

Di-n-amylamine
2050-92-2

Di-n-amylamine

pentane
109-66-0,8031-35-4,9078-70-0

pentane

Conditions
Conditions Yield
With hydrogen; sulphidized CoO-MoO3; at 300 ℃; for 8h; under 45003.6 - 90757.2 Torr; Mechanism; Product distribution;
5.8%
5.4%
3%
0.8%

143-16-8 Upstream products

  • 544-10-5
    544-10-5

    1-Chlorohexane

  • 111-26-2
    111-26-2

    hexan-1-amine

  • 111-25-1
    111-25-1

    1-bromo-hexane

  • 4393-08-2
    4393-08-2

    N,N-di(hexyl)benzylamine

143-16-8 Downstream products

  • 5468-40-6
    5468-40-6

    N,N-dihexyl-lactamide

  • 102457-29-4
    102457-29-4

    1-(2-chloro-phenoxy)-3-dihexylamino-propan-2-ol

  • 628-73-9
    628-73-9

    hexanenitrile

  • 102-86-3
    102-86-3

    tri-n-hexylamine

*Product Name
Cas No
Quantity
Company Name
Phone
*Email
*Description
*Code
Items marked with * are mandatory
Submit