Your Location:Home >111-86-4

111-86-4

  • Product Name:N-Octylamine
  • Molecular Formula:C8H19N
  • Molecular Weight:129.246
Inquiry

Product Details

Detail

  • Cas No: 111-86-4
  • Molecular Formula: C8H19N
  • Appearance: clear liquid with an ammonia-like odor
  • Purity: 99%
Product Name n-Octylamine
Alias 1-Aminooctane, n-Octylamine,  Caprylamine
English
Molecular formula

C8H19N

Molecular weight 129.24
CAS No 111-86-4
EINECS
Specification

Assay(GC)99%   

Water < 0.3%

color < 30 # (APHA)

Appearance traits
Use This product is mainly used as fungicide, pesticide, surfactant and pharmaceutical intermediates.
Package 160kg/drum
Other product information

Properties: 

Appearance:Colourless oil liquid,

Melting point:−4°C

Boiling point:179.4°C

Density:0.782 g/ml at 25 °C

Vapour pressure:1 mm hg ( 20 °C)

Refractive index:N20/D 1.432(lit.)

Flash(ing) point:145 °F

Water soluble properties:0.2 g/L (25 ºC)

Factory supply N-Octylamine 111-86-4 (Octylamine)  with low price

  • Molecular Formula:C8H19N
  • Molecular Weight:129.246
  • Appearance/Colour:clear liquid with an ammonia-like odor 
  • Vapor Pressure:1 mm Hg ( 20 °C) 
  • Melting Point:-5 - -1 °C(lit.) 
  • Refractive Index:n20/D 1.429(lit.)  
  • Boiling Point:179.4 °C at 760 mmHg 
  • PKA:10.65(at 25℃) 
  • Flash Point:62.8 °C 
  • PSA:26.02000 
  • Density:0.786 g/cm3 
  • LogP:3.00590 

Octylamine(Cas 111-86-4) Usage

Production Methods

Specific uses were not located in the literature. 1-Octylamine is manufactured under the tradenameArmeen8D(Armak).

Synthesis Reference(s)

Chemistry Letters, 7, p. 1057, 1978The Journal of Organic Chemistry, 47, p. 4327, 1982 DOI: 10.1021/jo00143a031Tetrahedron Letters, 11, p. 3411, 1970

Air & Water Reactions

Insoluble in water.

Reactivity Profile

OCTANAMINE 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.

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

Flammable

Definition

ChEBI: An 8-carbon primary aliphatic amine.

General Description

A yellow liquid with an ammonia-like odor. Insoluble in water and less dense than water. Hence floats on water. Contact may irritate skin, eyes and mucous membranes. May be toxic by ingestion. Used to make other chemicals.

InChI:InChI:1S/C8H19N/c1-2-3-4-5-6-7-8-9/h2-9H2,1H3

Companies adhering to the "science and technology aim, quality first, customer first, honest and trustworthy" business philosophy, in line with the "pragmatic, integrity, unity, innovation" spirit of enterprise, forge ahead, constantly pursuing higher levels of product quality and service. Warmly welcome customers at home and abroad to establish mutual trust, mutual benefit, and stable cooperation!

111-86-4 Relevant articles

Cs2CO3-promoted efficient carbonate and carbamate synthesis on solid phase

Salvatore, Ralph N.,Flanders, Vincent L.,Ha, Dang,Jung, Kyung Woon

, p. 2797 - 2800 (2000)

Mild and efficient preparation of alkyl ...

Self-assembly and characterization of a novel hydrogen-bonded nanostructure

Liu, Yang,Xiao, Shengqiang,Li, Hongmei,Li, Yuliang,Liu, Huibiao,Lu, Fushen,Zhuang, Junpeng,Zhu, Daoben

, p. 6256 - 6260 (2004)

A novel hydrogen-bonded supramolecular s...

-

Ralston

, (1940)

-

Reduction of azides to amines with borohydride exchange resin - Nickel acetate

Yoon,Choi,Shon

, p. 3047 - 3053 (1993)

Borohydride exchange resin (BER) - nicke...

Direct terminal alkylamino-functionalization via multistep biocatalysis in one recombinant whole-cell catalyst

Schrewe, Manfred,Ladkau, Nadine,Buehler, Bruno,Schmid, Andreas

, p. 1693 - 1697 (2013)

Direct and regiospecific amino-functiona...

Testing of microorganisms for ω-transaminase activity

Clay, Dorina,Koszelewski, Dominik,Grischek, Barbara,Gross, Johannes,Lavandera, Ivan,Kroutil, Wolfgang

, p. 2005 - 2009 (2010)

Various bacterial cells were tested to i...

Kinetic studies of the Hydrolysis of n-Octylamine on the Surface of a Sodium Dodecyl Sulfate Micelle by the Ultrasonic Absorption Method

Yamashita, Teruyo,Yano, Hiroshige,Harada, Shoji,Yasunaga, Tatsuya

, p. 5482 - 5485 (1983)

Ultrasonic relaxation absorption has bee...

Direct Enzymatic Synthesis of Fatty Amines from Renewable Triglycerides and Oils

Bevinakatti, Han,Citoler, Joan,Finnigan, William,Turner, Nicholas J.

, (2021/11/30)

Fatty amines represent an important clas...

PROCESS FOR CATALYTIC AMINATION OF ALCOHOL

-

Page/Page column 9; 10, (2021/06/26)

A process for catalytic amination of an ...

PROCESS FOR PRODUCING A CATALYST, CATALYST AND USE THEREOF

-

Page/Page column 13-16, (2021/06/26)

A process for producing a supported cata...

Highly selective synthesis of primary amines from amide over Ru-Nb2O5 catalysts

Guo, Wanjun,Guo, Yong,Jia, Hongyan,Liu, Xiaohui,Pan, Hu,Wang, Yangang,Wang, Yanqin,Xia, Qineng

, (2021/12/22)

Amines are an important class of compoun...

111-86-4 Process route

complex of α-cyclodextrin with n-octylamine

complex of α-cyclodextrin with n-octylamine

n-Octylamine
111-86-4

n-Octylamine

alpha cyclodextrin
10016-20-3

alpha cyclodextrin

Conditions
Conditions Yield
With phosphate buffer; In water-d2; at 25 ℃; Equilibrium constant; Thermodynamic data; standard molar enthalpy ΔrH0, standard molar Gibbs energy ΔrG0, standard molar entropy ΔrS0;
 
In alkaline aq. solution; at 25 ℃; pH=11.60; Equilibrium constant;
 
9-hydroxyimino-heptadecanoic acid

9-hydroxyimino-heptadecanoic acid

sulfuric acid
7664-93-9

sulfuric acid

azelaic acid
123-99-9,26776-28-3

azelaic acid

n-Octylamine
111-86-4

n-Octylamine

8-Aminooctanoic acid
1002-57-9

8-Aminooctanoic acid

Conditions
Conditions Yield
Erhitzen mit konz. Salzsaeure auf 180grad.Hydrolysis;
 

111-86-4 Upstream products

  • 111-85-3
    111-85-3

    n-chlorooctane

  • 629-27-6
    629-27-6

    1-Iodooctane

  • 1120-07-6
    1120-07-6

    nonanamide

  • 629-37-8
    629-37-8

    1-nitrooctane

111-86-4 Downstream products

  • 7261-59-8
    7261-59-8

    (2-amino-ethyl)-(2-octylamino-ethyl)-amine

  • 40510-21-2
    40510-21-2

    N-n-Octyl-diaminoethan-1,2

  • 855379-69-0
    855379-69-0

    octyl-[2]thienylmethyl-amine

  • 4080-76-6
    4080-76-6

    N-octylmaleimide

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