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1860-26-0

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1860-26-0 Usage

Chemical Properties

Colorless liquid

Uses

Tris(2-ethylhexyl)amine is a compound used in the extraction and stripping of inorganic acids.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 1860-26-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,6 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1860-26:
(6*1)+(5*8)+(4*6)+(3*0)+(2*2)+(1*6)=80
80 % 10 = 0
So 1860-26-0 is a valid CAS Registry Number.
InChI:InChI=1/C24H51N/c1-7-13-16-22(10-4)19-25(20-23(11-5)17-14-8-2)21-24(12-6)18-15-9-3/h22-24H,7-21H2,1-6H3

1860-26-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-N,N-bis(2-ethylhexyl)hexan-1-amine

1.2 Other means of identification

Product number -
Other names 2-ethyl-N,N-bis(2-ethylhexyl)hexylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1860-26-0 SDS

1860-26-0Synthetic route

d,l-2-ethylhexanal
123-05-7

d,l-2-ethylhexanal

2-ethyl-N-(2-ethylhexyl)-1-hexanamine
106-20-7

2-ethyl-N-(2-ethylhexyl)-1-hexanamine

A

2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

B

tri-(2-ethyl-n-hexyl)amine
1860-26-0

tri-(2-ethyl-n-hexyl)amine

Conditions
ConditionsYield
With hydrogen; 5% Pd(II)/C(eggshell) at 80℃; under 37503.8 Torr; for 52h; Product distribution / selectivity; Autoclave; Inert atmosphere; Industry scale;A 8.7 %Chromat.
B 86.2 %Chromat.
d,l-2-ethylhexanal
123-05-7

d,l-2-ethylhexanal

2-ethyl-N-(2-ethylhexyl)-1-hexanamine
106-20-7

2-ethyl-N-(2-ethylhexyl)-1-hexanamine

tri-(2-ethyl-n-hexyl)amine
1860-26-0

tri-(2-ethyl-n-hexyl)amine

Conditions
ConditionsYield
With hydrogen; 5% Pd(II)/C(eggshell) at 140℃; under 30003 Torr; for 14h; Product distribution / selectivity; Autoclave; Inert atmosphere; Industry scale;96.0 %Chromat.
tri-(2-ethyl-n-hexyl)amine
1860-26-0

tri-(2-ethyl-n-hexyl)amine

tris(2-ethylhexyl)amine N-oxide
1314607-57-2

tris(2-ethylhexyl)amine N-oxide

Conditions
ConditionsYield
With dihydrogen peroxide In acetic acid at 25℃; for 120h;80%
tri-(2-ethyl-n-hexyl)amine
1860-26-0

tri-(2-ethyl-n-hexyl)amine

2-isocyano-propionic acid butyl ester
33140-30-6

2-isocyano-propionic acid butyl ester

4-methyl-5-butoxy1,3-oxazole
24201-52-3

4-methyl-5-butoxy1,3-oxazole

tri-(2-ethyl-n-hexyl)amine
1860-26-0

tri-(2-ethyl-n-hexyl)amine

propyl bromide
106-94-5

propyl bromide

N,N,N-tri-2-ethylhexyl-N-propylammonium bromide

N,N,N-tri-2-ethylhexyl-N-propylammonium bromide

Conditions
ConditionsYield
In toluene for 48h; Reflux;
tri-(2-ethyl-n-hexyl)amine
1860-26-0

tri-(2-ethyl-n-hexyl)amine

trifluoroacetic acid
76-05-1

trifluoroacetic acid

tris(2-ethylhexyl)ammonium trifluoroacetate

tris(2-ethylhexyl)ammonium trifluoroacetate

Conditions
ConditionsYield
In water at 20℃;
methanesulfonic acid
75-75-2

methanesulfonic acid

tri-(2-ethyl-n-hexyl)amine
1860-26-0

tri-(2-ethyl-n-hexyl)amine

tris(2-ethylhexyl)ammonium methanesulfonate

tris(2-ethylhexyl)ammonium methanesulfonate

Conditions
ConditionsYield
In water at 20℃;
trifluorormethanesulfonic acid
1493-13-6

trifluorormethanesulfonic acid

tri-(2-ethyl-n-hexyl)amine
1860-26-0

tri-(2-ethyl-n-hexyl)amine

tris(2-ethylhexyl)ammonium trifluoromethanesulfonate

tris(2-ethylhexyl)ammonium trifluoromethanesulfonate

Conditions
ConditionsYield
In water at 20℃;
tri-(2-ethyl-n-hexyl)amine
1860-26-0

tri-(2-ethyl-n-hexyl)amine

toluene-4-sulfonic acid
104-15-4

toluene-4-sulfonic acid

tris(2-ethylhexyl)ammonium tosylate

tris(2-ethylhexyl)ammonium tosylate

Conditions
ConditionsYield
In water at 20℃;
tri-(2-ethyl-n-hexyl)amine
1860-26-0

tri-(2-ethyl-n-hexyl)amine

methyl iodide
74-88-4

methyl iodide

C25H54N(1+)*I(1-)

C25H54N(1+)*I(1-)

Conditions
ConditionsYield
at 120℃; for 240h;

1860-26-0Downstream Products

1860-26-0Relevant articles and documents

PROCESS FOR THE PREPARATION OF AN AMINE

-

Page/Page column 7, (2010/11/03)

Process for preparing an amine by reacting an aldehyde and/or ketone with hydrogen and a nitrogen compound selected from the group consisting of primary and secondary amines in the presence of a heterogeneous catalyst, wherein the reaction is carried out using a suspended catalyst as heterogeneous catalyst and is carried out in the semibatch mode in which the nitrogen compound as one reactant is placed in the reaction vessel and the aldehyde and/or the ketone as the other reactant is added during the course of the reaction and the aldehyde and/or the ketone is added in portions or continuously to the reaction mixture during the course of the reaction as a function of the achieved conversion of the nitrogen compound until a conversion of the nitrogen compound of at least 95% results, and all or part of the catalyst remains in the reaction vessel after the reaction batch and is reused for the next reaction batch.

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