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Di-n-butyl-hexadecylamin, also known as N,N-dibutyl-N-hexadecylamine, is a long-chain alkylamine with the chemical formula C32H69N. It is a colorless to pale yellow liquid at room temperature and is soluble in organic solvents. Di-n-butyl-hexadecylamin is primarily used as a corrosion inhibitor, emulsifier, and intermediate in the synthesis of various chemicals, including surfactants and lubricants. Its unique structure, featuring a long hydrocarbon chain and two butyl groups attached to the nitrogen atom, contributes to its surfactant properties and ability to form stable emulsions. Di-n-butyl-hexadecylamin is also known for its low toxicity and biodegradability, making it a preferred choice in various industrial applications where environmental impact is a concern.

5675-43-4

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5675-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5675-43-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,7 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5675-43:
(6*5)+(5*6)+(4*7)+(3*5)+(2*4)+(1*3)=114
114 % 10 = 4
So 5675-43-4 is a valid CAS Registry Number.

5675-43-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Di-n-butyl-hexadecylamin

1.2 Other means of identification

Product number -
Other names Dibutyl-hexadecyl-amin

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:5675-43-4 SDS

5675-43-4Relevant academic research and scientific papers

Joint Synthesis of Tertiary Unsymmetrical and Symmetrical Aliphatic Amines

Kozlov,Tereshko,Basalaeva,Tarasevich

, p. 1095 - 1098 (2007/10/03)

Tertiary unsymmetrical and symmetrical aliphatic amines were prepared by reaction of higher (C8-C16) and lower (C2-C4) aliphatic alcohols with nitriles containing the same number of carbon atoms as the lower aliphatic alcohols. Reaction conditions ensuring nearly quantitative yields of tertiary amines were determined.

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