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28947-77-5

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28947-77-5 Usage

Description

Tri-hexadecylamine, with the chemical formula C30H63N, is a long-chain amine characterized by a 16-carbon hydrophobic tail. This unique structure endows it with versatile properties, making it a valuable component in a wide range of industrial and commercial applications.

Uses

Used in Cosmetics Industry:
Tri-hexadecylamine is used as a surfactant and emulsifier for promoting the stability and consistency of cosmetic products. Its hydrophobic tail aids in the formation of stable emulsions, ensuring even distribution of ingredients and enhancing the product's performance.
Used in Pharmaceuticals Industry:
In the pharmaceutical sector, tri-hexadecylamine serves as a surfactant and emulsifier, improving the solubility and bioavailability of various drugs. Its ability to stabilize formulations contributes to the development of more effective and reliable medicinal products.
Used in Agrochemicals Industry:
Tri-hexadecylamine is utilized as a surfactant and emulsifier in agrochemicals, helping to create stable and effective formulations for agricultural applications. Its properties ensure even distribution and absorption of agrochemicals, promoting better crop protection and yield.
Used in Mining Industry:
As a flotation agent, tri-hexadecylamine plays a crucial role in the mining industry. It aids in the separation of valuable minerals from waste materials, improving the efficiency and productivity of mining operations.
Used in Paints and Coatings Industry:
Tri-hexadecylamine is employed as a dispersant in the production of paints and coatings. Its long-chain structure helps to prevent the aggregation of pigments and other components, ensuring a uniform and consistent finish.
Used in Polymer Production:
Tri-hexadecylamine has potential applications in the synthesis of polymers, where it can act as a catalyst or a structural component. Its hydrophobic nature can influence the properties of the resulting polymers, tailoring them for specific uses.
Used in Organic Synthesis:
As a catalyst in organic synthesis reactions, tri-hexadecylamine can facilitate various chemical transformations, improving the efficiency and selectivity of these processes. Its presence can help in achieving desired outcomes in the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 28947-77-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,4 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28947-77:
(7*2)+(6*8)+(5*9)+(4*4)+(3*7)+(2*7)+(1*7)=165
165 % 10 = 5
So 28947-77-5 is a valid CAS Registry Number.
InChI:InChI=1/C48H99N/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-46-49(47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2)48-45-42-39-36-33-30-27-24-21-18-15-12-9-6-3/h4-48H2,1-3H3

28947-77-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dihexadecylhexadecan-1-amine

1.2 Other means of identification

Product number -
Other names 1-Hexadecanamine,N,N-dihexadecyl

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:28947-77-5 SDS

28947-77-5Downstream Products

28947-77-5Relevant articles and documents

Conversion of Primary Amines to Symmetrical Secondary and Tertiary Amines using a Co-Rh Heterobimetallic Nanocatalyst

Chung, Hyunho,Han, Seulgi,Chung, Young Keun,Park, Ji Hoon

supporting information, p. 1267 - 1272 (2018/02/12)

Symmetrical tertiary amines have been efficiently realized from amine and secondary amines via deaminated homocoupling with heterogeneous bimetallic Co2Rh2/C as catalyst (molar ratio Co:Rh=2:2). Unsymmetric secondary anilines were produced from the reaction of anilines with symmetric tertiary amines. The Co2Rh2/C catalyst exhibited very high catalytic activity towards a wide range of amines and could be conveniently recycled ten times without considerable leaching. (Figure presented.).

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