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3-(Octadecyloxy)propylamine is a chemical compound with the molecular formula C21H43NO. It is an alkylamine derivative, characterized by an octadecyl (C18H37) group attached to a propylamine chain. 3-(octadecyloxy)propylamine is a colorless liquid with a density of approximately 0.82 g/cm3 and a melting point of around -35°C. It is soluble in water and is commonly used as a surfactant, emulsifier, and corrosion inhibitor in various industrial applications, such as in the manufacturing of lubricants, fuels, and metalworking fluids. Due to its amphiphilic nature, it can form micelles in aqueous solutions, making it effective in stabilizing emulsions and dispersing particles.

7617-75-6

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7617-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7617-75-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,1 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7617-75:
(6*7)+(5*6)+(4*1)+(3*7)+(2*7)+(1*5)=116
116 % 10 = 6
So 7617-75-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H45NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-23-21-18-19-22/h2-22H2,1H3

7617-75-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-octadecoxypropan-1-amine

1.2 Other means of identification

Product number -
Other names EINECS 231-529-7

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:7617-75-6 SDS

7617-75-6Relevant academic research and scientific papers

Hair cosmetic, aminocarboxylic acid amide and method for producing the same

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, (2008/06/13)

A hair cosmetic which can impart, to hairs, flexibility, smoothness and oily feeling when the hairs are wetted and smoothness, softness and combing easiness after the hairs are dried are provided, the hair cosmetic comprising an amine represented by the formula (I): Formula (I) (wherein R1 represents a C8-40 alkyl group or alkenyl group or a group represented by the formula R5O—(AO)n—CmH2m— (R5 represents a C8-40 alkyl group or alkenyl group having 8 to 40 carbon atoms, A represents a C2-3 alkylene group, n denotes a number from 0 to 30 in average and m denotes an integer of 2 or 3), R2 represents a C1-5 alkylene group, R3 represents H, a C1-24 alkyl group, alkenyl group or hydroxyalkyl group or a C6-28 aryl group or arylalkyl group, R4 represents H, a C1-5 alkyl group, alkylene group or hydroxyalkyl group or a C6-28 aryl group or arylalkyl group, p denotes an integer from 1 to 3, q and r denote integers from 0 to 2 and p+q+r is equal to 3. Also, the amine (I) can be produced with high selectivity and highly economically by reacting a primary amine with an aminocarboxylic acid to run amidation. An amine represented by the formula (1), its salt or quaternary ammonium salt are also provided: Formula (1)

Process for production of ether amine

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Example 1; comparative 1, (2008/06/13)

Disclosed herein are a process for producing an ether amine(3), which comprises reacting a primary or secondary alcohol(1),ROH, with acrylonitrile in an amount of 0.8 to 1.2 equivalents of the alcohol(1) in the presence of an alkali metal hydroxide in an amount of not less than 0.01 part by weight, but less than 0.05 part by weight per 100 parts by weight of the alcohol(1) to obtain an alkyloxypropionitrile(2),and then adding water to the reaction system without removing the alkali metal hydroxide therefrom and effecting hydrogenation using a hydrogenation catalyst:ROH(1)+ CH2=CHCN, ROCH2CH2CH2CN(2), ROCH2CH2CH2NH2(3) wherein R denotes a linear or branched alkyl or alkenyl group having 6 to 24 carbon atoms. Also disclosed are a process for producing an ether tertiary amine (5), R-O-CH2-CH2-CH2-N(CH2R1)2, which comprises adding an aldehyde to the resulting ether amine(3) in the presence of a metal catalyst or a Raney nickel catalyst, and a process for producing an ether quaternary ammonium salt (6), R-O-CH2-CH2-CH2-N(CH2R1)2(R2), which comprises reacting a quaternizing agent with the ether tertiary amine(5).

Poly-bis-triazinylimides, their preparation

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, (2008/06/13)

Poly-bis-triazinylimides of the formula STR1 are prepared from bis-(2,4-dichloro-1,3,5-triazin-6-yl)imides and polyalkylpiperidylamines. They are used as light stabilizers for polymers.

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