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N-[3-(dimethylamino)propyl]docosanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60270-33-9

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60270-33-9 Usage

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 60270-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,7 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60270-33:
(7*6)+(6*0)+(5*2)+(4*7)+(3*0)+(2*3)+(1*3)=89
89 % 10 = 9
So 60270-33-9 is a valid CAS Registry Number.
InChI:InChI=1/C27H56N2O/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-24-27(30)28-25-23-26-29(2)3/h4-26H2,1-3H3,(H,28,30)

60270-33-9SDS

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-[3-(Dimethylamino)propyl]docosanamide

1.2 Other means of identification

Product number -
Other names behenic acid dimethylaminopropylamide

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:60270-33-9 SDS

60270-33-9Downstream Products

60270-33-9Relevant academic research and scientific papers

HAIR TREATMENT AGENT

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Paragraph 0104, (2017/05/03)

PROBLEM TO BE SOLVED: To provide a hair treatment agent that can impart, even to damaged hair, excellent finger's running through properties, smoothness, and a coat feeling, both under wetness and after dryness. SOLUTION: A hair treatment agent comprises a compound or salt thereof. The compound has 1 or more and 5 or less amino group in a molecule, the amino group binds to a predetermined quaternary ammonium cation-containing group, the total of the number of the amino group(s) in the molecule and the number of the quaternary ammonium cation(s) are 2 or more and 10 or less, and the number of carbon in the molecule excluding carbon included in the quaternary ammonium cation-containing group is 0 or more and 24 or less. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPO&INPIT

A facile route towards the preparation of ultra-long-Chain amidosulfobetaine surfactants

Chu, Zonglin,Feng, Yujun

experimental part, p. 2655 - 2658 (2010/01/07)

A series of novel, ultra-long-chain amidosulfobetaine surfactants were prepared by amidation of ultra-long-chain fatty acids directly with N,N-dimethyl-1,3-propanediamine in the absence of solvents, followed by quaternization of the intermediates with 1,3-propanesultone in ethyl acetate.

Dimer poly-quaternary compounds

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Page/Page column 9, (2008/06/13)

The present invention relates to a novel class of polymeric compounds having specific quaternized amine based upon a dimer acid reacted with an dimethyl amino propyl amine to make an amido amine, which is subsequently reacted to make a polymeric quaternary compound. Dimer acid is a C-36 diacid having a cyclic structure and two amine groups that allow for the synthesis of a high molecular weight cationic compound which is extremely substantitive to human skin and are well tolerated by human tissue making them suitable for use preparation of barrier products for personal care applications.

HAIR COSMETIC

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Page/Page column 9, (2008/06/13)

The present invention provides hair cosmetics containing (a) an amideamine (I): wherein R1CO represents fatty acid residues among which C20 or more fatty acid residues account for 60 percent by weight or more, C20 fatty acid residues account for 3 percent by weight or more, and C22 fatty acid residues account for 50 to 95 percent by weight; (b) an organic acid; and (c) a C8 to C30 aliphatic alcohol, wherein the content of the component (b) is 1.5 to 10 times as many moles as the amine equivalent of the component (a).

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