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Octadecanamide, N,N-1,6-hexanediylbis12-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55349-01-4

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55349-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55349-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,4 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55349-01:
(7*5)+(6*5)+(5*3)+(4*4)+(3*9)+(2*0)+(1*1)=124
124 % 10 = 4
So 55349-01-4 is a valid CAS Registry Number.

55349-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(4-amino-3,5-dichlorophenyl)iminomethyl]phenol

1.2 Other means of identification

Product number -
Other names -

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:55349-01-4 SDS

55349-01-4Downstream Products

55349-01-4Relevant academic research and scientific papers

Comparison of structure/function correlational property of three kinds of gemini-type thixotropic surfactants capable of forming crystalline nanofiber based on hydrogen bonding-solid-state structure, two-dimensional molecular film forming, and epitaxial growth behavior

Iizuka, Manami,Nakagawa, Yuto,Moriya, Yuma,Satou, Eiichi,Fujimori, Atsuhiro

, p. 813 - 823 (2018)

In this study, we compare and investigate both microscopic molecular packing and mesoscopic morphogenetic behavior in two-dimensional (2D) organized films/three-dimensional (3D) solids of three kinds of Gemini-type diamide surfactants that systematically differ in terms of their chemical structure. The gelation of the surrounding medium is promoted by growing crystalline nanofibers of these surfactants, and the disappearance of these nanofibers and solvent reflow are caused by the application of a force on the corresponding gel because these surfactant molecules are considered potential thixotropic agents. The layer structure and sub-cell in the 3D crystals of surfactants are formed by the association of van derWaals force and hydrogen bonding because the mechanism responsible for crystalline nanofiber formation is intermolecular hydrogen bonding. In the monolayer on the water surface, only surfactant molecules having a hydroxyl group in the hydrophobic chain formed crystalline nanofibers. The introduction of hydroxyl groups into the hydrophobic chains also promoted a singlephase molecular conformation in 3D crystals. However, the absence of hydroxyl groups in the hydrophobic chain promoted the growth of the nanofibers in the cast film, whereas the introduction of hydroxyl groups in the hydrocarbons improves the thixotropic property itself. In addition, the epitaxial growth of nanofibers upon the addition of a growth aid was promoted by the absence of hydroxyl groups.

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