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20-(4-dodecylphenoxy)-3,6,9,12,15,18-hexaoxaicosan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67669-59-4

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67669-59-4 Usage

Chemical Classification

Aliphatic alcohol

Carbon Chain Length

20 carbon atoms

Functional Group

Hydroxyl (-OH)

Hydrophobic Tail

Comprised of 20 carbon atoms

Hydrophilic Head Group

Contains six ether oxygen atoms

Surfactant Properties

Due to its structure, it exhibits surfactant properties.

Applications

Emulsifying and stabilizing systems (e.g., creams, lotions)
Lubricant
Dispersant
Ingredient in cleaning products

Solubility

Soluble in nonpolar solvents

Potential Industrial and Agricultural Applications

Industrial processes
Agricultural formulations

Check Digit Verification of cas no

The CAS Registry Mumber 67669-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,6 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 67669-59:
(7*6)+(6*7)+(5*6)+(4*6)+(3*9)+(2*5)+(1*9)=184
184 % 10 = 4
So 67669-59-4 is a valid CAS Registry Number.
InChI:InChI=1/C32H58O8/c1-2-3-4-5-6-7-8-9-10-11-12-31-13-15-32(16-14-31)40-30-29-39-28-27-38-26-25-37-24-23-36-22-21-35-20-19-34-18-17-33/h13-16,33H,2-12,17-30H2,1H3

67669-59-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-[2-[2-[2-[2-[2-(4-dodecylphenoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol

1.2 Other means of identification

Product number -
Other names EINECS 266-852-2

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:67669-59-4 SDS

67669-59-4Downstream Products

67669-59-4Relevant academic research and scientific papers

Synthesis, characterization, and functional evaluation of branched dodecyl phenol polyoxyethylene ethers: A novel class of surfactants with excellent wetting properties

He, Mingyang,Qian, Junfeng,Sun, Zhonghua,Wang, Xing,Zhang, Zhihui

, p. 38054 - 38059 (2021/12/09)

A series of branched dodecyl phenol polyoxyethylene ethers (b-DPEOn) were successfully synthesized via alkylation and ethylene oxide addition reactions. The alkylation reaction was conducted by using a branched internal olefin as the raw material. Furthermore, the conversion rate of the branched dodecene was measured to be 98.1% and the selectivity towards branched dodecyl phenol (b-DP) was 95.9%. Moreover, b-DPEOn (b-DPEO7, b-DPEO10, b-DPEO12) were obtained via the reaction of ethylene oxide with b-DP. Notably, b-DPEO10 can efficiently reduce the surface tension of water below 31.55 mN m-1 at the critical micelle concentration (cmc) and the cmc value in water was approximately 1.3 × 10-2 g L-1 at 25 °C. The preferable wetting ability of b-DPEO10 was superior to that of commercialized dodecyl phenol polyoxyethylene ether (c-DPEOn), so it will be promoted and used in the textile and pesticide industries.

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