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DIETHYLENE GLYCOL MONOOCTADECYL ETHER, also known as octadecyl ethoxylate, is a non-ionic chemical compound that serves as an emulsifier, surfactant, and wetting agent. It is compatible with both water and oil-based substances due to its non-ionic nature, making it a versatile component in various industrial and household applications.

16057-43-5

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16057-43-5 Usage

Uses

Used in Detergent Industry:
DIETHYLENE GLYCOL MONOOCTADECYL ETHER is used as an emulsifier and surfactant for its ability to disperse and stabilize different components in detergents, enhancing their cleaning and spreading properties.
Used in Cosmetics Industry:
In cosmetics, DIETHYLENE GLYCOL MONOOCTADECYL ETHER is used as a wetting agent to improve the spreading and absorption of cosmetic products on the skin, providing a smooth and even application.
Used in Cleaning Agents Industry:
DIETHYLENE GLYCOL MONOOCTADECYL ETHER is utilized as a surfactant in cleaning agents to facilitate the dispersion of dirt and grime, making it easier to clean various surfaces.
Used in Pesticides Industry:
In the pesticides industry, DIETHYLENE GLYCOL MONOOCTADECYL ETHER is used as a surfactant to improve the spreading and wetting properties of the pesticide, ensuring even distribution and effective pest control.
It is important to handle and use DIETHYLENE GLYCOL MONOOCTADECYL ETHER with caution, as it can cause skin irritation and may be harmful if ingested or inhaled in high concentrations.

Check Digit Verification of cas no

The CAS Registry Mumber 16057-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,5 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16057-43:
(7*1)+(6*6)+(5*0)+(4*5)+(3*7)+(2*4)+(1*3)=95
95 % 10 = 5
So 16057-43-5 is a valid CAS Registry Number.
InChI:InChI=1/C22H46O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19-24-21-22-25-20-18-23/h23H,2-22H2,1H3

16057-43-5SDS

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 2-(2-octadecoxyethoxy)ethanol

1.2 Other means of identification

Product number -
Other names 3,6-dioxatetracosan-1-ol

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:16057-43-5 SDS

16057-43-5Relevant academic research and scientific papers

Drug carrier based on sulfonium lipidosome structure and preparation method and application of drug carrier

-

Paragraph 0049; 0058-0060, (2019/08/14)

The invention relates to the technical field of medicine, in particular to a sulfonium compound shown as a general formula (A), and discloses a preparation method of the compound. The compound is poly-condensed with genes to form a nanometer compound with the particle size of 100-300 nm and Zeta potential of +20-+40. The gene loading capability of the sulfonium compound enables the sulfonium compound to have potential application in gene transfer.

Combinatorial synthesis of PEG oligomer libraries

-

Page/Page column 9, (2010/02/15)

A simple chain-extending approach was established for the scale-up of the monoprotected monodisperse PEG diol materials. Reactions of THP-(OCH2CH2)n—OMs (n=4, 8, 12) with a large excess of commercially available H—(OCH2CH2)n—OH (n=1-4) under basic conditions led to THP-(OCH2CH2)n—OH (n=5-15). Similarly, Me-(OCH2CH2)n—OH (n=4-11, 13) were prepared from Me-(OCH2CH2)n—OMs (n=3, 7, 11). For the chain elongation steps, 40-80% yields were achieved through extraction purification. PEG oligomer libraries I and II were generated in 50-95% overall yields by alkylation or acylation of THP-(OCH2CH2)n—OH (n=1-15) followed by deprotection. Alkylation of Me-(OCH2CH2)n—OH (n=1-11, 13) with X—(CH2)m—CO2R (X=Br or OMs) and subsequent hydrolysis led to PEG oligomer library III in 30-60% overall yields. Combinatorial purification techniques were adapted to the larger-scale library synthesis. A total of 498 compounds, each with a weight of 2-5 g and a minimum purity of 90%, were synthesized.

2-picolylamine derivatives

-

, (2008/06/13)

The present invention relates to novel 2-picolylamine derivatives of general formula I STR1 wherein R1 represents an alkyl or phenylalkyl radical; R2 is hydrogen, C1 -C4 acyl or C1 -C4 alko

Synthesis of Hydroxyethyl Ethers from Long Chain Fatty Alcohols

Rao, Samala Jagadishwar,Bhalerao, Uday T.,Tilak, Bal Dattatreya

, p. 277 - 278 (2007/10/02)

A two-step facile synthesis of mono- and di-β-hydroxyethyl ethers of long chain fatty alcohols starting from alcohols and chloro/bromo acetic esters is described.These compounds, which are otherwise difficult to obtain in pure state, are of great interest as plant groth promoters.

Organotin-containing composition for the stabilization of polymers of vinyl chloride

-

, (2008/06/13)

An organotin-containing composition for the stabilization of polymers or copolymers of vinyl chloride in which there is incorporated a stabilizing amount of an organotin compound containing at least two tin atoms and which is a mercapto, hydroxy or alkoxy substituted ester of a mercapto acid substituted organotin mercapto acid diester.

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