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C18E3, also known as Ceteareth-3, is a non-ionic surfactant derived from coconut and palm kernel oils. It is a mixture of ethoxylated fatty alcohols with an average of 3 moles of ethylene oxide per molecule. C18E3 is widely used in the cosmetics and personal care industry as an emulsifier, solubilizer, and foam booster, providing stability and improving the texture of formulations. It is known for its mildness and compatibility with various ingredients, making it suitable for a range of products, including creams, lotions, and shampoos.

4439-32-1

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4439-32-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4439-32-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4439-32:
(6*4)+(5*4)+(4*3)+(3*9)+(2*3)+(1*2)=91
91 % 10 = 1
So 4439-32-1 is a valid CAS Registry Number.
InChI:InChI=1/C24H50O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19-26-21-23-28-24-22-27-20-18-25/h25H,2-24H2,1H3

4439-32-1SDS

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-octadecoxyethoxy)ethoxy]ethanol

1.2 Other means of identification

Product number -
Other names C18E3

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:4439-32-1 SDS

4439-32-1Downstream Products

4439-32-1Relevant academic research and scientific papers

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

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Paragraph 0049; 0067-0069, (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

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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.

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