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Triethylene glycol monostearate, also known as TEGMS, is a non-ionic chemical compound that is widely used as an emulsifier and surfactant in various industrial applications. It is synthesized through the esterification of stearic acid with triethylene glycol, making it a versatile and multifunctional chemical with a broad range of uses.

10233-24-6

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10233-24-6 Usage

Uses

Used in Personal Care and Cosmetics Industry:
TEGMS is used as a stabilizer and thickening agent in the production of personal care products and cosmetics. Its emulsifying and surfactant properties help to create stable formulations and improve the texture and consistency of these products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, TEGMS is utilized as a stabilizer and thickening agent in the formulation of various medications. Its ability to improve the stability and consistency of pharmaceutical products makes it an essential component in drug development.
Used in Food Production:
TEGMS is used as a food additive in food production. Its emulsifying properties help to improve the texture, consistency, and stability of various food products, enhancing their quality and shelf life.
Used in Plastics and Polymer Manufacturing:
In the manufacturing of plastics and polymers, TEGMS is employed as a plasticizer and surfactant. Its ability to improve the flexibility and processability of plastics and polymers makes it a valuable component in the production of various plastic materials.
Used in Lubricant Production:
TEGMS is used as a lubricant additive in the production of various types of lubricants. Its surfactant properties help to reduce friction and wear, improving the performance and longevity of lubricated components.
Used in Petroleum Industry:
In the petroleum industry, TEGMS is employed as an additive in drilling fluids and lubricants. Its emulsifying and surfactant properties help to improve the performance and stability of these fluids, enhancing the efficiency of drilling operations.
Overall, TEGMS is a versatile and multifunctional chemical compound with a wide range of industrial applications, making it an essential component in various industries, including personal care, cosmetics, pharmaceuticals, food production, plastics and polymer manufacturing, lubricant production, and the petroleum industry.

Check Digit Verification of cas no

The CAS Registry Mumber 10233-24-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,3 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10233-24:
(7*1)+(6*0)+(5*2)+(4*3)+(3*3)+(2*2)+(1*4)=46
46 % 10 = 6
So 10233-24-6 is a valid CAS Registry Number.
InChI:InChI=1/C24H48O5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-24(26)29-23-22-28-21-20-27-19-18-25/h25H,2-23H2,1H3

10233-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(2-hydroxyethoxy)ethoxy]ethyl octadecanoate

1.2 Other means of identification

Product number -
Other names PEG-3 Stearate

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:10233-24-6 SDS

10233-24-6Upstream product

10233-24-6Downstream Products

10233-24-6Relevant academic research and scientific papers

Combinatorial synthesis of PEG oligomer libraries

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Page/Page column 11, (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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