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2-(2-hydroxyethoxy)ethyl palmitate is a chemical compound derived from palmitic acid and ethylene oxide, commonly used in personal care products and cosmetics. It acts as an emollient, emulsifier, and moisturizer, known for its ability to deeply hydrate and soften the skin.
Used in Personal Care Industry:
2-(2-hydroxyethoxy)ethyl palmitate is used as an emollient, emulsifier, and moisturizer for its ability to deeply hydrate and soften the skin, making it a popular ingredient in lotions, creams, and anti-aging products.
Used in Cosmetics Industry:
2-(2-hydroxyethoxy)ethyl palmitate is used as an ingredient in various skincare products for its hydrating and softening properties, contributing to the overall effectiveness and quality of cosmetic formulations.

36381-62-1

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36381-62-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36381-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,8 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 36381-62:
(7*3)+(6*6)+(5*3)+(4*8)+(3*1)+(2*6)+(1*2)=121
121 % 10 = 1
So 36381-62-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H40O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-20(22)24-19-18-23-17-16-21/h21H,2-19H2,1H3

36381-62-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-hydroxyethoxy)ethyl hexadecanoate

1.2 Other means of identification

Product number -
Other names 2-(2-Hydroxyethoxy)ethyl palmitate

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:36381-62-1 SDS

36381-62-1Downstream Products

36381-62-1Relevant academic research and scientific papers

Synthesis of novel amphiphilic spin probes with the paramagnetic doxyl group in the polar region

Pajk, Stane,Pe?ar, Slavko

scheme or table, p. 659 - 665 (2009/04/07)

The use of ESR and specially designed spin probes has led to major breakthroughs in understanding the complexity of biological membranes. Research has been focused mainly on molecular events within the?lipid bilayer, and few probes have been designed for studying events in the extracellular space near the membrane surface. We have prepared a series of amphiphilic spin probes in which an ethylene glycol type hydrophilic spacer was introduced between a hydrophobic anchor and the doxyl group, placing the latter above the membrane in the extracellular space. Furthermore, the 2pπ orbital, containing the unpaired electron of the nitroxide group, would be orientated perpendicular to the membrane surface, making it more useful for ESR investigations of structural and dynamic properties close to the membrane surface in different situations of the cell life.

Combinatorial synthesis of PEG oligomer libraries

-

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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