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52849-47-5

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52849-47-5 Usage

General Description

2-(2-hydroxyethoxy)ethyl myristate is a chemical compound that is commonly used in the production of cosmetics and personal care products. It is a type of emollient and skin conditioning agent that helps to moisturize and soften the skin. The chemical is also used as a fragrance ingredient and a solvent in various products. 2-(2-hydroxyethoxy)ethyl myristate is derived from myristic acid, a saturated fatty acid found in natural sources such as coconut oil and palm oil, and it is known for its ability to improve the texture and feel of skincare and haircare products. This chemical is considered safe for use in cosmetics and personal care products when used in accordance with industry regulations and guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 52849-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,4 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52849-47:
(7*5)+(6*2)+(5*8)+(4*4)+(3*9)+(2*4)+(1*7)=145
145 % 10 = 5
So 52849-47-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H36O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-18(20)22-17-16-21-15-14-19/h19H,2-17H2,1H3

52849-47-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-hydroxyethoxy)ethyl tetradecanoate

1.2 Other means of identification

Product number -
Other names EINECS 258-223-6

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:52849-47-5 SDS

52849-47-5Downstream Products

52849-47-5Relevant articles and documents

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.

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