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2040-64-4

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2040-64-4 Usage

General Description

Myristic acid lauryl ester is a chemical compound derived from myristic acid and lauryl alcohol. It is commonly used in the production of cosmetics, personal care products, and household cleaners as an emollient and surfactant. The compound is valued for its ability to enhance the spreadability and texture of various formulations, and it also functions as a skin conditioning agent. Myristic acid lauryl ester is known for its mildness on the skin, making it suitable for use in products designed for sensitive or delicate skin. It also serves as an emulsifier, helping to blend oil and water-based ingredients in formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 2040-64-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,4 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2040-64:
(6*2)+(5*0)+(4*4)+(3*0)+(2*6)+(1*4)=44
44 % 10 = 4
So 2040-64-4 is a valid CAS Registry Number.
InChI:InChI=1/C26H52O2/c1-3-5-7-9-11-13-15-16-18-20-22-24-26(27)28-25-23-21-19-17-14-12-10-8-6-4-2/h3-25H2,1-2H3

2040-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dodecyl tetradecanoate

1.2 Other means of identification

Product number -
Other names Lauryl myristate

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:2040-64-4 SDS

2040-64-4Downstream Products

2040-64-4Relevant articles and documents

Efficient greener methodology for the preparation of bio-based phase change materials from lipids

Y?ld?r?m, Ayhan,K?raylar, Kaan

, p. 407 - 413 (2020/11/19)

In the present work, a new, highly efficient and simple strategy has been developed for the synthesis of long chain esters from fatty acids and fatty alcohols as phase change materials. Equivalent amounts of the selected starting compounds were taken to the esterification reaction at 110 °C in a solventless medium. In order to catalyze the esterification reaction, non-hygroscopic triphenylphosphine-sulfur trioxide adduct was used (0.83 mmol%) which is an easily accessible compound. The relevant reaction was completed in a very short time (2 h) and under optimized esterification conditions, excellent conversion were reached. The targeted mono ester compounds (15 examples) were obtained in good to excellent yields even after a simple crystallization step (72-99%). Additionally, a catalyst reuse investigation and study covering the scale-up production of stearyl stearate was also carried out. The triphenylphosphine-sulfur trioxide catalyzed solvent free process can compete with existing processes and proved to be a cheaper, practical and environmentally-friendly method for the esterification of fatty acids and alcohols.

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