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124-06-1

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124-06-1 Usage

General Description

Ethyl tetradecanoate, also known as ethyl myristate, is a fatty acid ester derived from myristic acid and ethanol. It has the chemical formula of C16H32O2. It is a colorless and odorless liquid that is found in some plants and animal fats. Ethyl tetradecanoate is used in various industries as an additive and ingredient in cosmetics, perfumes, and personal care products due to its lubricating properties and ability to provide a smooth skin feel. It is also utilized in the pharmaceutical industry as a penetration enhancer in transdermal drug delivery systems. Despite its wide usage, ethyl tetradecanoate is considered relatively safe as it's non-toxic and non-irritating.

Check Digit Verification of cas no

The CAS Registry Mumber 124-06-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 124-06:
(5*1)+(4*2)+(3*4)+(2*0)+(1*6)=31
31 % 10 = 1
So 124-06-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H32O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16(17)18-4-2/h3-15H2,1-2H3

124-06-1 Well-known Company Product Price

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  • Alfa Aesar

  • (A11646)  Ethyl tetradecanoate, 98%   

  • 124-06-1

  • 100ml

  • 537.0CNY

  • Detail
  • Alfa Aesar

  • (A11646)  Ethyl tetradecanoate, 98%   

  • 124-06-1

  • 500ml

  • 1647.0CNY

  • Detail

124-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl myristate

1.2 Other means of identification

Product number -
Other names Ethyl tetradecanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:124-06-1 SDS

124-06-1Relevant articles and documents

Electrochemical Tandem Olefination and Hydrogenation Reaction with Ammonia

Zhang, Xiaofeng,Jiang, Runze,Cheng, Xu

, p. 16016 - 16025 (2021/08/24)

An electrochemical Horner-Wadsworth-Emmons/hydrogenation tandem reaction was achieved using ammonia as electron and proton donors. The reaction could give two-carbon-elongated ester and nitrile from aldehyde or ketones directly. This reaction could proceed with a catalytic amount of base or even without a base. The ammonia provides both the electron and proton for this tandem reaction and enables the catalyst-free hydrogenation of an α,β-unsaturated HWE intermediate. More than 40 examples were reported, and functional groups, including heterocycles and hydroxyl, were tolerated.

NATURAL BIOSURFACTANT OF ESTER AND MANUFACTURING METHOD THEREOF

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Paragraph 0125; 0126; 0129-0132, (2020/12/11)

The present invention relates to an ester natural surfactant and a manufacturing method thereof. The present invention relates to an eco-friendly ester natural surfactant having excellent solubility in water and biodegradability, and a manufacturing method thereof. The present invention relates to an ester natural surfactant, and more particularly, to an ester natural surfactant and a method for preparing the same. (by machine translation)

Preparation method of long-chain ester

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Paragraph 0121; 0122; 0123, (2019/03/23)

The invention relates to the field of organic synthesis and provides a preparation method of long-chain ester, which comprises the following steps: carrying out esterification reaction of the carboxylic acid and the alcohol through a catalyst and obtaining a long-chain ester phase and a water phase post the standing and layering of the reaction liquid; the catalyst comprises ionic liquid or eutectic solvent; purifying and separating the long-chain ester phase to obtain high-purity long-chain ester; introducing the residual substance again into the esterification reaction system for reaction after the water in the water phase is removed. The yield and the purity of the long-chain ester prepared by the invented method are as high as 99.8% and 99% respectively as indicated by the embodiment of the preparation method.

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