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N-NONADECANOIC ACID ETHYL ESTER is a chemical compound that consists of a long chain fatty acid, n-nonadecanoic acid, esterified with ethyl alcohol. It is a colorless liquid with a mild odor and is known for its applications in the food, perfume, and biodiesel industries. N-NONADECANOIC ACID ETHYL ESTER is synthesized through the esterification of n-nonadecanoic acid with ethyl alcohol under specific reaction conditions and is considered safe for use in food and cosmetic products when used in accordance with regulations and guidelines.

18281-04-4

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18281-04-4 Usage

Uses

Used in Food Industry:
N-NONADECANOIC ACID ETHYL ESTER is used as a flavoring agent in food products for enhancing the taste and aroma of various dishes and ingredients.
Used in Perfume and Fragrance Industry:
N-NONADECANOIC ACID ETHYL ESTER is used as a component in the production of perfumes and other fragrance products, contributing to the creation of unique and pleasant scents.
Used in Biodiesel Production:
N-NONADECANOIC ACID ETHYL ESTER is recognized for its potential use in biodiesel production, offering an alternative and renewable source of energy.

Check Digit Verification of cas no

The CAS Registry Mumber 18281-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,8 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18281-04:
(7*1)+(6*8)+(5*2)+(4*8)+(3*1)+(2*0)+(1*4)=104
104 % 10 = 4
So 18281-04-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O/c1-2-3-4-5-6-7-8-9/h6-7,9H,2-5,8H2,1H3/b7-6+

18281-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl nonadecanoate

1.2 Other means of identification

Product number -
Other names Nonadecansaeure-aethylester

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:18281-04-4 SDS

18281-04-4Downstream Products

18281-04-4Relevant academic research and scientific papers

Solvent-free esterification of carboxylic acids and alcohols in the presence of silphos [PCl3-n(SiO2)n] as a heterogeneous phosphine reagent

Rao, Ambati Narasimha,Ganesan, Kumaran,Shinde, Chandra Kant

experimental part, p. 2299 - 2308 (2012/06/18)

An efficient solvent-free method for the preparation of esters from various aromatic and aliphatic acids with primary, secondary, and tertiary alcohols using a heterogeneous phosphine reagent, silphos [PCl3-n(SiO 2)n], in good yields is reported.

Selective Mono- and Bis(alkoxycarbonylation)s of Olefins Catalyzed by Palladium in the Presence of Cu(I) or Cu(II) Chloride under Remarkably Mild Conditions. Application to the Synthesis of γ-Butyrolactone Derivatives

Toda, Shiho,Miyamoto, Masanori,Kinoshita, Hideki,Inomata, Katsuhiko

, p. 3600 - 3606 (2007/10/02)

Palladium-catalyzed mono- and bis(alkoxycarbonylation)s of the olefins were controlled by the use of copper(II) and copper(I) chloride, respectively, in alcohol under normal pressure of carbon monoxide and oxygen at room temperature without any other additives. 3-Buten-1-ols gave the corresponding γ-butyrolactones and 2-oxotetrahydrofuran-3-acetic acid esters, respectively, in high yields.

Selective Mono- and Dicarbonylation of Terminal Olefins Catalyzed by Pd-C in the Presence of Cu(II) or Cu(I) Chloride under Mild Conditions

Inomata, Katsuhiko,Toda, Shiho,Kinoshita, Hideki

, p. 1567 - 1570 (2007/10/02)

Pd-C can catalyze the carbonylation of terminal olefins with normal pressure of carbon monoxide at room temperature.The corresponding mono- and diesters (succinates) were selectively formed in excellent yields using Cu(II) and Cu(I) chloride, respectively, in alcohol.

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