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Ethyl 3-(ethylsulfanyl)propanoate is a colorless liquid organic compound with the chemical formula C7H14O2S. It is an ester derived from 3-(ethylsulfanyl)propanoic acid and ethanol, featuring a sulfur atom in its structure. ethyl 3-(ethylsulfanyl)propanoate is characterized by a pleasant, fruity odor and is commonly used as a flavoring agent in the food and beverage industry, particularly in the production of beverages, confectionery, and dairy products. It is also employed as a fragrance ingredient in the cosmetics and perfumery sector. Ethyl 3-(ethylsulfanyl)propanoate is synthesized through the esterification of 3-(ethylsulfanyl)propanoic acid with ethanol, and it is known for its stability and low toxicity, making it a safe additive for various applications.

5402-68-6

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5402-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5402-68-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5402-68:
(6*5)+(5*4)+(4*0)+(3*2)+(2*6)+(1*8)=76
76 % 10 = 6
So 5402-68-6 is a valid CAS Registry Number.

5402-68-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-ethylsulfanylpropanoate

1.2 Other means of identification

Product number -
Other names 3-Aethylmercapto-propionsaeure-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:5402-68-6 SDS

5402-68-6Relevant academic research and scientific papers

Studies on umami taste. Synthesis of new guanosine 5′-phosphate derivatives and their synergistic effect with monosodium glutamate

Cairoli, Paola,Morelli, Carlo F.,Speranza, Giovanna,Manitto, Paolo,Pieraccini, Stefano,Sironi, Maurizio

supporting information; scheme or table, p. 1043 - 1050 (2009/05/08)

A number of N2-alkyl and N2-acyl derivatives of guanosine 5′-phosphate (GMP) have been synthesized and tested for their synergistic effect with monosodium L-glutamate (MSG), the prototypical substance imparting umami taste to savory-based foods. Capacities to enhance the taste intensity of MSG (γ values) were estimated through subjective comparisons of MSG/nucleotide mixtures in water with appropriate solutions of MSG alone. Assuming β = γ[nucleotide]/γ[IMP], β values of the N 2-substituted GMPs were found in the range 1.2-5.7. Such values appear to be related to the chain length of the substituent in the 2-position of the purine nucleus and dependent on the replacement of a CH2 group with an S atom and/or with an α-CO group. These findings indicate that the exocyclic NHR group of the guanine moiety is actively implicated in the synergism between GMP derivatives and MSG. Theoretical calculations suggest that an anti conformation is probably assumed by ribonucleotide molecules interacting with umami receptors.

Highly efficient KF/Al2O3-catalyzed versatile hetero-Michael addition of nitrogen, oxygen, and sulfur nucleophiles to α,β-ethylenic compounds

Yang, Lei,Xu, Li-Wen,Xia, Chun-Gu

, p. 3279 - 3282 (2007/10/03)

The first example of KF/Al2O3-catalyzed versatile hetero-Michael addition reaction of nitrogen, oxygen, and sulfur nucleophiles was developed for facile preparation of organic compounds of widely different structures. In contrast with the existing methods using many acidic catalysts, this method is very general, simple, high-yielding, environmentally friendly, and oxygen and moisture tolerant.

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