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Methylthiomethyl hexanoate, with the molecular formula C8H16O2S, is a chemical compound characterized by its clear, colorless liquid form and a distinctive fruity, sulfur-like odor. It is soluble in alcohol and oils, making it a versatile ingredient in various industries.

74758-91-1

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74758-91-1 Usage

Uses

Used in the Food Industry:
Methylthiomethyl hexanoate is used as a flavoring agent for its ability to impart a fruity and berry-like taste to food products, enhancing their overall flavor profile.
Used in the Fragrance Industry:
In the realm of perfumes and personal care products, methylthiomethyl hexanoate is utilized as a fragrance ingredient to provide a fruity and tropical scent, adding depth and complexity to the olfactory experience.
Used in Household Products:
Methylthiomethyl hexanoate's unique aroma profile also makes it suitable for use in household products such as air fresheners and cleaning agents, where it contributes a pleasant and refreshing scent to the environment.
Safety:
When used within the regulatory limits, methylthiomethyl hexanoate is considered safe for its intended applications across these industries.

Check Digit Verification of cas no

The CAS Registry Mumber 74758-91-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,5 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74758-91:
(7*7)+(6*4)+(5*7)+(4*5)+(3*8)+(2*9)+(1*1)=171
171 % 10 = 1
So 74758-91-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O2S/c1-3-4-5-6-8(9)10-7-11-2/h3-7H2,1-2H3

74758-91-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methylsulfanylmethyl hexanoate

1.2 Other means of identification

Product number -
Other names METHYLTHIOMETHYL HEXANOATE

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:74758-91-1 SDS

74758-91-1Downstream Products

74758-91-1Relevant articles and documents

Chemistry of peroxyacyl nitrates. Part III. The oxidation of thioethers by peroxyhexanoyl nitrate

Noort, Paul C. M. van,Vermeeren, Hans P. W.,Louw, Robert

, p. 312 - 321 (2007/10/02)

The reaction of peroxyhexanoyl nitrate, 1a, a homologue of the atmospheric pollutant "PAN", 1b, with some twenty thioethers, is described.At 0-25 deg C, common thioethers such as Et2S or PhSMe are rapidly converted into sulfoxides in high yields in a variety of solvents, ranging from pentane and chloroform to acetic acid, methanol and aqueous acetonitrile.Rates are essentially solvent-independent, although the reaction is subject to marked steric hindrance.Relative rates for five p-substituted thioanisoles in MeOH at 22 deg C, leading to a Hammett ρ-value of -1.7, show that the sulfur atoms display nucleophilic character.Electron-attracting groups on α-carbon, such as in PhSCCl3 and in MeSCH2OC(O)Ph, inhibit the formation of sulfoxide.Addition of EtSH lowers the yield of sulfoxide, producing instead EtSSEt and EtSNO.Oxidation of Me2S by 1a with the NO2 group labelled by 18O does not give rise to 18O-enriched DMSO.Comparison of (CH3)2S with (CD3)2S revealed an inverse kinetic H/D isotope effect.The products obtained from 1a vary with solvent.In the presence of water or EtSH, hexanoic acid is formed, while methanol gives rise to methyl hexanoate, and in pentane/hexanoic acid, hexanoic anhydride is produced.In aprotic solvents, significant amounts of CO2 are formed.These observations can best be rationalized on the basis of an intermediate sulfurane R1R2S(ONO2)(OCOR), (I), produced from thioether R1SR2 and 1a, in the first step.The fate of (I) under various conditions is discussed.Finally, the features of the oxidation of thioethers by peroxyacylnitrate are compared with those of acyl peroxides and peroxy esters.It is suggested that in each case formation of a sulfurane may well be the first step.

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