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666-15-9

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666-15-9 Usage

General Description

Methyl methanesulfinate, also known as MMS, is a chemical compound with the formula CH3SSO2CH3. It is a colorless liquid with a strong sulfurous odor. MMS is commonly used as a reagent in organic synthesis and as a flavoring agent in the food industry. It is known for its potent odor, which can be irritating to the eyes, skin, and respiratory system. Methyl methanesulfinate is also used as a preservative in the production of wine and beer to inhibit the growth of spoilage microorganisms. It is important to handle MMS with care and use proper protective equipment due to its hazardous fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 666-15-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,6 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 666-15:
(5*6)+(4*6)+(3*6)+(2*1)+(1*5)=79
79 % 10 = 9
So 666-15-9 is a valid CAS Registry Number.

666-15-9SDS

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 methyl methanesulfinate

1.2 Other means of identification

Product number -
Other names methylsulfinyloxymethane

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:666-15-9 SDS

666-15-9Relevant articles and documents

Unsensitized photooxidation of sulfur compounds with molecular oxygen in solution

Robert-Banchereau, Evelyne,Lacombe, Sylvie,Ollivier, Jean

, p. 2087 - 2102 (2007/10/03)

The short wavelength irradiation of aliphatic disulfides, sulfides and of n-butanethiol in alcohols or aqueous acetonitrile in the presence of oxygen was investigated: the corresponding sulfonic acids are produced in good yields for short alkyl chain compounds, together with smaller amounts of sulfuric and carboxylic acids. In acetonitrile, the influence of added water on the reaction course is evidenced: increased reaction rate and acid yields, control of sulfuric acid formation. Intermediates such as sulfinic acid and thiosulfonate were detected and their rates of formation were monitored. The reaction appears to involve thiyl radicals giving rise to sulfonyl radicals in the presence of oxygen. A first tentative hypothesis concerning the mechanism is advanced.

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