MMTS
MMTS Basic information
- Product Name:
- MMTS
- Synonyms:
-
- Formaldehyde dimethyl mercaptal S-oxide, Methyl methylmercaptomethyl sulfoxide, Methyl methylsulfinylmethyl sulfide, MMTS
- (Methylsulfinyl
- Methylsulfinylmethylsulfanylmethane
- Methyl methylsulfinylmethyl sulfide,97%
- methyl(methylsulfinylmethyl)sulfane
- FAMSO Formaldehyde Dimethyl Dithioacetal S-Oxide Methyl (Methylthio)methyl Sulfoxide
- FORMALDEHYDE DIMETHYL DITHIOACETAL S-OXIDE
- FAMSO
- CAS:
- 33577-16-1
- MF:
- C3H8OS2
- MW:
- 124.22
- EINECS:
- 251-577-2
- Product Categories:
-
- API intermediates
- Sulfur Compounds (for Synthesis)
- Synthetic Organic Chemistry
- Mol File:
- 33577-16-1.mol
MMTS Chemical Properties
- Melting point:
- 222-226°C
- Boiling point:
- 92 °C (2 mmHg)
- Density
- 1.22
- refractive index
- 1.548-1.558
- Flash point:
- >110°C
- solubility
- Soluble in acetic acid, alcohol, THF, CS2, CCl4, CHCl3, acetone, benzene, and DMSO; slightly soluble in cyclohexane and hexane.
- pka
- (DMSO) 29.0.
- form
- clear liquid
- color
- Colorless to Light yellow to Light orange
- Specific Gravity
- 1.22
- Sensitive
- Hygroscopic
- BRN
- 906789
- InChIKey
- OTKFCIVOVKCFHR-UHFFFAOYSA-N
- LogP
- -0.479 (est)
- CAS DataBase Reference
- 33577-16-1(CAS DataBase Reference)
- NIST Chemistry Reference
- Methane, (methylsulfinyl)(methylthio)-(33577-16-1)
- EPA Substance Registry System
- Methane, (methylsulfinyl)(methylthio)- (33577-16-1)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/38
- Safety Statements
- 37/39-26-24/25-23
- RIDADR
- 3334
- TSCA
- Yes
- HS Code
- 29309070
MMTS Usage And Synthesis
Chemical Properties
Clear colorless to yellow liquid
Uses
(Methylthio)dimethyl sulfoxide is a essential oil from fruit of Gallesia integrifolia exhibit antifungal activity against Aspergillus fumigatus, Aspergillus niger and Aspergillus ochraceus.
Definition
ChEBI: (Methylsulfinyl)(methylthio)methane is a sulfoxide.
Reactivity Profile
Formaldehyde Dimethyl Thioacetal Monoxide is a versatile synthetic reagent used to produce aldehydes, ketones, α-keto carboxylates, α-amino acid derivatives, and arylacetic acid derivatives.
Synthesis
Formaldehyde Dimethyl Thioacetal Monoxide could be preparative through the substitution of chloromethyl methyl sulfoxide with sodium methanethiol or the oxidation of formaldehyde dimethyl dithioacetal with hydrogen peroxide.
Precautions
The reagent decomposes slightly when heated under acidic conditions. It is stable in alkaline and neutral media. It is desirable to keep the reagent in a tightly sealed container over 4 ? molecular sieves.
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