Bis(methylthio)methane

98%

Reagent Code: #147848
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Alias Dimethylthiomethane; methylene bis(dimethylsulfide); bis(methylthio)methane
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CAS Number 1618-26-4
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Properties Specific gravity (20/20) 1.0620 to 1.0650

science Other reagents with same CAS 1618-26-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 108.23 g/mol
Formula CH₃SCH₂SCH₃
badge Registry Numbers
MDL Number MFCD00008564
thermostat Physical Properties
Boiling Point 152°C(lit.)
inventory_2 Storage & Handling
Density 1.06g/mL
Storage Room temperature, dry

description Product Description

Used as a sulfur-containing intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive thioether groups enable the construction of complex sulfur heterocycles and bioactive molecules. Also employed in the development of flavors and fragrances due to its ability to release sulfur notes under specific conditions. Additionally, it serves as a reagent in the synthesis of specialty polymers and ligands for catalysis.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿360.00
inventory 25g
10-20 days ฿1,150.00
inventory 100g
10-20 days ฿3,860.00
inventory 500g
10-20 days ฿12,680.00

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Bis(methylthio)methane
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Used as a sulfur-containing intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive thioether groups enable the construction of complex sulfur heterocycles and bioactive molecules. Also employed in the development of flavors and fragrances due to its ability to release sulfur notes under specific conditions. Additionally, it serves as a reagent in the synthesis of specialty polymers and ligands for catalysis.

Used as a sulfur-containing intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive thioether groups enable the construction of complex sulfur heterocycles and bioactive molecules. Also employed in the development of flavors and fragrances due to its ability to release sulfur notes under specific conditions. Additionally, it serves as a reagent in the synthesis of specialty polymers and ligands for catalysis.

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