Dimethyl sulfone
| Nom du produit | Dimethyl sulfone |
|---|---|
| Numéro CAS | 67-71-0 |
| Synonymes | Methyl sulfone, Methylsulfonylmethane, MSM, DMSO2 |
| Formule moléculaire | C2H6O2S |
| Poids moléculaire | 94.13 g/mol |
| Apparence | White crystalline solid |
| Assay (GC) | ≥99,01 TP3T |
| Point de fusion | 107–109 °C |
| Boiling Point | 238 °C |
| Solubilité | Soluble in water, methanol, ethanol; slightly soluble in acetone |
| Perte au séchage | ≤ 0,51 TP3T |
| Métaux lourds | ≤ 10 ppm |
| Colis | Fût en fibre de 25 kg avec double revêtement en polyéthylène |
| Spécifications | 99% |
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Synonymes : Methyl sulfone, Methylsulfonylmethane, MSM, DMSO2
Dimethyl sulfone is a small, highly polar organosulfur molecule with a sulfonyl group flanked by two methyl groups. This simple structure—often written as (CH3)2SO2—underpins its distinctive properties: thermal stability, high water solubility, and the ability to participate in hydrogen bonding without acting as a strong acid or base. Unlike its reduced analog dimethyl sulfoxide (DMSO), dimethyl sulfone is fully oxidized and chemically inert under normal conditions, which makes it an attractive building block for pharmaceutical and nutraceutical applications.
While the compound occurs naturally in trace amounts in certain plants, algae, and mammalian fluids, commercial supply relies on synthetic routes. Oxidation of dimethyl sulfide or DMSO yields high-purity dimethyl sulfone, which is then purified through crystallization to meet pharmacopeial standards. The resulting white crystalline solid is available in several grades, from technical to USP/EP, with assay values typically exceeding 99%.
In the pharmaceutical and dietary supplement sectors, dimethyl sulfone is best known as MSM. It serves as a sulfur donor in vivo, supporting the synthesis of connective tissue components such as collagen and keratin. Formulators also value it for its ability to improve the solubility and stability of other actives, while chemists use it as a mild oxidant or as an intermediate in organic synthesis. Its low toxicity and favorable safety profile have made it a staple in joint health products and sports nutrition.
Dimethyl sulfone crystallizes in a monoclinic system, forming colorless, odorless crystals that are stable at room temperature. The molecule is tetrahedral around the sulfur atom, with two methyl groups and two oxygen atoms arranged in a near-symmetric fashion. This geometry results in a significant dipole moment (≈4.4 D), which explains its high solubility in polar solvents like water (up to 150 g/L at 20 °C) and its low solubility in nonpolar media. The sulfonyl group is resistant to oxidation and reduction under mild conditions, contributing to the compound’s long shelf life. It has a melting point of 107–109 °C and boils at 238 °C, allowing for distillation if needed. The material is non-flammable and has a very low vapor pressure at ambient temperatures.
| Paramètre | Spécifications |
|---|---|
| Assay (GC) | ≥99,01 TP3T |
| Apparence | White crystalline solid |
| Identification | IR spectrum conforms to reference |
| Point de fusion | 107–109 °C |
| Perte au séchage | ≤ 0,51 TP3T |
| Métaux lourds | ≤ 10 ppm |
| Résidu au feu | ≤ 0,11 TP3T |
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