Dimethyl sulfide (CAS N° 75-18-3)​

Photo credits: ScenTree SAS

Sulfuric

Dimethyl sulfide

Methylsulfanylmethane ; Dimethyl monosulfide ; Dimethyl sulphyde ; Dimethyl thioether ; DMS ; Exact-S ; Methane thiomethane ; Methyl monosulfide ; Methyl sulfide ; Methyl thioether ; Methylsulfanylmethane ; 2-thiapropane ; Thiobismethane ; 2-thiopropane

Dimethyl sulfide (CAS N° 75-18-3)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
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METHYL SULPHIDE 'A'GRADE 441M250000 Visit website Je me procure cet ingrédient Synthetic Aroma Chemicals Certifications : Kasher - -

METHYL SULPHIDE 'A'GRADE

ID : 441M250000

UK

Certifications : Certifications : Kasher

Information Générales

General Presentation

  • CAS N° :

    75-18-3
  • EINECS number :

    200-846-2
  • FEMA number :

    2746
  • FLAVIS number :

    12.006
  • JECFA number :

    452
  • Volatility :

    Head
  • Price Range :

    €€€
Physico-chemical properties

Physico chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,846
  • Refractive Index @20°C :

    1,431 – 1,441 @25°C
  • Optical rotation :

    Data not available.
  • Vapor pressure :

    862,6 hPa @25°C
  • Flash Point :

    -36°C
  • Molecular formula :

    C2H6S
  • Molecular Weight :

    62,13 g/mol
  • Log P :

    0,84
  • Fusion Point :

    -98°C
  • Boiling Point :

    38°C
  • Detection Threshold :

    0,3 et 10 ppb
Utilisation

Chemistry & Uses

Uses in perfumery :

Dimethyl Sulfide is used in small quantities in exotic and red fruits, woody, green and eau fraiche notes. In low quantity, it brings a juicy and acidic effect to fruity notes, but an onion facet if overdosed.

Year of discovery :

Data not available.

Natural availability :

Dimethyl Sulfide is present in many foods consumed daily, but its synthetic version in most often used in perfumery.

Isomerism :

Dimethyl Sulfide does not have any isomer used in perfumery.

Synthesis precursor :

Dimethyl Sulfide is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

The synthesis of Dimethyl Sulfide consists of a single step: reacting two molar equivalents of bromomethane with one and a half equivalent of sodium sulfide, in a hydroalcoholic and hot medium.

Stability :

Stable in perfumes and diverse functional bases

Other comments :

Data not available.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

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