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Atomfair Dimethyl Sulfate DMS C2H6O4S

Description Dimethyl Sulfate (CAS No. 77-78-1) is a highly reactive organic compound with the molecular formula C2H6O4S . This colorless, oily liquid is widely recognized for its role as a potent methylating agent in organic synthesis and industrial applications. With an IUPAC name of dimethyl sulfate , it is characterized by its ability to transfer methyl groups to nucleophiles, making it invaluable in the production of pharmaceuticals, dyes, and agrochemicals. Due to its extreme toxicity and carcinogenic properties, Dimethyl Sulfate must be handled with stringent safety precautions, including the use of personal protective equipment (PPE) and proper ventilation. Available in…

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Description

Description

Dimethyl Sulfate (CAS No. 77-78-1) is a highly reactive organic compound with the molecular formula C2H6O4S. This colorless, oily liquid is widely recognized for its role as a potent methylating agent in organic synthesis and industrial applications. With an IUPAC name of dimethyl sulfate, it is characterized by its ability to transfer methyl groups to nucleophiles, making it invaluable in the production of pharmaceuticals, dyes, and agrochemicals. Due to its extreme toxicity and carcinogenic properties, Dimethyl Sulfate must be handled with stringent safety precautions, including the use of personal protective equipment (PPE) and proper ventilation. Available in high-purity grades, this chemical is essential for researchers and scientists requiring precise and efficient methylation reactions.

  • CAS No: 77-78-1
  • Molecular Formula: C2H6O4S
  • Molecular Weight: 126.13
  • Exact Mass: 125.99867984
  • Monoisotopic Mass: 125.99867984
  • IUPAC Name: dimethyl sulfate
  • SMILES: COS(=O)(=O)OC
  • Synonyms: DIMETHYL SULFATE, 77-78-1, Dimethyl sulphate, dimethylsulfate, Sulfuric acid, dimethyl ester

Application

Dimethyl Sulfate is primarily used as a methylating agent in the synthesis of pharmaceuticals, pesticides, and dyes. It is also employed in the preparation of quaternary ammonium compounds and other specialty chemicals. In laboratory settings, it serves as a reagent for introducing methyl groups into organic molecules under controlled conditions. Due to its hazardous nature, applications are strictly regulated to ensure safety and environmental compliance.

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