Basic information Safety Supplier Related

acetyl Methanesulfonate

Basic information Safety Supplier Related

acetyl Methanesulfonate Basic information

Product Name:
acetyl Methanesulfonate
Synonyms:
  • acetyl Methanesulfonate
  • Methanesulfonyl acetate
  • NSC 158252
  • Busulfan Impurity 6
  • Acetic acid, anhydride with methanesulfonic acid
  • Busulfan Impurity 10
CAS:
5539-53-7
MF:
C3H6O4S
MW:
138.14
Mol File:
5539-53-7.mol
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acetyl Methanesulfonate Chemical Properties

Boiling point:
56 °C(Press: 0.01 Torr)
Density 
1.346±0.06 g/cm3(Predicted)
storage temp. 
Hygroscopic, Refrigerator, under inert atmosphere
solubility 
Chloroform (Sparingly)
form 
Oil
color 
Yellow
Stability:
Extremely Moisture Sensitive
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acetyl Methanesulfonate Usage And Synthesis

Uses

Acetyl Methanesulfonate, is an impurity of Busulfan (B689900), an alkylating agent with antileukemic activity. Antineoplastic. It is a reagent for ether cleavage, for the cleavage of activated cyclopropanes as partial structures of cyclopropyl ketones, and for acetylation of aromatic rings.

Preparation

Preparative Methods: Acetyl Methanesulfonate can be prepared on a large scale (1 mol) from Acetyl Chloride and Methanesulfonic Acid by heating at reflux followed by fractional distillation (85% yield).

storage

Handling, Storage, and Precautions: slightly hygroscopic. However, no particular precautions are required  upon exposure to air for a short period of time. acetyl Methanesulfonate is stable if stored at 4 °C for several months. Use in a fume hood.

Purification Methods

The main impurity is methanesulfonic acid. Reflux it with redistilled acetyl chloride for 6-10hours, i.e. until no further HCl is absorbed in a trap, and exclude moisture. Distil off excess of AcCl and carefully distil it below 0.001mm with the bath temperature below 120o to give the anhydride as a pale yellow oil which solidifies below 0o. Below ~130o it gives the disulfonic anhydride, and above ~130o polymers are formed, and it is used for cleaving ethers [Preparation, IR, NMR: Karger & Mazur J Org Chem 36 528, 532 1971]. [Beilstein 2 H 166, 2 III 349.]

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