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2-Hydroxypropyl methanesulfonate

Base Information
  • Chemical Name:2-Hydroxypropyl methanesulfonate
  • CAS No.:113391-95-0
  • Molecular Formula:C4H10O4S
  • Molecular Weight:154.1848
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70550108
  • Mol file:113391-95-0.mol
2-Hydroxypropyl methanesulfonate

Synonyms:2-hydroxypropyl methanesulfonate;113391-95-0;2-HYDROXY-1-PROPYL METHANESULFONATE;starbld0006398;SCHEMBL8352021;DTXSID70550108

Suppliers and Price of 2-Hydroxypropyl methanesulfonate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 2-Hydroxy-1-propylMethanesulfonate
  • 1g
  • $ 1925.00
Total 2 raw suppliers
Chemical Property of 2-Hydroxypropyl methanesulfonate
Chemical Property:
  • PSA:71.98000 
  • LogP:0.42420 
  • XLogP3:-0.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:154.02997997
  • Heavy Atom Count:9
  • Complexity:154
Purity/Quality:

97% *data from raw suppliers

2-Hydroxy-1-propylMethanesulfonate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(COS(=O)(=O)C)O
  • Uses 2-Hydroxy-1-propyl Methanesulfonate is used in the preparation of labeled cocaine analogs.
Technology Process of 2-Hydroxypropyl methanesulfonate

There total 1 articles about 2-Hydroxypropyl methanesulfonate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With trifluoroacetic acid; In dichloromethane; at 25 ℃; for 3h; Title compound not separated from byproducts;
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