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Technology Process of 2-t-Butylamino-1-phenylethanol methanesulfonate

2-t-Butylamino-1-phenylethanol methanesulfonate

Base Information
  • Chemical Name:2-t-Butylamino-1-phenylethanol methanesulfonate
  • CAS No.:72156-37-7
  • Molecular Formula:C13H23NO4S
  • Molecular Weight:0
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70992882
  • Mol file:72156-37-7.mol
2-t-Butylamino-1-phenylethanol methanesulfonate

Synonyms:72156-37-7;2-t-Butylamino-1-phenylethanol methanesulfonate;CRL 40610E;2-Tertiobutylamino-1-phenyl-1-ethanol methanesulfonate [French];alpha-(((1,1-Dimethylethyl)amino)methyl)benzenemethanol methanesulfonate (salt);Benzenemethanol, alpha-(((1,1-dimethylethyl)amino)methyl)-, methanesulfonate (salt);2-Tertiobutylamino-1-phenyl-1-ethanol methanesulfonate;2-TERT-BUTYLAMINO-1-PHENYLETHANOL METHANESULFONATE;C12H19NO.CH4O3S;DTXSID70992882;C12-H19-N-O.C-H4-O3-S;LS-30729;Methanesulfonic acid--2-(tert-butylamino)-1-phenylethan-1-ol (1/1)

Suppliers and Price of 2-t-Butylamino-1-phenylethanol 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
  • American Custom Chemicals Corporation
  • 2-T-BUTYLAMINO-1-PHENYLETHANOL METHANESULFONATE 95.00%
  • 5MG
  • $ 496.90
Total 3 raw suppliers
Chemical Property of 2-t-Butylamino-1-phenylethanol methanesulfonate
Chemical Property:
  • Vapor Pressure:0.00144mmHg at 25°C 
  • Boiling Point:284°C at 760 mmHg 
  • Flash Point:80.7°C 
  • PSA：95.01000 
  • LogP:3.08380 
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:4
  • Exact Mass:289.13477939
  • Heavy Atom Count:19
  • Complexity:249
Purity/Quality:

99% *data from raw suppliers

2-T-BUTYLAMINO-1-PHENYLETHANOL METHANESULFONATE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)NCC(C1=CC=CC=C1)O.CS(=O)(=O)O
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