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Iodoethane-13C2

Base Information Edit
  • Chemical Name:Iodoethane-13C2
  • CAS No.:34189-74-7
  • Molecular Formula:C2H5 I
  • Molecular Weight:157.98
  • Hs Code.:
  • European Community (EC) Number:693-169-0
  • DSSTox Substance ID:DTXSID90445966
  • Wikidata:Q82264519
  • Mol file:34189-74-7.mol
Iodoethane-13C2

Synonyms:Iodoethane-13C2;34189-74-7;Ethyl-13C2 iodide;iodo(1,2-13C2)ethane;DTXSID90445966;Iodoethane-13C2 contains copper as stabilizer;J-019484;Iodoethane-13C2, 99 atom % 13C, contains copper as stabilizer

Suppliers and Price of Iodoethane-13C2
Supply Marketing:Edit
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
  • Iodoethane-13C2
  • 250mg
  • $ 1010.00
  • TRC
  • Iodoethane-13C2
  • 100mg
  • $ 460.00
  • Medical Isotopes, Inc.
  • Iodoethane-13C2
  • 0.25 g
  • $ 495.00
  • American Custom Chemicals Corporation
  • IODOETHANE-13C2 95.00%
  • 100MG
  • $ 789.51
Total 2 raw suppliers
Chemical Property of Iodoethane-13C2 Edit
Chemical Property:
  • Melting Point:-108 °C(lit.)
     
  • Refractive Index:n20/D 1.512(lit.)  
  • Boiling Point:69-73 °C(lit.)
     
  • Flash Point:>230 °F  
  • PSA:0.00000 
  • Density:1.975 g/mL at 25 °C  
  • LogP:1.44130 
  • Storage Temp.:2-8°C 
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:157.95031
  • Heavy Atom Count:3
  • Complexity:2.8
Purity/Quality:

99.90% *data from raw suppliers

Iodoethane-13C2 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:T,Xn 
  • Statements: 23/24/25-42/43-63-36/37/38-22 
  • Safety Statements: 23-26-36/37/39-45-36/37 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CCI
  • Isomeric SMILES:[13CH3][13CH2]I
  • Uses Iodoethane-13C2 is an isotopic analog of Iodoethane (I705870), which is used in a variety of organic chemical reactions including the synthesis of disubstituted α-amino acids through alkylation reaction. It is also used in electrochemical reduction reactions in the preparation of carbamates.
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