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1,2-Ethanedithiol

Base Information Edit
  • Chemical Name:1,2-Ethanedithiol
  • CAS No.:540-63-6
  • Molecular Formula:C2H6S2
  • Molecular Weight:94.2016
  • Hs Code.:29309070
  • European Community (EC) Number:208-752-3
  • NSC Number:60481
  • UNII:92T634FLAR
  • DSSTox Substance ID:DTXSID9052187
  • Nikkaji Number:J4.507A
  • Wikipedia:Ethane-1,2-dithiol
  • Wikidata:Q2738870
  • Metabolomics Workbench ID:45049
  • Mol file:540-63-6.mol
1,2-Ethanedithiol

Synonyms:s-Ethylene dimercaptan;Ethylenedithiol;Dithioglycol;Ethylene mercaptan;Dithioethyleneglycol;FEMA No. 3484;Ethylene dithioglycol;Ethylene dimercaptan;1,2-Dithiol ethane;ethane-1,2-dithiol;Ethylene glycol, dithio-;Ethylenedimercaptan;1,2-Dimercaptoethane;Ethyl hydropersulfide;1,2-dithioglycol;

Suppliers and Price of 1,2-Ethanedithiol
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
  • 1,2-Ethanedithiol
  • 100g
  • $ 360.00
  • TCI Chemical
  • 1,2-Ethanedithiol >99.0%(GC)
  • 25g
  • $ 25.00
  • TCI Chemical
  • 1,2-Ethanedithiol >99.0%(GC)
  • 100g
  • $ 100.00
  • TCI Chemical
  • 1,2-Ethanedithiol >99.0%(GC)
  • 500g
  • $ 311.00
  • Sigma-Aldrich
  • 1,2-Ethanedithiol ≥98.0% (GC)
  • 500ml
  • $ 292.00
  • Sigma-Aldrich
  • 1,2-Ethanedithiol for synthesis. CAS 540-63-6, chemical formula HSCH CH SH., for synthesis
  • 8007950500
  • $ 292.00
  • Sigma-Aldrich
  • 1,2-Ethanedithiol for synthesis
  • 500 mL
  • $ 279.35
  • Sigma-Aldrich
  • 1,2-Ethanedithiol technical grade, ≥90%
  • 500ml
  • $ 186.00
  • Sigma-Aldrich
  • 1,2-Ethanedithiol for synthesis. CAS 540-63-6, chemical formula HSCH CH SH., for synthesis
  • 8007950100
  • $ 139.00
  • Sigma-Aldrich
  • 1,2-Ethanedithiol for synthesis
  • 100 mL
  • $ 133.20
Total 165 raw suppliers
Chemical Property of 1,2-Ethanedithiol Edit
Chemical Property:
  • Appearance/Colour:Clear colorless solid 
  • Vapor Pressure:4.8 mm Hg ( 20 °C) 
  • Melting Point:?41 °C(lit.) 
  • Refractive Index:n20/D 1.558(lit.)  
  • Boiling Point:144.3 °C at 760 mmHg 
  • PKA:pK1:8.96;pK2:10.54 (25°C) 
  • Flash Point:44.4 °C 
  • PSA:77.60000 
  • Density:1.05 g/cm3 
  • LogP:0.84600 
  • Storage Temp.:Store at 0-5°C 
  • Sensitive.:Air Sensitive 
  • Water Solubility.:insoluble 
  • XLogP3:0.8
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:93.99109254
  • Heavy Atom Count:4
  • Complexity:6
Purity/Quality:

99% *data from raw suppliers

1,2-Ethanedithiol *data from reagent suppliers

Safty Information:
  • Pictogram(s): ToxicT; HarmfulXn; Flammable
  • Hazard Codes:T,Xn,F 
  • Statements: 10-23/24/25-23/25-21-36-23-21/22-36/37/38-20/21/22 
  • Safety Statements: 36/37/39-45-26-16-36/37-36-7/9 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Other Classes -> Thiols
  • Canonical SMILES:C(CS)S
  • Description 1,2-Ethanedithiol (EDT) is a colorless liquid with a characteristic odor that resembles that of rotten cabbage. It is widely used as a building block in organic synthesis, and it is also an effective ligand for metal ions. 1,2-ethanedithiol if applied as a flavoring agent and it is available in a variety of animal foods, in cooked beef and chicken.
  • Uses 1,2-Ethanedithiol is used as a reagent in organic synthesis to convert carbonyl compounds to thioacetals (1,3-dithiolanes). It replaces the toxic reagent arsenic tirchloride, which is involved in the synthesis of membrane-permeant fluorogenic biarsenicals from precursor dyes fluorescein and resorufin. It acts bidendate ligand to form complexes with metal ions. Metal-complexing agent. Reverses the inhibition by α-keto aldehydes on mitosis in E. coli.
Technology Process of 1,2-Ethanedithiol

There total 52 articles about 1,2-Ethanedithiol 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 magnesium(II) perchlorate; water; methylene green; In acetonitrile; Irradiation;
DOI:10.1016/S0040-4039(00)61086-9
Guidance literature:
With magnesium(II) perchlorate; water; methylene green; In acetonitrile; Irradiation;
DOI:10.1016/S0040-4039(00)61086-9
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