Ethanethiol

Synonym
Product Category
Product Code
CAS Number
MDL Number
Pubchem CID
Reaxys RN
Ethyl mercaptan, Mercaptan C2, EtSH
Nonfluorochemicals
KUMI0F341
75-08-1  
MFCD00004887
6343
773638
image-155171-Trimethyl(trifluoromethyl)silane_reagent.png
Chemical Name
Molecular Formula
Molecular Weight
Assay
Appearance
Boiling Point
Packaging
Storage
Ethanethiol
C2H6S
62.13
≥98%
Colorless to Almost Colorless Liquid
35°C
5g,10g,20g,50g,100g,500g,1kg and 25kg
Store at 2-8°C temp.
Ethanethiol (also named as Ethyl mercaptan, Mercaptan C2, EtSH) is a useful reagent in organic synthesis. e.g. in the selective Deprotection of TES Groups using Zinc(II) Triflate.
Advances in the o-phthalaldehyde derivatizations. Comeback to the o-phthalaldehyde-ethanethiol reagent. [1]
Protection for the Hydroxyl Group, Including 1,2- and 1,3-Diols. [2]
Functionalization of poly(3-hydroxybutyrate) with different thiol compounds inhibits MDM2–p53 interactions in MCF7 cells. [3]
References:
[1] R.Hanzeko, et al, J. Chromatogr. A., 2007, 1163(1-2), pp 25-42.
[2] P.G.M.Wuts, et al, Protective groups in organic synthesis, 5th Edition, 2014, Chap. 1, 17.
[3] M.A.Abdelwahab, et al, J. Appl. Polym. Sci., 2019, 136(2), art. no. 46924.
Signal Word
Hazard Statements
Precautionary Statements
HS Code
RIDADR
Legal Information
Danger
H224,H302+H332,H410
P210,P273,P501
2930909899
UN 2363 3/PG I

1. Product Specification
Available on request.
2. Safety Data Sheet
Available on request.
Please inquire for pricing and availability of this product by writing email to sales@kumidas.com.