Skip to Content
MilliporeSigma
All Photos(1)

Documents

516686

Sigma-Aldrich

Sodium thiomethoxide solution

21% in H2O

Synonym(s):

Sodium methanethiolate solution, Sodium methanethiolate, Sodium thiomethoxide solution

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
CH3NaS
Molecular Weight:
70.09
Beilstein/REAXYS Number:
3592983
UNSPSC Code:
12352100
PubChem Substance ID:
24873578
NACRES:
NA.22

concentration

21% in H2O

Looking for similar products? Visit Product Comparison Guide

Legal Information

Product of Arkema

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

80.6 °F - closed cup

flash_point_c

27 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Y P Pang et al.
FEBS letters, 502(3), 93-97 (2001-10-05)
Using the computer docking program EUDOC, in silico screening of a chemical database for inhibitors of human adenovirus cysteine proteinase (hAVCP) identified 2,4,5,7-tetranitro-9-fluorenone that selectively and irreversibly inhibits hAVCP in a two-step reaction: reversible binding (Ki = 3.09 microM) followed
Surface-initiated reversible addition-fragmentation chain transfer (RAFT) polymerization from fine particles functionalized with trithiocarbonates.
Ohno K, et al.
Macromolecules, 44(22), 8944-8953 (2011)
Mild, selective deprotection of thioacetates using sodium thiomethoxide.
Wallace OB and Springer DM.
Tetrahedron Letters, 39(18), 2693-2694 (1998)
Peter C Tyler et al.
Journal of the American Chemical Society, 129(21), 6872-6879 (2007-05-10)
Transition state theory suggests that enzymatic rate acceleration (kcat/knon) is related to the stabilization of the transition state for a given reaction. Chemically stable analogues of a transition state complex are predicted to convert catalytic energy into binding energy. Because

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service