Skip to Content
Merck
All Photos(1)

Documents

Safety Information

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:
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

Signal Word

Danger

Hazard Statements

H226,H302,H314

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

80.6 °F - closed cup

Flash Point(C)

27 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

516686-VAR:
516686-1L:
516686-5L:
516686-25ML:
516686-100ML:
516686-BULK:

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

Customers Also Viewed

Slide 1 of 2

1 of 2

Trimethylacetyl chloride 99%

Sigma-Aldrich

T72605

Trimethylacetyl chloride

Tetrahydrofuran anhydrous, ≥99.9%, inhibitor-free

Sigma-Aldrich

401757

Tetrahydrofuran

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
Mild, selective deprotection of thioacetates using sodium thiomethoxide.
Wallace OB and Springer DM.
Tetrahedron Letters, 39(18), 2693-2694 (1998)
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)
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

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