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mercury - methane (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51176-12-6

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51176-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51176-12-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,7 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51176-12:
(7*5)+(6*1)+(5*1)+(4*7)+(3*6)+(2*1)+(1*2)=96
96 % 10 = 6
So 51176-12-6 is a valid CAS Registry Number.

51176-12-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name mercury,methane

1.2 Other means of identification

Product number -
Other names mercury-methyl hydride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:51176-12-6 SDS

51176-12-6Relevant academic research and scientific papers

Mass spectroscopic and nuclear magnetic resonance evidence confirming the existence of methyl mercury hydride

Craig, Peter J.,Mennie, Darren,Needham, Michael,Oshah, Naman,Donard, Olivier F.X.,Martin, Fabienne

, p. 5 - 8 (1993)

Mass spectroscopic and NMR evidence involving deuterium labelling is presented for the existence of CH3HgH.

Vinylmercury Hydrides: Synthesis and Spectroscopic Characterization

Guillemin, Jean-Claude,Bellec, Nathalie,Szetsi, Sandor Kis,Nyulaszi, Laszlo,Veszpremi, Tamas

, p. 6586 - 6591 (2008/10/09)

The first vinylmercury hydrides, and among them the parent compound, have been prepared by a chemoselective reduction of the corresponding vinylmercury chlorides with tributylstannane in the presence of a radical inhibitor. These hydrides have been characterized on the basis of their spectral data (1H, 13C, and 199Hg NMR spectroscopy and mass spectrometry). The photoelectron spectra of the ethenylmercury hydride displays bands at 9.79,10.13, 11.41, and 13.20 eV. On the basis of photoelectron spectra and ab initio quantum chemical calculations some (d-p)π interaction between the vinyl π-system and the mercury d-orbitals could be concluded. Vinylmercury hydrides have been condensed and then revaporized in vacuum at low temperature, but they exhibit a very low stability at room temperature even diluted in toluene (τ1/2 ≈ l min); elemental mercury and the corresponding divinylmercury were formed under these conditions.

Nuclear magnetic resonance and mass spectra of organomercury hydrides and deuterides

Craig, Peter J.,Needham, Michael I.,Ostah, Naaman,Stojak, Grace H.,Symons, Martyn,Teesdale-Spittle, Paul

, p. 153 - 156 (2007/10/03)

A series of new organomercury hydrides, including aromatic and fluoroaromatic compounds, have been characterised by mass and NMR spectroscopy. Unusual features of these compounds included an unusually downfield chemical shift for the Hg-H proton, confirmed by deuterium substitution, and a high value for the 199Hg-H coupling constant. The half-life for dilute solutions of methylmercury hydride was in the region of 1-3 h.

Characterization of Alkyl- and Aryl-mercuric Hydrides by NMR Spectroscopy

Kwetkat, Klaus,Kitching, William

, p. 345 - 348 (2007/10/02)

Low-temperature NMR measurements (1H, 13C, 199Hg) confirm that organomercuric hydrides (RHgH; R=alkyl, cycloalkyl, phenyl) are characterisable species in solution.

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