Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

176109

Sigma-Aldrich

Mercury(II) acetate

ACS reagent, ≥98.0%

Synonym(s):

Mercuric acetate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3COO)2Hg
CAS Number:
Molecular Weight:
318.68
Beilstein:
3563831
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NB.24

grade

ACS reagent

Assay

≥98.0%

form

powder

reaction suitability

reagent type: catalyst
core: mercury

impurities

≤0.01% insolubles

reduction residue

≤0.02%

mp

179-182 °C (lit.)

anion traces

chloride (Cl-): ≤0.005%
nitrate (NO3-): ≤0.005%
sulfate (SO42-): ≤0.005%

cation traces

Fe: ≤0.001%
Hg+: ≤0.4%
other heavy metals (as Pb): ≤0.002%

SMILES string

CC(=O)O[Hg]OC(C)=O

InChI

1S/2C2H4O2.Hg/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2

InChI key

BRMYZIKAHFEUFJ-UHFFFAOYSA-L

Looking for similar products? Visit Product Comparison Guide

General description

Mercury(II) acetate forms various addition compounds with olefins. Polarographic evaluation of these addition compounds has been proposed. It participates in the synthesis of nitrate esters, acetate esters, alcohols and ethers.
Mercury(II) acetate is a reagent mainly used in oxymercuration-demercuration reaction.

Application

Due to its strong affinity towards sulfur, it finds application as a reagent in desulfurization reactions. Mercury(II) acetate may be used in the preparation of mercury(II) acetate-Nafion modified electrode, which can be used in anodic stripping voltammetry for the analysis of lead and copper ions in waste water samples.
Mercury(II) acetate may be used in the preparation of 2-benzylidene-3(2H)-benzofuran-3-ones (aurones). It may be used in the hydrothermal synthesis of [Hg2(apca)2]n [apca = 3-aminopyrazine-2-carboxylate], a new mercury(I)-organic framework based on Hg22 + dumbbell.

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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

Polarography of olefin-mercury (II) acetate addition compounds.
Fleet B and Jee RD.
J. Electroanal. Chem. Interfac. Electrochem., 25(3), 397-408 (1973)
In situ hydrothermal synthesis of 2D mercury (I)-organic framework from 3-aminopyrazine-2-carboxylic acid and mercury (II) acetate.
Dehghanpour S, et al.
Inorganic Chemistry Communications, 25, 79-82 (2012)
Mercury (II) acetate-Nafion modified electrode for anodic stripping voltammetry of lead and copper with flow-injection analysis.
Dalangin RR and Gunasingham H.
Analytica Chimica Acta, 291(1), 81-87 (1994)
Mercury (II) Acetate.
Dejmek M.
Synlett, 23(19), 2867-2868 (2012)
Synthesis of 2-benzylidene-3 (2H)-benzofuran-3-ones (aurones) by oxidation of 2'-hydroxychalcones with mercury (II) acetate.
Sekizaki H.
Bulletin of the Chemical Society of Japan, 61(4), 1407-1409 (1988)

Protocols

Overcome challenges in synthesis and disulfide bond formation with protocols for Fmoc solid-phase peptide synthesis of peptides with cysteine and methionine.

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