Skip to Content
Merck
CN

200085

Mercury(II) bromide

ACS reagent

Synonym(s):

Mercuric bromide

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
HgBr2
CAS Number:
Molecular Weight:
360.40
NACRES:
NB.24
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
232-169-3
MDL number:
Grade:
ACS reagent
Form:
powder
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Mercury(II) bromide, ACS reagent

InChI key

NGYIMTKLQULBOO-UHFFFAOYSA-L

InChI

1S/2BrH.Hg/h2*1H;/q;;+2/p-2

SMILES string

Br[Hg]Br

grade

ACS reagent

vapor pressure

1 mmHg ( 136.5 °C)

form

powder

reaction suitability

reagent type: catalyst
core: mercury

impurities

≤0.05% insol. CH3OH

reduction residue

≤0.02%

color

white to very faintly yellow

bp

322 °C (lit.)

mp

236 °C (lit.)

anion traces

chloride (Cl-): ≤0.25%

Quality Level

Looking for similar products? Visit Product Comparison Guide

Application

Mercury(II) bromide (HgBr2) may be used in the preparation of mononuclear [Hg(L1)Br2] and 1D polymer [Hg2(L2)Br4]n [L1 = (N,N-diethyl,N′-(pyridin-2-yl)formylidene)ethane-1,2-diamine and L2 = (N,N-diethyl,N′-(pyridin-2-yl)benzylidene)ethane-1,2-diamine]. It may also be used as a promoter in the glycoslyation reaction of alcohols.

General description

Mercury(II) bromide (HgBr2) affords 1:1 adducts on reaction with N,N,N′,N′- tetramethyl-o-phenylenediamine. Single-crystal X-ray diffraction studies of these adducts have been reported. It forms complexes by reacting with 3,12-dimethylbenzo[a]quinoxalino[2,3-c]phenazine ligand.

signalword

Danger

Hazard Classifications

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

Storage Class

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

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-?-d-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters.
Carvalho I, et al.
Carbohydrate Research, 338(10), 1039-1043 (2003)
Syntheses, Structures and Properties of Two Luminous Mercury (II) Bromides Containing Tridentate N-Donor Schiff Bases: Control of Coordination Number and Nuclearity by Varying Ligand Matrices.
Satapathi S, et al.
Journal of Chemical Crystallography, 42(10), 1060-1066 (2012)
Synthesis of Quinoxalinophenazine Derivatives and Reaction of 3, 12-Dimethylbenzo [a] quinoxalino [2, 3-c] phenazine with Mercury (II) Bromide: Spectral and Structural Characterization.
Marjani AP, et al.
Chinese Journal of Structural Chemistry / Jie Gou Hua Xue, 33(10), 1460-1466 (2014)
Crystal Structures of the 1: 1 Adducts of N, N, N', N'-Tetramethyl-o-phenylenediamine with Zinc (II) Bromide and Mercury (II) Bromide and Iodide.
Hughes CM, et al.
Australian Journal of Chemistry, 38(10), 1521-1527 (1985)
M E Goodsite et al.
Environmental science & technology, 38(6), 1772-1776 (2004-04-13)
The oxidation of elemental mercury (Hg0) to the divalent gaseous mercury dibromide (HgBr2) has been proposed to account for the removal of Hg0 during depletion events in the springtime Arctic. The mechanism of this process is explored in this paper

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