Skip to Content
Merck
CN
All Photos(1)

Key Documents

Safety Information

760625

Sigma-Aldrich

Zinc bromide

crystalline, anhydrous, beads, -10 mesh, 99.999% trace metals basis

Synonym(s):

Zinc dibromide

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
ZnBr2
CAS Number:
Molecular Weight:
225.20
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:

grade

anhydrous

Assay

99.999% trace metals basis

form

beads
crystalline

particle size

-10 mesh

mp

394 °C (lit.)

SMILES string

Br[Zn]Br

InChI

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

InChI key

VNDYJBBGRKZCSX-UHFFFAOYSA-L

Looking for similar products? Visit Product Comparison Guide

Application

Anhydrous crystalline zinc bromide is used for the synthesis of ZnS based composite semiconductor photocatalyst. It is also widely studied to understand the structure-property relationships in zinc bromide and hence predict its different applications. Zinc bromide is a widely used catalyst for stereochemical reactions and is also an important brominating agent.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Corr. 1B - Skin Sens. 1

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

新产品

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

Chieh; C.; et al.
Zeitschrift fur Kristallographie, 166, 189-189 (1984)
Batsanov; S. S.; et al.
Journal of Molecular Structure, 980, 225-225 (2010)
Yasuhiro Inui et al.
Chemical & pharmaceutical bulletin, 57(10), 1158-1160 (2009-10-06)
Asymmetric intermolecular hydroacylation between salicylaldehyde (1) and 1,5-hexadiene (2) using a combination of [RhCl(C(8)H(14))(2)](2) (0.10 eq), (S)-BINAP (0.10 eq), and ZnBr(2) (0.20 eq) afforded an enantiomerically enriched hydroacylated product iso-3 of 84% ee, along with an achiral product normal-3.
Biswajit Kalita et al.
Chemical communications (Cambridge, England), (36)(36), 4291-4293 (2008-09-20)
Benzylic and allylic hydrocarbons are selectively converted to the corresponding sulfonamides by a ZnBr2-H2O-catalyzed reaction with PhI=NTs; saturated adamantane is aminosulfonated at the tertiary C-H bond.
Yu Sung Chun et al.
Organic letters, 11(15), 3414-3417 (2009-07-04)
The in situ generated Blaise reaction intermediate, a zinc bromide complex of beta-enaminoester, reacts with various unactivated terminal alkynes and an internal alkyne under mild conditions to afford alpha-vinylated beta-enaminoesters in good to excellent yields.

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