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230022

Sigma-Aldrich

Zinc bromide

99.999% trace metals basis

Synonym(s):

Zinc dibromide

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About This Item

Linear Formula:
ZnBr2
CAS Number:
7699-45-8
Molecular Weight:
225.20
EC Number:
231-718-4
MDL number:
MFCD00011294
UNSPSC Code:
12352302
eCl@ss:
38150410
PubChem Substance ID:
24853770
NACRES:
NA.23

Assay

99.999% trace metals basis

form

powder and chunks

reaction suitability

reagent type: catalyst
core: zinc

impurities

≤15.0 ppm Trace Metal Analysis

bp

~670 °C/1 atm (lit.)

mp

394 °C (lit.)

solubility

diethyl ether: slightly soluble(lit.)
ethanol: very soluble(lit.)

SMILES string

Br[Zn]Br

InChI

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

InChI key

VNDYJBBGRKZCSX-UHFFFAOYSA-L

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Application

Zinc bromide supported on silica or montmorillonite can be used as a selective catalyst for the bromination of aromatic substrates.

It can be used as starting material to prepare poly(ethylene oxide)/ zinc salt systems, which can be used as polymer electrolytes.

Itcan also be used to prepare ZnO nanoparticles.

Signal Word

Danger

Hazard Statements

H302,H314,H317,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - 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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

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Franz, A.K. Woerpel, K.A.
Journal of the American Chemical Society, 121, 949-949 (1999)
Yang Yu et al.
Preparative biochemistry & biotechnology, 37(4), 381-387 (2007-09-13)
Zinc bromide catalyzes the three component condensation reaction of an aldehyde, urea, and beta-ketoester or beta-diketone under solvent-free conditions to afford the corresponding dihydropyrimidinones (DHPMs) with moderate to high yields in short reaction time. The present method is very effective
Facile preparation of phenyl 1-thioglycosides of partially methylated maltooligosaccharides by restricted thiolysis of fully methylated cyclodextrins.
N Sakairi et al.
Carbohydrate research, 280(1), 139-143 (1996-01-04)
Carles Rodríguez-Escrich et al.
Organic letters, 9(6), 989-992 (2007-02-14)
The key THF derivative (9a) for an enantioselective synthesis of amphidinolide X/Y was obtained from 1a via a selenoetherification reaction. In fact, among the cyclization methods investigated, the highest yield and stereocontrol were achieved at -78 degrees C with PhSeCl/EtiPr2N
Kathleen Simis et al.
Drug development and industrial pharmacy, 34(9), 936-942 (2008-09-19)
Application of the Staccato system to liquid drugs presents unique technological challenges. Liquids, such as nicotine, do not form physically stable films on vaporization substrates. We identified two thermally reversible zinc halides (ZnCl2 and ZnBr2) that complex with nicotine in
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