221864
Potassium bromide
≥99% trace metals basis
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About This Item
Linear Formula:
KBr
CAS Number:
Molecular Weight:
119.00
PubChem Substance ID:
eCl@ss:
38050405
UNSPSC Code:
12352302
NACRES:
NA.21
EC Number:
231-830-3
MDL number:
Assay:
≥99% trace metals basis
Form:
powder or crystals
Product Name
Potassium bromide, ≥99% trace metals basis
InChI key
IOLCXVTUBQKXJR-UHFFFAOYSA-M
InChI
1S/BrH.K/h1H;/q;+1/p-1
SMILES string
[K+].[Br-]
vapor pressure
<0.01 mmHg ( 20 °C)
1 mmHg ( 795 °C)
assay
≥99% trace metals basis
form
powder or crystals
technique(s)
FTIR: suitable
pH
5-6 (25 °C, 119 g/L)
mp
734 °C (lit.)
Quality Level
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Application
May be used for removal of peripheral membrane proteins.
Potassium bromide may be used along with:
- Cerium(IV) ammonium nitrate (CAN) for synthesizing dibromides via alkene bromination.
- Sodium perborate for synthesizing brominated anilines via oxidative bromination of unprotected aromatic amines.
- Hydrochloric acid and hydrogen peroxide for the bromination of active methylene and methyne compounds with high chemoselectivity.
Suitable for use with FT-IR spectrometers
General description
Potassium bromide, a water-soluble inorganic salt, is redox reagent.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Chemoselective bromination of active methylene and methyne compounds by potassium bromide, hydrochloric acid and hydrogen peroxide.
Shimosaki R, et al.
Synlett, 2006(14), 2287-2289 (2006)
Mild and regioselective oxidative bromination of anilines using potassium bromide and sodium perborate.
Roche D, et al.
Tetrahedron Letters, 41(13), 2083-2085 (2000)
Madhusmita Dhupal et al.
International journal of nanomedicine, 13, 6735-6750 (2018-11-15)
Titanium dioxide nanoparticles (TiO2 NPs) represent a scientific breakthrough in the areas of biological and medicinal applications. Interaction of TiO2 NPs with components of innate immune system remains elusive. This study explored in vitro immunotoxicity of murine macrophage RAW 264.7
Ville Petteri Heljo et al.
Pharmaceutical research, 28(3), 540-552 (2010-10-23)
The purpose of this study is to show how disaccharides differ in their ability to protect lyophilized β-galactosidase from enzymatic activity loss and secondary structure changes during storage. β-galactosidase was lyophilized with trehalose, sucrose, cellobiose or melibiose at 2:1, 20:1
An efficient bromination of alkenes using cerium (IV) ammonium nitrate (CAN) and potassium bromide.
Nair V, et al.
Tetrahedron, 57(34), 7417-7422 (2001)
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