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P9881

Sigma-Aldrich

Potassium bromide

ReagentPlus®, ≥99.0%

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About This Item

Linear Formula:
KBr
CAS Number:
Molecular Weight:
119.00
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.55

vapor pressure

<0.01 mmHg ( 20 °C)
1 mmHg ( 795 °C)

product line

ReagentPlus®

assay

≥99.0%

form

powder

pH

5-6 (25 °C, 119 g/L)

mp

734 °C (lit.)

SMILES string

[K+].[Br-]

InChI

1S/BrH.K/h1H;/q;+1/p-1

InChI key

IOLCXVTUBQKXJR-UHFFFAOYSA-M

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Application

May be used for removal of peripheral membrane proteins.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Jun Pan et al.
Organic letters, 13(18), 4974-4976 (2011-08-26)
A facile Pd-catalyzed conversion of aryl and vinyl triflates to aryl and vinyl halides (bromides and chlorides) is described. This method allows convenient access to a variety of aryl, heteroaryl, and vinyl halides in good to excellent yields and with
Kazue Kurihara
Advances in colloid and interface science, 158(1-2), 130-138 (2010-05-11)
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Keiichiro Hayashi et al.
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Mutations in the SCN1A gene, which encodes the α1 subunit of voltage-gated sodium channels, cause generalized epilepsy with febrile seizures plus (GEFS+) and severe myoclonic epilepsy of infancy (SMEI). N1417H-Scn1a mutant rats are considered to be an animal model of
Pascal Miéville et al.
Magnetic resonance in chemistry : MRC, 49(11), 689-692 (2011-10-18)
As previously demonstrated by Thurber and Tycko, the peak position of (79)Br in potassium bromide (KBr) allows one to determine the temperature of a spinning sample. We propose to adapt the original design by using a compact KBr tablet placed
Hitesh Kulhari et al.
Nanomedicine : nanotechnology, biology, and medicine, 11(6), 1511-1520 (2015-05-03)
Docetaxel (DTX) is an anticancer drug that is used alone and in combination with other drugs to treat tumours. However, it suffers from the drawback of non-specific cytotoxicity. To improve the therapeutic potential of DTX, we report the synthesis of

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