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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

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Thomas Trevethan et al.
Small (Weinheim an der Bergstrasse, Germany), 7(9), 1264-1270 (2011-04-13)
Modification and functionalization of the atomic-scale structure of insulating surfaces is fundamental to catalysis, self-assembly, and single-molecule technologies. Specially designed syn-5,10,15-tris(4-cyanophenylmethyl)truxene molecules can reshape features on an ionic KBr (001) surface. Atomic force microscopy images demonstrate that both KBr monolayer
Kazue Kurihara
Advances in colloid and interface science, 158(1-2), 130-138 (2010-05-11)
Brush layers of polyelectrolytes, ionized chains of poly(glutamic acid) (PLGA) and poly(lysine) (PLL), prepared by the Langmuir-Blodgett method, were characterized using the surface forces measurements at various pHs, salt concentrations and chain densities. This paper reviews the major results: (1)
Keiichiro Hayashi et al.
Epilepsia, 52(5), 1010-1017 (2011-04-13)
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
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
David C Fabry et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(35), 10834-10838 (2012-07-13)
"I" did it: An iodine(III)-mediated bromocarbocyclization was elaborated as an efficient tool for the synthesis of oxoindoles. This method is applicable to a variety of structurally different substrates, also with chemically sensitive groups, and gives access to the heterocycles in

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