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460591

Sigma-Aldrich

Sodium bromide

AnhydroBeads, −10 mesh, 99.999% trace metals basis

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About This Item

Linear Formula:
NaBr
CAS Number:
Molecular Weight:
102.89
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23

vapor pressure

1 mmHg ( 806 °C)

product line

AnhydroBeads

assay

99.999% trace metals basis

impurities

≤15.0 ppm Trace Metal Analysis

particle size

−10 mesh

mp

755 °C (lit.)

SMILES string

[Na+].[Br-]

InChI

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

InChI key

JHJLBTNAGRQEKS-UHFFFAOYSA-M

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Legal Information

AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC

pictograms

Health hazardExclamation mark

signalword

Warning

Hazard Classifications

Repr. 2 - STOT RE 2 - STOT SE 3

target_organs

Central nervous system

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

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David G Levitt et al.
Journal of applied physiology (Bethesda, Md. : 1985), 109(3), 786-795 (2010-06-19)
Measurement of body composition changes following bariatric surgery is complicated because of the difficulty of measuring body fat in highly obese individuals that have increased photon absorption and are too large for the standard dual-energy X-ray absorptiometry (DXA) table. We
Julian Holley et al.
Physical review. E, Statistical, nonlinear, and soft matter physics, 84(5 Pt 2), 056110-056110 (2011-12-21)
Excitation waves on a subexcitable Belousov-Zhabotinsky (BZ) substrate can be manipulated by chemical variations in the substrate and by interactions with other waves. Symbolic assignment and interpretation of wave dynamics can be used to perform logical and arithmetic computations. We
Jun Huang et al.
Carbohydrate polymers, 91(1), 191-197 (2012-10-10)
TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl radical)-mediated 6-carboxy β-chitin derivatives (T-chitin) with different carboxylate content were successfully synthesized by controlling the addition level of NaClO as the primary oxidant. The structural and biochemical properties of the derivatives were investigated. The carboxylate contents of the
Carlos Barata et al.
Environmental science & technology, 46(17), 9663-9672 (2012-07-26)
When considering joint toxic apical effects at higher levels of biological organization, such as the growth of populations, the so-called pharmacological mode of action that relies on toxicological mechanistic effects on molecular target sites may not be relevant. Such effects
Kajari Maiti et al.
The journal of physical chemistry. B, 114(22), 7499-7508 (2010-05-19)
Bolaforms B(1), B(2), and B(3) of the formulas, Br(-)Me(3)N(+)(CH(2))(10)N(+)Me(3)Br(-), Br(-)Me(3)N(+)(CH(2))(10)OH, and Br(-)Me(3)N(+)(CH(2))(10)COO(-)Na(+), respectively, were synthesized, and their properties in the bulk as well as at the air/aqueous NaBr (10 mM) solution interface have been studied. Their interactions with sodium dodecyl

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