V900057
Sodium bromide
Vetec™, reagent grade, 98%
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About This Item
Linear Formula:
NaBr
CAS Number:
Molecular Weight:
102.89
UNSPSC Code:
12352302
PubChem Substance ID:
EC Number:
231-599-9
MDL number:
Assay:
98%
Grade:
reagent grade
Form:
powder, crystals or chunks
InChI key
JHJLBTNAGRQEKS-UHFFFAOYSA-M
InChI
1S/BrH.Na/h1H;/q;+1/p-1
SMILES string
[Na+].[Br-]
grade
reagent grade
vapor pressure
1 mmHg ( 806 °C)
product line
Vetec™
assay
98%
form
powder, crystals or chunks
pH
5.4 (20 °C, 50 g/L)
mp
755 °C (lit.)
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Repr. 2 - STOT RE 2 - STOT SE 3
target_organs
Central nervous system
Storage Class
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Majda Mekic et al.
Environmental science & technology, 52(21), 12306-12315 (2018-10-06)
A vertical wetted-wall flow-tube technique was used to explore the ionic strength effects at the air-water interface in mediating the sea-surface reaction between ozone (O3) and pyruvic acid (PA). The uptake coefficients of ozone on aqueous PA increase substantially with
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
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
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
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