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28-2060
Natriumbromid
JIS special grade, 99.5-100.3%
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About This Item
Lineare Formel:
NaBr
CAS-Nummer:
Molekulargewicht:
102.89
MDL-Nummer:
UNSPSC-Code:
12352302
PubChem Substanz-ID:
Assay:
99.5-100.3%
Qualität:
JIS special grade
Form:
solid
Empfohlene Produkte
Qualität
JIS special grade
Dampfdruck
1 mmHg ( 806 °C)
Assay
99.5-100.3%
Form
solid
Verfügbarkeit
available only in Japan
pH-Wert
5.4 (20 °C, 50 g/L)
mp (Schmelzpunkt)
755 °C (lit.)
Lagertemp.
15-25°C
SMILES String
[Na+].[Br-]
InChI
1S/BrH.Na/h1H;/q;+1/p-1
InChIKey
JHJLBTNAGRQEKS-UHFFFAOYSA-M
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Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Repr. 2 - STOT RE 2 - STOT SE 3
Zielorgane
Central nervous system
Lagerklassenschlüssel
13 - Non Combustible Solids
WGK
WGK 1
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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David G Levitt et al.
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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
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
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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