28-2070
Sodium bromide
SAJ first grade, ≥99.0%
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About This Item
Formula condensata:
NaBr
Numero CAS:
Peso molecolare:
102.89
Numero MDL:
Codice UNSPSC:
12352302
ID PubChem:
Saggio:
≥99.0%
Grado:
SAJ first grade
Stato:
solid
Prodotti consigliati
Grado
SAJ first grade
Tensione di vapore
1 mmHg ( 806 °C)
Saggio
≥99.0%
Stato
solid
Disponibilità
available only in Japan
pH
5.4 (20 °C, 50 g/L)
Punto di fusione
755 °C (lit.)
Temperatura di conservazione
15-25°C
Stringa SMILE
[Na+].[Br-]
InChI
1S/BrH.Na/h1H;/q;+1/p-1
JHJLBTNAGRQEKS-UHFFFAOYSA-M
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Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Repr. 2 - STOT RE 2 - STOT SE 3
Organi bersaglio
Central nervous system
Codice della classe di stoccaggio
13 - Non Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 1
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
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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
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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
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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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