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About This Item
Linear Formula:
NaBr
CAS Number:
Molecular Weight:
102.89
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
Assay:
99.5-100.3%
grade:
JIS special grade
form:
solid
Recommended Products
grade
JIS special grade
vapor pressure
1 mmHg ( 806 °C)
Assay
99.5-100.3%
form
solid
availability
available only in Japan
pH
5.4 (20 °C, 50 g/L)
mp
755 °C (lit.)
storage temp.
15-25°C
SMILES string
[Na+].[Br-]
InChI
1S/BrH.Na/h1H;/q;+1/p-1
InChI key
JHJLBTNAGRQEKS-UHFFFAOYSA-M
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Repr. 2 - STOT RE 2 - STOT SE 3
Target Organs
Central nervous system
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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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
David G Levitt et al.
Journal of applied physiology (Bethesda, Md. : 1985), 109(3), 786-795 (2010-06-19)
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Julian Holley et al.
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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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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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