14714
Cesium
purum, ≥99.5%
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About This Item
Empirical Formula (Hill Notation):
Cs
CAS Number:
Molecular Weight:
132.91
UNSPSC Code:
12352300
PubChem Substance ID:
EC Number:
231-155-4
MDL number:
Assay:
≥99.5%
InChI key
TVFDJXOCXUVLDH-UHFFFAOYSA-N
InChI
1S/Cs
SMILES string
[Cs]
vapor pressure
1 mmHg ( 279 °C)
grade
purum
assay
≥99.5%
reaction suitability
reagent type: reductant
resistivity
19 μΩ-cm, 0°C
bp
705 °C (lit.)
mp
28.5 °C (lit.)
density
1.873 g/mL at 25 °C (lit.)
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Application
Investigations studying scattering effects on quantum efficiency and response time for cesiated metal photocathodes
Alkali modifier for hydrogenation catalysts
Reactant involved in synthesis of pseudo-hollandite chromium tellurides
Catalyst for ammonia synthesis, investigations of in situ cesium reduction
Alkali modifier for hydrogenation catalysts
Reactant involved in synthesis of pseudo-hollandite chromium tellurides
Catalyst for ammonia synthesis, investigations of in situ cesium reduction
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B - Water-react 1
supp_hazards
Storage Class
4.3 - Hazardous materials which set free flammable gases upon contact with water
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
监管及禁止进口产品
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R. Kosydar, et al.,
Applied Catalysis, 402, 121-131 (2011)
K. L. Jensen, et al.,
Journal of Applied Physics, 110 (2011)
Ying Wang et al.
Chemical communications (Cambridge, England), 49(3), 306-308 (2012-11-28)
A noncentrosymmetric chiral Strandberg-type polyoxometalate based material, Cs(4)Mo(5)P(2)O(22), that contains unusual one dimensional chains constructed from [Mo(5)P(2)O(23)](6-) units has been reported. Cs(4)Mo(5)P(2)O(22) shows a moderate SHG response, and is phase-matchable.
Ilenia Rossetti et al.
Inorganic chemistry, 50(8), 3757-3765 (2011-03-26)
We present here a X-ray absorption spectroscopy (XAS) investigation on the local chemical order and electronic structure of Cs and Ba, promoters of the Ru/C catalysts for ammonia synthesis that attracted interest because of highly increased productivity. The role of
Min Lu et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(6), 2099-2104 (2013-01-24)
Multidrug transporters belonging to the multidrug and toxic compound extrusion (MATE) family expel dissimilar lipophilic and cationic drugs across cell membranes by dissipating a preexisting Na(+) or H(+) gradient. Despite its clinical relevance, the transport mechanism of MATE proteins remains
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