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About This Item
Linear Formula:
CsCl
CAS Number:
Molecular Weight:
168.36
EC Number:
MDL number:
UNSPSC Code:
12352207
PubChem Substance ID:
NACRES:
NA.75
Assay:
≥99.5% (titration)
form:
powder
solubility:
H2O: 3 M at 20 °C, clear, colorless
Recommended Products
product line
BioXtra
Quality Level
Assay
≥99.5% (titration)
form
powder
impurities
Insoluble matter, passes filter test
loss
≤0.5% loss on drying, 110 °C
pH
5.0-7.5 (20 °C, 3 M in H2O)
mp
645 °C (lit.)
solubility
H2O: 3 M at 20 °C, clear, colorless
anion traces
sulfate (SO42-): ≤0.002%
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Application
Used for the preparation of electrically conducting glasses.Used to make solutions for the separation of RNA from DNA by density gradient centrifugation.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Repr. 2
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Takafumi Yamamoto et al.
Inorganic chemistry, 50(22), 11787-11794 (2011-10-25)
The rock salt (B1) structure of binary oxides or chalcogenides transforms to the CsCl (B2) structure under high pressure, with critical pressures P(s) depending on the cation to anion size ratio (R(c)/R(a)). We investigated structural changes of A(2)MO(3) (A =
Structure, dynamics, and hydration of POPC/POPS bilayers suspended in NaCl, KCl, and CsCl solutions.
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Effects of alkali metal chlorides on the properties of mixed negatively charged lipid bilayers are experimentally measured and numerically simulated. Addition of 20mol% of negatively charged phosphatidylserine to zwitterionic phosphatidylcholine strengthens adsorption of monovalent cations revealing their specificity, in the
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Munc13 proteins play several roles in regulating short-term synaptic plasticity. However, the underlying molecular mechanisms remain largely unclear. Here we report that C. elegans UNC-13L, a Munc13-1 ortholog, has three domains that inhibit synaptic vesicle (SV) exocytosis. These include the X
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DNA topoisomerases are important targets in anticancer and antibacterial therapy because drugs can initiate cell death by stabilizing the transient covalent topoisomerase-DNA complex. In this study, we employed a method that uses CsCl density gradient centrifugation to separate unbound from
Philip A Gurnev et al.
Langmuir : the ACS journal of surfaces and colloids, 28(45), 15824-15830 (2012-10-24)
We demonstrate that the cation-selective channel formed by gramicidin A can be used as a reliable sensor for studying the multivalent ion accumulation at the surfaces of charged lipid membranes and the "charge inversion" phenomenon. In asymmetrically charged membranes with
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