等级
reagent grade
产品线
Vetec™
方案
≥99%
mp
645 °C (lit.)
SMILES字符串
[Cl-].[Cs+]
InChI
1S/ClH.Cs/h1H;/q;+1/p-1
InChI key
AIYUHDOJVYHVIT-UHFFFAOYSA-M
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应用
用于制造导电玻璃。用于制备将RNA与DNA分离的密度梯度离心溶液。
法律信息
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
警示用语：
Warning
危险声明
危险分类
Repr. 2
储存分类代码
13 - Non Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Tuan A Ho et al.
Langmuir : the ACS journal of surfaces and colloids, 28(2), 1256-1266 (2011-12-14)
All-atom molecular dynamics simulations were conducted to study the dynamics of aqueous electrolyte solutions confined in slit-shaped silica nanopores of various degrees of protonation. Five degrees of protonation were prepared by randomly removing surface hydrogen atoms from fully protonated crystalline
Travis A Hage et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 32(8), 2714-2721 (2012-02-24)
We report a novel coupled system of sodium-activated potassium currents (I(KNa)) and persistent sodium currents (I(NaP)), the components of which are widely distributed throughout the brain. Its existence and importance has not been previously recognized. Although I(KNa) was known to
Structure, dynamics, and hydration of POPC/POPS bilayers suspended in NaCl, KCl, and CsCl solutions.
Piotr Jurkiewicz et al.
Biochimica et biophysica acta, 1818(3), 609-616 (2011-12-14)
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
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 =
Sandra Aedo et al.
Antimicrobial agents and chemotherapy, 56(11), 5458-5464 (2012-08-08)
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
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