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Krypton-84Kr
90 atom %
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About This Item
Lineare Formel:
84Kr
CAS-Nummer:
Molekulargewicht:
83.91
MDL-Nummer:
UNSPSC-Code:
12142003
PubChem Substanz-ID:
Note: This product can be packaged on demand. For information on pricing, availability and packaging of custom sizes, please contact Stable Isotopes Customer Service
Empfohlene Produkte
Isotopenreinheit
90 atom %
Assay
≥99.5% (Total Krypton)
Form
gas
Verunreinigungen
<0.5% Total others
Massenverschiebung
depleted
SMILES String
[84Kr]
InChI
1S/Kr/i1+0
InChIKey
DNNSSWSSYDEUBZ-IGMARMGPSA-N
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Verpackung
Dieses Produkt kann auch als Bulk verfügbar sein und wird dann auf Anfrage abgefüllt. Für weitere Informationen über Preis, Verfügbarkeit und Verpackung kontaktieren Sie bitte Stable Isotopes Customer Service.
All gas volumes are quoted at Standard Temperature and Pressure (STP) and not at Normal Temperature and Pressure (NTP). One STP Liter is 7.7% more gas than one NTP Liter.
Signalwort
Warning
H-Sätze
P-Sätze
Gefahreneinstufungen
Press. Gas Compr. Gas
Lagerklassenschlüssel
2B - Aerosol cans and lighters
WGK
nwg
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves
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Xavier Devaux et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 16(12), 2692-2701 (2015-07-03)
The results of a study on the evolution of HiPco single-walled carbon nanotubes during the oxidizing action of H2 SO4 and HNO3 are presented. The process conditions used have been chosen so as to avoid any significant damage to the
Gamil A Guirgis et al.
The journal of physical chemistry. A, 119(47), 11532-11547 (2015-10-06)
The FT-microwave spectrum (6.5-26 GHz) of (chloromethyl)fluorosilane (ClCH2-SiH2F) has been recorded and 250 transitions for the parent species along with (13)C, (37)Cl, (29)Si, and (30)Si isotopologues have been assigned for trans conformer. Infrared spectra (3100 to 400 cm(-1)) of gas
James G Carter et al.
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Anti-VEGF-A therapy has become a mainstay of treatment for ocular neovascularisation and in cancer; however, their effectiveness is not universal, in some cases only benefiting a minority of patients. Anti-VEGF-A therapies bind and block both pro-angiogenic VEGF-Axxx and the partial
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