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蒸汽壓力
1.23 psi ( 20 °C)
3.55 psi ( 55 °C)
品質等級
形狀
liquid
反應適用性
reagent type: oxidant
濃度
3.5-4.5% (OsO4)
4 wt. % in H2O
密度
1.0 g/mL at 20 °C
1.04 g/mL at 25 °C
儲存溫度
2-8°C
SMILES 字串
O=[Os](=O)(=O)=O
InChI
1S/4O.Os
InChI 密鑰
VUVGYHUDAICLFK-UHFFFAOYSA-N
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一般說明
OsO4(4wt%,溶于 H2O)广泛应用于有机合成,特别是羟基化反应。此外,它还参与烯烃的氧化裂解。
應用
- In situ X-ray-assisted electron microscopy staining for large biological samples.: This study explores the use of osmium tetroxide solution for X-ray-assisted electron microscopy staining, enhancing the visualization of large biological samples (Ströh et al., 2022).
- Application of the electron microscope to the cytochemical peroxidase reaction in salamander leukocytes.: The use of osmium tetroxide solution in electron microscopy enhances the cytochemical analysis of peroxidase reactions in salamander leukocytes, providing clear and detailed images (MITSUI, 1960).
訊號詞
Danger
危險分類
Acute Tox. 2 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
儲存類別代碼
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
其他客户在看
On stereochemistry of osmium tetroxide oxidation of allylic alcohol systems: empirical rule.
Tetrahedron Letters, 24(37), 3943-3946 (1983)
Kinetics of Oxidation of Some Fluoroquinolones by Hexacyanoferrate (III) in Alkaline Medium.
International Journal of Chemistry (Canadian Center of Science and Education), 34(2), 1388-1388 (2013)
Asymmetric induction in the reaction of osmium tetroxide with olefins.
Journal of the American Chemical Society, 102(12), 4263-4265 (1980)
The Journal of general virology, 92(Pt 11), 2485-2493 (2011-07-29)
Negatively stained influenza virions sometimes show irregular morphology and are often referred to as pleomorphic. However, this irregular morphology has not been visualized when ultrathin-section transmission and scanning electron microscopies are used. This study focused on the effects of ultracentrifugation
OsO4·streptavidin: a tunable hybrid catalyst for the enantioselective cis-dihydroxylation of olefins.
Angewandte Chemie (International ed. in English), 50(46), 10863-10866 (2011-09-29)
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