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About This Item
Linear Formula:
OsO4
CAS Number:
Molecular Weight:
254.23
NACRES:
NB.24
PubChem Substance ID:
UNSPSC Code:
12352303
EC Number:
244-058-7
MDL number:
Assay:
≥98.0%
Grade:
ACS reagent
Form:
crystalline
Solubility:
acetone: soluble(lit.), carbon tetrachloride: soluble(lit.), methyl tert-butyl ether: soluble(lit.), toluene: soluble(lit.), water: soluble(lit.)
grade
ACS reagent
Quality Level
vapor density
8.8 (vs air)
vapor pressure
7 mmHg ( 20 °C)
description
identification passes test
assay
≥98.0%
form
crystalline
reaction suitability
reagent type: oxidant
clarity of soln
passes test
bp
130 °C (lit.)
mp
39.5-41 °C (lit.)
solubility
acetone: soluble(lit.), carbon tetrachloride: soluble(lit.), methyl tert-butyl ether: soluble(lit.), toluene: soluble(lit.), water: soluble(lit.)
storage temp.
2-8°C
SMILES string
O=[Os](=O)(=O)=O
InChI
1S/4O.Os
InChI key
VUVGYHUDAICLFK-UHFFFAOYSA-N
Application
Osmium tetroxide may be used in the following processes:
- As a tissue-staining contrast agent for staining tissues.
- Lactonization of alkenols to lactones by oxidation.
- Synthesis of the corresponding tetrols from 1,5-cycloocatdiene by bishydroxylation.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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On the Stereoselectivity in Bisdihydroxylation of 1,5-cyclooctadiene with Osmium Tetroxide.
Kawazoe K, et al.
Synthetic Communications, 31(14), 2107-2112 (2001)
P Maupin-Szamier et al.
The Journal of cell biology, 77(3), 837-852 (1978-06-01)
We have studied the destruction of purified muscle actin filaments by osmium tetroxide (OsO4) to develop methods to preserve actin filaments during preparation for electron microscopy. Actin filaments are fragmented during exposure to OsO4. This causes the viscosity of solutions
Direct Lactonization of Alkenols via Osmium Tetroxide-Mediated Oxidative Cleavage.
Schomaker JM, et al.
Organic Letters, 5(17), 3089-3092 (2003)

