All Photos(2)
About This Item
Empirical Formula (Hill Notation):
Os
CAS Number:
Molecular Weight:
190.23
EC Number:
MDL number:
UNSPSC Code:
11101711
PubChem Substance ID:
NACRES:
NA.23
Recommended Products
Quality Level
assay
99.9% trace metals basis
form
powder
resistivity
8.12 μΩ-cm, 20°C
bp
5027 °C (lit.)
mp
3045 °C (lit.)
density
22.61 g/cm3 (lit.)
SMILES string
[Os]
InChI
1S/Os
InChI key
SYQBFIAQOQZEGI-UHFFFAOYSA-N
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Sol. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
4.1B - Flammable solid hazardous materials
wgk_germany
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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Michael H Stewart et al.
ACS nano, 6(6), 5330-5347 (2012-06-08)
The ability of luminescent semiconductor quantum dots (QDs) to engage in diverse energy transfer processes with organic dyes, light-harvesting proteins, metal complexes, and redox-active labels continues to stimulate interest in developing them for biosensing and light-harvesting applications. Within biosensing configurations
Gabriel E Büchel et al.
Journal of inorganic biochemistry, 113, 47-54 (2012-06-13)
A one-pot synthesis of osmium(IV) complexes with two different tautomers of indazole, 1H-indazole and 2H-indazole, namely (H(2)ind)[Os(IV)Cl(5)(2H-ind)] (1) and (H(2)ind)[Os(IV)Cl(5)(1H-ind)] (2) is reported. Both compounds have been comprehensively characterized by NMR spectroscopy, ESI (electrospray ionization) mass spectrometry, electronic absorption spectroscopy
Sunil A Patil et al.
Chemical communications (Cambridge, England), 48(82), 10183-10185 (2012-09-13)
Using the well-known exoelectrogen Shewanella oneidensis MR-1, an osmium redox polymer modified anode exhibited ca. 4-fold increase in current generation. Additionally, a significant decrease in the start-up time for electrocatalysis was observed. The findings suggest that the inherent extracellular electron
Carole J R Bataille et al.
Chemical Society reviews, 40(1), 114-128 (2010-11-05)
Numerous synthetic protocols for producing syn-diols from the corresponding alkenes have been developed and published over recent years. It is the intent of the following tutorial review to present a concise summary of the main methods used to prepare syn-diol
Hideki Sugimoto et al.
Inorganic chemistry, 52(2), 543-545 (2013-01-01)
Oxidation of the hydroxoosmium(III) complex resulted in C-H bond activation of the methyl group of the supporting ligand (N,N'-dimethyl-2,11-diaza[3.3](2,6)pyridinophane). The product was an osmium(IV) complex exhibiting a seven-coordinate structure with an additional Os-CH(2) bond.
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