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Sigma-Aldrich

Osmium

powder, 99.9% trace metals basis

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About This Item

Empirical Formula (Hill Notation):
Os
CAS Number:
7440-04-2
Molecular Weight:
190.23
EC Number:
231-114-0
MDL number:
MFCD00011147
UNSPSC Code:
11101711
PubChem Substance ID:
24855959
NACRES:
NA.23

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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Related Categories

signalword

Danger

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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Kilian Muñiz
Chemical Society reviews, 33(3), 166-174 (2004-03-18)
Imido complexes of osmium tetroxide are versatile compounds for olefin functionalisation. This tutorial review offers a brief historical overview on these compounds and discusses the electronic properties and reactivities of isolated imido osmium compounds in what had been the original
Isolda Romero-Canelón et al.
Journal of medicinal chemistry, 56(3), 1291-1300 (2013-02-02)
Organometallic half-sandwich complexes [M(p-cymene)(azo/imino-pyridine)X](+) where M = Ru(II) or Os(II) and X ═ Cl or I, exhibit potent antiproliferative activity toward a range of cancer cells. Not only are the iodido complexes more potent than the chlorido analogues, but they
Bastien Boff et al.
Inorganic chemistry, 52(5), 2705-2715 (2013-02-23)
A library of 29 organoosmium compounds has been built up with known and novel cyclometalated compounds obtained with C-N, N(∧)C(∧)N, and C(∧)N(∧)N ligands. All compounds have been tested for their in vitro cytotoxic properties against A172, a tumor cell line
Hideki Sugimoto et al.
Journal of the American Chemical Society, 134(46), 19270-19280 (2012-11-02)
For the synthesis of the 1,2-diols, cis-1,2-dihydroxylation of alkenes catalyzed by osmium(VIII) tetroxide (OsO(4)) is a powerful method. However, OsO(4) is quite toxic due to its highly volatile and sublimable nature. Thus, the development of alternative catalysts for cis-1,2-dihydroxylation of
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
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