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60811

Sigma-Aldrich

Cobalt carbonyl

moistened with hexane (hexane 1-10%), ≥90% (Co)

Synonym(s):

Cobalt tetracarbonyl dimer, Di-μ-carbonylhexacarbonyldicobal, Octacarbonyldicobalt, Dicobalt octacarbonyl

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About This Item

Linear Formula:
Co2(CO)8
CAS Number:
10210-68-1
Molecular Weight:
341.95
MDL number:
MFCD00016024
UNSPSC Code:
12352300
PubChem Substance ID:
57651787
NACRES:
NA.22

Quality Level

100

assay

≥90% (Co)

form

solid

quality

moistened with hexane (hexane 1-10%)

reaction suitability

core: cobalt
reagent type: catalyst

storage temp.

2-8°C

SMILES string

[Co++].[Co++].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+]

InChI

1S/8CO.2Co/c8*1-2;;/q;;;;;;;;2*+2

InChI key

MQIKJSYMMJWAMP-UHFFFAOYSA-N

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Application

  • Cobalt carbonyl [Co2(CO)8] is commonly used as a catalyst in the hydroformylation (oxo reaction) of alkenes.
  • Along with pyridine, it can be used as a catalyst in the carboxylation of alkenes into corresponding acids and esters.
  • It is employed as a key precursor in the preparation of cobalt platinum (CoPt3), cobalt sulfide (Co3S4) and cobalt selenide (CoSe2) nanocrystals.
  • It is also used as a reagent in Pauson-Khand cyclizations and Nicholas reaction.

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Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2 - Repr. 2 - Self-heat. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 Inhalation

target_organs

Nervous system

Storage Class

4.2 - Pyrophoric and self-heating hazardous materials

wgk_germany

WGK 3

flash_point_f

-9.4 °F

flash_point_c

-23 °C

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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In situ free-surfactant synthesis and ORR-electrochemistry of carbon-supported Co3S4 and CoSe2 nanoparticles.
Feng Y, et al.
Chemistry of Materials, 20(1), 26-28 (2007)
Dicobalt octacarbonyl.
Fischer S.
Synlett, 2002(09), 1558-1559 (2002)
Octacarbonyldicobalt.
Encyclopedia of Reagents for Organic Synthesis, Second Edition, 1-26 (2014)
M Varón et al.
Scientific reports, 3, 1234-1234 (2013-02-08)
Magnetostatic (dipolar) interactions between nanoparticles promise to open new ways to design nanocrystalline magnetic materials and devices if the collective magnetic properties can be controlled at the nanoparticle level. Magnetic dipolar interactions are sufficiently strong to sustain magnetic order at
A Lewis acid-mediated version of the Nicholas reaction: Synthesis of syn-alkylated products and cobalt-complexed cycloalkynes.
Schreiber SL, et al.
Journal of the American Chemical Society, 108(11), 3128-3130 (1986)
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