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232696

Sigma-Aldrich

Cobalt(II) chloride

97%

Synonym(s):

Cobalt dichloride, Cobalt muriate, Cobaltous chloride, Dichlorocobalt

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About This Item

Linear Formula:
CoCl2
CAS Number:
7646-79-9
Molecular Weight:
129.84
EC Number:
231-589-4
MDL number:
MFCD00010938
UNSPSC Code:
12352302
PubChem Substance ID:
329752407
NACRES:
NA.55

vapor pressure

40 mmHg ( 0 °C)

Assay

97%

form

powder

mp

724 °C (lit.)

SMILES string

Cl[Co]Cl

InChI

1S/2ClH.Co/h2*1H;/q;;+2/p-2

InChI key

GVPFVAHMJGGAJG-UHFFFAOYSA-L

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Application

The vapor-phase co-reductions with other metal halides by hydrogen results in finely divided intermetallics with applications as structural materials or compounds with useful thermoelectric, magnetic, and oxidation-resistance properties.

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B Inhalation - Eye Dam. 1 - Muta. 2 - Repr. 1B - Resp. Sens. 1 - Skin Sens. 1

Storage Class Code

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Sabra I Djomehri et al.
Journal of cell communication and signaling, 13(1), 129-143 (2018-12-06)
While 3D cellular models are useful to study biological processes, gel-embedded organoids have large variability. This paper describes high-yield production of large (~1 mm diameter), scaffold-free, highly-spherical organoids in a one drop-one organoid format using MCF10A cells, a non-tumorigenic breast cell
Cobalt (II) chloride-mediated synthesis of β-enamino compounds under solvent-free conditions.
Zhang ZH and Hu JY.
Journal of the Brazilian Chemical Society, 17(7), 1447-1451 (2006)
Cobalt (II) chloride catalysed cleavage of ethers with acyl halides: Scope and mechanism.
Iqbal J and Srivastava RR.
Tetrahedron, 47(18), 3155-3170 (1991)
Cobalt (II) chloride catalyzed acylation of alcohols with acetic anhydride: scope and mechanism.
Iqbal J and Srivastava RR.
The Journal of Organic Chemistry, 57(7), 2001-2007 (1997)
An unusual chemoselectivity in cobalt (II) chloride catalysed cleavage of oxiranes with anilines: A highly regioselective synthesis of β-amino alcohols.
Iqbal J and Pandey A.
Tetrahedron Letters, 31(4), 575-576 (1990)
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