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Cupric acetate

Copper(II) acetate
Copper(II)-acetate.jpg
Small crystals of copper(II) acetate
Copper(II)acetate crystal 01.jpg
Copper(II) acetate crystals on copper wire
Names
IUPAC name
Tetra-μ2-acetatodiaquadicopper(II)
Other names
Copper(II) ethanoate
Cupric acetate
Copper Acetate
Verdigris
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.005.049
PubChem CID
UNII
Properties
Cu(CH3COO)2
Molar mass 181.63 g/mol (anhydrous)
199.65 g/mol (hydrate)
Appearance Dark green crystalline solid
Odor odorless (hydrate)
Density 1.882 g/cm3 (hydrate)
Melting point Undetermined
Boiling point 240 °C (464 °F; 513 K)
hydrate:
7.2 g/100 mL (cold water)
20 g/100 mL (hot water)
Solubility Soluble in alcohol
Slightly soluble in ether and glycerol
1.545 (hydrate)
Structure
Monoclinic
Hazards
Safety data sheet Baker MSDS
R-phrases (outdated) 22-36/37/38-50/53
S-phrases (outdated) 26-60-61
NFPA 704
Flammability code 0: Will not burn. E.g., water Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point Non-flammable
Lethal dose or concentration (LD, LC):
LD50 (median dose)
710mg/kg oral rat
US health exposure limits (NIOSH):
PEL (Permissible)
TWA 1 mg/m3 (as Cu)
REL (Recommended)
TWA 1 mg/m3 (as Cu)
IDLH (Immediate danger)
TWA 100 mg/m3 (as Cu)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Copper(II) acetate, also referred to as cupric acetate, is the chemical compound with the formula Cu(OAc)2 where AcO is acetate (CH
3
CO
2
). The hydrated derivative, which contains one molecule of water for each Cu atom, is available commercially. Anhydrous Cu(OAc)2 is a dark green crystalline solid, whereas Cu2(OAc)4(H2O)2 is more bluish-green. Since ancient times, copper acetates of some form have been used as fungicides and green pigments. Today, copper acetates are used as reagents for the synthesis of various inorganic and organic compounds. Copper acetate, like all copper compounds, emits a blue-green glow in a flame.

Copper acetate hydrate adopts the paddle wheel structure seen also for related Rh(II) and Cr(II) tetraacetates. One oxygen atom on each acetate is bound to one copper at 1.97 Å (197 pm). Completing the coordination sphere are two water ligands, with Cu–O distances of 2.20 Å (220 pm). The two five-coordinate copper atoms are separated by only 2.62 Å (262 pm), which is close to the Cu–Cu separation in metallic copper. The two copper centers interact resulting in a diminishing of the magnetic moment such that near 90 K, Cu2(OAc)4(H2O)2 is essentially diamagnetic due to cancellation of the two opposing spins. Cu2(OAc)4(H2O)2 was a critical step in the development of modern theories for antiferromagnetic coupling.


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