Copper benzoate

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Copper benzoate
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Names
IUPAC name
copper dibenzoate
Other names
cupric benzoate
Identifiers
3D model (JSmol)
ChemSpider
UNII
Properties
  • C
    14
    H
    10
    CuO
    4
    [1]
  • C
    14
    H
    12
    CuO
    5
    (dihydrate)[2]
Molar mass
  • 305.77 g/mol[1]
  • 323.795 g/mol (dihydrate)[2]
Appearance blue solid
Density 1.197 g/cm3
Hazards
GHS pictograms GHS07: Harmful
GHS Signal word Warning
H315, H319, H335
PP261Script error: No such module "Preview warning".Category:GHS errors, PP305+P351+P338Script error: No such module "Preview warning".Category:GHS errors
Flash point 111.4 °C (232.5 °F; 384.5 K)
NIOSH (US health exposure limits):Template:Chembox NIOSH (set)/formatPocketGuideLink
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)
Related compounds
Other cations
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
Tracking categories (test):

Copper benzoate is the chemical compound with the formula Cu
2
(C
6
H
5
CO
2
)
4
(H
2
O)
2
. These coordination complexes are derived from the cupric ion and the conjugate base of benzoic acid. Many derivatives are known with diverse ancillary ligands.[citation needed] It has found some niche use as a combination fuel and source of copper ion for blue light production in fireworks.[3]

Preparation

In laboratory, copper benzoate can be made by combining aqueous solutions of potassium benzoate with copper sulfate. Hydrated copper benzoate precipitates as a pale blue solid:[citation needed]

4 K(C
6
H
5
CO
2
) + 2 CuSO
4
 · 5H2O → Cu
2
(C
6
H
5
CO
2
)
4
(H
2
O)
2
+ 2 K
2
SO
4
+ 8 H
2
O

Uses

It is sometimes used by hobbyists as a fuel and blue flame colorant in pyrotechnics, but it is not on the list of chemicals approved in consumer fireworks in the US.[4]

It is also used in two-part dental adhesives, in polyester resin compositions to increase thermal resistance and decrease gelation, and as a metal-based hydrogen sulfide scavenger in asphalt.[1]

Structure

Structure of one form of copper(II) benzoate.

Copper(II) benzoate exists in at least two structural forms, depending on the degree of hydration. As in copper(II) acetate, one form of copper benzoate adopts a "Chinese lantern" structure,[5] wherein a pair of copper centers are linked by four bridging carboxylate ligands. Typically, one site on each copper center is occupied by water, which can be replaced by other ligands.[6] A hydrated form is also known, wherein each Cu(II) centre is bound to four water ligands and a bidentate O,O-benzoate.[7]

References

  1. 1.0 1.1 1.2 1.3 "Copper Benzoate SDS". Dr. J. Pharmachem Pvt. Ltd.. https://www.jpharmachem.com/content/uploads/2023/12/copper-benzoate-msds.pdf. 
  2. 2.0 2.1 Sigma-Aldrich Co., Benzoic acid, copper (II) salt dihydrate.
  3. "Formulas For Firework Stars Using Copper Benzoate" (in en). https://www.skylighter.com/blogs/how-to-make-fireworks/copper-benzoate-blue-fireworks-stars. 
  4. "Approved and Prohibited Fireworks Chemicals". US Department of Transportation. https://www.phmsa.dot.gov/sites/phmsa.dot.gov/files/docs/approvals-and-permits/hazmat/energetic-materials-approvals/18306/list-approved-and-prohibited-fireworks-chemicals.pdf. 
  5. Wells, A. F. (1984). Structural inorganic chemistry (5th ed.). Oxford [Oxfordshire] : New York: Clarendon Press ; Oxford University Press. ISBN 0-19-855370-6. 
  6. Kawata, T.; Uekusa, H.; Ohba, S.; Furukawa, T.; Tokii, T.; Muto, Y.; Kato, M. (1 June 1992). "Magneto-structural correlation in dimeric copper(II) benzoates". Acta Crystallographica Section B Structural Science 48 (3): 253–261. doi:10.1107/S0108768191012697. 
  7. Koizumi, Hideo; Osaki, Kenji; Watanabé, Tokunosuké (1963). "Crystal Structure of Cupric Benzoate Trihydrate Cu(C6H5COO)23H2O". Journal of the Physical Society of Japan 18 (1): 117–124. doi:10.1143/JPSJ.18.117. Bibcode1963JPSJ...18..117K. 




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