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Other names
Cupric bromide
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Identifiers | |
3D model (Jmol)
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ChemSpider | |
ECHA InfoCard | 100.029.243 |
PubChem CID
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Properties | |
CuBr2 | |
Molar mass | 223.37 g/mol |
Appearance | grayish black crystals deliquescent |
Density | 4.710 g/cm3, solid |
Melting point | 498 °C (928 °F; 771 K) |
Boiling point | 900 °C (1,650 °F; 1,170 K) |
55.7 g/100 mL (20 °C) | |
Solubility in [[alcohol, acetone, ammonia]] | soluble |
Solubility in [[benzene, ether, ethyl ether, sulfuric acid]] | insoluble |
+685.5·10−6 cm3/mol | |
Structure | |
monoclinic | |
Hazards | |
NFPA 704 | |
US health exposure limits (NIOSH): | |
PEL (Permissible)
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TWA 1 mg/m3 (as Cu) |
REL (Recommended)
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TWA 1 mg/m3 (as Cu) |
IDLH (Immediate danger)
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TWA 100 mg/m3 (as Cu) |
Related compounds | |
Other anions
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Copper(II) fluoride Copper(II) chloride |
Other cations
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Nickel(II) bromide Copper(I) bromide Zinc bromide Cadmium bromide Mercury(II) fluoride |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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what is ?) | (|
Infobox references | |
Copper(II) bromide (CuBr2) is a chemical compound. It is used in photographic processing as an intensifier and as a brominating agent in organic synthesis.
It is also used in the copper vapor laser, a class of laser where the medium is copper bromide vapour formed in-situ from hydrogen bromide reacting with the copper discharge tube. Producing yellow or green light, it is used in dermatological applications.
Copper(II) bromide can be obtained by combining copper oxide and hydrobromic acid:
Copper(II) bromide is purified by crystallisation twice from water, filtration to remove any CuBr and concentration under vacuum. This product is dehydrated using phosphorus pentoxide.
In the solid state CuBr2 has a polymeric structure, with CuBr4 planar units connected on opposite sides to form chains. The crystal structure is monoclinic, space group C2/m, with lattice constants a = 714 pm, b = 346 pm, c = 718 pm, e ß = 121° 15'. CuBr2 monomeric units are present in the gas phase at high temperature.
Copper (II) bromide in chloroform-ethyl acetate reacts with ketones resulting in the formation of alpha-bromo ketones. The resulting product can be directly used for the preparation of derivatives. This heterogeneous method is reported to be the most selective and direct method of formation of α-bromo ketones.
Dibromination of NPGs, n-pentenyl glycosides, using CuBr2/LiBr reagent combination was performed in order for an NPG to serve as a glycosyl acceptor during halonium-promoted couplings. Such reaction gives high yield of the dibromides from alkenyl sugars that are resistant to a direct reaction with molecular bromine.
Copper(II) bromide lasers produce pulsed yellow and green light and have been studied as a possible treatment for cutaneous lesions. Experiments have also shown copper bromide treatment to be beneficial for skin rejuvenation. It has been widely used in photography as its solution was used as the bleaching step for intensifying collodion and gelatin negatives. Copper(II)bromide has also been proposed as a possible material in humidity indicator cards.