What Is Copper Solvent?
Copper acetate, monohydrate is blue-green powdery crystals. The crystal water is removed at 240 ° C. It is soluble in ethanol and slightly soluble in ether and glycerol. Used as analytical reagent, chromatographic analysis reagent, and also used as organic synthesis catalyst, paint fast-drying agent, pesticide auxiliary, raw material of enamel pigment, etc.
- Chinese name
- Copper acetate
- English name
- Cupric Acetate Monohydrate
- nickname
- Copper acetate
- Chemical formula
- Cu (CH3COO) 2 · H2O
- Molecular weight
- 199.65
- CAS Registry Number
- 6046-93-1
- EINECS registration number
- 205-553-3
- Melting point
- 115
- Water soluble
- 7.2g / 100mL (cold water), 20g / 100ml (hot water)
- Density
- 1.882 g / cm3
- Exterior
- Blue-green crystal
- Application
- Chromatographic analysis, organic synthesis, etc.
- Danger symbol
- N, Xn
- Risk description
- Environmentally hazardous substances
- Dangerous Goods Transport Number
- UN 9106/3077
- Copper acetate, monohydrate is blue-green powdery crystals. The crystal water is removed at 240 ° C. It is soluble in ethanol and slightly soluble in ether and glycerol. Used as analytical reagent, chromatographic analysis reagent, and also used as organic synthesis catalyst, paint fast-drying agent, pesticide auxiliary, raw material of enamel pigment, etc.
Copper acetate structure
- The two copper atoms interact with each other. At room temperature, the magnetic moment is 1.40BM, but decreases with decreasing temperature (such as 0.36BM at 93K). At 253K, the magnetic susceptibility exhibits a maximum value. From this, the adjacent The exchange between copper atoms is 286 cm-1, indicating that the copper atoms in the dimer are bonded by a weak covalent bond. Due to the opposite cancellation of the spin directions, Cu2 (OAc) 4 (H2O) 2 is essentially antimagnetic, and this structure has made an important contribution to the development of modern antiferromagnetic coupling theory. [1]
Synthetic method and properties of copper acetate
Copper acetate synthesis method
- Preparation method in the laboratory:
- Dissolve 50 g of copper sulfate pentahydrate in 500 ml of water, filter, dissolve another 57 g of sodium carbonate decahydrate in 240 ml of water, heat to 60 ° C, slowly add the copper sulfate solution, and keep stirring. Let it stand, filter out the precipitate, wash it with hot water until there is no sulfuric acid, put the precipitate in 300 ml of water, add 2 ml of ammonia water and stir, let it stand, pour out the upper solution, and wash and precipitate several times. Add 180 ml of water to a beaker, heat to 60 ° C, add 22 g of glacial acetic acid, and then add the washed basic copper carbonate until there is a little left at the bottom of the container. After filtration, the filtrate was concentrated by evaporation to 1/3 of the original volume, cooled, filtered, washed with 2 ml of water, and dried at room temperature to obtain a finished product. The mother liquor continues to evaporate, and 5ml of 25% acetic acid is added when the crystals are about to come out, and part of the finished product can be obtained. It was 32-35 g. [2]
- The total response is:
- 2 CuSO4 · 5H2O + 4 NH3 + 4 HOAc Cu2 (OAc) 4 (H2O) 2 + 2 (NH4) 2SO4 + 8 H2O
Copper acetate properties
- Monohydrate will lose water under vacuum at 100 ° C:
- Cu2 (OAc) 4 (H2O) 2 Cu2 (OAc) 4 + 2 H2O
- Reduction of copper acetate with copper, hydrazine hydrate, etc. in a non-aqueous solvent will give colorless and volatile cuprous acetate:
- 2 Cu + Cu2 (OAc) 4 2 Cu2 (OAc) 2
- 2 Cu2 (OAc) 4 + N2H4 · H2O == 2 Cu2 (OAc) 2 + 4 HOAc + N2 [1]
- Note: Acetic acid (CH3COOH) can be expressed as HOAc
Copper acetate application
Organic Synthesis of Copper Acetate
- Copper acetate is used more as a catalyst or oxidant in organic synthesis. For example, Cu2 (OAc) 4 can catalyze the coupling of two terminal alkynes, and the product is 1,3-diyne:
- Cu2 (OAc) 4 + 2 RCCH 2 CuOAc + RCCCCR + 2 HOAc
- The intermediates of the reaction include copper acetylene and the like, and then oxidized with copper acetate to obtain alkynyl radicals.
- In addition, the synthesis of alkynamines (terminal alkynes containing amino groups) from copper acetate also involves copper acetylene intermediates.
Copper acetate
- Reaction principle:
- Making specimens from copper acetate (2 photos)
- The H + in the demagnesium chlorophyll is replaced by Cu2 + again to form a copper-substituted chlorophyll, which is more bright and stable than the original chlorophyll. According to this principle, green plant specimens can be preserved by treatment with copper acetate.
- Specimen method:
- Plant specimens are impregnated with a saturated copper acetate solution prepared in 50% acetic acid solution (heatable during processing)
Copper acetate technical index
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Copper acetate substance toxicity
- Non-toxic to mildly toxic, with LD50 (oral, rodent-rat) 710 mg / kg [3] and LDLo (oral, rodent-rat) 1600 mg / kg [4]
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2. Hepatotoxicity-other changes 3. Kidney, ureter and bladder toxicity-other changes |
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2. Hepatotoxicity-jaundice, others not classified 3. Chronic disease-related toxicity-death |
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3. Endocrine toxicity-changes in spleen weight |
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- [5-12]
Copper acetate precautions
- It should be stored in a ventilated and dry warehouse. The mouth of the bag must be tightly sealed to prevent moisture. Open flames and flammable materials are strictly prohibited.