Calcium acetate
Chemical compound From Wikipedia, the free encyclopedia
Calcium acetate is a chemical compound which is a calcium salt of acetic acid. It has the formula Ca(C2H3O2)2. Its standard name is calcium acetate, while calcium ethanoate is the systematic name. An older name is acetate of lime. The anhydrous form is very hygroscopic; therefore the monohydrate (Ca(CH3COO)2•H2O) is the common form.
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![]() Calcium acetate crystals | |
Names | |
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Preferred IUPAC name
Calcium diacetate[1] | |
Other names
Acetate of lime Calcium ethanoate | |
Identifiers | |
3D model (JSmol) |
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Abbreviations | Ca(OAc)2 |
3692527 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
DrugBank | |
ECHA InfoCard | 100.000.492 |
EC Number |
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E number | E263 (preservatives) |
22320 | |
KEGG | |
PubChem CID |
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RTECS number |
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UNII |
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CompTox Dashboard (EPA) |
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Properties | |
C4H6CaO4 | |
Molar mass | 158.166 g/mol (anhydrous) 176.181 g/mol (monohydrate) |
Appearance | White solid hygroscopic |
Odor | slight acetic acid odor |
Density | 1.509 g/cm3 |
Melting point | 160 °C (320 °F; 433 K)[2] decomposition to CaCO3 + acetone |
37.4 g/100 mL (0 °C) 34.7 g/100 mL (20 °C) 29.7 g/100 mL (100 °C) | |
Solubility | slightly soluble in methanol, hydrazine insoluble in acetone, ethanol and benzene |
Acidity (pKa) | ca. 0.7 |
−70.7·10−6 cm3/mol | |
Refractive index (nD) |
1.55 |
Pharmacology | |
V03AE07 (WHO) | |
Hazards | |
NFPA 704 (fire diamond) | |
680 to 730 °C (1,256 to 1,346 °F; 953 to 1,003 K) | |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose) |
4280 mg/kg (oral, rat) |
Related compounds | |
Other cations |
Magnesium acetate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Production
Calcium acetate can be prepared by soaking calcium carbonate (found in eggshells, or in common carbonate rocks such as limestone or marble) or hydrated lime in vinegar:
- CaCO3(s) + 2CH3COOH(aq) → Ca(CH3COO)2(aq) + H2O(l) + CO2(g)
- Ca(OH)2(s) + 2CH3COOH(aq) → Ca(CH3COO)2(aq) + 2H2O(l)
Since both reagents would have been available pre-historically, the chemical would have been observable as crystals then.
Uses
- In kidney disease, blood levels of phosphate may rise (called hyperphosphatemia) leading to bone problems. Calcium acetate binds phosphate in the diet to lower blood phosphate levels.[3]
- Calcium acetate is used as a food additive, as a stabilizer, buffer and sequestrant, mainly in candy products under the number E263.
- Tofu is traditionally obtained by coagulating soy milk with calcium sulfate. Calcium acetate has been found to be a better alternative; being soluble, it requires less skill and a smaller amount.[4]
- Because it is inexpensive, calcium acetate was once a common starting material for the synthesis of acetone before the development of the cumene process:[5][6]
- Ca(CH3COO)2 → CaCO3(s) + (CH3)2CO
- A saturated solution of calcium acetate in alcohol forms a semisolid, flammable gel that is much like "canned heat" products such as Sterno.[7] Chemistry teachers often prepare "California Snowballs", a mixture of calcium acetate solution and ethanol.[8] The resulting gel is whitish in color, resembling a snowball and can be lit on fire; it will burn for around 20 minutes.[9]
Natural occurrence
Pure calcium acetate is yet unknown among minerals. Calclacite—calcium acetate chloride pentahydrate—is listed as a known mineral,[10] but its genesis is anthropogenic (human-generated, as opposed to naturally occurring).[11]
References
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