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Calcium Acetate

Ca(C2H3O2)2 salt

Properties

StateSolid (white hygroscopic powder or crystals)
ColorWhite
SolubilityVery soluble in water (347 g/L at 20°C); slightly soluble in ethanol
Melting Point160°C (monohydrate decomposes)
Boiling PointDecomposes before boiling

About Calcium Acetate

Calcium acetate is the calcium salt of acetic acid, and it sits at an interesting crossroads of pharmacology, food chemistry, and the history of organic synthesis. The chemistry that matters: Ca(C2H3O2)2 dissolves in water at about 347 g/L without needing the acidic stomach environment that calcium carbonate requires, which is why it is preferred over CaCO3 as a phosphate binder in dialysis patients. In the gut, the released Ca²⁺ ion grabs dietary phosphate (PO4³⁻) and precipitates as insoluble calcium phosphate, which then leaves the body unabsorbed — the mechanism of action behind the brand name PhosLo. The pyrolysis chemistry is the historically interesting part. Heat dry calcium acetate to roughly 400 °C and it decarboxylates and rearranges to give acetone and calcium carbonate: Ca(CH3COO)2 → CaCO3 + CH3COCH3. From the 1860s through the early 20th century this was how the world made acetone, until the cumene-from-propylene route quietly displaced it. The compound is also a buffer (pKa of acetic acid is 4.76), which is why it shows up in food technology as E263 — it controls pH in baked goods and processed cheese.

Where you'll encounter it

If you work in nephrology or pharmacy you encounter calcium acetate as PhosLo tablets — patients with end-stage renal disease take them with meals to keep serum phosphate from climbing into the range that drives vascular calcification. In a food-processing plant, it is the white powder added to control acidity in baked goods or sequester metal ions that would otherwise catalyze rancidity. Brewers and cheesemakers use it to tweak water hardness. Around the lab, you see it occasionally as a calcium source for assays where chloride or sulfate would interfere, and once in a while as a starting material for niche organic-synthesis demos that retrace the dry-distillation route to acetone.

Common Uses

  • Phosphate binder in dialysis patients with end-stage renal disease (PhosLo)
  • Food sequestrant and buffer (E263) in baked goods and processed cheese
  • Calcium magnesium acetate alternative for environmentally sensitive road de-icing
  • Starting material in the historical dry-distillation route to acetone
  • Calcium source for biochemical assays where Cl⁻ or SO4²⁻ would interfere
  • Stabilizer to suppress recrystallization in some confectionery and dairy products
  • Cheesemaking adjunct to firm curd and adjust calcium balance

Safety Information

Food-grade calcium acetate is GRAS at typical use concentrations and not classified hazardous under GHS. The clinically meaningful risk is hypercalcemia in PhosLo patients — serum Ca should be monitored, and patients are kept under roughly 1.5 g elemental Ca per day from binders. Bulk powder is mildly irritating to eyes (H319-like) and the respiratory tract on inhalation; gloves and a dust mask handle it adequately. No significant fire or reactivity hazard.

This safety summary is for educational reference only and may not be complete. It is not a substitute for Safety Data Sheets (SDS), medical advice, or professional chemical safety guidance. Always consult appropriate SDS and qualified professionals before handling chemicals.

Constituent Elements

Frequently Asked Questions

What is the molar mass of calcium acetate?
Anhydrous Ca(CH3COO)2 comes out to 158.167 g/mol: one Ca at 40.078, four carbons at 12.011 each (48.044), six hydrogens at 1.008 (6.048), and four oxygens at 15.999 (63.996). Most reagent-grade material is actually the monohydrate at 176.18 g/mol, so check the label before weighing out a stoichiometric amount.
How does calcium acetate work as a phosphate binder?
Once swallowed with food, it dissociates and releases Ca²⁺. The free calcium meets dietary phosphate in the gut lumen and precipitates as insoluble calcium phosphate, which is excreted in the stool. Unlike calcium carbonate, this happens efficiently across the full pH range of the GI tract, so it works even in patients on proton-pump inhibitors with elevated gastric pH.
How was acetone historically made from calcium acetate?
Dry distillation around 400 °C: Ca(CH3COO)2 → CaCO3 + CH3COCH3. Mechanistically the two acetate ligands lose their carboxyl carbons as carbonate while the remaining methyl groups couple through a ketonization to give acetone. From the 1860s through about 1960 this was the dominant industrial route, until the cumene process and direct propene oxidation made acetone a byproduct of phenol manufacture.