Iodine Number (Chemistry) Calculators
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Iodine Value Test
Standard method: Wijs reagent (ICl in glacial acetic acid) + fat sample → react for 30 min in dark. Add KI solution → ICl + KI → I₂ + KCl. Titrate excess I₂ with Na₂S₂O₃ (sodium thiosulfate) to starch endpoint. Iodine value = [(blank − sample) mL × N_Na₂S₂O₃ × 12.69] / sample mass (g). Where 12.69 = milliequivalent weight of I₂ × 1.269.
Typical Iodine Values
- Linseed (flaxseed) oil: 170–204 (drying oil; polymerizes in air)
- Sunflower oil: 120–145
- Soybean oil: 117–141
- Olive oil: 75–90 (mainly monounsaturated)
- Palm oil: 44–58
- Coconut oil: 6–11 (highly saturated)
- Butter: 25–40
- Lard: 45–75
Significance
Drying oils (IV > 130): cross-link and polymerize when exposed to O₂ → used in oil-based paints, varnishes, linoleum. Semi-drying oils (IV 100–130): partial drying properties. Non-drying oils (IV < 100): do not polymerize; used as lubricants and in food.
Glossary
Frequently Asked Questions
The iodine number (iodine value, IV) = grams of I₂ that react with 100 g of a fat or oil. Each C=C double bond in a fatty acid reacts with exactly one mole of I₂ (or ICl in the Wijs method). Therefore: IV directly measures the total number of double bonds per unit mass. Higher IV = more double bonds = more unsaturated fatty acids. A fat with IV = 150 has more than twice the unsaturation of a fat with IV = 70. Used to characterize: edible fats and oils quality control; classification as saturated (IV < 20), monounsaturated (IV 75–100), polyunsaturated (IV > 100); drying ability of industrial oils.
The Wijs method (AOCS Cd 1d-92; ISO 3961): (1) Weigh ~0.25–0.5 g of fat/oil into a glass-stoppered flask. (2) Add 20 mL Wijs reagent (ICl in glacial acetic acid). (3) Allow to react 30 min in the dark (protect from light — photocatalyzed decomposition would occur). (4) Add 20 mL 15% KI solution → reacts with excess ICl: ICl + KI → I₂ + KCl. (5) Add 100 mL water. (6) Titrate the liberated I₂ with standardized 0.1 M Na₂S₂O₃ to a pale yellow endpoint, then add starch indicator → titrate to colorless. (7) Run a blank (same procedure without fat). IV = (blank volume − sample volume) × N × 12.69 / sample mass.
Drying oils: IV > 130. These polymerize when exposed to air oxygen — a process called auto-oxidation followed by cross-linking. The polyunsaturated fatty acids (especially linolenic acid with 3 double bonds and linoleic acid with 2) in drying oils react with O₂ to form hydroperoxides → radical chain reactions → polymer network. Linseed oil (IV ≈ 180): rich in α-linolenic acid (C18:3) → fastest drying. Tung oil (IV ≈ 160): extremely fast drying. Applications: oil-based paints, varnishes, wood stains, linoleum, printing inks, artist oils. Semi-drying oils (IV 100–130): soybean, sunflower, corn — partial drying. Non-drying (IV < 100): olive, coconut, palm — don't polymerize; used in food and cosmetics.
Iodine value correlates directly with the proportion of unsaturated fatty acids: Each C=C double bond in one mole of fatty acid contributes 254 g/mol (1 mol I₂) to IV. For a pure fatty acid, IV = (number of double bonds × 253.8) / molar mass × 100. Stearic acid (C18:0): IV = 0 (no double bonds). Oleic acid (C18:1): theoretical IV = 253.8/282.5 × 100 = 89.9. Linoleic acid (C18:2): theoretical IV = 2 × 253.8/280.5 × 100 = 181. Actual oil IV = weighted average of fatty acid contributions. Example: sunflower oil is ~65% linoleic acid (C18:2) → high IV ≈ 130. Olive oil is ~72% oleic acid (C18:1) → lower IV ≈ 80.