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Smoke point

From Wikipedia, the free encyclopedia
Burning point of oils and fats
"Burning point" redirects here. For the Finnish band, seeBurning Point.
"Burning point" redirects here. For the lowest temperature at which a substance starts burning, seeAutoignition temperature.

Thesmoke point, also referred to as theburning point, is the temperature at which anoil or fat begins to produce a continuous bluish smoke that becomes clearly visible, dependent upon specific and defined conditions.[1] This happens when one or multiple substances in the oil start to chemically react with oxygen and burn, which can include the oil itself, proteins, sugars, or other organic material.[2] It is distinct from theflash point andfire point, which denote the temperatures at which the oil itself (specifically, vaporized oil, which is distinct from the smoke produced at the smoke point) begins to burn.[2]

Smoke point values can vary greatly.[3] The most important factor determining the smoke point of an oil is the amount of proteins andfree fatty acids (FFAs).[2] Higher quantities of these lower the smoke point.[2] The FFA content typically represents less than 1% of the total oil and consequently renders smoke point a poor indicator of the capacity of a fat or oil to withstand heat, in a non-cuisine related sense.[4][5][6] Virgin (raw) oils, which contain various flavorful organic compounds, have lower smoke points than refined oils because the organic compounds burn.[2] Animal-based fats and oils tend to have lower smoke points than vegetable-based ones, as well.[2] Oils made of polyunsaturated fats have lower smoke points, those made of monounsaturated fats have middling smoke points, and oils made of saturated fats have even higher smoke points.[2] The level of refinement, seed variety, and climate and weather of growth of the source plants also significantly affect its smoke point.[2]

Factors unrelated to the oil's composition are also important, such as the volume of oil utilized, the size of the container, the presence of air currents, and the type and source of light.[3] And practically, even when smoke is cooked in ovens set to above its true smoke point, moisture and other objects can prevent it from reaching the full temperature.[2] The smoke point also decreases over time when oil is reused.[2] Cooks in practice tend to avoid the smoke point by noticing when the oil begins to shimmer, which happens just before it begins to smoke; adding food (to absorb heat) or lowering the temperature will prevent smoking.[7]

Acrolein, a potential carcinogen, is often present in the smoke, but this is only an issue to, for example, line cooks burning large quantities of food who breathe in large quantities of smoke over long periods, and not for home cooks.[2] This is because oil chemically decomposes into free fatty acids and glycerol, and at sufficiently high temperatures glycerol with burn to form acrolein.[7] Free radicals produced by the high temperatures, although much reported on, are not dangerous.[2]

Temperature

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The smoke point of an oil correlates with its level of refinement.[8][9] Many cooking oils have smoke points above standard home cooking temperatures:[10]

  • Pan frying (sauté) on stove top heat: 120 °C (248 °F)
  • Deep frying: 160–180 °C (320–356 °F)
  • Oven baking: Average of 180 °C (356 °F)

Smoke point decreases at a different pace in different oils.[11]

Considerably above the temperature of the smoke point is theflash point, the point at which the vapours from the oil can ignite in air, given an ignition source.

The following table presents smoke points of various fats and oils.

FatQualitySmoke point[caution 1]
Almond oil221 °C430 °F[12]
Avocado oilRefined271 °C520 °F[13][14]
Avocado oilVirgin (unrefined)200 °C392 °F[15]
Avocado oilExtra virgin (unrefined)250 °C482 °F[15]
Beef tallow250 °C480 °F
ButterUnrefined150 °C302 °F[16]
Butter, clarified (ghee)Clarified250 °C482 °F[17]
Castor oilRefined200 °C[18]392 °F
Coconut oilRefined, dry204 °C400 °F[19]
Coconut oilUnrefined, dry expeller pressed, virgin177 °C350 °F[19]
Corn oil230–238 °C[20]446–460 °F
Corn oilUnrefined178 °C[18]352 °F
Cottonseed oilRefined, bleached, deodorized220–230 °C[21]428–446 °F
Flaxseed oilUnrefined107 °C225 °F[14]
Grapeseed oil216 °C421 °F
Lard190 °C374 °F[16]
Mustard oil250 °C480 °F[22]
Olive oilRefined199–243 °C390–470 °F[23][failed verification]
Olive oilVirgin210 °C410 °F
Olive oilExtra virgin, low acidity, high quality207 °C405 °F[14][24]
Olive oilExtra virgin190 °C374 °F[24]
Palm oilFractionated235 °C[25]455 °F
Peanut oilRefined232 °C[14]450 °F
Peanut oil227–229 °C[14][26]441–445 °F
Peanut oilUnrefined160 °C[14]320 °F
Pecan oil243 °C[27]470 °F
Rapeseed oil (Canola)220–230 °C[28]428–446 °F
Rapeseed oil (Canola)Expeller press (unrefined)190–232 °C375–450 °F[29]
Rapeseed oil (Canola)Refined204 °C400 °F
Rice bran oilRefined232 °C[30]450 °F
Safflower oilUnrefined107 °C225 °F[14]
Safflower oilSemirefined160 °C320 °F[14]
Safflower oilRefined266 °C510 °F[14]
Sesame oilUnrefined177 °C350 °F[14]
Sesame oilSemirefined232 °C450 °F[14]
Soybean oil234 °C[31]453 °F
Sunflower oilNeutralized, dewaxed, bleached & deodorized252–254 °C[32]486–489 °F
Sunflower oilSemirefined232 °C[14]450 °F
Sunflower oil227 °C[14]441 °F
Sunflower oilUnrefined, first cold-pressed, raw107 °C[33]225 °F
Sunflower oil, high oleicRefined232 °C450 °F[14]
Sunflower oil, high oleicUnrefined160 °C320 °F[14]
Vegetable oil blendRefined220 °C[24]428 °F
  1. ^Specified smoke, fire, and flash points of any fat and oil can be misleading: they depend almost entirely upon the free fatty acid content, which increases during storage or use. The smoke point of fats and oils decreases when they are at least partially split into free fatty acids and glycerol; the glycerol portion decomposes to form acrolein, which is the major source of the smoke evolved from heated fats and oils. A partially hydrolyzed oil therefore smokes at a lower temperature than non-hydrolyzed oil. (Adapted fromGunstone, Frank D., ed. (17 March 2011).Vegetable Oils in Food Technology: Composition, Properties and Uses. Wiley, Inc.OCLC 1083187382.)

Oxidative stability

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Main article:Rancidification

Hydrolysis and oxidation are the two primary degradation processes that occur in an oil during cooking.[11] Oxidative stability is how resistant an oil is to reacting with oxygen, breaking down and potentially producing harmful compounds while exposed to continuous heat. Oxidative stability is the best predictor of how an oil behaves during cooking.[34][35][36]

TheRancimat method is one of the most common methods for testing oxidative stability in oils.[36] This determination entails speeding up the oxidation process in the oil (under heat and forced air), which enables its stability to be evaluated by monitoring volatile substances associated with rancidity. It is measured as "induction time" and recorded as total hours before the oil breaks down. Canola oil requires 7.5 hours, for example, whereas extra virgin olive oil (EVOO) and virgin coconut oil will last over a day at 110 °C (230 °F) of continuous heat.[10] The differing stabilities correlate with lower levels of polyunsaturated fatty acids, which are more prone to oxidation. EVOO is high in monounsaturated fatty acids and antioxidants, conferring stability. Some plant cultivars have been bred to produce "high-oleic" oils with more monounsaturatedoleic acid and less polyunsaturatedlinoleic acid for enhanced stability.[10]

The oxidative stability does not directly correspond to the smoke point and thus the latter cannot be used as a reference for safe and healthy cooking.[37]

See also

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References

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  1. ^American Oil Chemists' Society (2011)."AOCS Official Method Cc 9a-48, Smoke, Flash and Fire Points Cleveland Open Cup Method".Official methods and recommended practices of the AOCS - (6th ed.). Champaign, Ill. : American Oil Chemists' Society.
  2. ^abcdefghijklKrystal, Becky (2020-03-09)."What you should know about oil smoke points — and why they're not as scary as you might think".The Washington Post.ISSN 0190-8286. Retrieved2025-06-17.
  3. ^abThomas, Alfred (2002).Fats and Fatty Oils. Ullmann's Encyclopedia of Industrial Chemistry. Wenheim: Wiley-VCH.ISBN 978-3-527-30673-2.
  4. ^Gennaro, L.; et al. (1998). "Effect of biophenols on olive oil stability evaluated by thermogravimetric analysis".Journal of Agricultural and Food Chemistry.46 (11):4465–4469.Bibcode:1998JAFC...46.4465G.doi:10.1021/jf980562q.
  5. ^Gomez-Alonso, S.; et al. (2003). "Changes in phenolic composition and antioxidant activity of virgin olive oil during frying".J Agric Food Chem.51 (3):667–72.Bibcode:2003JAFC...51..667G.doi:10.1021/jf025932w.PMID 12537439.
  6. ^Chen, W.; et al. (2013)."Total polar compounds and acid values of repeatedly used frying oils measured by standard and rapid methods"(PDF).J Food Drug Anal.21 (1): 85.
  7. ^abHowell, Daedalus (2024-09-10)."Why We Can All Stop Worrying About Cooking Oil Smoke Points".Organic Authority. Retrieved2025-06-17.
  8. ^Boickish, Michael (1998).Fats and oils handbook. Champaign, IL: AOCS Press. pp. 95–96.ISBN 978-0-935315-82-0.
  9. ^Morgan, D.A. (1942). "Smoke, fire, and flash points of cottonseed, peanut, and other vegetable oils".Oil & Soap.19 (11):193–198.doi:10.1007/BF02545481.S2CID 93662177.
  10. ^abcGray, S (June 2015)."Cooking with extra virgin olive oil"(PDF).ACNEM Journal.34 (2):8–12. Archived fromthe original(PDF) on 2020-11-12. Retrieved2016-12-18.
  11. ^abMonoj K. Gupta; Kathleen Warner;Pamela J. White (2004).Frying technology and Practices. AOCS Press, Champaign, Illinois.
  12. ^Marcus, Jacqueline B. (2013).Culinary Nutrition: The Science and Practice of Healthy Cooking. Academic Press. p. 61.ISBN 978-012-391882-6.Table 2-3 Smoke Points of Common Fats and Oils.
  13. ^"Smoking Points of Fats and Oils".What’s Cooking America.
  14. ^abcdefghijklmno"Smoke Point of Oils".Baseline of Health. Jonbarron.org. 2012-04-17. Retrieved2019-12-26.
  15. ^abMarie Wong; Cecilia Requejo-Jackman; Allan Woolf (April 2010)."What is unrefined, extra virgin cold-pressed avocado oil?".Aocs.org. Retrieved26 December 2019.
  16. ^abThe Culinary Institute of America (2011). The Professional Chef (9th ed.). Hoboken, New Jersey: John Wiley & Sons.ISBN 978-0-470-42135-2. OCLC 707248142.
  17. ^"Smoke Point of different Cooking Oils".Charts Bin. 2011.
  18. ^abDetwiler, S. B.; Markley, K. S. (1940). "Smoke, flash, and fire points of soybean and other vegetable oils".Oil & Soap.17 (2):39–40.doi:10.1007/BF02543003.
  19. ^ab"Introducing Nutiva Organic Refined Coconut Oil".Nutiva. Archived fromthe original on 2015-02-14.
  20. ^Vegetable Oils in Food Technology (2011), p. 284.
  21. ^Vegetable Oils in Food Technology (2011), p. 214.
  22. ^"Mustard Seed Oil".Clovegarden.
  23. ^"Olive Oil Smoke Point". Retrieved2016-08-25.
  24. ^abcGray, S (June 2015)."Cooking with extra virgin olive oil"(PDF).ACNEM Journal.34 (2):8–12.
  25. ^(in Italian)Scheda tecnica dell'olio di palma bifrazionato PO 64.
  26. ^Vegetable Oils in Food Technology (2011), p. 234.
  27. ^Ranalli N, Andres SC, Califano AN (Jul 2017)."Dulce de leche‐like product enriched with emulsified pecan oil: Assessment of physicochemical characteristics, quality attributes, and shelf‐life".European Journal of Lipid Science and Technology.doi:10.1002/ejlt.201600377. Retrieved15 January 2021.
  28. ^Vegetable Oils in Food Technology (2011), p. 121.
  29. ^"What is the "truth" about canola oil?". Spectrum Organics, Canola Oil Manufacturer. Archived fromthe original on April 13, 2014.
  30. ^Vegetable Oils in Food Technology (2011), p. 303.
  31. ^Vegetable Oils in Food Technology (2011), p. 92.
  32. ^Vegetable Oils in Food Technology (2011), p. 153.
  33. ^"Organic unrefined sunflower oil". Retrieved18 December 2016.
  34. ^Fats and oils in human nutrition. Food and Agriculture Organization of the United Nations and the World Health Organization. 1994.ISBN 978-92-5-103621-1. Archived fromthe original on November 29, 2013.
  35. ^Nwosu, V.; et al.Oxidative Stability of various oils as determined by Rancimat Method. Department of Food Science.: North Carolina State University.
  36. ^abMethrom. "Oxidative stability of oils and fats - Rancimat method".Application Bulletin. 204/2 e.
  37. ^"Evaluation of Chemical and Physical Changes in Different Commercial Oils during Heating"(PDF).

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