Rapeseed oil

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Rapeseed oil is one of the oldest known vegetable oils. There are both edible and industrial forms produced from rapeseed, the seed of several cultivars of the plant family Brassicaceae (mustards). The term "rapeseed" applies to oilseeds from the species Brassica napus and Brassica rapa, while the term canola refers to specific rapeseed varieties bred to produce oil for use in human and animal foods. [1] In manufacturing, the edible varieties of canola are required to contain less than 2% erucic acid in Canada, the United States, European Union, and many other countries. [1] [2] [3]

Contents

Canola is produced as low erucic acid rapeseed (LEAR) oil and is generally recognized as safe (GRAS) by the United States Food and Drug Administration (FDA). [2] [4]

In commerce, non-food varieties are typically called colza oil. [5] In 2022, Canada, Germany, China, and India were the leading producers of rapeseed oil, accounting together for 41% of the world total.

History

The name for rapeseed comes from the Latin word rapum meaning turnip. Turnip, rutabaga (swede), cabbage, Brussels sprouts, and mustard are related to rapeseed. Rapeseed belongs to the genus Brassica . Brassica oilseed varieties are some of the oldest plants cultivated, with documentation of its use tracing back to India from 4,000 years ago, and use in China and Japan 2,000 years ago. [6] :55 Its use in Northern Europe for oil lamps is documented to have started in the 13th century. [6] Rapeseed oil extracts were first put on the market in 1956–1957 as food products, but these had several unacceptable properties. That form of rapeseed oil had a distinctive taste and a greenish colour due to the presence of chlorophyll, and still contained a higher concentration of erucic acid. [7]

Canola field Waldo Hills Drive - DPLA - 65febc8b1ee46c1437870b42a0eb9606.jpg
Canola field
Canola oil Canola Oil (4107885913).jpg
Canola oil

Canola was bred from rapeseed cultivars of B. napus and B. rapa at the University of Manitoba in the early 1970s. [8] [9] Its nutritional profile was then different from present-day oil, as well as containing much less[ more? ] erucic acid. [10] This work was performed at the National Research Council of Canada laboratories in Saskatoon using gas liquid chromatography. [11] Canola was originally a trademark name of the Rapeseed Association of Canada; the name is a portmanteau of "can" from Canada and "ola" from "oil". [12] [13] Canola is now a generic term for edible varieties of rapeseed oil in North America and Australasia; [14] the change in name also serves to distinguish it from natural rapeseed oil, which has much higher erucic acid content. [15]

A genetically engineered rapeseed that is tolerant to the herbicide Roundup (glyphosate) was first introduced to Canada in 1995 (Roundup Ready). A genetically modified variety developed in 1998 is considered to be the most disease- and drought-resistant canola variety to date. In 2009, 90% of the Canadian crop was herbicide-tolerant. [16] In 2005, 87% of the canola grown in the US was genetically modified. [17] In 2011, out of the 31 million hectares of canola grown worldwide, 8.2 million (26%) were genetically modified. [18]

A 2010 study conducted in North Dakota found glyphosate- or glufosinate-resistance transgenes in 80% of wild natural rapeseed plants, and a few plants that were resistant to both herbicides. This may reduce the effectiveness of the herbicide tolerance trait for weed control over time, as the weed species could also become tolerant to the herbicide. However, one of the researchers agrees that "feral populations could have become established after trucks carrying cultivated GM seeds spilled some of their load during transportation". She also notes that the GM canola results they found may have been biased as they only sampled along roadsides. [19]

Genetically modified canola attracts a price penalty compared to non-GM canola; in Western Australia, it is estimated to be 7.2% on average. [20]

Production

Rapeseed oil production
2022, millions of tonnes
Flag of Canada (Pantone).svg  Canada 3.7
Flag of Germany.svg  Germany 3.7
Flag of the People's Republic of China.svg  China 3.6
Flag of India.svg  India 3.4
Flag of France.svg  France 1.8
Flag of Poland.svg  Poland 1.4
World26.7
Source: FAOSTAT of the United Nations [21]

In 2022, world production of rapeseed oil was 27 million tonnes, led by Canada, Germany, China, and India as the largest producers, accounting for 41% of the total when combined (table).

Production process

Canola oil is made at a processing facility by slightly heating and then crushing the seed. [22] Almost all commercial canola oil is then extracted using hexane solvent, [23] which is recovered at the end of processing. Finally, the canola oil is refined using water precipitation and organic acid to remove gums and free fatty acids, filtering to remove color, and deodorizing using steam distillation. [22] Sometimes the oil is also bleached for a lighter color. [24] The average density of canola oil is 0.92 g/ml (7.7 lb/US gal; 9.2 lb/imp gal). [25]

Cold-pressed and expeller-pressed canola oil are also produced on a more limited basis. About 44% of a seed is oil, with the remainder as a canola meal used for animal feed. [22] About 23 kg (51 lb) of canola seed makes 10 L (2.64 US gal) of canola oil. Canola oil is a key ingredient in many foods. Its reputation as a healthful oil has created high demand in markets around the world, [26] and overall it is the third-most widely consumed vegetable oil, after soybean oil and palm oil. [27]

The oil has many non-food uses and, like soybean oil, is often used interchangeably with non-renewable petroleum-based oils in products, [26] including industrial lubricants, biodiesel, candles, lipsticks, and newspaper inks.[ citation needed ]

Canola vegetable oils certified as organic are required to be from non-GMO rapeseed. [28]

Nutrition and health

Canola oil
Nutritional value per 100 g
Energy 3,700 kJ (880 kcal)
0 g
Starch 0 g
Sugars 0 g
Dietary fiber 0 g
Fat
100 g
Saturated 7.4 g
Trans 0.4 g
Monounsaturated 63.3 g
Polyunsaturated 28.1 g
9.1 g
18.6 g
0 g
Vitamins and minerals
Vitamins Quantity
%DV
Vitamin A equiv.
0%
0 μg
0%
0 μg
0 μg
Vitamin A 0 IU
Thiamine (B1)
0%
0 mg
Riboflavin (B2)
0%
0 mg
Niacin (B3)
0%
0 mg
Pantothenic acid (B5)
0%
0 mg
Vitamin B6
0%
0 mg
Folate (B9)
0%
0 μg
Vitamin B12
0%
0 μg
Vitamin C
0%
0 mg
Vitamin E
117%
17.5 mg
Vitamin K
59%
71.3 μg
Minerals Quantity
%DV
Calcium
0%
0 mg
Iron
0%
0 mg
Magnesium
0%
0 mg
Manganese
0%
0 mg
Phosphorus
0%
0 mg
Potassium
0%
0 mg
Sodium
0%
0 mg
Zinc
0%
0 mg
Other constituentsQuantity
Water0 g

Percentages estimated using US recommendations for adults, [29] except for potassium, which is estimated based on expert recommendation from the National Academies [30]

Nutritional content

Canola oil is 100% fat, composed of 63% monounsaturated fat, 28% polyunsaturated fat, and 7% saturated fat (table). The ratio of linoleic acid (an omega-6 fatty acid) to alpha-linolenic acid (an omega-3 fatty acid) is 2:1 (table). A 100 g (3.5 oz) reference amount of canola oil provides 880 calories of food energy and is a rich source of vitamin E (117% of the Daily Value, DV) and vitamin K (59% DV) (table).

Health research

Reviews indicate that consumption of canola oil can reduce blood levels of cholesterol and low-density lipoprotein (LDL) two risk factors for cardiovascular diseases and may help reduce body weight. [31] [32] [33] [34]

In 2006, canola oil was given a qualified health claim by the United States Food and Drug Administration for lowering the risk of coronary heart disease, resulting from its significant content of unsaturated fats; the allowed claim for food labels states: [35]

"Limited and not conclusive scientific evidence suggests that eating about 1 12 tablespoons (19 grams) of canola oil daily may reduce the risk of coronary heart disease due to the unsaturated fat content in canola oil. To achieve this possible benefit, canola oil is to replace a similar amount of saturated fat and not increase the total number of calories you eat in a day. One serving of this product contains [x] grams of canola oil."

Erucic acid

CompoundFamily% of total
Oleic acid ω-961% [36]
Linoleic acid ω-621% [36]
Alpha-linolenic acid ω-311% [36]
9% [37] [38]
Saturated fatty acids 7% [36]
Palmitic acid 4% [37]
Stearic acid 2% [37]
Trans fat 0.4% [39]
Erucic acid 0.01% [40]
<0.1% [41] [42]

Although wild rapeseed oil contains significant amounts of erucic acid, [43] the cultivars used to produce commercial, food-grade canola oil were bred to contain less than 2% erucic acid, [2] an amount deemed not significant as a health risk. The low-erucic trait was due to two mutations changing the activity of LEA1 and KCS17. [44] [45]

The erucic acid content in canola oil has been reduced over the years. In western Canada, a reduction occurred from the average content of 0.5% between 1987 and 1996 [46] to a current content of 0.01% from 2008 to 2015. [40] Other reports also show a content lower than 0.1% in Australia [41] and Brazil. [42]

To date, no health effects have been associated with dietary consumption of erucic acid by humans; but tests of erucic acid metabolism in other species imply that higher levels may be detrimental. [47] [48] Canola oil produced using genetically modified plants has also not been shown to explicitly produce adverse effects. [49]

Canola oil is generally recognized as safe. [2]

Glucosinolates

Another chemical change in canola is the reduction of glucosinolates. [44] As the oil is extracted, most of the glucosinolates are concentrated into the seed meal, an otherwise rich source of protein. Livestock have varying levels of tolerance to glucosinolates intake, with some being poisoned relatively easily. [50] [51] A small amount of glucosinolates also enters the oil, imparting a pungent odor. [52]

Further reduction of glucosinolate levels remains important for the use of rapeseed meal in animal feed. [53] [54]

It is not completely clear which genetic changes from plant breeding resulted in the current reduction in this group of chemicals. [44]

Uses

B. napus is the source for canola as a high quality vegetable oil for human food products, and as a high-protein pomace to feed fish and farm animals. [1] Canola oil is favored for its culinary qualities, and is used widely as a salad oil, for shortening, margarine, in deep frying, baking, sandwich spreads, and non-dairy creamers. [1]

Apart from its use for human consumption, rapeseed oil is extensively used as a lubricant for machinery, in cosmetics, printing inks, fabrics, plastic products, and pesticides. [1] It was widely used in European domestic lighting before the advent of coal (city) gas or kerosene. It was the preferred oil for train pot lamps, and was used for lighting railway coaches in the United Kingdom before gas lighting, and later electric lighting, were adopted. Burned in a Carcel lamp, it was part of the definition of the French standard measure for illumination, the carcel, for most of the nineteenth century. In lighthouses, such as in early Canada, rapeseed oil was used before the introduction of mineral oil. Rapeseed oil was used with the Argand burner because it was cheaper than whale oil. [84] Rapeseed oil was burned to a limited extent in the Confederacy during the American Civil War. [85]

Biodiesel

Rapeseed oil is used as diesel fuel, either as biodiesel, straight in heated fuel systems, or blended with petroleum distillates for powering motor vehicles. [1] Biodiesel may be used in pure form in newer engines without engine damage and is frequently combined with fossil-fuel diesel in ratios varying from 2% to 20% biodiesel.

Rapeseed oil is the preferred oil stock for biodiesel production in Europe, Canada, and the United States, partly because rapeseed produces more oil per unit of land area compared to other oil sources, such as soybeans, but primarily because canola oil has a carbon footprint substantially lower than conventional diesel fuel. [86]

Other edible rapeseed oils

Some less-processed versions of rapeseed oil are used for flavor in some countries. Chinese rapeseed oil was originally extracted from the field mustard. In the 19th century, rapeseed (B. rapa) was introduced by European traders, and local farmers crossed the new plant with field mustard to produce semi-winter rapeseed. [87] Their erucic acid content was reduced to modern "canola" levels by breeding with Canadian low-erucic acid cultivar "ORO". [45] [88] Chinese rapeseed oil has a distinctive taste and a greenish colour due to the different processing method: seeds are roasted and expeller-pressed to obtain the oil. A centrifuge is used to remove solids, followed by a heating step. The resultant oil is heat-stable and fundamental to Sichuan cuisine.

In India, mustard oil is used in cooking. [89] In the United Kingdom and Ireland, some chefs use a "cabbagey"-tasting rapeseed oil processed by cold-pressing. [90] This cold process means that the oil has a low smoke point, and is therefore unsuitable for frying in Sichuan cuisine, for example. [91]

Spanish rapeseed poisoning outbreak

In 1981, there was an oil poisoning outbreak, later known as toxic oil syndrome that was attributed to people consuming what they thought was olive oil but turned out to be rapeseed oil that had been denatured with 2% aniline (phenylamine). The substance was intended for industrial use but had been illegally refined in an attempt to remove the aniline. [92] It was then fraudulently sold as olive oil, mainly in street markets, mostly in the Madrid area. [93] [94]

See also

Notes

    References

    1. 1 2 3 4 5 6 "The Biology of Brassica napus L. (Canola/Rapeseed)". Plant and Biotechnology Risk Assessment Unit Plant Health Science Division, Canadian Food Inspection Agency, Government of Canada. 22 December 2017. Retrieved 18 September 2025.
    2. 1 2 3 4 "21 CFR 184.1555 "Rapeseed oil"". US Food and Drug Administration. 1 April 2010. Retrieved 19 April 2020. (ecfr.gov version)
    3. Corrigendum to Commission Regulation (EC) No 2019/1870 of 7 November 2019 amending and correcting Regulation (EC) No 1881/2006 as regards maximum levels of erucic acid and hydrocyanic acid in certain foodstuffs
    4. "Rapeseed oil, Low erucic acid". US Food and Drug Administration. 13 February 2025. Retrieved 18 September 2025.
    5. Velíšek J (2013). The Chemistry of Food. Wiley. p. 102. ISBN   978-1-118-38383-4.
    6. 1 2 Snowdon R, Lühs W, Friedt W (2007). "Oilseed Rape". Oilseeds. Genome Mapping and Molecular Breeding in Plants. Vol. 2. pp. 55–114. doi:10.1007/978-3-540-34388-2_2. ISBN   978-3-540-34387-5.
    7. Fan L, Eskin NM (2015). "The use of antioxidants in the preservation of edible oils". Handbook of Antioxidants for Food Preservation. pp. 373–388. doi:10.1016/B978-1-78242-089-7.00015-4. ISBN   978-1-78242-089-7.
    8. "Richard Keith Downey: Genetics". science.ca. 2007. Retrieved 29 December 2008.
    9. Pederson Am, Storgaard A (15 December 2015). "Baldur Rosmund Stefansson". The Canadian Encyclopedia . Retrieved 4 September 2019.
    10. Barthet V. "Canola". The Canadian Encyclopedia . Archived from the original on 27 February 2014. Retrieved 29 December 2008.
    11. Lawrence K (1992). From Rapeseed to Canola: The Billion Dollar Success Story. Saskatoon, Saskatchewan: National Research Council Plant Biotechnology Institute. p. 41.
    12. Wrigley CW, Corke H, Seetharaman K, et al. (17 December 2015). Encyclopedia of Food Grains. Academic Press. p. 238. ISBN   978-1785397622.
    13. Canola Council of Canada (2016). "What is Canola?" . Retrieved 16 December 2013.
    14. "Has canola become a generic trademark?". genericides.org. 21 April 2021. Archived from the original on 20 October 2021. Retrieved 13 May 2021.
    15. Kazaz S, Miray R, Lepiniec L, et al. (January 2022). "Plant monounsaturated fatty acids: Diversity, biosynthesis, functions and uses" (PDF). Progress in Lipid Research. 85: 101138. doi:10.1016/j.plipres.2021.101138. PMID   34774919.{{cite journal}}: CS1 maint: article number as page number (link)
    16. Beckie HJ, Harker KN, Légère A, et al. (Autumn 2011). "GM Canola: The Canadian Experience". Farm Policy Journal. 8 (1): 43–49. S2CID   13980244.
    17. Johnson, Stanley R. et al Quantification of the Impacts on US Agriculture of Biotechnology-Derived Crops Planted in 2006 National Center for Food and Agricultural Policy, Washington DC, February 2008. Retrieved 12 August 2010.
    18. "Biotech Canola – Annual Update 2011" (PDF). International Service for the Acquisition of Agri-Biotech Applications. Archived from the original (PDF) on 30 May 2013. Retrieved 26 May 2013.
    19. Gilbert N (6 August 2010). "GM crop escapes into the American wild". Nature. doi: 10.1038/news.2010.393 .
    20. Paull J (2019). "Genetically Modified (GM) Canola: Price Penalties and Contaminations". Biomedical Journal of Scientific & Technical Research. 17 (2): 1–4. doi: 10.26717/BJSTR.2019.17.002965 .
    21. "Production of rapeseed oil (canola) in 2022, Crops/Regions/World list/Production Quantity/Year (pick lists)". UN Food and Agriculture Organization, Corporate Statistical Database (FAOSTAT). 2025. Retrieved 10 July 2025.
    22. 1 2 3 "Steps in Oil and Meal Processing". Canola Council of Canada. 2016. Retrieved 30 April 2016.
    23. Crosby G (2017). "Ask the Expert: Concerns about canola oil". The Nutrition Source. Harvard T.H. Chan School of Public Health . Retrieved 23 April 2017.
    24. "How It's Made - Canola Oil". YouTube . 11 March 2012.
    25. "Section 3.1: Leaking Tank Experiments with Orimulsion and Canola Oil" (PDF). NOAA Technical Memorandum NOS OR&R 6. National Ocean Service. December 2001.
    26. 1 2 "What is canola oil?". Canola Council of Canada. 2016. Retrieved 30 April 2016.
    27. Ash M (15 March 2016). "Soybeans & Oil Crops". Economic Research Service, US Department of Agriculture. Archived from the original on 23 April 2016. Retrieved 30 April 2016.
    28. "Canola Oil Myths and Truths". UC Berkeley School of Public Health. 17 February 2015. Retrieved 23 April 2017.
    29. United States Food and Drug Administration (2024). "Daily Value on the Nutrition and Supplement Facts Labels". FDA. Archived from the original on 27 March 2024. Retrieved 28 March 2024.
    30. "TABLE 4-7 Comparison of Potassium Adequate Intakes Established in This Report to Potassium Adequate Intakes Established in the 2005 DRI Report". p. 120. In: Stallings VA, Harrison M, Oria M, eds. (2019). "Potassium: Dietary Reference Intakes for Adequacy". Dietary Reference Intakes for Sodium and Potassium. pp. 101–124. doi:10.17226/25353. ISBN   978-0-309-48834-1. PMID   30844154. NCBI   NBK545428.
    31. Rosqvist F, Niinistö S (2024). "Fats and oils - a scoping review for Nordic Nutrition Recommendations 2023". Food and Nutrition Research. 68. doi:10.29219/fnr.v68.10487. PMC   10870979 . PMID   38370114.
    32. Voon PT, Ng CM, Ng YT, et al. (September 2024). "Health Effects of Various Edible Vegetable Oil: An Umbrella Review". Advances in Nutrition. 15 (9): 100276. doi:10.1016/j.advnut.2024.100276. PMC   11374968 . PMID   39053603.{{cite journal}}: CS1 maint: article number as page number (link)
    33. Ghobadi S, Hassanzadeh-Rostami Z, Mohammadian F, et al. (2019). "Effects of Canola Oil Consumption on Lipid Profile: A Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials". Journal of the American College of Nutrition. 38 (2): 185–196. doi:10.1080/07315724.2018.1475270. PMID   30381009. S2CID   53177789.
    34. Raeisi-Dehkordi H, Amiri M, Humphries KH, et al. (2019). "The Effect of Canola Oil on Body Weight and Composition: A Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials". Advances in Nutrition. 10 (3): 419–432. doi:10.1093/advances/nmy108. PMC   6520036 . PMID   30809634.
    35. Schneeman, B.O. (6 October 2006). "Qualified Health Claims, Letter of Enforcement Discretion U.S. Food and Drug Administration: Unsaturated Fatty Acids from Canola Oil and Reduced Risk of Coronary Heart Disease". US Food and Drug Administration. Archived from the original on 2 October 2013. Retrieved 3 September 2008.
    36. 1 2 3 4 "Comparison of Dietary Fats Chart" (PDF). Canola Council of Canada. Archived from the original (PDF) on 23 September 2006. Retrieved 3 September 2008.
    37. 1 2 3 USDA National Nutrient Database for Standard Reference, Release 21 (2008)
    38. DeFilippis AP, Sperling LS (2006). "Understanding omega-3's" (PDF). American Heart Journal. 151 (3): 564–570. doi:10.1016/j.ahj.2005.03.051. PMID   16504616. Archived from the original (PDF) on 22 October 2007.
    39. USDA National Nutrient Database for Standard Reference, Release 22 (2009)
    40. 1 2 J Barthet VJ (2015). "Quality of western Canadian Canola 2015" (PDF) (Press release). Canadian Grain Research Laboratory: Canadian Grain Commission. ISSN   1700-2222 . Retrieved 21 December 2016.
    41. 1 2 DE S, DW M, TM K (2016). "Quality of Australian canola 2015–16" (PDF) (Press release). Australia: NSW Department of Primary Industries – Australian Oilseeds Federation. ISSN   1322-9397. Archived from the original (PDF) on 8 May 2023. Retrieved 21 December 2016.
    42. 1 2 Heidy Aguilera Fuentes P, Jose Ogliaria P, Carlos Deschamps F, et al. (2011). "Centro de Ciências Agrárias" [Agricultural Science Center]. Avaliação da Qualidade de Óleos de Soja, Canola, Milho e Girassol Durante o Armazenamento (PDF) (Thesis) (in Portuguese). Florianópolis, Brazil: Universidade Federal de Santa Catarina. OCLC   817268651 . Retrieved 21 December 2016.
    43. Sahasrabudhe MR (1977). "Crismer values and erucic acid contents of rapeseed oils". Journal of the American Oil Chemists' Society. 54 (8): 323–324. doi:10.1007/BF02672436. S2CID   84400266.
    44. 1 2 3 Hu J, Chen B, Zhao J, et al. (May 2022). "Genomic selection and genetic architecture of agronomic traits during modern rapeseed breeding". Nature Genetics. 54 (5): 694–704. doi:10.1038/s41588-022-01055-6. PMID   35484301. S2CID   248430415. We found that FAE1 (BnaA08g11130D) and KCS17 (BnaA08g11140D) were the genes associated with fatty acid elongation for erucic acid (C22:1) (–log 10(P) = 10.997) ...
    45. 1 2 Wu G, Wu Y, Xiao L, et al. (February 2008). "Zero erucic acid trait of rapeseed (Brassica napus L.) results from a deletion of four base pairs in the fatty acid elongase 1 gene". Theoretical and Applied Genetics. 116 (4): 491–499. doi:10.1007/s00122-007-0685-z. PMID   18075728. Since then almost all of the LEA rapeseed cultivars have been developed in China and other countries by traditional crossing method with the LEA gene source from the ORO (Harvey and Downey 1963).{{cite journal}}: CS1 maint: overridden setting (link)
    46. DeClercq D, Daun J, Tipples K (1997). "Quality of Western Canadian Canola 1997" (PDF) (Press release). Canadian Grain Research Laboratory: Canadian Grain Commission. ISSN   0836-1657 . Retrieved 21 December 2016.
    47. Food Standards Australia New Zealand (June 2003) Erucic acid in food: A Toxicological Review and Risk Assessment Archived 23 November 2018 at the Wayback Machine Technical report series No. 21; Page 4 paragraph 1; ISBN   0-642-34526-0, ISSN   1448-3017
    48. Wallace HA, Tetyana K (2023). "Food Safety and Foodborne Toxicants". Hayes' Principles and Methods of Toxicology. Vol. 1. pp. 701–754. doi:10.1201/9781003390008-14. ISBN   978-1-003-39000-8.
    49. Reddy CS, Hayes AW (2007). "Foodborne Toxicants". In Hayes AW (ed.). Principles and methods of toxicology (5th ed.). London, UK: Informa Healthcare. p. 640. ISBN   978-0-8493-3778-9.
    50. "Glucosinolates as undesirable substances in animal feed - Scientific Opinion of the Panel on Contaminants in the Food Chain". EFSA Journal. 6 (1): 590. January 2008. doi: 10.2903/j.efsa.2008.590 .
    51. O'Brien 2008, p. 37.
    52. Zhou Q, Tang H, Jia X, et al. (2018). "Distribution of glucosinolate and pungent odors in rapeseed oils from raw and microwaved seeds". International Journal of Food Properties. 21 (1): 2296–2308. doi: 10.1080/10942912.2018.1514632 .
    53. Shahidi F, Naczk M (1990). "Removal of Glucosinolates and Other Antinutrients from Canola and Rapeseed by Methanol/Ammonia Processing". Canola and Rapeseed. pp. 291–306. doi:10.1007/978-1-4615-3912-4_17. ISBN   978-1-4613-6744-4.
    54. Jhingan S, Harloff HJ, Abbadi A, et al. (9 February 2023). "Reduced glucosinolate content in oilseed rape (Brassica napus L.) by random mutagenesis of BnMYB28 and BnCYP79F1 genes". Scientific Reports. 13 (1): 2344. Bibcode:2023NatSR..13.2344J. doi:10.1038/s41598-023-28661-6. PMC   9911628 . PMID   36759657.
    55. 1 2 3 "FoodData Central". United States Department of Agriculture. 1 April 2019. All values in this table are from this database unless otherwise cited or when italicized as the simple arithmetic sum of other component columns.
    56. "USDA Specifications for Vegetable Oil Margarine Effective August 28, 1996" (PDF).
    57. "Avocado oil, fat composition, 100 g". FoodData Central, United States Department of Agriculture. 1 April 2019. Retrieved 23 February 2025.
    58. Wong M, Requejo-Jackman C, Woolf A (April 2010). "What is unrefined, extra virgin cold-pressed avocado oil?". Aocs.org. The American Oil Chemists' Society. Retrieved 26 December 2019.
    59. "Brazil nut oil, fat composition, 100 g". US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
    60. 1 2 3 4 Katragadda HR, Fullana A, Sidhu S, et al. (May 2010). "Emissions of volatile aldehydes from heated cooking oils". Food Chemistry. 120 (1): 59–65. doi:10.1016/j.foodchem.2009.09.070.
    61. "Canola oil, fat composition, 100 g". US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
    62. 1 2 3 4 5 6 Wolke RL (16 May 2007). "Where There's Smoke, There's a Fryer". The Washington Post. Retrieved 5 March 2011.
    63. "Coconut oil, fat composition, 100 g". US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
    64. "Corn oil, industrial and retail, all purpose salad or cooking, fat composition, 100 g". US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
    65. "Cottonseed oil, salad or cooking, fat composition, 100 g". US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
    66. "Cottonseed oil, industrial, fully hydrogenated, fat composition, 100 g". US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
    67. "Linseed/Flaxseed oil, cold pressed, fat composition, 100 g". US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
    68. "Grape seed oil, fat composition, 100 g". FoodData Central, United States Department of Agriculture. 1 April 2019. Retrieved 23 February 2025.
    69. Callaway J, Schwab U, Harvima I, et al. (April 2005). "Efficacy of dietary hempseed oil in patients with atopic dermatitis". Journal of Dermatological Treatment. 16 (2): 87–94. doi:10.1080/09546630510035832. PMID   16019622.
    70. Melina V. "Smoke points of oils" (PDF). veghealth.com. The Vegetarian Health Institute.
    71. "Safflower oil, salad or cooking, high oleic, primary commerce, fat composition, 100 g". US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
    72. "Olive oil, salad or cooking, fat composition, 100 g". US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
    73. "Palm oil, fat composition, 100 g". US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
    74. "Palm oil, industrial, fully hydrogenated, filling fat, fat composition, 100 g". US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
    75. "Oil, peanut". FoodData Central. usda.gov.
    76. Orthoefer FT (2020). "Rice Bran Oil". Bailey's Industrial Oil and Fat Products. pp. 1–25. doi:10.1002/047167849X.bio015.pub2. ISBN   978-0-471-38460-1.
    77. "Rice bran oil". RITO Partnership. Retrieved 22 January 2021.
    78. "Oil, sesame, salad or cooking". FoodData Central. fdc.nal.usda.gov. 1 April 2019.
    79. "Soybean oil, salad or cooking, fat composition, 100 g". US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
    80. "Soybean oil, salad or cooking, (partially hydrogenated), fat composition, 100 g". US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
    81. "FoodData Central". fdc.nal.usda.gov.
    82. "Walnut oil, fat composition, 100 g". US National Nutrient Database, United States Department of Agriculture.
    83. "Smoke Point of Oils". Baseline of Health. Jonbarron.org.
    84. "USQUE AD MARE - Early Lights - Canadian Coast Guard". Ccg-gcc.gc.ca. 31 March 2008. Retrieved 14 March 2010.
    85. Mallett JW. "How the South got chemicals during the war". Southern Historical Society Papers. 31: 101.
    86. Norman D (29 February 2024). "Canola sector anticipates major biofuel boom". The Western Producer. Retrieved 18 September 2025.
    87. "Southwest China's Foundational Rapeseed Oil". New Cookery Recipes. Archived from the original on 17 January 2024. Retrieved 6 April 2021.
    88. Hu S, Yu C, Zhao H, et al. (March 2007). "Genetic diversity of Brassica napus L. Germplasm from China and Europe assessed by some agronomically important characters". Euphytica. 154 (1–2): 9–16. doi:10.1007/s10681-006-9263-8. Using these canola varieties as parents, Chinese breeders have successively developed a series of new varieties adapted to local condition.{{cite journal}}: CS1 maint: overridden setting (link)
    89. Sen I (1 November 2011). "American Chefs Discover Mustard Oil". The New York Times.
    90. Thring O (12 June 2012). "The rise of rapeseed oil". The Guardian.
    91. "Which oil should I use for frying?". AkerCare. Aker Solutions. Archived from the original on 2 December 2016. Retrieved 6 April 2021.
    92. Gelpí E, de la Paz MP, Terracini B, et al. (May 2002). "The Spanish toxic oil syndrome 20 years after its onset: a multidisciplinary review of scientific knowledge". Environmental Health Perspectives. 110 (5). US National Library of Medicine National Institutes of Health: 457–464. doi:10.1289/ehp.110-1240833. PMC   1240833 . PMID   12003748.
    93. "Factbox: Fake olive oil scandal that caused Spain's worst food poisoning epidemic in 1981". Reuters. 19 October 2021.
    94. Westfall, Sammy (19 October 2021). "Victims of a 1981 mass cooking-oil poisoning occupy Madrid museum". Washington Post.

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