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Rapeseed oil

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(Redirected from Canola oil)
"Canola" redirects here. For other uses, see Canola (disambiguation).
Not to be confused with grape seed oil.

Close-up of canola blooms
Canola flower
Rapeseed oil
Canola field, Willamette Valley, Oregon, May 2017

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. Historically, it was restricted as a food oil due to its content of erucic acid. Laboratory studies about this acid have shown damage to the cardiac muscle of laboratory animals in high quantities. It also imparts a bitter taste, and glucosinolates, which made many parts of the plant less nutritious in animal feed.[1][2] Rapeseed oil from standard cultivars can contain up to 54% erucic acid.[3]

Canola oil is a food-grade version derived from rapeseed cultivars specifically bred for low acid content. It is also known as low erucic acid rapeseed (LEAR) oil and is generally recognized as safe by the United States Food and Drug Administration.[a][4] Canola oil is limited by government regulation to a maximum of 2% erucic acid by weight in the US[4] and the EU,[7] with special regulations for infant food. These low levels of erucic acid do not cause harm in humans.[4][10]

In commerce, non-food varieties are typically called colza oil.[11]

Rapeseed is extensively cultivated in Canada, India, France, Belgium, Ireland, the United Kingdom, the United States, the Netherlands, Germany, Denmark, Poland, Japan and Slovenia. In France and Denmark especially, the extraction of the oil is an important industry.[citation needed]

History

[edit]

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.[12]: 55  Its use in Northern Europe for oil lamps is documented to have started since the 13th century.[12] Rapeseed oil extracts were first put on the market in 1956–1957 as food products, but these suffered from several unacceptable characteristics. 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.[13]

Canola was bred from rapeseed cultivars of B. napus and B. rapa at the University of Manitoba, Canada, by Keith Downey and Baldur R. Stefansson in the early 1970s,[14][15] having then a different nutritional profile than present-day oil in addition to much less erucic acid.[16] 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".[17][18] Canola is now a generic term for edible varieties of rapeseed oil in North America and Australasia;[19] the change in name also serves to distinguish it from natural rapeseed oil, which has much higher erucic acid content.[20]

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.[21] In 2005, 87% of the canola grown in the US was genetically modified.[22] In 2011, out of the 31 million hectares of canola grown worldwide, 8.2 million (26%) were genetically modified.[23]

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.[24]

Genetically modified canola attracts a price penalty compared to non-GM canola; in Western Australia, it is estimated to be 7.2% on average.[25]

Production and trade

[edit]
Rapeseed oil production – 2021[26]
Country millions of tonnes
 Canada 4.2
 Germany 4.0
 China 3.3
 India 3.0
 France 1.8
World total 26.6
Canola field in Manitoba, Canada
Rapeseed oil is one of the most commonly produced vegetable oils globally.

In 2021, world production of rapeseed oil was 26 million tonnes, led by Canada, Germany and China as the largest producers, accounting together for 43% of the world total.[26] Canada was the world's largest exporter of rapeseed oil in 2021, shipping 3.1 million tonnes or approximately 74% of its total production.[26]

The benchmark price for worldwide canola trade is the ICE Futures Canada (formerly Winnipeg Commodity Exchange) canola futures contract.[27]

In China, rapeseed meal is mostly used as a soil fertilizer rather than for animal feed,[28] while canola is used mainly for frying food. In the words of one observer, "China has a vegetable oil supply shortage of 20 million tonnes per year. It covers a large percentage of that shortage with soybean imports from Brazil, the U.S. and Argentina."[29]

GMO regulation

[edit]
See also: Regulation of the release of genetically modified organisms

There are several forms of genetic modification, such as herbicide (glyphosate and glufosinate, for example) tolerance and different qualities in canola oil. Regulation varies from country to country; for example, glyphosate-resistant canola has been approved in Australia, Canada, China, Korea, Mexico, Philippines, and the US, while Laurical, a product with a different oil composition, has been approved for growing only in Canada and the US.[30]

In 2003, Australia's gene technology regulator approved the release of canola genetically modified to make it resistant to glufosinate ammonium, a herbicide.[31] The introduction of the genetically modified crop to Australia generated considerable controversy.[32] Canola is Australia's third biggest crop, and is used often by wheat farmers as a break crop to improve soil quality. As of 2008, the only genetically modified crops in Australia were canola, cotton, and carnations.[33][34]

GMO litigation

[edit]

Genetically modified canola has become a point of controversy and contentious legal battles. In one high-profile case (Monsanto Canada Inc v. Schmeiser) the Monsanto Company sued Percy Schmeiser for patent infringement after he replanted canola seed he had harvested from his field, which he discovered was contaminated with Monsanto's patented glyphosate-tolerant canola by spraying it with glyphosate, leaving only the resistant plants. The Canadian Supreme Court ruled that Percy was in violation of Monsanto's patent because he knowingly isolated and replanted the resistant seed that he had harvested.[35][dubious – discuss] On 19 March 2008, Schmeiser and Monsanto Canada Inc. came to an out-of-court settlement whereby Monsanto would pay for the clean-up costs of the contamination, which came to a total of C$660.[36] In Western Australia, in the Marsh v Baxter case, a GM canola farmer was sued by his organic neighbour because GM canola contamination led to the loss of organic certification. Although the facts of the case and the losses to the organic farmer were agreed between the parties, the judge did not find the GM farmer liable for the losses.[37]

Production process

[edit]
Canola oil

Canola oil is made at a processing facility by slightly heating and then crushing the seed.[38] Almost all commercial canola oil is then extracted using hexane solvent,[39] 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.[38] Sometimes the oil is also bleached for a lighter color.[40] The average density of canola oil is 0.92 g/ml (7.7 lb/US gal; 9.2 lb/imp gal).[41]

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.[38] 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,[42] and overall it is the third-most widely consumed vegetable oil, after soybean oil and palm oil.[43]

The oil has many non-food uses and, like soybean oil, is often used interchangeably with non-renewable petroleum-based oils in products,[42] 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.[44]

Nutrition and health

[edit]
Canola oil
Nutritional value per 100 grams
Energy3,701 kJ (885 kcal)
0 g
Starch0 g
Sugars0 g
Dietary fiber0 g
100 g
Saturated7.4 g
Trans0.4 g
Monounsaturated63.3 g
Polyunsaturated28.1 g
8 g
20 g
0 g
Vitamins and minerals
VitaminsQuantity
%DV†
Vitamin A equiv.
0%
0 μg
0%
0 μg
0 μg
Vitamin A0 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
MineralsQuantity
%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
Nutrition Data
†Percentages estimated using US recommendations for adults,[45] except for potassium, which is estimated based on expert recommendation from the National Academies.[46]

Canola oil is considered safe for human consumption,[47][48] and has a relatively low amount of saturated fat, a substantial amount of monounsaturated fat, with roughly a 2:1 mono- to polyunsaturated fats ratio.[49]

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:[50]

"Limited and not conclusive scientific evidence suggests that eating about 1 1⁄2 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."

A 2013 review, sponsored by the Canola Council of Canada and the U.S. Canola Association, concluded there was a substantial reduction in total cholesterol and low-density lipoprotein (LDL) cholesterol, and an increase in tocopherol levels and improved insulin sensitivity, compared with other sources of dietary fat.[49] A 2014 review of health effects from consuming plant oils rich in alpha-linolenic acid, including canola, stated that there was moderate benefit for lower risk of cardiovascular diseases, bone fractures, and type-2 diabetes.[51]

A 2019 review of randomized clinical trials found that canola oil consumption reduces total cholesterol (TC) and LDL compared to sunflower oil and saturated fat.[52] Consumption of canola oil has been shown to reduce body weight when compared with saturated fat.[53]

Regarding individual components, canola oil is low in saturated fat and contains both omega-6 and omega-3 fatty acids in a ratio of 2:1. It is high in monounsaturated fats, which may decrease the risk of heart disease.[54]

Erucic acid

[edit]
Main article: Erucic acid
Compound Family % of total
Oleic acid ω-9 61%[55]
Linoleic acid ω-6 21%[55]
Alpha-linolenic acid ω-3 11%[55]
9%[56][57]
Saturated fatty acids 7%[55]
Palmitic acid 4%[56]
Stearic acid 2%[56]
Trans fat 0.4%[58]
Erucic acid 0.01%[59]
<0.1%[60][61]

Although wild rapeseed oil contains significant amounts of erucic acid,[62] the cultivars used to produce commercial, food-grade canola oil were bred to contain less than 2% erucic acid,[4] 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.[63][64]

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[65] to a current content of 0.01% from 2008 to 2015.[59] Other reports also show a content lower than 0.1% in Australia[60] and Brazil.[61]

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.[66][67] Canola oil produced using genetically modified plants has also not been shown to explicitly produce adverse effects.[68]

It is usually accepted that canola oil poses no unusual health risks for humans.[67] Canola oil is generally recognized as safe by the United States Food and Drug Administration.[4][48]

Glucosinolates

[edit]
Main article: Glucosinolates

Another chemical change in canola is the reduction of glucosinolates.[63] 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.[69][1] A small amount of glucosinolates also enters the oil, imparting a pungent odor.[70]

Further reduction of glucosinolate levels remains important for the use of rapeseed meal in animal feed.[71][72]

It is not completely clear which genetic changes from plant breeding resulted in the current reduction in this group of chemicals.[63]

Comparison to other vegetable oils

[edit]
Properties of vegetable oils[73][74]
The nutritional values are expressed as percent (%) by mass of total fat.
Type Processing
treatment[75]		 Saturated
fatty acids		 Monounsaturated
fatty acids		 Polyunsaturated
fatty acids		 Smoke point
Total[73] Oleic
acid
(ω−9)		 Total[73] α-Linolenic
acid
(ω−3)		 Linoleic
acid
(ω−6)		 ω−6:3
ratio
Avocado[76] 11.6 70.6 52–66
[77]		 13.5 1 12.5 12.5:1 250 °C (482 °F)[78]
Brazil nut[79] 24.8 32.7 31.3 42.0 0.1 41.9 419:1 208 °C (406 °F)[80]
Canola[81] 7.4 63.3 61.8 28.1 9.1 18.6 2:1 204 °C (400 °F)[82]
Coconut[83] 82.5 6.3 6 1.7 0.019 1.68 88:1 175 °C (347 °F)[80]
Corn[84] 12.9 27.6 27.3 54.7 1 58 58:1 232 °C (450 °F)[82]
Cottonseed[85] 25.9 17.8 19 51.9 1 54 54:1 216 °C (420 °F)[82]
Cottonseed[86] hydrogenated 93.6 1.5 0.6 0.2 0.3 1.5:1
Flaxseed/linseed[87] 9.0 18.4 18 67.8 53 13 0.2:1 107 °C (225 °F)
Grape seed   10.4 14.8 14.3   74.9 0.15 74.7 very high 216 °C (421 °F)[88]
Hemp seed[89] 7.0 9.0 9.0 82.0 22.0 54.0 2.5:1 166 °C (330 °F)[90]
High-oleic safflower oil[91] 7.5 75.2 75.2 12.8 0 12.8 very high 212 °C (414 °F)[80]
Olive (extra virgin)[92] 13.8 73.0 71.3 10.5 0.7 9.8 14:1 193 °C (380 °F)[80]
Palm[93] 49.3 37.0 40 9.3 0.2 9.1 45.5:1 235 °C (455 °F)
Palm[94] hydrogenated 88.2 5.7 0
Peanut[95] 16.2 57.1 55.4 19.9 0.318 19.6 61.6:1 232 °C (450 °F)[82]
Rice bran oil 25 38.4 38.4 36.6 2.2 34.4[96] 15.6:1 232 °C (450 °F)[97]
Sesame[98] 14.2 39.7 39.3 41.7 0.3 41.3 138:1
Soybean[99] 15.6 22.8 22.6 57.7 7 51 7.3:1 238 °C (460 °F)[82]
Soybean[100] partially hydrogenated 14.9 43.0 42.5 37.6 2.6 34.9 13.4:1
Sunflower[101] 8.99 63.4 62.9 20.7 0.16 20.5 128:1 227 °C (440 °F)[82]
Walnut oil[102] unrefined 9.1 22.8 22.2 63.3 10.4 52.9 5:1 160 °C (320 °F)[103]

Uses

[edit]

Apart from its use for human consumption, rapeseed oil is extensively used as a lubricant for machinery. 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, for example 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.[104] Rapeseed oil was burned to a limited extent in the Confederacy during the American Civil War.[105]

Rapeseed oil was used in Gombault's Caustic Balsam,[106] a popular horse and human liniment at the turn of the 20th century.

Among the more unusual applications of rapeseed oil is the calming of choppy seas, where the oil modifies the surface tension of the water and rapidly smooths the surface. For this purpose, rapeseed oil was carried in ship's lifeboats.[107][better source needed]

Biodiesel

[edit]
Main article: 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. 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. Owing to the costs of growing, crushing, and refining rapeseed biodiesel, rapeseed-derived biodiesel from new oil costs more to produce than standard diesel fuel, so diesel fuels are commonly made from the used oil. Rapeseed oil is the preferred oil stock for biodiesel production in most of Europe, accounting for about 80% of the feedstock,[citation needed] 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 significantly lower gel point than most other vegetable oils.[citation needed]

Other edible rapeseed oils

[edit]

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.[108] Their erucic acid content was reduced to modern "canola" levels by breeding with Canadian low-erucic acid cultivar "ORO".[64][109] 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.[110]

In India, mustard oil is used in cooking.[111] In the United Kingdom and Ireland, some chefs use a "cabbagey"-tasting rapeseed oil processed by cold-pressing.[112] This cold process means that the oil has a low smoke point, and is therefore unsuitable for frying in Sichuan cuisine, for example.[113]

Spanish rapeseed poisoning outbreak

[edit]
Main article: Toxic oil syndrome

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.[114] It was then fraudulently sold as olive oil, mainly in street markets, mostly in the Madrid area.[115][116]

See also

[edit]
Wikimedia Commons has media related to Rapeseed oil.

References

[edit]
  1. ^ 21 CFR 184.1555 also recognizes fully-hydrogenated rapeseed oil and superglycerinated fully hydrogenated rapeseed oil as GRAS, without limits on erucic acid levels. However, these two are not to be used as a regular cooking oil, but as an emusifier in foods in limited quantities.[4]
  1. ^ a b O'Brien 2008, p. 37.
  2. ^ Balakhial, Amir; Naserian, Abasali; Heravi moussavi, Alireza; Valizadeh, Reza (2022). "Effect of Replacing Corn Silage with Canola Silage on Feed Intake, Nutrient Digestibility, Milk Yield, and Thyroid Hormones of Lactating Dairy Cows". Farm Animal Health and Nutrition. 1 (1): 1–5. doi:10.58803/fahn.v1i1.2.
  3. ^ Sahasrabudhe 1977, p. 323.
  4. ^ a b c d e f "21 CFR 184.1555 "Rapeseed oil"". US Food and Drug Administration. 1 April 2010. Retrieved 19 April 2020. (ecfr.gov version)
  5. ^ 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
  6. ^ Consolidated text: Commission Regulation (EU) 2023/915 of 25 April 2023 on maximum levels for certain contaminants in food and repealing Regulation (EC) No 1881/2006
  7. ^ Commission Regulation (EC) No 1881/2006 of 19 December 2006 setting maximum levels for certain contaminants in foodstuffs.[5] No longer in force, Date of end of validity: 24/05/2023; Repealed by 32023R0915.[6]
  8. ^ Commission Implementing Regulation (EU) 2023/2783 of 14 December 2023 laying down the methods of sampling and analysis for the control of the levels of plant toxins in food and repealing Regulation (EU) 2015/705
  9. ^ Commission Regulation (EU) 2015/705 of 30 April 2015 laying down methods of sampling and performance criteria for the methods of analysis for the official control of the levels of erucic acid in foodstuffs and repealing Commission Directive 80/891/EEC. No longer in force, Date of end of validity: 31/03/2024; Repealed by 32023R2783.[8]
  10. ^ Commission Directive 80/891/EEC of 25 July 1980 relating to the Community method of analysis for determining the erucic acid content in oils and fats intended to be used as such for human consumption and foodstuffs containing added oils or fats. No longer in force, Date of end of validity: 21/05/2015; Repealed by 32015R0705.[9]
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    "Greenpeace has the last laugh on genetic grains talks". Australian Broadcasting Corporation. 13 March 2003. Archived from the original on 5 May 2004.
    Cauchi, Stephen (25 October 2003). "GM: food for thought". The Age. Retrieved 20 October 2007.<
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Sources

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