Erucic acid

Erucic acid is a monounsaturated omega-9 fatty acid, denoted 22:1ω9. It has the chemical formula CH3(CH2)7CH=CH(CH2)11COOH. It is prevalent in wallflower seed and other plants in the family Brassicaceae, with a reported content of 20 to 54% in high erucic acid rapeseed oil[2] and 42% in mustard oil. Erucic acid is also known as cis-13-docosenoic acid and the trans isomer is known as brassidic acid.

Erucic acid
Erucic acid.png
Names
Preferred IUPAC name
(13Z)-Docos-13-enoic acid
Other names
C22:1 (Lipid numbers)
Identifiers
CAS Number
  • 112-86-7 check
3D model (JSmol)
  • Interactive image
Beilstein Reference
1728049
ChEBI
  • CHEBI:28792 check
ChEMBL
  • ChEMBL1173380 check
ChemSpider
  • 4444561 check
ECHA InfoCard100.003.647 Edit this at Wikidata
EC Number
  • 204-011-3
Gmelin Reference
177365
KEGG
  • C08316 check
PubChem CID
  • 5281116
UNII
  • 075441GMF2 check
CompTox Dashboard (EPA)
  • DTXSID8026931 Edit this at Wikidata
InChI
  • InChI=1S/C22H42O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h9-10H,2-8,11-21H2,1H3,(H,23,24)/b10-9- check
    Key: DPUOLQHDNGRHBS-KTKRTIGZSA-N check
  • InChI=1/C22H42O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h9-10H,2-8,11-21H2,1H3,(H,23,24)/b10-9-
    Key: DPUOLQHDNGRHBS-KTKRTIGZBD
SMILES
  • O=C(O)CCCCCCCCCCC\C=C/CCCCCCCC
Properties
Chemical formula
C22H42O2
Molar mass338.576 g·mol−1
AppearanceWhite waxy solid
Density0.860 g/cm3
Melting point33.8 °C (92.8 °F; 306.9 K)
Boiling point381.5 °C (718.7 °F; 654.6 K) (decomposes)
Solubility in water
Insoluble
Solubility in methanol and ethanolSoluble
Hazards
GHS labelling:[1]
Pictograms
GHS07: Exclamation mark
Signal word
Warning
Hazard statements
H315H319H335
Precautionary statements
P261P264P271P280P302+P352P304+P340P305+P351+P338P312P321P332+P313P337+P313P362P403+P233P405P501
Flash point349.9 °C (661.8 °F; 623.0 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

UsesEdit

Erucic acid has many of the same uses as mineral oils, but it is more readily biodegradable than some. It has limited ability to polymerize and dry for use in oil paints. Like other fatty acids, it can be converted into surfactants or lubricants, and can be used as a precursor to biodiesel fuel.

Derivatives of erucic acid have many further uses, such as behenyl alcohol (CH3(CH2)21OH), a pour point depressant (enabling liquids to flow at a lower temperature), and silver behenate, for use in photography.[3]

Sources of erucic acidEdit

The seed oil of the rape plant is rich in erucic acid.

The name erucic means "of or pertaining to Eruca", which is a genus of flowering plants in the family Brassicaceae. The genus includes colewort (E. sativa), which today is better known as arugula (US) or rocket (UK).

Erucic acid is produced naturally (together with other fatty acids) across a great range of green plants, but especially so in members of the genus Brassica. For industrial purposes and production of erucic acid, rapeseed is used; for food purposes a 'low-erucic acid rapeseed' (LEAR) has been developed (canola), which contains fats derived from oleic acid instead of erucic acid.[4]

BiochemistryEdit

Erucic acid is produced by elongation of oleic acid via oleoyl-coenzyme A and malonyl-CoA.[5] Erucic acid is broken down into shorter-chain fatty acids in the human liver by the long-chain acyl CoA dehydrogenase enzyme.

Health effectsEdit

Studies done on laboratory animals in the early 1970s[6] show that erucic acid appears to have toxic effects on the heart at high enough doses. However, more recent research has cast doubt on the relevance of rat studies to the human health of erucic acid. Rats are unusual in their inability to process erucic acid, and the symptoms in rats caused by a diet with high levels of erucic acid has not been observed in pigs, primates, or any other animals.[7] An association between the consumption of rapeseed oil and increased myocardial lipidosis, or heart disease, has not been established for humans.[8] While there are reports of toxicity from long-term use of Lorenzo's oil (which contains erucic acid and other ingredients), there are no reports of harm to people from dietary consumption of erucic acid.[9]: 646–657 

Publication of animal studies with erucic acid through the 1970s led to governments worldwide moving away from oils with high levels of erucic acid,[6] and tolerance levels for human exposure to erucic acid have been established based on the animal studies.[8][10][11]

In 2003, Food Standards Australia set a provisional tolerable daily intake (PTDI) for an average adult of about 500 mg/day of erucic acid, extrapolated based on "the level that is associated with increased myocardial lipidosis in nursing pigs."[8] "There is a 120-fold safety margin between this level and the level that is associated with increased myocardial lipidosis in nursing pigs. The dietary exposure assessment has concluded that the majority of exposure to erucic acid by the general population would come from the consumption of colza oil. The dietary intake of erucic acid by an individual consuming at the average level is well below the PTDI; therefore, there is no cause for concern in terms of public health and safety. However, the individual consuming at a high level has the potential to approach the PTDI. This would be particularly so if the level of erucic acid in colza oil were to exceed 2% of the total fatty acids."[8]

Food-grade rapeseed oil (also known as canola oil, rapeseed 00 oil, low erucic acid rapeseed oil, LEAR oil, and rapeseed canola-equivalent oil) is regulated to a maximum of 2% erucic acid by weight in the US[10] and 2% in the EU[12] (was 5%[11] before 2019-11-19), with special regulations for infant food. Canola was bred from rapeseed cultivars of B. napus and B. rapa by Dr. Baldur Stefansson at the Univqersity of Manitoba, Canada. Canola oil is derived from a variety of rapeseed that is low in erucic acid, as opposed to colza oil. 


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