Oleic acid |

Last updated: 25/08/2025
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(Not known by any other names) |
The following alerts are based on the data in the tables below. An absence of an alert does not imply the substance has no implications for human health, biodiversity or the environment but just that we do not have the data to form a judgement. These hazard alerts do not take account of usage patterns or exposure, thus do not represent risk.
Environmental fate |
Ecotoxicity |
Human health |
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A naturally occuring monounsaturated omega-9 fatty acid abundant in olive oil, various nuts and seeds, and animal fat that has some insecticidal activity |
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Cockroaches; Spider mites; Beetles including Asian cabinet beetle (Trogoderma granarium) |
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Stored grain; Ornamentals; Cucumber; Strawberry; Tomato |
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- |
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- |
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- |
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Approved (as fatty acid C7-C20) |
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31/08/2029 |
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None |
EC Regulation 1107/2009 (repealing 91/414) |
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Not approved |
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Not applicable |
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Not applicable |
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No |
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Yes |
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ATAustria |
BEBelgium |
BGBulgaria |
CYCyprus |
CZCzech Republic |
DEGermany |
DKDenmark |
EEEstonia |
ELGreece |
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ESSpain |
FIFinland |
FRFrance |
HRCroatia |
HUHungary |
IEIreland |
ITItaly |
LTLithuania |
LULuxembourg |
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LVLatvia |
MTMalta |
NLNetherlands |
PLPoland |
PTPortugal |
RORomania |
SESweden |
SISlovenia |
SKSlovakia |
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ISIceland |
NONorway |
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Isomeric. Oleic acid is the cis-isomer and occurs naturally. The trans-isomer is known as elaidic acid and is abundant in diet as a major component of partially hydrogenated vegetable oils. |
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C₁₈H₃₄O₂ |
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CCCCCCCC/C=C\CCCCCCCC(=O)O |
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ZQPPMHVWECSIRJ-KTKRTIGZSA-N |
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InChI=1S/C18H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h9-10H,2-8,11-17H2,1H3,(H,19,20)/b10-9- |
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Yes |
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Insecticide; Other substance |
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Surfactant; Antimicrobial; Antiviral |
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Plant-derived substance; Animal-derived substance |
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- |
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Natural |
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No direct insecticidal activity but can disrupt the lipid structure of insect cuticles, making it easier for other chemicals to penetrate. It may also influence insect behaviour making them better exposed ro control. |
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A naturally occuring monounsaturated omega-9 fatty acid abundant in olive oil, various nuts and seeds, and animal fat that has some insecticidal activity |
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Crop protection |
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Cockroaches; Spider mites; Beetles including Asian cabinet beetle (Trogoderma granarium) |
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Stored grain; Ornamentals; Cucumber; Strawberry; Tomato |
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- |
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112-80-1 |
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204-007-1 |
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- |
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- |
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445639 |
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282.47 |
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(Z)-octadec-9-enoic acid |
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(Z)-octadec-9-enoic acid |
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- |
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- |
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GRAS |
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- |
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Not applicable |
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Not applicable |
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Not classified |
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Not applicable |
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- |
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Colourless to pale yellow, visous oily liquid |
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Current |
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late 19th century, first agricultural use |
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- Bayer CropScience
- Evergreen Garden Care UK
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Often supplied as ready-to-use formulations and as liquid concentrates |
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Commercial production of oleic acid involves extracting this monounsaturated fatty acid primarily from vegetable oils such as olive, sunflower, and canola oil, though animal fats like tallow and lard are also used in some regions. The process typically begins with hydrolysis, where triglycerides in the oils or fats are broken down into glycerol and free fatty acids. Oleic acid is then isolated and purified using fractionation techniques like distillation and crystallisation. In some cases, chemical catalysis, including hydrogenation and esterification, is employed to convert other fatty acids into oleic acid. |
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GHG emissions during the production of oleic acid vary significantly depending on the feedstock and processing method. Based on GREET model data and similar LCAs Vegetable oil-derived oleic acid emits approximately 1.5–3.5 kg CO₂e per kg; tallow-derived oleic acid emits slightly higher GHG due to methane emissions from livestock. Petroleum-derived oleic acid , a less common production approach, has estimated emissions of 5–7 kg CO₂e per kg. These estimates include agricultural emissions, oil extraction and refining and fatty acid distillation and purification where appropriate. |
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16.3 |
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286 |
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113 |
(closed cup) |
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5.37 X 1007 |
Calculated |
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7.73 |
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
High |
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As this parameter is not normally measured directly, a surrogate measure is used: ‘Photochemical oxidative DT₅₀’. Where data is available, this can be found in the Fate Indices section below. |
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Soil adsorption and mobility |
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None
Terrestrial ecotoxicology |
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> 10000 |
Rat |
Low |
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205 |
Pimephales promelas |
Low |
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2.8 |
Daphnia magna |
Moderate |
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HUMAN HEALTH AND PROTECTION |
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> 10000 |
Rat |
Low |
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Intravenous LD₅₀ = 2.4 mg kg⁻¹ |
Rat |
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Carcinogen |
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Endocrine disruptor |
XNo, known not to cause a problem |
A0 A = Chromosome aberration (EFSA database) 0 = No data ; B0 B = DNA damage/repair (EFSA database) 0 = No data ; C0 C = Gene mutation (EFSA database) 0 = No data ; D0 D = Genome mutation (EFSA database) 0 = No data ; E0 E = Unspecified genotoxicity type (miscellaneous data source) 0 = No data |
XNo, known not to cause a problem |
Reproduction / development effects |
Acetyl cholinesterase inhibitor |
Neurotoxicant |
No data found |
No data found |
No data found |
Respiratory tract irritant |
Skin irritant |
Skin sensitiser |
No data found |
✓Yes, known to cause a problem |
XNo, known not to cause a problem |
Eye irritant |
Phototoxicant |
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✓Yes, known to cause a problem |
No data found |
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May offer health benefits including preventing cardiovascular issues and Type 2 diabetes |
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Not explosive or oxidising Combustable liquid |
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Not regulated |
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Substance is light and air sensitive - store in the dark and in air tight container at 15-25 DegC. Non-reactive. |
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oleic acid |
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Record last updated: |
25/08/2025 |
Contact: |
aeru@herts.ac.uk |
Please cite as: |
Lewis, K.A., Tzilivakis, J., Warner, D. and Green, A. (2016) An international database for pesticide risk assessments and management. Human and Ecological Risk Assessment: An International Journal, 22(4), 1050-1064. DOI: 10.1080/10807039.2015.1133242 |