Clove oil

Clove oil	Last updated: 31/10/2024
(Also known as: Essential clove oil; Eugenol; Clove bud oil)

Data alerts

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.

Environmental fate	Ecotoxicity	Human health
Environmental fate Low alert: Non-persistent Warning: Significant data are missing	Ecotoxicity Moderate alert: Fish acute ecotoxicity: Moderate; Daphnia acute ecotoxicity: Moderate	Human health High alert: Neurotoxicant Warning: Significant data are missing

GENERAL INFORMATION

Description

A plant-based oil, of which the main consituents are eugenol and 4-allyl-2-methoxyphenol, which has fungicidal, herbicidal and insecticidal activity.

Example pests controlled

Gloeosporium spp,; Penicillium spp.; Cacopsylla chinensis; Poison ivy (Rhus radicans L.); Ants; Rodents; Cockroaches; Root knot nematodes

Example applications

Apple; Pear; Cucumber; Tomato; Melon; Vegetable crops; Ornamentals; Domestic situations

Efficacy & activity

Efficacy demonstrated via field rials.

Appearance and life cycle

Availability status

Current

Introduction & key dates

Taxonomic classification

Class: Magnoliopsida; Order: Myrtales; Order: Myrtaceae

GB regulatory status

GB COPR regulatory status

Approved

Date COPR inclusion expires

31/08/2031

GB LERAP status

None

EC Regulation 1107/2009 (repealing 91/414)

EC Regulation 1107/2009 status

Approved

Dossier rapporteur/co-rapporteur

Malta

Date EC 1107/2009 inclusion expires

31/01/2026

EU Candidate for substitution (CfS)

Listed in EU database

Yes

Approved for use (✓) under EC 1107/2009 in the following EU Member States

ATAustria	BEBelgium	BGBulgaria	CYCyprus	CZCzech Republic	DEGermany	DKDenmark	EEEstonia	ELGreece
		✓	✓					✓
ESSpain	FIFinland	FRFrance	HRCroatia	HUHungary	IEIreland	ITItaly	LTLithuania	LULuxembourg
✓		✓				✓
LVLatvia	MTMalta	NLNetherlands	PLPoland	PTPortugal	RORomania	SESweden	SISlovenia	SKSlovakia

Approved for use (✓) under EC 1107/2009 by Mutual Recognition of Authorisation and/or national regulations in the following EEA countries

ISIceland	NONorway

Additional information

Known to be also used in the following countries

Morocco

Chemical structure

Isomerism

Chemical formula

Canonical SMILES

Isomeric SMILES

International Chemical Identifier key (InChIKey)

VEEIFXWJNCAVEQ-FYZOBXCZSA-N

International Chemical Identifier (InChI)

2D structure diagram/image available?

Yes

General status

Biopesticide type

Insecticide, Herbicide, Fungicide, Rodenticide, Nematicide, Other substance

Other bioactivity & uses

Bactericide

Substance groups

Plant-derived substance; Plant oil

Minimum active substance purity

>800 g kg⁻¹ eugenol

Known relevant impurities

Substance origin

Natural; Complex mixture

Mode of action

Contact, non-selective, causes breakdown of cell structure

Substance source

Plant oil from the buds, leaves and stem of clove (Eugenia caryophyllus, Syzygium aromaticum, Caryophyllus aromaticus Spreng) plants

Substance production

Manufactured by steam distillation or by water distillation.

Uses

Harvest and crop protection

Target pests

Gloeosporium spp,; Penicillium spp.; Cacopsylla chinensis; Poison ivy (Rhus radicans L.); Ants; Rodents; Cockroaches; Root knot nematodes

Target host

Apple; Pear; Cucumber; Tomato; Melon; Vegetable crops; Ornamentals; Domestic situations

Farming system suitability

IFM - where regulatory approvals exist

CAS RN

84961-50-2

Alternative/old CAS RN

8000-34-8

EC number

284-638-7

CIPAC number

906

US EPA chemical code

PubChem CID

Molecular mass

Chemical name

clove oil

PIN (Preferred Identification Name)

IUPAC name

CAS name

Other status information

Highly phytotoxic; FEMA=2323

Relevant Environmental Water Quality Standards

Herbicide Resistance Class (HRAC MoA class)

Not applicable

Herbicide Resistance Class (WSSA MoA class)

Not applicable

Insecticide Resistance Class (IRAC MoA class)

Not known

Fungicide Resistance Class (FRAC MOA class)

Not applicable

Examples of recorded resistance

Physical state

Pale yellow oily liquid that is a complex chemical mixture which includes eugenol (~80-95%), beta-caryophyllene (~5-17%) and alpha-humulene (~2%)

Related substances & organisms

eugenol

Formulations

Property

Product

Manufacturer

Example products

Bioxeda

Xeda International

Matran EC

Ecosmart

Poison Ivy Defoliant

St Gabriel Laboratories

Formulation and application details

Usually applied as a post-harvest drench. The commercial product is an oil emulsion.

ENVIRONMENTAL FATE

Property

Value

Source; quality score; and other information

Interpretation

Solubility - In water at 20 °C (mg l⁻¹)

2170

High

Solubility - In organic solvents at 20 °C (mg l⁻¹)

Miscible

Ethanol

Miscible

Methanol

Miscible

Ether

Miscible

Chloroform

Melting point (°C)

-21.2

Boiling point (°C)

232.9

Degradation point (°C)

Flashpoint (°C)

121

Eugenol

Octanol-water partition coefficient at pH 7, 20 °C

1.10 X 10⁰²

Calculated

Log P

2.04

Low

Fat solubility of residues

Solubility

Data type

Density (g ml⁻¹)

1.04

Dissociation constant pKa) at 25 °C

at 25 °C

Vapour pressure at 20 °C (mPa)

12200

Highly volatile. If applied directly to plants or soil, drift is a concern & mitigation is advisable

Henry's law constant at 25 °C (Pa m³ mol⁻¹)

0.9

Moderately volatile

Volatilisation as max % of applied dose lost

From plant surface

From soil surface

Maximum UV-vis absorption L mol⁻¹ cm⁻¹

Surface tension (mN m⁻¹)

35.1

undiluted

Degradation

Property

Value

Source; quality score; and other information

Interpretation

General biodegradability

Readily biodegradable

Soil degradation (days) (aerobic)

DT₅₀ (typical)

1.08

Non-persistent

DT₅₀ (lab at 20 °C)

2.09

Non-persistent

DT₅₀ (field)

DT₉₀ (lab at 20 °C)

DT₉₀ (field)

DT₅₀ modelling endpoint

1.08

Geometric mean

Note

EU 2021 dossier Lab studies DT₅₀ (normalised) range 0.99-1.16 days, Soils=4

Dissipation rate RL₅₀ (days) on plant matrix

Value

Note

Dissipation rate RL₅₀ (days) on and in plant matrix

Value

Note

Aqueous photolysis DT₅₀ (days) at pH 7

Value

Note

Aqueous hydrolysis DT₅₀ (days) at 20 °C and pH 7

Value

Note

Water-sediment DT₅₀ (days)

Water phase only DT₅₀ (days)

Air degradation

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.

Decay in stored produce DT₅₀

Soil adsorption and mobility

Property

Value

Source; quality score; and other information

Interpretation

Linear

K_d (mL g⁻¹)

K_oc (mL g⁻¹)

Notes and range

Freundlich

K_f (mL g⁻¹)

K_foc (mL g⁻¹)

¹/_n

Notes and range

pH sensitivity

Known metabolites

None

ECOTOXICOLOGY

Terrestrial ecotoxicology

Property

Value

Source; quality score; and other information

Interpretation

Mammals - Acute oral LD₅₀ (mg kg⁻¹)

> 1930

Rat as Eugenol

Moderate

Mammals - Short term dietary NOEL

(mg kg⁻¹)

(ppm diet)

Mammals - Chronic 21d NOAEL (mg kg⁻¹ bw d⁻¹)

Birds - Acute LD₅₀ (mg kg⁻¹)

Birds - Short term dietary (LC₅₀/LD₅₀)

Birds - Chronic 21d NOEL (mg kg⁻¹ bw d⁻¹)

Earthworms - Acute 14 day LC₅₀ (mg kg⁻¹)

> 1000

Eisenia foetida

Low

Earthworms - Chronic NOEC, reproduction (mg kg⁻¹)

> 1000

Eisenia foetida

Low

Soil micro-organisms

Nitrogen mineralisation: No significant adverse effect

Dose 112.5 mg product/kg soil 28 Day

Collembola

Acute LC₅₀ (mg kg⁻¹)

191.4

Folsomia candida as product (Bioxeda 18% Eugenol)

Chronic NOEC (mg kg⁻¹)

46.32

Folsomia candida as product (Bioxeda 18% Eugenol)

Non-target plants

Honeybees (Apis spp.)

Contact acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Oral acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Unknown mode acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Chronic

Bumblebees (Bombus spp.)

Contact acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Oral acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Mason bees (Osmia spp.)

Contact acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Oral acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Other bee species (1)

Acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg insect⁻¹)

Mode of exposure

Other bee species (2)

Acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg insect⁻¹)

Mode of exposure

Beneficial insects (Ladybirds)

Beneficial insects (Lacewings)

Beneficial insects (Parasitic wasps) as Mortality LR₅₀ g ha⁻¹

185.25

Aphidius rhopalosiphi as product Bioxeda 18% Eugenol

Beneficial insects (Predatory mites)

Beneficial insects (Ground beetles)

Aquatic ecotoxicology

Property

Value

Source; quality score; and other information

Interpretation

Temperate Freshwater Fish - Acute 96 hour LC₅₀ (mg l⁻¹)

7.5

Oncorhynchus mykiss as Eugenol

Moderate

Temperate Freshwater Fish - Chronic 21 day NOEC (mg l⁻¹)

Tropical Freshwater Fish - Acute 96 hour LC₅₀ (mg l⁻¹)

13.0

Danio rerio as Eugenol

Moderate

Temperate Freshwater Aquatic invertebrates - Acute 48 hour EC₅₀ (mg l⁻¹)

1.9

Daphnia magna as Eugenol

Moderate

Temperate Freshwater Aquatic invertebrates - Chronic 21 day NOEC (mg l⁻¹)

Tropical Freshwater Aquatic invertebrates - Acute 48 hour EC₅₀ (mg l⁻¹)

Aquatic crustaceans - Acute 96 hour LC₅₀ (mg l⁻¹)

Sediment dwelling organisms - Acute 96 hour LC₅₀ (mg l⁻¹)

Sediment dwelling organisms - Chronic 28 day NOEC, static, water (mg l⁻¹)

Sediment dwelling organisms - Chronic 28 day NOEC, sediment (mg kg⁻¹)

Aquatic plants - Acute 7 day EC₅₀, biomass (mg l⁻¹)

Algae - Acute 72 hour EC₅₀, growth (mg l⁻¹)

41.0

Scenedesmus subspicatus as Eugenol

Low

Algae - Chronic 96 hour NOEC, growth (mg l⁻¹)

Mesocosm study data

NOEAEC mg l⁻¹

Marine bivalves – Acute EC₅₀ development (mg l⁻¹)

HUMAN HEALTH AND PROTECTION

General

Property

Value

Source; quality score; and other information

Interpretation

Threshold of Toxicological Concern (Cramer Class)

Low (class I)

Mammals - Acute oral LD₅₀ (mg kg⁻¹)

> 1930

Rat as Eugenol

Moderate

Mammals - Dermal LD₅₀ (mg kg⁻¹ body weight)

Mammals - Inhalation LC₅₀ (mg l⁻¹)

Other Mammal toxicity endpoints

ADI - Acceptable Daily Intake (mg kg⁻¹ bw day⁻¹)

1.0

ARfD - Acute Reference Dose (mg kg⁻¹ bw day⁻¹)

None allocated

AAOEL - Acute Acceptable Operator Exposure Level (mg kg⁻¹ bw day⁻¹)

None allocated

AOEL - Acceptable Operator Exposure Level - Systemic (mg kg⁻¹ bw day⁻¹)

1.0

Dermal penetration studies (%)

25-70

concentration dependent

Dangerous Substances Directive 76/464

Exposure Routes

Public

Acceptable for proposed uses

Occupational

Acceptable for proposed uses

Mammalian dose elimination route and rate

Rapid and extensive urinary excretion approx.94.5 % within 24 h in humans

Health issues

Specific human health issues

Carcinogen

Genotoxic

Endocrine disruptor

; ; ; ;

No data found

Reproduction / development effects

Acetyl cholinesterase inhibitor

Neurotoxicant

No data found

Respiratory tract irritant

Skin irritant

Skin sensitiser

Eye irritant

Phototoxicant

No data found

General human health issues

Major consitituent Eugenol may be a skin sensitiser; Toxic
Cytotoxic
Potential liver toxicant
May cause acute respiratory distress at high doses
CNS depression at high doses

Handling issues

Property

Value and interpretation

General

Not highly flammable
Not explosive or oxidising

CLP classification 2013

Health: H302, H315, H319, H317

WHO Classification

Not listed (Not listed)

UN Number

Waste disposal & packaging

Shelf-life, storage, stability and reactivity

TRANSLATIONS

Language

Name

English

clove oil

French

Huile essentielle de Clous de Girofle

German

Danish

Italian

Spanish

Greek

Polish

Swedish

Hungarian

Dutch

Norwegian

Record last updated:	31/10/2024
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