(Also known as: Palo santo oil; oil of guaiac; guaiacum sanctum l. gum oil; bulnesia sarmienti extract)
Hazard alerts
The following Pesticide Hazard Tricolour (PHT) 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. The alerts for Highly Hazardous Pesticides (HHPs) are based on applying the FAO/WHO (Type 1) and the PAN (Type II) criteria to PPDB data. Further details on the HHP indicators are given in the tables below. Neither the PHT nor the HHP hazard alerts take account of usage patterns or exposure, thus they do not represent risk.
No UK approval for use as a plant protection agent
EC Regulation 1107/2009 (repealing 91/414)
EC Regulation 1107/2009 status
Not approved
Dossier rapporteur/co-rapporteur
Not applicable
Date EC 1107/2009 inclusion expires
Not applicable
EU Candidate for substitution (CfS)
Not applicable
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
Also used in
USA
Chemical structure
Isomerism
Guaiacwood oil contains isomeric compounds, particularly among its sesquiterpene constituents. One of its major components, guaiol, is known to exhibit isomerism. Guaiol is chiral, existing in enantiomeric forms. The most common form is (-)-guaiol, but other stereoisomers (like epimers) may also occur naturally or be synthesised.
Chemical formula
-
Canonical SMILES
-
Isomeric SMILES
-
International Chemical Identifier key (InChIKey)
-
International Chemical Identifier (InChI)
-
2D structure diagram/image available?
No
General status
Biopesticide type
Insecticide; Repellent
Substance groups
Plant-derived substance; Plant oil
Minimum active substance purity
-
Known relevant impurities
-
Substance origin
Natural; Complex mixture
Mode of action
Non-toxic mode of action - repellency via odour
Insecticide behavioural & physiological effects
-
Substance source
An oil from the Palosanto tree (Bulnesia sarmienti) found in Latin America
Mixture composition
The chemical composition of Guaiacwood oil chemical is dominated by sesquiterpenoids, particularly tertiary sesquiterpene alcohols, with major constituents including bulnesol (typically 40-45%, sometimes up to higher ranges) and guaiol (25-30%, with combined guaiol + bulnesol often 65–85% or more), alongside supporting compounds such as guaiacol (variable, reported 20–30% in some sources but lower in others), gamma-eudesmol (~2%), elemol (~1%), beta-elemol, alpha- and beta-eudesmol, 10-epi-gamma-eudesmol, and various guaiane/eudesmane hydrocarbons and oxides like alpha-guaiene, bulnesene, guaioxide, and beta-patchoulene. Composition varies by source, distillation method, and processing but bulnesol and guaiol are the defining bioactive markers.
It is a yellow to greenish yellow semi-solid mass with a rose-like odour. is primarily composed of guaiol (40-70%), bulnesol, bulnesene, alpha-guaiene, guaioxide and beta-patchoulene.
Used traditionally for centuries; 2000s, recognised for pest management benefits
Example manufacturers & suppliers of products using this active now or historically
Heffner Oil, Argentina
Nelixia
Example products using this active
Formulation and application details
Ready-to-use formulations
Commercial production
Commercial production of guaiacwood oil begins with the sustainable harvesting of the dense, resin-rich wood, which is then chipped and subjected to steam distillation to extract the essential oil. This method captures key aromatic compounds like guaiol and bulnesol. After distillation, the oil is filtered and tested for purity before being packaged for use.
Impact on climate of production and use
Data for specific plant oils is scarce. However, from publicly available data the carbon footprint of plant oils has been estimated at between 1.0 and 4.0 kg CO₂e per kg of oil. This depends on the plant oil content, agricultural practices and processing methods used.
ENVIRONMENTAL FATE
Property
Value
Source; quality score; and other information
Interpretation
Solubility - In water at 20 °C at pH 7 (mg l⁻¹)
1.27
A3 A = EU regulatory and evaluation data as published by EC, EFSA (RAR, DAR & Conclusion dossiers), EMA (e.g. EU Annex III PIC DGD) (EU - Pesticides database; EFSA Scientific Publications ) 3 = Unverified data of known source
Low
Solubility - In organic solvents at 20 °C (mg l⁻¹)
-
-
-
Melting point (°C)
42
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source
Octanol-water partition coefficient at pH 7, 20 °C
P
3.72 X 1004
Calculated
-
Log P
4.57
A3 A = EU regulatory and evaluation data as published by EC, EFSA (RAR, DAR & Conclusion dossiers), EMA (e.g. EU Annex III PIC DGD) (EU - Pesticides database; EFSA Scientific Publications ) 3 = Unverified data of known source
High
Fat solubility of residues
Solubility
-
-
-
Data type
-
-
-
Density (g ml⁻¹)
0.965
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source
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)
-
-
-
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)
-
-
-
Degradation
Property
Value
Source; quality score; and other information
Interpretation
General biodegradability
-
Soil degradation (days)
DT₅₀ (typical)
-
-
-
DT₅₀ (lab at 20 °C)
-
-
-
DT₅₀ (field)
-
-
-
DT₉₀ (lab at 20 °C)
-
-
-
DT₉₀ (field)
-
-
-
DT₅₀ modelling endpoint
-
-
-
Note
-
Soil mineralisation
Aerobic (at 20 °C)
-
-
-
Anaerobic (at 20 °C)
-
-
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)
-
-
-
Sediment 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.
Tzilivakis, J., Lewis, K.A., Green, A. and Warner, D.J. (2026) A decade of growth and impact of the Pesticide Properties Database (PPDB). Human and Ecological Risk Assessment: An International Journal, 1–26. DOI: 10.1080/10807039.2026.2702066
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
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