Triacontanol
Last updated: 14/09/2023
(Also known as: melissyl alcohol; myricyl alcohol; 1-hydroxytriacontane )
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
 
 
 
A natural chemical that acts as a phytohormone which is used in commercial horticulture as a plant growth regulator
Growth
Ornamental plants including roses; Cotton; Tomato; Chilli peppers; Rice; Peanuts; Potato
-
Current
1934, first lab synthesis
Not approved
Not applicable
No UK approval for use
EC Regulation 1107/2009 (repealing 91/414)
Not approved
Not applicable
Not applicable
Not applicable
No
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
 
 
 
 
 
 
 
 
 
ISIceland
NONorway
 
 
 
 
 
 
 
 
 
None
C₃₀H₆₂O
CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO
-
REZQBEBOWJAQKS-UHFFFAOYSA-N
InChI=1S/C30H62O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31/h31H,2-30H2,1H3
Yes
Plant Growth Regulator
Fatty alcohol PGR
>98%
-
Natural
Effects photosynthesis, plant metabolism, and can increase the growth of roots, shoots and flower production. Influences nutrient uptake.
593-50-0
209-794-5
-
-
68972
No data found
438.81
triacontan-1-ol
triacontan-1-ol
n-triacontanol
-
-
Not applicable
Not applicable
Not applicable
Not applicable
-
White powdery solid
Shogun Caymen Chemical Co., Dow Agrosiences
Sumoboost Miraculan Well-Bloom
Normally mixed with an emulsifying agent and water to form a suspension and used as a foliar spray. Also available as an emulsifiable concentrate.
Insoluble
Insoluble
1700
Chloroform
-
80
-
-
-
-
-
-
-
-
-
-
4.07 X 1013
Calculated
-
13.61
High
-
-
-
-
-
-
0.777
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
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-
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-
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-
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-
-
-
-
-
-
-
-
-
-
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Soil adsorption and mobility
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-
-
Cannot be calculated
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-
-
-
-
-
-
-
-
-
-
-
-
-
None
Terrestrial ecotoxicology
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-
-
-
-
-
-
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-
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HUMAN HEALTH AND PROTECTION
Low (class I)
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-
-
-
-
2000
Rabbit
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EU MRL pesticide database 
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Carcinogen
Endocrine disruptor
No data found
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
No data found
Reproduction / development effects
Acetyl cholinesterase inhibitor
Neurotoxicant
No data found
No data found
No data found
Respiratory tract irritant
Skin irritant
Skin sensitiser
✓Yes, known to cause a problem
✓Yes, known to cause a problem
No data found
Eye irritant
Phototoxicant
 
✓Yes, known to cause a problem
No data found
 
May be harmful by inhalation, ingestion, or skin absorption
Not compatible with oxidising agents
None currently allocated
Not listed (Not listed)
Not regulated
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triacontanol
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Record last updated:
14/09/2023
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