(Also known as: aceto-caustin; trichloracetic acid; trichloroacetic acid)
SUMMARY
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.
Example manufacturers & suppliers of products using this active now or historically
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Example products using this active
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Formulation and application details
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ENVIRONMENTAL FATE
Property
Value
Source; quality score; and other information
Interpretation
Solubility - In water at 20 °C (mg l⁻¹)
44000
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source
High
Solubility - In organic solvents at 20 °C (mg l⁻¹)
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Melting point (°C)
57
V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) 3 = Unverified data of known source
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Boiling point (°C)
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Degradation point (°C)
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Flashpoint (°C)
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Octanol-water partition coefficient at pH 7, 20 °C
P
2.14 X 1001
Calculated
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Log P
1.33
V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) 3 = Unverified data of known source
Low
Fat solubility of residues
Solubility
-
-
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Data type
-
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Density (g ml⁻¹)
1.63
V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) 3 = Unverified data of known source
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Dissociation constant pKa) at 25 °C
0.77
V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) 3 = Unverified data of known source
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Strong acid
Vapour pressure at 20 °C (mPa)
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Henry's law constant at 25 °C (Pa m³ mol⁻¹)
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Maximum UV-vis absorption L mol⁻¹ cm⁻¹
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Surface tension (mN m⁻¹)
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Degradation
Property
Value
Source; quality score; and other information
Interpretation
General biodegradability
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Soil degradation (days) (aerobic)
DT₅₀ (typical)
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DT₅₀ (lab at 20 °C)
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DT₅₀ (field)
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DT₉₀ (lab at 20 °C)
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DT₉₀ (field)
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DT₅₀ modelling endpoint
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Note
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Dissipation rate RL₅₀ on plant matrix
Value
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Note
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Dissipation rate RL₅₀ on and in plant matrix
Value
-
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Note
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Aqueous photolysis DT₅₀ (days) at pH 7
Value
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Note
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Aqueous hydrolysis DT₅₀ (days) at 20 °C and pH 7
Value
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Note
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Water-sediment DT₅₀ (days)
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Water phase only DT₅₀ (days)
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Soil adsorption and mobility
Property
Value
Source; quality score; and other information
Interpretation
Linear
Kd
-
Q2 Q = Miscellaneous data from online sources 2 = Unverified data of unknown source
Very mobile
Koc
1
Notes and range
Estimated
Freundlich
Kf
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Kfoc
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1/n
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Notes and range
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pH sensitivity
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Fate indices
Property
Value
Source; quality score; and other information
Interpretation
GUS leaching potential index
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SCI-GROW groundwater index (μg l⁻¹) for a 1 kg ha⁻¹ or 1 l ha⁻¹ application rate
Value
Cannot be calculated
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Note
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Potential for particle bound transport index
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Potential for loss via drain flow
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Bio-concentration factor
BCF (l kg⁻¹)
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CT₅₀ (days)
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Known metabolites
None
ECOTOXICOLOGY
Terrestrial ecotoxicology
Property
Value
Source; quality score; and other information
Interpretation
Mammals - Acute oral LD₅₀ (mg kg⁻¹)
400
F3 F = U.S. EPA ECOTOX database / U.S. EPA pesticide fate database / Miscellaneous WHO documents / FAO data, IPCS INCHEM data (US EPA Databases Related to Pesticide Risk Assessment ) 3 = Unverified data of known source
Aquatic plants - Acute 7 day EC₅₀, biomass (mg l⁻¹)
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Algae - Acute 72 hour EC₅₀, growth (mg l⁻¹)
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Algae - Chronic 96 hour NOEC, growth (mg l⁻¹)
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Mesocosm study data
NOEAEC mg l⁻¹
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NOEAEC mg l⁻¹
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HUMAN HEALTH AND PROTECTION
General
Property
Value
Source; quality score; and other information
Interpretation
Threshold of Toxicological Concern (Cramer Class)
High (class III)
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Mammals - Acute oral LD₅₀ (mg kg⁻¹)
400
F3 F = U.S. EPA ECOTOX database / U.S. EPA pesticide fate database / Miscellaneous WHO documents / FAO data, IPCS INCHEM data (US EPA Databases Related to Pesticide Risk Assessment ) 3 = Unverified data of known source
Non-statutory WHO drinking water guideline 0.2 mg l⁻¹
B5 B = UK CRD and ACP Evaluation Documents / and other DEFRA (UK) documents; Also Chemicals Regulation Division, Health and Safety Executive (HSE), UK (click here ) 5 = Verified data used for regulatory purposes
UK EA QS database 2018
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Drinking Water MAC (μg l⁻¹)
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Mammalian dose elimination route and rate
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Health issues
Specific human health issues
Carcinogen
Genotoxic
Endocrine disruptor
?Possibly, status not identified
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
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E0 E = Unspecified genotoxicity type (miscellaneous data source) 0 = No data
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
Ecotoxicity
Human health
Warning:
