(Also known as: 1,3,5-trioxane; S-trioxane; metaformaldehyde; trioxin; paraformaldehyde; aldeform; trioxymethylen)
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)
221000
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source
High
Solubility - In organic solvents at 20 °C (mg l⁻¹)
Insoluble
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source
Ethanol
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Insoluble
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source
Ether
-
Melting point (°C)
62
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source
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Boiling point (°C)
115
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source
Sublimes
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Degradation point (°C)
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-
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Flashpoint (°C)
45
E4 E = Manufacturers safety data sheets 4 = Verified data
(closed cup)
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Octanol-water partition coefficient at pH 7, 20 °C
P
3.72 X 10-01
Calculated
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Log P
-0.43
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)
1.17
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source
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Dissociation constant pKa) at 25 °C
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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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Volatilisation as max % of applied dose lost
From plant surface
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From soil surface
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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 (days) on plant matrix
Value
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Note
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Dissipation rate RL₅₀ (days) 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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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
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Soil adsorption and mobility
Property
Value
Source; quality score; and other information
Interpretation
Linear
Kd (mL g⁻¹)
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Koc (mL g⁻¹)
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Notes and range
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Freundlich
Kf (mL g⁻¹)
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Kfoc (mL g⁻¹)
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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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Photochemical oxidative DT₅₀ (hrs) as indicator of long-range air transport risk
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Bio-concentration factor
BCF (l kg⁻¹)
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CT₅₀ (days)
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Known soil metabolites
None
Known groundwater metabolites
None
Other known metabolites
Metabolite name and reference
Aliases
Formation medium / Rate
Estimated maximum occurrence fraction
Formic acid
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Air (oxidation)
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ECOTOXICOLOGY
Terrestrial ecotoxicology
Property
Value
Source; quality score; and other information
Interpretation
Mammals - Acute oral LD₅₀ (mg kg⁻¹)
> 550
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source
Rat
Moderate
Mammals - Short term dietary NOEL
(mg kg⁻¹)
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(ppm diet)
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Mammals - Chronic 21d NOAEL (mg kg⁻¹ bw d⁻¹)
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Birds - Acute LD₅₀ (mg kg⁻¹)
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Birds - Short term dietary (LC₅₀/LD₅₀)
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Birds - Chronic 21d NOEL (mg kg⁻¹ bw d⁻¹)
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Earthworms - Acute 14 day LC₅₀ (mg kg⁻¹)
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Earthworms - Chronic NOEC, reproduction (mg kg⁻¹)
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Soil micro-organisms
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Collembola
Acute LC₅₀ (mg kg⁻¹)
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Chronic NOEC (mg kg⁻¹)
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Non-target plants
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Honeybees (Apis spp.)
Contact acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)
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Oral acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)
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Unknown mode acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)
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Chronic
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Bumblebees (Bombus spp.)
Contact acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)
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Oral acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)
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Mason bees (Osmia spp.)
Contact acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)
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-
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Oral acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)
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-
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Other bee species (1)
Acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg insect⁻¹)
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Mode of exposure
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Other bee species (2)
Acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg insect⁻¹)
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Mode of exposure
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Beneficial insects (Ladybirds)
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-
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Beneficial insects (Lacewings)
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Beneficial insects (Parasitic wasps)
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Beneficial insects (Predatory mites)
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Beneficial insects (Ground beetles)
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Aquatic ecotoxicology
Property
Value
Source; quality score; and other information
Interpretation
Temperate Freshwater Fish - Acute 96 hour LC₅₀ (mg l⁻¹)
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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Marine bivalves
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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)
> 550
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source
Rat
Moderate
Mammals - Dermal LD₅₀ (mg kg⁻¹ body weight)
-
-
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Mammals - Inhalation LC₅₀ (mg l⁻¹)
0.203
E3 E = Manufacturers safety data sheets 3 = Unverified data of known source
Rat
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Other Mammal toxicity endpoints
Intraperitoneal LD₅₀ = 425 mg kg⁻¹
A5 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 ) 5 = Verified data used for regulatory purposes
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
Warning:
Human health
