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Diss Factsheets
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EC number: 206-022-9 | CAS number: 288-88-0
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Toxicological Summary
- Administrative data
- Workers - Hazard via inhalation route
- Workers - Hazard via dermal route
- Workers - Hazard for the eyes
- Additional information - workers
- General Population - Hazard via inhalation route
- General Population - Hazard via dermal route
- General Population - Hazard via oral route
- General Population - Hazard for the eyes
- Additional information - General Population
Administrative data
Workers - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 0.65 mg/m³
- Most sensitive endpoint:
- developmental toxicity / teratogenicity
- Route of original study:
- Oral
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Overall assessment factor (AF):
- 25
- Modified dose descriptor starting point:
- LOAEC
- Value:
- 16
- Explanation for the modification of the dose descriptor starting point:
- No inhalation repeated toxicity study available.
- AF for dose response relationship:
- 1
- AF for differences in duration of exposure:
- 2
- Justification:
- DNEL based on a 2 generation study.
- AF for interspecies differences (allometric scaling):
- 1
- Justification:
- Extrapolation from oral to inhalation
- AF for other interspecies differences:
- 2.5
- AF for intraspecies differences:
- 5
- AF for the quality of the whole database:
- 1
- AF for remaining uncertainties:
- 1
Acute/short term exposure
- Hazard assessment conclusion:
- insufficient hazard data available (further information necessary)
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- insufficient hazard data available (further information necessary)
Acute/short term exposure
- Hazard assessment conclusion:
- insufficient hazard data available (further information necessary)
DNEL related information
Workers - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 5.86 mg/kg bw/day
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- Oral
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Overall assessment factor (AF):
- 100
- Modified dose descriptor starting point:
- LOAEL
- Value:
- 16 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
No repeated dose toxicity study by dermal route is available. A
safety factor of 3 is used to derive the NOAEL from the LOAEL.
- AF for dose response relationship:
- 1
- AF for differences in duration of exposure:
- 2
- Justification:
- Based on the 2-generation study.
- AF for interspecies differences (allometric scaling):
- 4
- AF for other interspecies differences:
- 2.5
- AF for intraspecies differences:
- 5
- AF for the quality of the whole database:
- 1
- AF for remaining uncertainties:
- 1
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- insufficient hazard data available (further information necessary)
Acute/short term exposure
- Hazard assessment conclusion:
- low hazard (no threshold derived)
Workers - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- low hazard (no threshold derived)
Additional information - workers
- Corrected dermal NOAEL, route = oral NOAEL x (ABSoral-rat/ABSderm-rat) x (ABSderm-rat/ ABSderm-human)
- = oral NOAEL x (ABSoral-rat/ABSderm-human)
- Corrected dermal LOAEL = 16 x 100/2.73 =586 mg/kg/day
WORKERS /DNELs Long-term exposure - systemic effects
Key study for DNELs calculation:
In the two-generation reproductive toxicity study reported in the US EPA dossier, rats (30/sex/dose) were exposed to 1,2,4-triazole continuously via the feed at nominal concentrations of 0, 250, 500 and 3000 ppm(US EPA HPV 2009, Pesticide fact sheet 2006)*.
In this two-generation study, there were no test substance-related effects on food consumption or clinical signs effects in either generation at any dietary level.
However, 1,2,4-triazole produced evidence of toxicity in P-generation animals at a dietary level of 3,000 ppm (188.6 and 217.9 mg/kg/day for males and females, respectively), including reduced fertility and neuropathology.
In F1-generation: the only evidence of toxicity at lower dietary levels of 250 and 500 ppm (16 and 32 mg/kg bw/d) was slightly reduced body weight in F1- males. This effect was observed at 500 ppm (37.5 mg/kg bw/d) in F1-females.
The combined (male and female) F2-pup body weights for the 250- and 500-ppm dietary groups were significantly decreased from control and are considered to be due to the incidental difference in the time of delivery and not exposure to the test substance.
Based on the slight decrease in body weight in the F1-males, the LOAEL is 16 mg/kg bw/d (it’s a smallest tested concentration). It’s the only observed effect.
Based on the marked reduction in fertility in P-generation animals, the reproductive (fertility) NOAEL is 34.4 mg/kg bw/day (500 ppm) and the LOAEL for this endpoint is 231.7 mg/kg bw/day (3000 ppm).
The critical effect was the decrease of body weight (-4.38% to –6.38% compared to control) in males F1 generation, therefore the LOAEL was 16.0 mg/kg bw/d (250 ppm).
In the Pesticide dossier(Pesticide fact sheet 2006), the same LOAEL (16.0 mg/kg bw/d) was used to calculate the Chronic Reference dose (cRfD).
1 Dermal DNEL
Step 1) Relevant dose-descriptor:LOAEL, rat = 16.0 mg/kg bw/d.
We have selected the Lowest Adverse Effect Level (LOAEL) of 16.0 mg/kg bw/d based on theslightdecrease in body weight in males (F1-generation) :decrease of 4.38 to 6.38% compared to control
Step 2) Modification of starting point:
* Correction for absorption difference between rat and human, and between dermal and oral absorption: The results of a recent in vitro dermal absorption study revealed an absorption of 2.73 % though human skin. As no available data is reported for oral absorption in rats, the oral aborption is considered to be 100 %
Step 3) Assessment factors:
*LOAEL to NOEL: 1 : An additional safety factor of 1 (instead of 3) is proposed for LOAEL to NOAEL conversion. According to the guidance on information requirements and chemical safety assessement (Chapter R8): The size of an assessment effect factor should take into account [...] the extent and severity of the effects seen at the LOAEL.
* Interspecies : 4 x 2.5= 10
* Intraspecies : 5(factor for workers)
* Exposure duration : 2 (subchronic to chronic exposure)
* Quality of database : 1
* Dose response: 1 (LOAEL > NOAEL)
AF total = 3x 10x5x2x1x1 = 100
Step 4) DNEL calculation:
DNEL value = 586 mg/kg/day/100= 5.86 mg/kg
DNEL Long-term Dermal value based on LOAEL(oral) is 5.86 mg/kg bw
2 Inhalation DNEL
Step 1) Relevant dose-descriptor:LOAEL, rat = 16.0 mg/kg bw/d
Step 2) Modification of starting point:
* Correction for absorption difference between rat and human, and between inhalation and oral absorption:No available data is reported for oral and inhalation absorption, the oral and inhalation absorptions are therefore estimated to 100%.The correction factor is 1.
* Correction of respiratory volume for relevant duration:For 8h of exposure, the respiratory volume of humans is 6.7m3/ person, and the respiratory volume light activity for worker (8h exposure) is 10 m3/person.The correction factor is 6.7/10.
* Correction or exposure duration in study (24h/d, 7d/wk) to default worker exposure (8h/d, 5d/wk):The correction factor is 24/8 x 7/5.
Step 3) Assessment factors:
* Interspecies: 2.5
* Intraspecies : 5(factor for workers)
* Exposure duration : 2 (subchronic to chronic exposure)
* Dose response: 1 (LOAEL > NOAEL)
* Quality of database: 1
AF total = 2.5x5x2x1x1 = 25
Step 4) DNEL calculation:
DNEL value = 16.0 x (6.7/10 x 24/8 x 7/5) / 25 = 0.65 mg/m3
DNEL Long-term Inhalation value based on LOAEL(oral) is 0.65 mg/m3
*Bibliographie :
-US EPA HPV Challenge program, 1H-1,2,4-triazole (TA) Cas number 288-88-0, July 2009
-1,2,4-Triazole, Triazole Alanine, Triazole Acetic Acid: Human Health Aggregate Risk Assessment in Support of Reregistration and Registration Actions for Triazole-derivative Fungicide Compounds. US EPA, office of prevention, pesticides and toxic substances, February 7, 2006
General Population - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- exposure based waiving
Acute/short term exposure
- Hazard assessment conclusion:
- exposure based waiving
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- exposure based waiving
Acute/short term exposure
- Hazard assessment conclusion:
- exposure based waiving
DNEL related information
General Population - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- exposure based waiving
Acute/short term exposure
- Hazard assessment conclusion:
- exposure based waiving
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- exposure based waiving
Acute/short term exposure
- Hazard assessment conclusion:
- exposure based waiving
General Population - Hazard via oral route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 0.08 mg/kg bw/day
- Most sensitive endpoint:
- developmental toxicity / teratogenicity
- Route of original study:
- Oral
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Overall assessment factor (AF):
- 200
- Modified dose descriptor starting point:
- LOAEL
- Value:
- 16 mg/kg bw/day
- AF for dose response relationship:
- 1
- AF for differences in duration of exposure:
- 2
- Justification:
- subchronic to chronic
- AF for interspecies differences (allometric scaling):
- 4
- AF for other interspecies differences:
- 2.5
- AF for intraspecies differences:
- 10
- AF for the quality of the whole database:
- 1
- AF for remaining uncertainties:
- 1
Acute/short term exposure
- Hazard assessment conclusion:
- exposure based waiving
DNEL related information
General Population - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- low hazard (no threshold derived)
Additional information - General Population
General population
Key study for DNELs calculation:
In the two-generation reproductive toxicity study reported in the US EPA dossier, rats (30/sex/dose) were exposed to 1,2,4-triazole continuously via the feed at nominal concentrations of 0, 250, 500 and 3000 ppm(US EPA HPV 2009, Pesticide fact sheet 2006)*.
In this two-generation study, there were no test substance-related effects on food consumption or clinical signs effects in either generation at any dietary level.
However, 1,2,4-triazole produced evidence of toxicity in P-generation animals at a dietary level of 3,000 ppm (188.6 and 217.9 mg/kg/day for males and females, respectively), including reduced fertility and neuropathology.
In F1-generation: the only evidence of toxicity at lower dietary levels of 250 and 500 ppm (16 and 32 mg/kg bw/d) was slightly reduced body weight in F1- males. This effect was observed at 500 ppm (37.5 mg/kg bw/d) in F1-females.
The combined (male and female) F2-pup body weights for the 250- and 500-ppm dietary groups were significantly decreased from control and are considered to be due to the incidental difference in the time of delivery and not exposure to the test substance.
Based on the slight decrease in body weight in the F1-males, the LOAEL is 16 mg/kg bw/d (it’s a smallest tested concentration). It’s the only observed effect.
Based on the marked reduction in fertility in P-generation animals, the reproductive (fertility) NOAEL is 34.4 mg/kg bw/day (500 ppm) and the LOAEL for this endpoint is 231.7 mg/kg bw/day (3000 ppm).
The critical effect was the decrease of body weight (-4.38% to –6.38% compared to control) in males F1 generation, therefore the LOAEL was 16.0 mg/kg bw/d (250 ppm).
In the Pesticide dossier(Pesticide fact sheet 2006), the same LOAEL (16.0 mg/kg bw/d) was used to calculate the Chronic Reference dose (cRfD).
Step 1) Relevant dose-descriptor: LOAEL, rat = 16.0 mg/kg bw/d.
Step 2: Modification of the starting point: No
No difference absorption are expected between rats and humans.
Step 3: Assessment factors:
-LOAEL to NOAEL= 1 An additional safety factor of 1 (instead of 3) is proposed for LOAEL to NOAEL conversion. According to the guidance on information requirements and chemical safety assessement (Chapter R8): The size of an assessment effect factor should take into account [...] the extent and severity of the effects seen at the LOAEL.
- Interspecies differences: an allometric scaling factor of 4(standard for rats) is applied because no route-to-route extrapolation is performed. A factor of 2.5to correct for differences other than differences in metabolic rate is also applied.
- Intraspecies differences: the default assessment factor of 10 is applied.
- Differences in exposure duration: as the exposure in rats was around 18 months (2 generation study) a factor of 2 for subacute-to-chronic extrapolation is applied.
- Dose-response relationship: a factor of 1 is applied due to the use of a NOAEL as dose descriptor and the low toxicity of the test substance.
- Quality of whole database: 1
- Global assessment factor: 1x4 x 2.5 x 10 x 2 x 1 x 1 =200
Step 4: DNEL derivation:
General population DNEL (long term, systemic effects) = 16/ 200 = 0.08 mg/kg bw/day
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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