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Diss Factsheets
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EC number: 443-870-0 | CAS number: 163520-33-0
- 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:
- 1.13 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- Oral
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Dose descriptor starting point:
- NOAEL
- Value:
- 8 mg/kg bw/day
- Modified dose descriptor starting point:
- NOAEC
- Value:
- 14.11 mg/m³
- Explanation for the modification of the dose descriptor starting point:
Inhalation N(L)OAEC= oral N(L)OAEL*(1/0.38 m³/kg bw/d)*0.67*1
In the ECHA Guidance a factor of 2 is suggested for the extrapolation from oral to inhalation absorption. On the contrary, the Technical guidance document on risk assessment in support of Commission directive 93/67/EEC, 2003 appendix IV A and B gives a number of physico-chemical properties that normally determine oral, inhalation and dermal absorption. These parameters include molecular weight, log Kow, pKa values and for inhalation also particle size distribution, vapour pressure etc. Molecules with a molecular weight < 500 and a log KOW between 0 and 4 can be assumed to be well absorbed equivalently by the oral and inhalation route. Oral absorption may be reduced for acids and bases depending on their pKa value and their possibility of absorption in the GI tract. More lipophilic substances may be better absorbed in the GI tract due to the solubilisation with bile acids and thus oral absorption may be higher than inhalation absorption. The consideration of physico-chemical parameters should be performed before using default assumptions. In an acute inhalation study no mortalities occurred up to the limit dose whereas mortality was observed in the acute oral toxicity study. Unless valid data suggest that inhalation leads to higher absorption than oral ingestion, equal absorption will be assumed when extrapolating from oral to inhalation route.
- Justification:
- The dose descriptor starting point is a NOAEL
- Justification:
- The DNEL is based on a chronic study.
- Justification:
- Allometric scaling not necessary for inhalation because it was included in the modification of the dose descriptor
- Justification:
- Default value according to ECHA REACh Guidance
- Justification:
- Default value for workers according to ECHA REACh Guidance
- Justification:
- The DNEL is based on a high-quality study.
- Justification:
- No remaining uncertainties.
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- hazard unknown but no further hazard information necessary as no exposure expected
Acute/short term exposure
- Hazard assessment conclusion:
- hazard unknown but no further hazard information necessary as no exposure expected
DNEL related information
Workers - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 3.333 mg/kg bw/day
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- Dermal
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Dose descriptor starting point:
- NOAEL
- Value:
- 1 000 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
- No route-to-route extrapolation needed.
- Justification:
- The dose descriptor starting point is based on a NOAEL.
- Justification:
- The DNEL is based on a subacute study.
- Justification:
- Rat to human
- Justification:
- Default value according to ECHA REACh Guidance
- Justification:
- Default value for workers according to ECHA REACh Guidance
- Justification:
- The DNEL is based on a high-quality study.
- Justification:
- No remaining uncertainties.
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- sensitisation (skin)
Acute/short term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- sensitisation (skin)
Workers - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- no hazard identified
Additional information - workers
No DNELs have been derived for systemic effects after short-term dermal and inhalation exposure of the test substance for workers, as it is assumed that the assessment of hazard is sufficiently covered by deriving the respective DNELs for long-term exposure. Even though a local NOAEL was observed in the dermal 28-day study it was not considered in the hazard assessment as the existing sensitising properties of the registered substance were not addressed in this study. No threshold can be derived for sensitisation.
Reliable studies with dietary administration of the test substance have been conducted in mice, rats and dogs on a subacute to chronic basis. For risk assessment the chronic oral studies are considered.
One of the two chronic studies was carried out in dogs. For 12 months 4 animals/sex/group received dose levels of 20, 100 and 700 ppm (corresponding to 0.7, 3.5 and 24 mg/kg bw/day for combined sexes). The kidney as target organ showed a tubular increase in the incidence and severity of vacuolation in the highest dose group. Hence, the NO(A)EL was set to 3.5 mg/kg bw/day.
In the second chronic study 70 rats/sex/dose received 20, 200, 2000 and 4000 ppm (corresponding to 1.0, 10, 101 and 210 mg/kg bw/day for combined sexes) continuously for 104 weeks. This combined chronic/carcinogenicity study showed an increased incidence of ketones in the urine as well as decreased absolute and relative kidney and increased relative liver weights. Hence, the NO(A)EL was set at 8 and 12 mg/kg bw/day for males and females, respectively.
Dogs are the most sensitive species among all species tested, providing the lowest NOAELs in subacute, subchronic and chronic studies. Due to the fact that dog studies are less covered from a statistical point of view due to the amount of animals used, the second chronic study with rats is considered as well. Taken into account that the scaling factor for rat is 4 instead of 1.4 for the dog both NOAELs result in the same NOAEL (3.5/1.4 = 2.5 mg/kg bw/day vs. 10/4 = 2.5 mg/kg bw/day).
Hence, for a conservative approach, the NOAEL of the chronic rat study (i.e. 8 mg/kg bw/day) was chosen for the risk assessment.
Regarding the dermal route one subacute study was conducted in rats. In a 28 day-study, the test substance was administered to 5 animals/sex/group at dose levels of 10, 100 and 1000 mg/kg bw/day for 5 days/week. The study was performed in accordance with OECD 410 and revealed a systemic NOAEL of 1000 mg/kg bw/day and a local NOAEL of 0.5 mg/cm²/day (calculated as follows 10 mg/kg bw*0.2 kg bw rat/4 cm²).
Determination of corrected starting point for DNEL derivation
Repeated dose toxicity – systemic effects – inhalation route – worker:
The DNEL for systemic effects via the inhalation route for worker is determined on the basis of route-to-route extrapolation from the OECD 453 oral study on the test substance, which established a NOAEL of 8 mg/kg bw day for males. In contrast to the recommendations of the ECHA Guidance, a factor of 1 (equal absorption of 100% assumed for the oral and the inhalative route for animals and humans) was included for the extrapolation from oral to inhalation absorption, as there is no valid data suggesting that inhalation leads to higher absorption than oral ingestion (recommendation of the VCI Working group "Toxicology", 2008). Molecules with a molecular weight <500 and a log Kow between 0 and 4 can be assumed to be well absorbed equivalently by the oral and inhalation route. Oral absorption may be reduced for acids and bases depending on their pKa value and their electric charge in the GI tract. More lipophilic substances may be better absorbed in the GI tract due to solubilisation with bile acids, and thus oral absorption may be higher than inhalation absorption (VCI Working group "Toxicology", 2008). Unless valid data suggest that inhalation leads to higher absorption than oral ingestion, equal absorption will be assumed when extrapolating from oral to inhalation route. The following corrections were made:
No correction for relative absorption oral vs. inhalation: 1; Correction for respiratory volume (standard breathing volume for the rat, 8 h): 0.38 m³/kg; Correction for respiratory volume (worker, light physical activity): 6.7 m³/day /10 m³/day
Therefore the corrected NOAEC for repeated dose systemic effects via the inhalation route is: 8 mg/kg bw/day / 0.38 m³/kg bw × 6.7 m³ /10 m³ × 1= 14.11 mg/m³
Repeated dose toxicity – systemic effects – dermal route – worker:
The DNEL for systemic effects via the dermal route for worker is determined from the OECD 410 dermal study on the test substance, which established a NOAEL of 1000 mg/kg bw/day. No corrections were made to the NOAEL.
General Population - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 0.28 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- Oral
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Dose descriptor starting point:
- NOAEL
- Value:
- 8 mg/kg bw/day
- Modified dose descriptor starting point:
- NOAEC
- Value:
- 6.96 mg/m³
- Explanation for the modification of the dose descriptor starting point:
Inhalation NOAEC= oral NOAEL*(1/1.15 m3/kg/d)*1
In the ECHA Guidance a factor of 2 is suggested for the extrapolation from oral to inhalation absorption. On the contrary, the Technical guidance document on risk assessment in support of Commission directive 93/67/EEC, 2003 appendix IV A and B gives a number of physico-chemical properties that normally determine oral, inhalation and dermal absorption. These parameters include molecular weight, log Kow, pKa values and for inhalation also particle size distribution, vapour pressure etc. Molecules with a molecular weight < 500 and a log KOW between 0 and 4 can be assumed to be well absorbed equivalently by the oral and inhalation route. Oral absorption may be reduced for acids and bases depending on their pKa value and their possibility of absorption in the GI tract. More lipophilic substances may be better absorbed in the GI tract due to the solubilisation with bile acids and thus oral absorption may be higher than inhalation absorption. The consideration of physico-chemical parameters should be performed before using default assumptions. In an acute inhalation study no mortalities occurred up to the limit dose whereas mortality was observed in the acute oral toxicity study. Unless valid data suggest that inhalation leads to higher absorption than oral ingestion, equal absorption will be assumed when extrapolating from oral to inhalation route.
- Justification:
- The dose descriptor starting point is a NOAEL
- Justification:
- The DNEL is based on a chronic study.
- Justification:
- Allometric scaling not necessary for inhalation because it was included in the modification of the dose descriptor
- Justification:
- Default value according to ECHA REACh Guidance
- Justification:
- Default value for general population according to ECHA REACh Guidance
- Justification:
- The DNEL is based on a high-quality study.
- Justification:
- No remaining uncertainties.
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- hazard unknown but no further hazard information necessary as no exposure expected
Acute/short term exposure
- Hazard assessment conclusion:
- hazard unknown but no further hazard information necessary as no exposure expected
DNEL related information
General Population - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 1.67 mg/kg bw/day
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- Dermal
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Dose descriptor starting point:
- NOAEL
- Value:
- 1 000 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
- No route-to-route extrapolation needed.
- Justification:
- The dose descriptor starting point is based on a NOAEL.
- Justification:
- The DNEL is based on a subacute study.
- Justification:
- Rat to human
- Justification:
- Default value according to ECHA REACh Guidance
- Justification:
- Default value for general population according to ECHA REACh Guidance
- Justification:
- The DNEL is based on a high-quality study.
- Justification:
- No remaining uncertainties.
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- sensitisation (skin)
Acute/short term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- sensitisation (skin)
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:
- repeated dose toxicity
- Route of original study:
- Oral
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Dose descriptor starting point:
- NOAEL
- Value:
- 8 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
- No route-to-route extrapolation needed.
- Justification:
- The dose descriptor starting point is based on a NOAEL.
- Justification:
- The DNEL is based on a chronic study.
- Justification:
- Rat to human
- Justification:
- Default value according to ECHA REACh Guidance
- Justification:
- Default value for general population according to ECHA REACh Guidance
- Justification:
- The DNEL is based on a high-quality study.
- Justification:
- No remaining uncertainties.
Acute/short term exposure
- Hazard assessment conclusion:
- low hazard (no threshold derived)
DNEL related information
General Population - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- no hazard identified
Additional information - General Population
No DNELs have been derived for systemic effects after short-term dermal and inhalation exposure of the test substance for the general population, as it is assumed that the assessment of hazard is sufficiently covered by deriving the respective DNELs for long-term exposure. Even though a local NOAEL was observed in a dermal 28-day study it was not considered in the hazard assessment as the existing sensitising properties of the registered substance were not addressed in this study. No threshold can be derived for sensitisation.
Reliable studies with dietary administration of isoxadiphen-ethyl have been conducted in mice, rats and dogs on a subacute to chronic basis. For risk assessment the chronic oral studies are considered.
One of the two chronic studies was carried out in dogs. For 12 months 4 animals/sex/group received dose levels of 20, 100 and 700 ppm (corresponding to 0.7, 3.5 and 24 mg/kg bw/day for combined sexes). The kidney as target organ showed a tubular increase in the incidence and severity of vacuolation in the highest dose group. Hence, the NO(A)EL was set to 3.5mg/kg bw/day.
In the second chronic study 70 rats/sex/dose received 20, 200, 2000 and 4000 ppm (corresponding to 1.0, 10, 101 and 210 mg/kg bw/day for combined sexes) continuously for 104 weeks. This combined chronic/carcinogenicity study showed an increased incidence of ketones in the urine as well as decreased absolute and relative kidney and increased relative liver weights. Hence, the NO(A)EL was set at 8 and 12 mg/kg bw/day for males and females, respectively.
Dogs are the most sensitive species among all species tested, providing the lowest NOAELs in subacute, subchronic and chronic studies. Due to the fact that dog studies are less covered from a statistical point of view due to the amount of animals used, the second chronic study with rats is considered as well. Taken into account that the scaling factor for rat is 4 instead of 1.4 for the dog both NOAELs result in the same NAEL (3.5/1.4 = 2.5 mg/kg bw/day vs. 10/4 = 2.5 mg/kg bw/day).
Hence, for a conservative approach, the NOAEL of the chronic rat study (i.e. 8 mg/kg bw/day) was chosen for the risk assessment.
Regarding the dermal route one subacute study was conducted in rats. In a 28 day-study, isoxadiphen-ethyl was administered to 5 animals/sex/group at dose levels of 10, 100 and 1000 mg/kg bw/day for 5 days/week. The study was performed in accordance with OECD 410 and revealed a systemic NOAEL of 1000 mg/kg bw/day and a local NOAEL of 0.5 mg/cm²/day (calculated as follows 10 mg/kg bw*0.2 kg bw rat/4 cm²).
Determination of corrected starting point for DNEL derivation
Repeated dose toxicity – systemic effects – inhalation route – general population:
The DNEL for systemic effects via the inhalation route for the general population is determined on the basis of route-to-route extrapolation from the OECD 453 oral study on isoxadiphen-ethyl, which established a NOAEL of 8 mg/kg bw day. In contrast to the recommendations of the ECHA Guidance, a factor of 1 (equal absorption of 100% assumed for the oral and the inhalative route for animals and humans) was included for the extrapolation from oral to inhalation absorption, as there is no valid data suggesting that inhalation leads to higher absorption than oral ingestion (recommendation of the VCI Working group "Toxicology", 2008). Molecules with a molecular weight <500 and a log Kow between 0 and 4 can be assumed to be well absorbed equivalently by the oral and inhalation route. Oral absorption may be reduced for acids and bases depending on their pKa value and their electric charge in the GI tract. More lipophilic substances may be better absorbed in the GI tract due to solubilisation with bile acids, and thus oral absorption may be higher than inhalation absorption (VCI Working group "Toxicology", 2008). Unless valid data suggest that inhalation leads to higher absorption than oral ingestion, equal absorption will be assumed when extrapolating from oral to inhalation route. The following corrections were made:
No correction for relative absorption oral vs. inhalation: 1
Correction for respiratory volume (standard breathing volume for the
rat, 24 h): 1.15m³/kg
Therefore the corrected NOAEC for repeated dose systemic effects via the inhalation route is:
8 mg/kg bw/day / 1.15 m³/kg bw = 6.96 mg/m³
Repeated dose toxicity – systemic effects – dermal route – general population:
The DNEL for systemic effects via the dermal route for worker is determined from the OECD 410 dermal study on isoxadiphen-ethyl, which established a NOAEL of 1000 mg/kg bw day. No corrections were made to the NOAEL.
Repeated dose toxicity – systemic effects – oral route – general population:
The DNEL for systemic effects via the oral route for the general population is determined from the OECD 453 oral study on isoxadiphen-ethyl, which established a NOAEL of 8 mg/kg bw day. No corrections were made to the NOAEL.
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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