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Diss Factsheets
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EC number: 203-826-1 | CAS number: 111-02-4
- 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:
- 27.17 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- Oral
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Overall assessment factor (AF):
- 42.5
- Modified dose descriptor starting point:
- other: NAEC
- Value:
- 577.5 mg/m³
- Explanation for the modification of the dose descriptor starting point:
- NAEC: [(660/4) x 70)/10]; NOAEL = 660 mg/kg on rat (Channon, 1926); 4 = allometric scaling factor rat; 70 kg/bw= standard human body weight; 10 m^3/person= default human breathing volume for workers in 8 h.
- AF for dose response relationship:
- 1
- Justification:
- No scaling needed
- AF for differences in duration of exposure:
- 3.4
- Justification:
- * ERASM Project: lower factor found based on RepDose study (factor 3.4 instead of 6 from subacute to chronic exposure). ** In addition, the study duratios is 42 days instead of 28. Then it is proposed to start from the NOAEL of the 42-day study, but to apply a lower duration factor of 3,4 instead of 6.
- AF for interspecies differences (allometric scaling):
- 1
- Justification:
- No allometric scaling needed because the starting point (NAEC) has just been corrected for the human evaluation.
- AF for other interspecies differences:
- 2.5
- AF for intraspecies differences:
- 5
- Justification:
- Based on the surfactant effect on epithelial tissues and absence of systemic effects, differences within species are expected to be limited. Therefore informed assessment factors of 3 and 5 are proposed instead of ECHA default values of 5 and 10 for workers and general population.
- AF for the quality of the whole database:
- 1
- Justification:
- No GLP studies compliant, but many qualitative evaluations to support the end point
- AF for remaining uncertainties:
- 1
- Justification:
- 100% conservative adsorption for inhalative route for animal and human is assumed
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
- Most sensitive endpoint:
- acute toxicity
- Route of original study:
- By inhalation
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Workers - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 38.8 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):
- 170
- Modified dose descriptor starting point:
- NOAEL
- Value:
- 6 600 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
- Oral to dermal AF = 10
- AF for dose response relationship:
- 1
- Justification:
- No scaling needed
- AF for differences in duration of exposure:
- 3.4
- Justification:
- * ERASM Project: lower factor found based on RepDose study (factor 3.4 instead of 6 from subacute to chronic exposure). ** In addition, the study duratios is 42 days instead of 28. Then it is proposed to start from the NOAEL of the 42-day study, but to apply a lower duration factor of 3,4 instead of 6.
- AF for interspecies differences (allometric scaling):
- 4
- Justification:
- rat to human
- AF for other interspecies differences:
- 2.5
- AF for intraspecies differences:
- 5
- Justification:
- Workers
- AF for the quality of the whole database:
- 1
- Justification:
- No GLP studies compliant, but many qualitative evaluations to support the end point
- AF for remaining uncertainties:
- 1
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
- Most sensitive endpoint:
- acute toxicity
- Route of original study:
- Dermal
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
Workers - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- no hazard identified
Additional information - workers
General Population - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 6.8 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- Oral
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Overall assessment factor (AF):
- 85
- Modified dose descriptor starting point:
- other: NAEC
- Value:
- 577.5 mg/m³
- Explanation for the modification of the dose descriptor starting point:
- NAEC= ((660 /4) x 70) /20; NOAEL = 660 mg/kg on rat (Channon, 1926); 4 = allometric scaling factor rat; 70 kg/bw= standard human body weight; 20 m^3/person= default human breathing volume for general population 24h.
- AF for dose response relationship:
- 1
- Justification:
- No scaling needed
- AF for differences in duration of exposure:
- 3.4
- Justification:
- * ERASM Project: lower factor found based on RepDose study (factor 3.4 instead of 6 from subacute to chronic exposure). ** In addition, the study duratios is 42 days instead of 28. Then it is proposed to start from the NOAEL of the 42-day study, but to apply a lower duration factor of 3,4 instead of 6.
- AF for interspecies differences (allometric scaling):
- 1
- Justification:
- No allometric scaling needed because the starting point (NAEC) has just been corrected for the human evaluation.
- AF for other interspecies differences:
- 2.5
- AF for intraspecies differences:
- 10
- Justification:
- General population
- AF for the quality of the whole database:
- 1
- AF for remaining uncertainties:
- 1
- Justification:
- 100% adsorption for inhalative route for animal and human is assumed
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
General Population - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 19.4 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):
- 340
- Modified dose descriptor starting point:
- NOAEL
- Value:
- 6 600 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
- Oral to dermal AF = 10
- AF for dose response relationship:
- 1
- Justification:
- No scaling needed
- AF for differences in duration of exposure:
- 3.4
- Justification:
- * ERASM Project: lower factor found based on RepDose study (factor 3.4 instead of 6 from subacute to chronic exposure). ** In addition, the study duratios is 42 days instead of 28. Then it is proposed to start from the NOAEL of the 42-day study, but to apply a lower duration factor of 3,4 instead of 6.
- AF for interspecies differences (allometric scaling):
- 4
- Justification:
- Rat
- AF for other interspecies differences:
- 2.5
- AF for intraspecies differences:
- 10
- Justification:
- Based on the surfactant effect on epithelial tissues and absence of systemic effects, differences within species are expected to be limited. Therefore informed assessment factors of 3 and 5 are proposed instead of ECHA default values of 5 and 10 for workers and general population.
- AF for the quality of the whole database:
- 1
- Justification:
- No GLP studies compliant, but many qualitative evaluations to support the end point
- AF for remaining uncertainties:
- 1
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
- Most sensitive endpoint:
- acute toxicity
- Route of original study:
- Dermal
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
General Population - Hazard via oral route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 1.94 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):
- 340
- Modified dose descriptor starting point:
- NOAEL
- Value:
- 660 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
- No modification necessary
- AF for dose response relationship:
- 1
- Justification:
- No scaling needing
- AF for differences in duration of exposure:
- 3.4
- Justification:
- * ERASM Project: lower factor found based on RepDose study (factor 3.4 instead of 6 from subacute to chronic exposure). ** In addition, the study duratios is 42 days instead of 28. Then it is proposed to start from the NOAEL of the 42-day study, but to apply a lower duration factor of 3,4 instead of 6.
- AF for interspecies differences (allometric scaling):
- 4
- Justification:
- Rat to human
- AF for other interspecies differences:
- 2.5
- AF for intraspecies differences:
- 10
- Justification:
- General population
- AF for the quality of the whole database:
- 1
- Justification:
- Data on structural similar substances
- AF for remaining uncertainties:
- 1
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
- Most sensitive endpoint:
- acute toxicity
- Route of original study:
- Oral
DNEL related information
General Population - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- no hazard identified
Additional information - General Population
References
[1] Kroes R, Renwick AG,*, Feron V, Galli CL, Gibney M, Greim H,Guy RH, Lhuguenot JC, van de Sandt JJM. Application of the threshold of toxicological
concern (TTC) to the safety evaluation of cosmetic ingredients. Food and Chemical Toxicology 45 (2007) 2533–2562
[2] Bartek, M J ; Labudde, J A ; Maibach, H I. Skin permeability in vivo: comparison in rat, rabbit, pig and man.The Journal of investigative
dermatology, 1972, Vol.58(3), pp.114-23.
[3] SchenkL and Gunnar J. A Quantitative Comparison of the Safety Margins in the European Indicative Occupational Exposure Limits and the
Derived No-Effect Levels for Workers under REACH. Toxicological Sciences 2011, 12(12), 408-416.
[4] ERASM Project: Safety Factors under REACH (June 2012); publications in progress.
[5] Batke M, Escher S, Hoffmann-Doerr S, Melber C, Messinger H, Mangelsdorf I. Evaluation of time extrapolation factors based on the database RepDose. Toxicology Letters 205 (2011) 122– 129Information 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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.