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Diss Factsheets
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EC number: 920-008-6 | CAS number: -
- 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:
- 330 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- By inhalation
DNEL related information
- DNEL derivation method:
- other: ECETOC
- Overall assessment factor (AF):
- 6
- Dose descriptor starting point:
- NOAEC
- Value:
- 3 950 mg/m³
- Modified dose descriptor starting point:
- NOAEC
- Value:
- 1 985 mg/m³
- Explanation for the modification of the dose descriptor starting point:
Dose descriptor starting value of 3950 mg/m3 was modified to account for duration adjustment and differences in breathing volume in rats and humans with light worker activity.
Modified dose = 3950 mg/m3 x (6h/8h) x (6.7 m3 / 10 m3).
- AF for dose response relationship:
- 1
- Justification:
- Point of departure is based on a NOAEC
- AF for differences in duration of exposure:
- 2
- Justification:
- Factor of 2 is appropriate when extrapolating from a subchronic to a chronic duration of exposure [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
- AF for interspecies differences (allometric scaling):
- 1
- Justification:
- Allometric scaling is not appropriate when extrapolating inhalation to inhalation exposure [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
- AF for intraspecies differences:
- 3
- Justification:
- Worker population [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
Acute/short term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 570 mg/m³
- Most sensitive endpoint:
- neurotoxicity
- Route of original study:
- By inhalation
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Overall assessment factor (AF):
- 1
- Dose descriptor starting point:
- NOAEC
- Value:
- 570 mg/m³
- Explanation for the modification of the dose descriptor starting point:
Since the study was conducted with human volunteers exposed for 4 hours, no modification of the dose descriptor was considered to be necessary.
- AF for dose response relationship:
- 1
- Justification:
- NOAEC Point of departure is based on a NOAEC
- AF for intraspecies differences:
- 1
- Justification:
- 12 healthy male volunteers were utilized in the study. The healthy subjects are representative of a healthy worker population. The critical endpoint for acute exposures to hydrocarbon solvents is transient nervous system depression. This endpoint is not expected to vary significantly within the healthy worker population.
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:
- 21 mg/kg bw/day
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- Dermal
DNEL related information
- DNEL derivation method:
- other: ECETOC
- Overall assessment factor (AF):
- 24
- Dose descriptor starting point:
- NOAEL
- Value:
- 495 mg/kg bw/day
- Modified dose descriptor starting point:
- NOAEL
- Value:
- 495 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
Although human skin is considered to be less permeable than rat skin, a species-specific absorption factor was not used in the rat to human dermal DNEL calculations. Also 100% absorption through dermal application was assumed.
- AF for dose response relationship:
- 1
- Justification:
- Point of departure is based on a NOAEL
- AF for differences in duration of exposure:
- 2
- Justification:
- AF of 2 is appropriate when extrapolating from subchronic to chronic duration [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
- AF for interspecies differences (allometric scaling):
- 4
- Justification:
- Allometric scaling (rat to humans) is appropriate when extrapolating from dermal exposures [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
- AF for intraspecies differences:
- 3
- Justification:
- Worker population [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
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
Workers - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- no hazard identified
Additional information - workers
The potential exposure to the test material indicates that long-term exposure DNELs need to be derived for workers and for the general population. No acute toxicity was noted in any of the toxicological studies conducted. As noted in existing human volunteer studies, DNELs derived for chronic exposures are typically lower than those calculated for acute exposures and would therefore be protective of human for both the acute and chronic exposures. Dermal and inhalation are the relevant routes of exposure. Aspiration is a potential hazard, but a DNEL calculation is not appropriate for an aspiration hazard.In instances where stable aerosol formation is expected, a value of 10 mg/m3 will be used as an operational control limit for inhalation exposure.Workers are expected to have infrequent and short-term exposures; however, for calculation of the DNEL for REACH purposes it is assumed that workers have maximal repeated exposure for 8 hr/day for 5 day/wk.
General Population - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 71 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- By inhalation
DNEL related information
- DNEL derivation method:
- other: ECETOC
- Overall assessment factor (AF):
- 10
- Dose descriptor starting point:
- NOAEC
- Value:
- 3 950 mg/m³
- Modified dose descriptor starting point:
- NOAEC
- Value:
- 705 mg/m³
- Explanation for the modification of the dose descriptor starting point:
Dose descriptor starting value of 3950 mg/m3 was modified to account for duration adjustment.
Modified dose = 3950 mg/m3 x (6h/24h) x (5 days/7 days).
- AF for dose response relationship:
- 1
- Justification:
- Point of departure is based on a NOAEC
- AF for differences in duration of exposure:
- 2
- Justification:
- AF of 2 is appropriate when extrapolating from subchronic to chronic duration [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
- AF for interspecies differences (allometric scaling):
- 1
- Justification:
- Allometric scaling is not appropriate when extrapolating dermal to dermal exposure [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
- AF for intraspecies differences:
- 5
- Justification:
- General Population [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
Acute/short term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 570 mg/m³
- Most sensitive endpoint:
- neurotoxicity
- Route of original study:
- By inhalation
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Overall assessment factor (AF):
- 1
- Dose descriptor starting point:
- NOAEC
- Value:
- 570 mg/m³
- Explanation for the modification of the dose descriptor starting point:
Since the study was conducted with human volunteers exposed for 4 hours, no modification of the dose descriptor was considered to be necessary.
- AF for dose response relationship:
- 1
- Justification:
- Point of departure is based on a NOAEC
- AF for intraspecies differences:
- 1
- Justification:
- 12 healthy male volunteers were utilized in the study. The critical endpoint for acute exposures to hydrocarbon solvents is transient nervous system depression. This endpoint is not expected to vary significantly within the general population.
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:
- 12 mg/kg bw/day
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- Dermal
DNEL related information
- DNEL derivation method:
- other: ECETOC
- Overall assessment factor (AF):
- 40
- Dose descriptor starting point:
- NOAEL
- Value:
- 495 mg/kg bw/day
- Modified dose descriptor starting point:
- NOAEL
- Value:
- 495 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
Although human skin is considered to be less permeable than rat skin, a species-specific absorption factor was not used in the rat to human dermal DNEL calculations. Also 100% absorption through dermal application was assumed.
- AF for dose response relationship:
- 1
- Justification:
- Point of departure is based on a NOAEC
- AF for differences in duration of exposure:
- 2
- Justification:
- AF of 2 is appropriate when extrapolating from subchronic to chronic duration [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
- AF for interspecies differences (allometric scaling):
- 4
- Justification:
- Allometric scaling (rat to humans) is appropriate when extrapolating from oral exposures [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
- AF for intraspecies differences:
- 5
- Justification:
- General population [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
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
General Population - Hazard via oral route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 21 mg/kg bw/day
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- By inhalation
DNEL related information
- DNEL derivation method:
- other: ECETOC
- Overall assessment factor (AF):
- 40
- Dose descriptor starting point:
- NOAEC
- Value:
- 3 950
- Modified dose descriptor starting point:
- NOAEL
- Value:
- 818.2 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
No long term or subchronic oral toxicity data on C9 -C14 aliphatics (2-25% aromatics) was available. Hence, an oral DNEL for general population was obtained by route to route exptrapolation from the available inhalation toxicity data. The NOAEC for a 90 -day exposure to C9 -C14 aliphatics (2 -25% aromatics) in rats was 690 ppm (3950 mg/m3). This value was converted to an oral NOAEL using the ECHA guidance. First the rat inhalation NOAEC was converted to a rat daily oral dose/NOAEL, taking into account the rat 6 -hr breathing volume/kg bw (0.29 m3/kg bw) and the difference in duration of exposure:
Rat oral NOAEL = 3950 mg/m3 x 0.29 mg/m3 x (5 days/7 days) = 818.2 mg/kg
- AF for dose response relationship:
- 1
- Justification:
- Point of departure is based on a NOAEC
- AF for differences in duration of exposure:
- 2
- Justification:
- AF of 2 is appropriate when extrapolating from subchronic to chronic duration [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
- AF for interspecies differences (allometric scaling):
- 4
- Justification:
- Allometric scaling (rat to humans) is appropriate when extrapolating from oral exposures [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
- AF for intraspecies differences:
- 5
- Justification:
- General population [ECETOC. (2003). Derivation of Assessment Factors for Human Health Risk Assessment. Technical Report No. 86].
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
General Population - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- no hazard identified
Additional information - General Population
The potential exposure to the test material indicates that long-term exposure DNELs need to be derived for general population. No acute toxicity was noted in any of the toxicological studies conducted. Additionally, DNELs derived for chronic exposures are typically lower than those calculated for acute exposures and would therefore be protective of human for both the acute and chronic exposures. Dermal and inhalation are the relevant routes of exposure. An oral DNEL was calculated for use in an indirect exposure assessment; the oral route is not expected to be a significant exposure route. Aspiration is a potential hazard, but a DNEL calculation is not appropriate for an aspiration hazard. Consumers in the general population are expected to have infrequent and short-term exposures. However, for calculation of DNELs for REACH, it is assumed that consumers have a maximal repeated dose for 24 hr/day for 7 day/wk.
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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