Registration Dossier
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 225-590-9 | CAS number: 4948-15-6
Toxicological Summary
Administrative data
Workers - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 1.25 mg/m³
DNEL related information
- DNEL derivation method:
- other: The general exposure limit for inhalable dust was applied
Acute/short term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 1.25 mg/m³
DNEL related information
- DNEL derivation method:
- other: The general exposure limit for inhalable dust is applied
Local effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 1.25 mg/m³
DNEL related information
- DNEL derivation method:
- other: The general exposure limit for inhalable dust is applied
Acute/short term exposure
- Hazard assessment conclusion:
- hazard unknown (no 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:
- 33.3 mg/kg bw/day
- Route of original study:
- Oral
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Overall assessment factor (AF):
- 300
- Dose descriptor starting point:
- NOAEL
- Value:
- 1 000 mg/kg bw/day
- Modified dose descriptor starting point:
- NOAEL
- Value:
- 10 000 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
The dermal route is typically covered by oral route information in the absence of data for this administration route. Since no data on penetration through skin are available, the dermal absorption property is evaluated based on physico-chemical parameters. The test substance is practically insoluble in both water and organic solvents with a rather large molecular weight (Mw= 598). As a result, absorption via the dermal route is expected to be below 10%. This is taken into account by modifying the NOAEL with a factor of 10 (ECHA GD chapter R7c).
- AF for dose response relationship:
- 1
- Justification:
- The dose discriptor used was already a NOAEL.
- AF for differences in duration of exposure:
- 6
- Justification:
- Default value compensating for chronic studies by using sub-acute study values.
- AF for interspecies differences (allometric scaling):
- 4
- Justification:
- Default value extrapolating from rat to human.
- AF for other interspecies differences:
- 2.5
- Justification:
- Default value.
- AF for intraspecies differences:
- 5
- Justification:
- Default value used for workers.
- AF for the quality of the whole database:
- 1
- Justification:
- Reliable and adequate guideline study.
- AF for remaining uncertainties:
- 1
- Justification:
- The approach used for DNEL derivation is conservative. No further assessment factors are required.
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
Identification of relevant dose descriptor
The test substance belongs to a category of organic pigments that all share a similar chemical structure (see CSR for category justification). Within this category, several substances were selected for testing in repeated dose toxicity studies. None of these studies revealed adverse effects for any tested substance up to the highest doses tested. Based on these results, together with toxicokinetic considerations, it was concluded that the members of this category are not taken up by the body after oral ingestion and are therefore not systemically available. Nevertheless, as worst case assessment, DNELs for systemic effects were established. In the available 28-day and 90-day repeated dose studies performed with several category members, NOAELs ranging from 1000 mg/kg to 5000 mg/kg body weight were established (highest doses tested). Since the data obtained with individual category members were shared within the category, it was chosen to select the lowest NOAEL of 1000 mg/kg obtained after 28-day administration as common dose descriptor for every substance within the group. This value was therefore used as starting point to derive the DNELs.
General Population - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
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:
- 16.7 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):
- 600
- Dose descriptor starting point:
- NOAEL
- Value:
- 1 000 mg/kg bw/day
- Modified dose descriptor starting point:
- NOAEL
- Value:
- 10 000 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
The dermal route is typically covered by oral route information in the absence of data for this administration route. Since no data on penetration through skin are available, the dermal absorption property is evaluated based on physico-chemical parameters. The test substance is practically insoluble in both water and organic solvents with a rather large molecular weight (Mw= 598). As a result, absorption via the dermal route is expected to be below 10%. This is taken into account by modifying the NOAEL with a factor of 10 (ECHA GD chapter R7c).
- AF for dose response relationship:
- 1
- Justification:
- The dose discriptor used was already a NOAEL.
- AF for differences in duration of exposure:
- 6
- Justification:
- Default value compensating for chronic studies by using sub-acute study values.
- AF for interspecies differences (allometric scaling):
- 4
- Justification:
- Default value extrapolating from rat to human.
- AF for other interspecies differences:
- 2.5
- Justification:
- Default value
- AF for intraspecies differences:
- 10
- Justification:
- Default value for general population
- AF for the quality of the whole database:
- 1
- Justification:
- Reliable and adequate guideline study.
- AF for remaining uncertainties:
- 1
- Justification:
- The approach used for DNEL derivation is conservative. No further assessment factors are required.
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:
- 10 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
- Dose descriptor starting point:
- NOAEL
- Value:
- 1 000 mg/kg bw/day
- AF for dose response relationship:
- 1
- Justification:
- The dose discriptor used was already a NOAEL.
- AF for differences in duration of exposure:
- 6
- Justification:
- No time extrapolation was necessary.
- AF for interspecies differences (allometric scaling):
- 4
- Justification:
- Default value extrapolating from rat to human.
- AF for other interspecies differences:
- 2.5
- Justification:
- Default value
- AF for intraspecies differences:
- 10
- Justification:
- Default value for general population
- AF for the quality of the whole database:
- 1
- Justification:
- Reliable and adequate guideline study
- AF for remaining uncertainties:
- 1
- Justification:
- No remaining uncertainties
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
Identification of relevant dose descriptor
The dose descriptor chosen is the same as for workers (see above). The NOAEL of 1000 mg/kg was used as starting point to derive the DNELs.
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.
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.
Route: .live1