Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
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: 233-899-5 | CAS number: 10421-48-4
- 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:
- 12 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):
- 25
- Modified dose descriptor starting point:
- NOAEC
- Value:
- 304 mg/m³
- Explanation for the modification of the dose descriptor starting point:
- No inhalation data available. The oral NOAEL of 57 mg/kg bw/d (Fe) is equivalent to 246 mg/kg bw/d iron trinitrate. Correction for breathing rate (/0.38) and actviity level (*6.7/10) and the extent of oral absorption (70%) and inhalation absorption (100% assumed) results in an inhalation NOAEC of 304 mg/m3.
- AF for dose response relationship:
- 1
- Justification:
- default value
- AF for differences in duration of exposure:
- 2
- Justification:
- extrapolation from a sub-chronic study to chronic exposure
- AF for interspecies differences (allometric scaling):
- 1
- Justification:
- not required - already accounted for
- AF for other interspecies differences:
- 2.5
- Justification:
- default value
- AF for intraspecies differences:
- 5
- Justification:
- default value for workers
- AF for the quality of the whole database:
- 1
- Justification:
- default value: reliable database
- AF for remaining uncertainties:
- 1
- Justification:
- default value: no other 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)
Acute/short term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
DNEL related information
Workers - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 17 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:
- NOAEL
- Value:
- 1 722 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
- Data for repeated dermal exposure are not available. The oral NOAEL of 57 mg/kg bw/d (Fe) is equivalent to 246 mg/kg bw/d iron trinitrate. Correction for the extent of oral absorption (70%) and dermal absorption (10%) gives a dermal NOAEL of 1722 mg/kg bw/d.
- AF for dose response relationship:
- 1
- Justification:
- default value
- AF for differences in duration of exposure:
- 2
- Justification:
- extrapolation from a sub-chronic study to chronic exposure
- AF for interspecies differences (allometric scaling):
- 4
- Justification:
- standard value (rat study)
- AF for other interspecies differences:
- 2.5
- Justification:
- default value
- AF for intraspecies differences:
- 5
- Justification:
- default value: workers
- AF for the quality of the whole database:
- 1
- Justification:
- default value: reliable database
- AF for remaining uncertainties:
- 1
- Justification:
- default value: no other 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:
- skin irritation/corrosion
Acute/short term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- skin irritation/corrosion
Workers - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
Additional information - workers
The relevant starting point for the derivation of systemic DNEL values is the oral NOAEL of 57 mg/kg bw/d (Fe) from a 90 -day oral toxicity study with ferric chloride.
The oral NOAEL of 57 mg/kg bw/d (Fe) is equivalent to 246 mg/kg bw/d iron trinitrate. Correction for breathing rate (/0.38) and activity level (*6.7/10) and the extent of oral absorption (70%) and inhalation absorption (100% assumed) results in an inhalation NOAEC of 304 mg/m3. A long-term systemic inhalation DNEL for workers of 12 mg/m3 is derived following the application of an overall assessment factor of 25, according to REACH guidance.
A short-term systemic inhalation DNEL for workers is not derived in the absence of any identified acute systemic hazard.
Local inhalation DNEL values for workers are not derived. The substance is of low pH and is therefore considered to be a potential respiratory irritant. Inhalation exposure should be controlled through the use of appropriate RMMs (engineering controls and/or RPE) where significant exposure is possible.
Correction of the oral NOAEL of 246 mg/kg bw/d for the extent of oral absorption (70%) and dermal absorption (10%) gives a dermal NOAEL of 1722 mg/kg bw/d. Application of an overall assessment factor of 100, according to REACH guidance gives a long-term systemic dermal DNEL for workers of 17 mg/kg bw/d.
A short-term systemic dermal DNEL for workers is not derived in the absence of any identified acute systemic hazard.
Local dermal DNEL values for workers are not derived. Skin corrosivity is assumed based on the low pH of the substance. Dermal exposure should therefore be minimised.
General Population - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 3 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):
- 50
- Modified dose descriptor starting point:
- NOAEC
- Value:
- 150 mg/m³
- Explanation for the modification of the dose descriptor starting point:
- No inhalation data available. The oral NOAEL of 57 mg/kg bw/d (Fe) is equivalent to 246 mg/kg bw/d iron trinitrate. Correction for breathing rate (/1.15) and the extent of oral absorption (70%) and inhalation absorption (100% assumed) results in an inhalation NOAEC of 150 mg/m3.
- AF for dose response relationship:
- 1
- Justification:
- default value
- AF for differences in duration of exposure:
- 2
- Justification:
- default value: extrapolation from sub-chronic study to chronic exposure
- AF for interspecies differences (allometric scaling):
- 1
- Justification:
- not required: already accounted for
- AF for other interspecies differences:
- 2.5
- Justification:
- default value
- AF for intraspecies differences:
- 10
- Justification:
- default value: general population
- AF for the quality of the whole database:
- 1
- Justification:
- default value: reliable database
- AF for remaining uncertainties:
- 1
- Justification:
- default: value no other 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)
Acute/short term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
DNEL related information
General Population - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 8.6 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):
- 200
- Modified dose descriptor starting point:
- NOAEL
- Value:
- 1 722 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
- Data for repeated dermal exposure are not available. The oral NOAEL of 57 mg/kg bw/d (Fe) is equivalent to 246 mg/kg bw/d iron trinitrate. Correction for the extent of oral absorption (70%) and dermal absorption (10%) gives a dermal NOAEL of 1722 mg/kg bw/d.
- AF for dose response relationship:
- 1
- Justification:
- default value
- AF for differences in duration of exposure:
- 2
- Justification:
- default value: extrapolation from sub-chronic study to chronic exposure
- AF for interspecies differences (allometric scaling):
- 4
- Justification:
- standard factor: rat study
- AF for other interspecies differences:
- 2.5
- Justification:
- default value
- AF for intraspecies differences:
- 10
- Justification:
- default value: general population
- AF for the quality of the whole database:
- 1
- Justification:
- default value: reliable database
- AF for remaining uncertainties:
- 1
- Justification:
- default value: no other 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:
- skin irritation/corrosion
Acute/short term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- skin irritation/corrosion
General Population - Hazard via oral route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 1.2 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):
- 200
- Modified dose descriptor starting point:
- NOAEL
- Value:
- 246 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
- Not required
- AF for dose response relationship:
- 1
- Justification:
- default value
- AF for differences in duration of exposure:
- 2
- Justification:
- default value: extrapolation from sub-chronic study to chronic exposure
- AF for interspecies differences (allometric scaling):
- 4
- Justification:
- standard factor: rat study
- AF for other interspecies differences:
- 2.5
- Justification:
- default value
- AF for intraspecies differences:
- 10
- Justification:
- default value: general population
- AF for the quality of the whole database:
- 1
- Justification:
- default value: reliable database
- AF for remaining uncertainties:
- 1
- Justification:
- default value: no other uncertainties
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
- Most sensitive endpoint:
- repeated dose toxicity
DNEL related information
General Population - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
Additional information - General Population
The relevant starting point for the derivation of systemic DNEL values is the oral NOAEL of 57 mg/kg bw/d (Fe) from a 90 -day oral toxicity study with ferric chloride.
The oral NOAEL of 57 mg/kg bw/d (Fe) is equivalent to 246 mg/kg bw/d iron trinitrate. Correction for breathing rate (/1.15) and the extent of oral absorption (70%) and inhalation absorption (100% assumed) results in an inhalation NOAEC of 150 mg/m3. A long-term systemic inhalation DNEL for the general population of 3 mg/m3 is derived following the application of an overall assessment factor of 50, according to REACH guidance.
A short-term systemic inhalation DNEL for the general population is not derived in the absence of any identified acute systemic hazard.
Local inhalation DNEL values for the general population are not derived. The substance is of low pH and is therefore considered to be a potential respiratory irritant. Inhalation exposure to high concentrations should be minimised.
Correction of the oral NOAEL of 246 mg/kg bw/d for the extent of oral absorption (70%) and dermal absorption (10%) gives a dermal NOAEL of 1722 mg/kg bw/d. Application of an overall assessment factor of 200, according to REACH guidance gives a long-term systemic dermal DNEL for the general population of 8.6 mg/kg bw/d.
A short-term systemic dermal DNEL for the general population is not derived in the absence of any identified acute systemic hazard.
Local dermal DNEL values for the general population are not derived. Skin corrosivity is assumed based on the low pH of the substance. Dermal exposure to high concentrations of the substance should be avoided.
Application of an overall assessment factor of 200, according to REACH guidance gives a long-term systemic oral DNEL for the general population of 1.2 mg/kg bw/d.
A short-term systemic oral DNEL for the general population is not derived in the absence of any identified acute systemic hazard
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.