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Diss Factsheets
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EC number: 234-390-0 | CAS number: 11138-47-9
- 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:
- 2 mg/m³
- Most sensitive endpoint:
- irritation (respiratory tract)
DNEL related information
- Overall assessment factor (AF):
- 1
- Modified dose descriptor starting point:
- NOAEC
Acute/short term exposure
- Hazard assessment conclusion:
- exposure based waiving
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 2 mg/m³
- Most sensitive endpoint:
- irritation (respiratory tract)
DNEL related information
- Overall assessment factor (AF):
- 1
- Dose descriptor:
- NOAEC
Acute/short term exposure
- Hazard assessment conclusion:
- exposure based waiving
DNEL related information
Workers - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 101 mg/kg bw/day
- Most sensitive endpoint:
- repeated dose toxicity
DNEL related information
- Overall assessment factor (AF):
- 9
- Modified dose descriptor starting point:
- LOAEL
Acute/short term exposure
- Hazard assessment conclusion:
- exposure based waiving
DNEL related information
Workers - Hazard for the eyes
Additional information - workers
DNELs for acute effects are not considered since long-term DNELs are sufficient to ensure that these effects do not occur.
DNEL long-term – systemic effects – dermal
Relevant dose-descriptor for the endpoint concerned: LOAEL of 1000 mg/kg bw in a 4 w oral Guideline study with rats (Degussa, 1989)
Correction of starting point:
Bioavailability in humans: assumed to be comparable with rats (no correction)
Exposure conditions: daily exposure over 4 weeks. Conversion factor for workplace exposure (5 d/w): 1.4
Conversion factor (PBS4 <--> PBS1): 0.65
Overall correction factor: 1.4 * 0.65 = 0.91
Corrected starting point: 1000 mg/kg bw * 0.91 = 910 mg/kg bw
Assessment factors:
Starting point: LOAEL; assessment factor of 3 (LOAEL → NOAEL)
Route to route extrapolation (oral → dermal): default assessment factor of 1
Duration extrapolation (subacute → chronic): default assessment factor of 6
Interspecies differences (rat → human): default assessment factor of 4
Interspecies differences (remaining differences): default assessment factor of 2.5
Intraspecies differences (workers): default assessment factor of 5
Quality of whole database: sufficient (no additional assessment factor)
Overall assessment factor: 3 * 1 * 6 * 4 * 2.5 * 5 = 900
DNEL long-term – systemic effects – dermal: 910 mg/kg bw ÷ 900 = 1.01 mg/kg bw/d
As for the dermal route 1 % absorption can be assumed, the external DNEL is about 101 mg/kg bw/d
DNEL long-term – local effects – inhalation
There are no studies with repeated exposure via inhalation available and also no extrapolation from a subacute oral study can be made for the local effects in the airways. In the EU RAR (ECB, 2007), several studies concerning workplace surveillance were described in detail and from these data a typical exposure concentration of 1 mg/m3 was derived, which gave no indication for adverse effects even after long-exposure. Therefore, no additional assessment factors have to be addressed. Assuming an amount of the respirable fraction in workplace air of about 30 – 50 % of the inhalable fraction (ECB, 2007), a DNEL of 2 mg/m3 can be derived.
General Population - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 0.5 mg/m³
- Most sensitive endpoint:
- irritation (respiratory tract)
DNEL related information
- Overall assessment factor (AF):
- 4
- Modified dose descriptor starting point:
- NOAEC
Acute/short term exposure
- Hazard assessment conclusion:
- exposure based waiving
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 0.5 mg/m³
- Most sensitive endpoint:
- irritation (respiratory tract)
DNEL related information
- Overall assessment factor (AF):
- 4
- Dose descriptor:
- NOAEC
Acute/short term exposure
- Hazard assessment conclusion:
- exposure based waiving
DNEL related information
General Population - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 36 mg/kg bw/day
- Most sensitive endpoint:
- repeated dose toxicity
DNEL related information
- Overall assessment factor (AF):
- 18
- Modified dose descriptor starting point:
- LOAEL
Acute/short term exposure
- Hazard assessment conclusion:
- exposure based waiving
DNEL related information
General Population - Hazard via oral route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 0.36 mg/kg bw/day
- Most sensitive endpoint:
- repeated dose toxicity
DNEL related information
- Overall assessment factor (AF):
- 1 800
- Modified dose descriptor starting point:
- NOAEL
Acute/short term exposure
- Hazard assessment conclusion:
- exposure based waiving
DNEL related information
General Population - Hazard for the eyes
Additional information - General Population
DNELs for acute effects are not considered since long-term DNELs are sufficient to ensure that these effects do not occur.
DNEL long-term – systemic effects – dermal
Relevant dose-descriptor for the endpoint concerned: LOAEL of 1000 mg/kg bw in a 4 w oral Guideline study with rats (Degussa, 1989)
Correction of starting point:
Bioavailability in humans: assumed to be comparable with rats (no correction)
Exposure conditions: daily exposure over 4 weeks (no correction)
Conversion factor (PBS4 <--> PBS1): 0.65
Overall correction factor: 0.65
Corrected starting point: 1000 mg/kg bw * 0.65 = 650 mg/kg bw
Assessment factors:
Starting point: LOAEL; assessment factor of 3 (LOAEL → NOAEL)
Route to route extrapolation: default assessment factor of 1 (oral → dermal)
Duration extrapolation: default assessment factor of 6 (subacute → chronic)
Interspecies differences: default assessment factor of 4 (rat → human)
Interspecies differences: default assessment factor of 2.5 (remaining differences)
Intraspecies differences: default assessment factor of 10 (general population)
Quality of whole database: sufficient (no additional assessment factor)
Overall assessment factor: 3 * 1 * 6 * 4 * 2.5 * 10 = 1800
DNEL long-term – systemic effects – dermal: 650 ÷ 1800 = 0.36 mg/kg bw/d
As for the dermal route 1 % absorption can be assumed, the external DNEL is about 36 mg/kg bw/d
DNEL long-term – systemic effects – inhalation
There are no studies with repeated exposure via inhalation available and also no extrapolation from a subacute oral study can be made for the local effects in the airways. For workers (see above) the DNEL is calculated with 2 mg/m3.
Correction of starting point:
Exposure conditions: breathing volume for general population 20 m3/d vs. 10 m3/d in workers: 2
Corrected starting point: 2 mg/m3 ÷ 2 = 1 mg/m3
Assessment factors:
Intraspecies differences: assessment factor of 2 (general population)
Overall assessment factor: 2
DNEL long-term – systemic effects – inhalation: 1 mg/m3 ÷ 2 = 0.5 mg/m3
DNEL long-term – systemic effects – oral
Relevant dose-descriptor for the endpoint concerned: LOAEL of 1000 mg/kg bw in a 4 w oral Guideline study with rats (Degussa, 1989)
Correction of starting point:
Bioavailability in humans: assumed to be comparable with rats (no correction)
Exposure conditions: daily exposure over 4 weeks (no correction)
Conversion factor (PBS4 <--> PBS1): 0.65
Overall correction factor: 0.65
Corrected starting point: 1000 mg/kg bw * 0.65 = 650 mg/kg bw
Assessment factors:
Starting point: LOAEL: default assessment factor of 3 (LOAEL → NOAEL)
Same route of exposure: no additional assessment factor
Duration extrapolation: default assessment factor of 6 (subacute → chronic)
Interspecies differences: default assessment factor of 4 (rat → human)
Interspecies differences: default assessment factor of 2.5 (remaining differences)
Intraspecies differences: default assessment factor of 10 (general population)
Quality of whole database: sufficient (no additional assessment factor)
Overall assessment factor: 3 * 6 * 4 * 2.5 * 10 = 1800
DNEL long-term – systemic effects – oral: 650 mg/kg bw ÷ 1800 = 0.36 mg/kg bw/d
DNEL long-term – local effects – inhalation
There are no studies with repeated exposure via inhalation available and also no extrapolation from a subacute oral study can be made for the local effects in the airways. For workers (see above) the DNEL is calculated with 2 mg/m3.
Correction of starting point:
Exposure conditions: breathing volume for general population 20 m3/d vs. 10 m3/d in workers: 2
Corrected starting point: 2 mg/m3 ÷ 2 = 1 mg/m3
Assessment factors:
Intraspecies differences: assessment factor of 2 (general population)
Overall assessment factor: 2
DNEL long-term – local effects – inhalation: 1 mg/m3 ÷ 2 = 0.5 mg/m3
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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