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EC number: 202-854-1 | CAS number: 100-46-9
- 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:
- 14.7 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- Oral
DNEL related information
- DNEL derivation method:
- other: ECHA REACH Guidance and ECETOC Technical Report No. 110
- Overall assessment factor (AF):
- 18
- Modified dose descriptor starting point:
- NOAEC
- Value:
- 264.5 mg/m³
- Explanation for the modification of the dose descriptor starting point:
- There are no relevant experimental data on repeated exposure by the inhalation route available.
- AF for dose response relationship:
- 1
- Justification:
- The dose response relationship is considered unremarkable, therefore no additional factor is used.
- AF for differences in duration of exposure:
- 6
- Justification:
- The default extrapolation factor for exposure duration is used: subacute (starting point) to chronic (end point).
- AF for interspecies differences (allometric scaling):
- 1
- Justification:
- Respiratory interspecies differences are fully covered by the factors used for route to route extrapolation.
- AF for other interspecies differences:
- 1
- Justification:
- There is no additional evidence for species differences including toxicodynamics (ECETOC). Therefore, no additional factor is used.
- AF for intraspecies differences:
- 3
- Justification:
- The (ECETOC) default value for the relatively homogenous group "worker" is used.
- AF for the quality of the whole database:
- 1
- Justification:
- The quality of the whole data base is considered to be sufficient and uncritical.
- AF for remaining uncertainties:
- 1
- Justification:
- The approach of the DNEL derivation is conservative. No further assessment factors are required.
Acute/short term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 44.1 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- Oral
DNEL related information
- DNEL derivation method:
- other: ECHA REACH Guidance and ECETOC Technical Report No. 110
- Overall assessment factor (AF):
- 3
- DNEL extrapolated from long term DNEL
Local effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 1 mg/m³
DNEL related information
- DNEL derivation method:
- other: VCI (2010)
Acute/short term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 3 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
DNEL related information
- DNEL derivation method:
- other: ECHA REACH Guidance and ECETOC Technical Report No. 110
- Overall assessment factor (AF):
- 3
- DNEL extrapolated from long term DNEL
Workers - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 8.3 mg/kg bw/day
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- Oral
DNEL related information
- DNEL derivation method:
- other: ECHA REACH Guidance and ECETOC Technical Report No. 110
- Overall assessment factor (AF):
- 72
- Modified dose descriptor starting point:
- NOAEL
- Value:
- 600 mg/kg bw/day
- Explanation for the modification of the dose descriptor starting point:
- There are no relevant experimental data on repeated exposure by the dermal route available.
- AF for dose response relationship:
- 1
- Justification:
- The dose response relationship is considered unremarkable, therefore no additional factor is used.
- AF for differences in duration of exposure:
- 6
- Justification:
- The default extrapolation factor for exposure duration is used: subacute (starting point) to chronic (end point).
- AF for interspecies differences (allometric scaling):
- 4
- Justification:
- The default allometric scaling factor for the differences between rats and humans is used.
- AF for other interspecies differences:
- 1
- Justification:
- Interspecies differences including toxicokinetics are fully covered by the allometric scaling. There is no additional evidance for species differences including toxicodynamics. Therefore, no additional factor is used.
- AF for intraspecies differences:
- 3
- Justification:
- The (ECETOC) default value for the relatively homogenous group "worker" is used.
- AF for the quality of the whole database:
- 1
- Justification:
- The quality of the whole data base is considered to be sufficient and uncritical.
- 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 DNEL required: short term exposure controlled by conditions for long-term
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- Oral
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 information related to acute/short-term and long-term exposure hazards via the different exposure routes has been commented/discussed above. For exposure hazards, where a more detailed discussion is appropriate, additional information is provided below.
Local effects via inhalation route
Long term exposure
The worker-DNEL long-term for inhalation route - local below was calculated with a LOAEL obtained in a combined repeated dose toxicity study with the reproduction/developmental toxicity screening test (OECD 422, BASF SE, 2013) performed with Benzylamine and compared with the above generic DNEL of 1 mg/m³ in order to justify the selection on the basis of the most conservative approach.
Hazard assessment conclusion: DNEL (Derived No Effect Level) = 5.9 mg/m³
Most sensitive endpoint: repeated dose toxicity (OECD 422); Route of original study: Oral
DNEL related information
DNEL derivation method: ECHA REACH Guidance and ECETOC Technical Report No. 110
Overall assessment factor (AF): 3
Dose descriptor starting point (after route to route extrapolation): NOAEC = 17.6 mg/m³
AF for dose response relationship: 1
Justification: The dose response relationship is considered unremarkable, therefore no additional factor is used.
AF for differences in duration of exposure: 1
Justification: When comparing subacute to chronic exposure duration, irritation responses are considered to be mostly concentration dependent; no duration-based difference between subacute and chronic exposure is assumed.
AF for interspecies differences (allometric scalling): 1
Justification: Respiratory interspecies differences are fully covered by the factors used for route to route extrapolation.
AF for other interspecies differences: 1
Justification: There is no additional evidence for species differences including toxicodynamics (ECETOC). Therefore, no additional factor is used.
AF for intraspecies differences: 3
Justification: The (ECETOC) default value for the relatively homogenous group "worker" is used.
AF for the quality of the whole database: 1
Justification: The quality of the whole data base is considered to be sufficient and uncritical.
AF for remaining uncertainties: 1
Justification: The approach of the DNEL derivation is conservative. No further assessment factors are required.
Justification and comments: The worker-DNEL long-term for inhalation route - local is derived from the LOAEL for local effects of 30 mg/kg bw/day, obtained in the key subacute oral repeated dose study in Wistar rats (BASF SE, 2013), where histological lesions in the stomach occurred down to the lowest dose level tested (30 mg/kg bw/d). The NOAECcorr is calculated as follows: NOAECcorr = 30 mg/kg bw/day*(1/0.38 m³/kg bw/d)*(6.7 m³ (8h)/10 m³ (8h))/3 = 17.6 mg/m³, with: 30 mg/kg bw/day: LOAEL (local effects), (1/0.38 m³/kg bw/d): correction factor for sRVrat, (6.7 m³ (8h)/10 m³ (8h)): correction factor for physical activity, 3: factor for LOAEL-to-NOAEL extrapolation.
Acute/short term exposure
The worker-DNEL acute for inhalation route - local of 3 mg/m³ has been set at three times of the corresponding long-term DNEL derived by the recommended VCI DNEL of 1 mg/m³ for test substances classified with R34 (causes burns) according to Directive 67/548/EEC.
With regard to local effects after acute inhalation exposure a Protective Action Criteria 1 (PAC-1) value of 2 mg/m³ is published for Benzylamine. The PAC-1 value is the airborne concentration of a substance above which it is predicted that the general population, including susceptible individuals, could experience notable discomfort, irritation, or certain asymptomatic, nonsensory effects. These effects are not disabling and are transient and reversible upon cessation of exposure. The PAC-1 value is a conservative value with regard to the acute exposure situation at the workplace as workers represent a more homogenous and less susceptible population group than the general population and peak exposure of workers is limited to 15 min whereas the PAC-1 value covers peak exposure up to 60 min.
The worker-DNEL acute for inhalation route - local of 3 mg/m³ derived on the basis of the generic DNEL of 1 mg/m³ (VCI, 2010) for workers is in the same range as the PAC-1 value of 2 mg/m³ for the general population group, and is, in view of the different underlying exposure durations, considered as the more conservative value. Therefore the selection of the worker-DNEL acute inhalation route - local of 3 mg/m³ is justified.
Conclusion
On this basis, the worker-DNEL long-term for inhalation route - local and the worker-DNEL acute for inhalation route - local are set at 1 and 3 mg/m³, respectively.
References:
- VCI (Verband der Chemischen Industrie e.V.) (2010). Ableitung von DNEL für lokal reizende Stoffe mit guter Datenlage zur systemischen Toxizität, aber limitierter Datenlage zur Inhalationstoxizität. Published 21.01.2010.
- PAC (Protective Action Criteria). Rev. 27, February 2012. 2012.http://www.atlintl.com/DOE/teels/teel.html.
- ECHA (2012). ECHA Guidance on IR/CSR Part E
General Population - Hazard via inhalation route
Systemic effects
Acute/short term exposure
DNEL related information
Local effects
Acute/short term exposure
DNEL related information
General Population - Hazard via dermal route
Systemic effects
Acute/short term exposure
DNEL related information
General Population - Hazard via oral route
Systemic effects
Acute/short term exposure
DNEL related information
General Population - Hazard for the eyes
Additional information - General Population
Benzylamine is neither marketed to the general public nor intentionally added to consumer products. Also, consumer products do not contain substances from which Benzylamine is intended to be released. Thus the derivation of general population DNELs is not required.
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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