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EC number: 614-144-2 | CAS number: 67800-94-6
- 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
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- 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
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- 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
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- Endpoint summary
- Stability
- Biodegradation
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- 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
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- Additional toxicological data

Endpoint summary
Administrative data
Description of key information
28-day oral (gavage) NOAEL for both sexes was concluded as 40 mg/kg b.w./d ( based on nominal) based on histopathological changes in the liver and thyroids (read across from oTDA, propoxylated).
Key value for chemical safety assessment
Repeated dose toxicity: via oral route - systemic effects
Endpoint conclusion
- Dose descriptor:
- NOAEL
- 40 mg/kg bw/day
Additional information
Results 'read across' from study on oTDA, propxylated, as permitted by Annex XI para 1.5, based on the justification in the report by Paul Illing Consultancy Services Ltd. and Marlin Consultancy (Illing and Barratt, 2010). Thus, on animal welfare grounds this test should not be undertaken on oTDA, ethoxylated and propoxylated. For further details concerning the grouping, consult Illing and Barratt, 2010.
The NOAEL for both sexes was concluded as 40 mg/kg b.w. /d (based on nominal).
Repeated dose toxicity: inhalation - systemic effects (target organ) digestive: liver; glandular: thyroids
Justification for classification or non-classification
According to Regulation (EC) No 1272/2008, Annex I, chapter 3.9 classification of Diaminotoluene, propoxylated as STOT RE cat. 2 is not recommended.Although the LOAEL (160 mg/kg) is below the guidance value for 28-day studies (300 mg/kg), the nature and severity of the adverse effects at this dose level do not support classification. Hematological changes at 160 mg/kg (females) and even at 640 mg/kg (females/males) give no conclusive evidence of consistent and significant adverse effect in hematology. The periportal hepatocellular changes observed at 160 mg/kg (2/5 males and 5/5 females grade 2) and even at 640 mg/kg (5/5 male and 5/5 female, grade 3) give no evidence of multifocal or diffuse necrosis, fibrosis or granuloma formation. The morphological alterations comply with those typical for reversible hepatic changes due to liver enzymes induction reflecting increased metabolism and hepatic clearance of Diaminotoluene, propoxylated. The follicular cell hyperthrophy/hyperplasie in the thyroids, observed in both genders up to a moderate degree at 160 mg/kg (grade 2) and 640 mg/kg (grade 3), are interpreted as being a specific thyroid toxicity via liver enzyme induction.The species-specific mechanism/effect of toxicity observed in this study cannot be directly extrapolated to humans, i.e. these effects are therefore considered of insufficient concern for classification.
On the basis of 'read across' from oTDA, propoxylated, the findings in the available study do not warrant classification ofDiaminotoluene, ethoxylated and propoxylated according to the EU criteria.
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