Registration Dossier
Registration Dossier
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: - | CAS number: -
- 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

Endpoint summary
Administrative data
Description of key information
Based on the available data, FAT 41045 is considered to be not irritating to rabbits' skin and eyes.
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Single dose, in vivo skin irritation (OECD 404) and eye irritation (OECD 405) studies in the rabbit were performed in compliance with GLP with FAT 41030 a structural analogue of FAT 41045. Both substances are very similar in their chemical structure and, as demonstrated, in a number of physicochemical properties. Therefore, the use of these studies for read-across is considered to be appropriate, thus avoiding duplicate tests. In addition, availability of these two in vivo studies facilitated waiving of the respective in vitro corrosion/irritation studies.
In vivo skin irritation:
Topical, semi-occlusive 4 hour application of FAT 41030 to intact rabbit skin did not elicit any oedema throughout the 15 day observation period (overall mean score at 24, 48 and 72 hours after patch removal in 3 animals = 0.0). Erythema or other signs of irritation were not evident whenever evaluation of the treated skin was possible. Marked, red staining of the treated skin by the dark red coloured test material prevented erythema reading in all animals at 1 and 24 hours and in 2 animals at 48 hours after patch removal). The red staining had not fully disappeared by the end of the observation period, but a trend to reversibility was evident in all animals.Corrosive effects on the treated skin were not evident throughout the study.
In vivo eye irritation
Instillation of FAT 41030 into the conjunctival sac of rabbit eye produced mild, early-onset and transient ocular changes such as slight watery discharge, swelling and reddening of the conjunctivae and sclerae. These effects were reversible and were no longer evident at 48 hours after treatment. In addition, red staining of the treated eyes seen until the 48-hour reading was attributed to the test material. Cornea or iris were unaffected in all animals. Corrosion was not seen at any observation time point. Overall ocular mean scores at 24, 48 and 72 hours after instillation in 3 animals were 0.00 for corneal lesions, 0.00 for iris lesions, 0.33 for conjunctival redness and 0.00 for chemosis. Thus toxicologically significant or irreversible damage to the rabbit eye were not evident.
Respiratory irritation
Data on respiratory irritation are unavailable.
Justification for classification or non-classification
FAT 41045 is not subject to classification according to the CLP (Reg. 1272/2008) or DSD (Dir. 67/548/EEC) regulations regarding skin or eye irritation, as skin reactions indicative of irritation or corrosion or ocular findings necessitating classification were not evident in the two in vivo irritation studies with FAT 41030.
The finding of staining of the skin by FAT 41030 is considered to be inherent with the nature of the test material being a dye rather than representing a toxicologically relevant effect. In addition, a trend to reversibility of this finding was evident in all animals. The findings of red remnants in or staining of the treated eye in the eye irritation study had fully disappeared in all animals, at the latest, by 72 hours after instillation and therefore, do not pose a finding requiring classification.
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.
