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Diss Factsheets
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EC number: 403-800-1 | CAS number: 103597-45-1 EVERSORB 78; LOWILITE 36; LS.BT.620; MIXXIM BB/100; TINUVIN 360
- 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
Toxicity to reproduction
Administrative data
- Endpoint:
- one-generation reproductive toxicity
- Remarks:
- based on test type (migrated information)
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- other:
- Rationale for reliability incl. deficiencies:
- other: Body responsible for the test
Data source
Reference
- Reference Type:
- other: Body responsible for the test
- Title:
- Unnamed
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 415 [One-Generation Reproduction Toxicity Study (before 9 October 2017)]
- Deviations:
- not specified
- GLP compliance:
- yes
- Limit test:
- no
Test material
- Reference substance name:
- Body responsible for the test
- IUPAC Name:
- Body responsible for the test
Constituent 1
Test animals
- Species:
- other: SD rats
- Strain:
- not specified
- Sex:
- male/female
Administration / exposure
- Route of administration:
- oral: unspecified
- Type of inhalation exposure (if applicable):
- not specified
- Vehicle:
- not specified
- Details on mating procedure:
- no data
- Analytical verification of doses or concentrations:
- not specified
- Duration of treatment / exposure:
- no data
- Frequency of treatment:
- Dosing regime (males): 7 days/week
Dosing regime (females): 7 days/week - Details on study schedule:
- no data
- No. of animals per sex per dose:
- Male: 24 animals at 0 mg/kg or mg/L
Male: 24 animals at 100 mg/kg or mg/L
Male: 24 animals at 300 mg/kg or mg/L
Male: 24 animals at 1000 mg/kg or mg/L
Female: 24 animals at 0 mg/kg or mg/L
Female: 24 animals at 100 mg/kg or mg/L
Female: 24 animals at 300 mg/kg or mg/L
Female: 24 animals at 1000 mg/kg or mg/L
Results and discussion
Results: P0 (first parental generation)
Effect levels (P0)
- Dose descriptor:
- NOAEL
- Effect level:
- 1 000 mg/kg bw/day
- Sex:
- not specified
Results: F1 generation
Effect levels (F1)
- Dose descriptor:
- NOAEL
- Generation:
- F1
- Effect level:
- 300 mg/kg bw/day
- Sex:
- not specified
- Basis for effect level:
- other: based on equivocal findings on pup survival in the high dose group
Overall reproductive toxicity
- Reproductive effects observed:
- not specified
Any other information on results incl. tables
Details on results (parental animals)
No clinical observations were related to the substance. No effects on the body weight or body weight gain were observed. Food consumption was not affected by the treatment. No effect of the treatment could be observed on mating and pregnancy rates.
Gross pathology findings occured sporadically, without any dose-response relationship and were not considered treatment
related.
Details on results (offspring)
Effects on F1 generation:
In the high and low dose group, the total number of dead/missing pups during lactation was significantly increased compared to the untreated controls. This was mainly due to the fact that in both groups all pups of one litter died to the lack of maternal care. This resulted in 17 dead pups in the low dose group and 13 in the high dose group. If the values are corrected for these numbers, this results in 8,10,6 and 10 dead/missing pups respectively. In addition, the relevance of this observation is strongly limited by the lack of any dose response relationship.
No effect of the test item treatment was found on pup weight or sex ratio. Clinical findings observed in pups were considered to be treatment related. The only remarkable finding was one pupshowing anuria in the high dose group.
Summarizing these findings, it seems most unlikely that any observation was substance related induced. However, a bordeline effectin the high dose group cannot be excluded with certainty.
The NOAEL is a very conservative value given that this finding is highly unlikely treatment related.
Applicant's summary and conclusion
- Conclusions:
- NOAEL = 1000mg/kg/d (parental animal)
NOAEL = 300 mg/kg/d (parental animal)
It seems most unlikely that any observation was substance related induced. However, a bordeline effect in the high dose group cannot be excluded
with certainty.
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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