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EC number: 269-056-3 | CAS number: 68186-94-7 This substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 77494.
- 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
Developmental toxicity / teratogenicity
Administrative data
- Endpoint:
- developmental toxicity
- Type of information:
- experimental study
- Adequacy of study:
- disregarded due to major methodological deficiencies
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- abstract
- Remarks:
- Abstract in English language only
Data source
Reference
- Reference Type:
- publication
- Title:
- Teratogenicity studies of Slow-Fe in mice and rats
- Author:
- Tadokoro, T. et al.
- Year:
- 1 979
- Bibliographic source:
- Oyo Yakuri 17 (3): 483 - 495.
Materials and methods
- Principles of method if other than guideline:
- The influence of iron sulfate (Slow Fe) on the foetuses and offspring of pregnant mice was studied. The mice were dosed p.o. once a day for 6 consecutive days. The dosages were 0, 120, 380 and 1200 mg/kg/day.
- Limit test:
- no
Test material
Test animals
- Species:
- mouse
Administration / exposure
- Details on exposure:
- Pregnant mice were dosed p.o. once a day for 6 consecutive days.
- Duration of treatment / exposure:
- 6 consecutive days (gestation days: 7 to 12)
- Frequency of treatment:
- once a day
- Duration of test:
- at least 61 days
Doses / concentrationsopen allclose all
- Dose / conc.:
- 120 mg/kg bw/day
- Dose / conc.:
- 380 mg/kg bw/day
- Dose / conc.:
- 1 200 mg/kg bw/day
- No. of animals per sex per dose:
- at least 15 pregnant females
- Control animals:
- yes
- Details on study design:
- A pilot study was conducted in female mice. The mice received 0, 300, 600 and 1200 mg/kg/day of the test item via oral administration. No mortality was observed during a two week observation period. The body weight was also determined during the observation period.
Examinations
- Maternal examinations:
- BODY WEIGHT CHANGE: Yes
- Time schedule for examinations: each day during gestation and at birth as well as on lactation days 7, 14 and 21. - Ovaries and uterine content:
- For the following examinations 15 dams were investigated at term:
The uterine content was examined after termination: Yes
Examinations included:
- Number of implants (% of implants)
- Number of dead implants
- Number of litters
- Number of dams without live foetuses
For the following examinations 5 dams were investigated after birth:
- Number of litters
- Length of gestation period
- Number and percentage of implantation sites - Fetal examinations:
- For the following examinations 15 litters were investigated at term:
- External examinations: Yes, all foetuses
- Soft tissue examinations: Yes, half of all foetuses
- Skeletal examinations: Yes, half of all foetuses
- Number of live male and female foetuses
- Sex ratio was determined.
- mean body weight at term.
For the following examinations 5 litters were investigated after birth:
- Mean body weight change of male and female offspring on lactation day 0, 7, 14 , 21, 28, 35 and 42.
- Number of delivered foetuses (male/female, stillborn).
- Number of surviving offsprings on lactation days 0, 7, 14, 21, 28, 35 and 42 days (% of delivered foetuses).
- Developmental index of offspring was determined after birth.
- Number sexual matured male and female offspring (% of survived offspring)
- Number of Preyer's reflex (% of survived offspring)
Results and discussion
Results: maternal animals
General toxicity (maternal animals)
- Details on results:
- The results of the present experiment showed no influence on survival of dams.
Please also refer to the field "Attached background material".
Effect levels (maternal animals)
- Remarks on result:
- other: The results of the present experiment showed no influence on survival of dams.
Results (fetuses)
- Details on embryotoxic / teratogenic effects:
- The teratogenicity was not revealed by dosing of the test item in mice in the present experiment.
Please also refer to the field "Attached background material".
Effect levels (fetuses)
- Remarks on result:
- other: The teratogenicity was not revealed by dosing of the test item in mice in the present experiment.
Applicant's summary and conclusion
- Conclusions:
- According to the authors, the results of the present experiment showed no influence on survival of dams. Furthermore, the teratogenicity was not revealed by dosing of the test item in mice in the present experiment. However, no conclusion can be drawn for this publication, since the reference is written in Japanese language and an abstract in English language is only available, which does not allow a review of the study. Furthermore, the number of dams per group is too low and the exposure duration is too short.
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