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EC number: 256-851-5 | CAS number: 50925-42-3
- 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
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1990
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 990
- Report date:
- 1990
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 401 (Acute Oral Toxicity)
- Principles of method if other than guideline:
- 5 male and 5 female rats were dosed with 2000 mg/kg Bayscript Yellow CA 51069 by gavage. Mortality, clinical signs and body weight were recorded for 14 days.
- GLP compliance:
- yes
- Test type:
- standard acute method
- Limit test:
- yes
Test material
- Reference substance name:
- Tetrasodium 3,3'-[[6-[(2-hydroxyethyl)amino]-1,3,5-triazine-2,4-diyl]bis[imino(2-methyl-4,1-phenylene)azo]]bisnaphthalene-1,5-disulphonate
- EC Number:
- 256-851-5
- EC Name:
- Tetrasodium 3,3'-[[6-[(2-hydroxyethyl)amino]-1,3,5-triazine-2,4-diyl]bis[imino(2-methyl-4,1-phenylene)azo]]bisnaphthalene-1,5-disulphonate
- Cas Number:
- 50925-42-3
- Molecular formula:
- C39H30N10Na4O13S4
- IUPAC Name:
- tetrasodium 3,3'-({6-[(2-hydroxyethyl)amino]-1,3,5-triazine-2,4-diyl}bis[imino(2-methyl-4,1-phenylene)diazene-2,1-diyl])dinaphthalene-1,5-disulfonate
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- At the start of the experiment, male rats were about 8 weeks of age and females about 9 weeks. The average initial weight of males was 184 g and of females 164 g. The mean deviation in animal weights was less than 20%. Females were nulliparous and non-pregnant.
Prior to study initiation the condition of the animals' health was checked. Only healthy animals without any clinical signs were included in the study. Animals were acclimated for at least 4 days before application. Five rats were used per dose and sex.
The rats were housed individually under conventional conditions in Makrolon® Type-III cages on low-dust wood granules, at a room temperature of 22 ± 2° C, with a 12-hour light/dark cycle (artificial lighting), relative humidity of about 50 ± 10% and approximately ten air changes per hour in groups of 5 animals.
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- water
- Details on oral exposure:
- The test substance was suspended under stirring on a magnetic stirrer in tap water at room temperature and intragastrically applied at a constant application volume of 10 ml/kg body weight. A rigid metal gavage was used for that purpose.
The test substance was formulated in the vehicle immediately before the start of the study. Because of the short time between preparation and application of the test substance analytical investigations on stability and homogeneity have not been performed. - Doses:
- 2000 mg/kg
- No. of animals per sex per dose:
- 5 male and 5 female rats/dose
- Control animals:
- no
- Details on study design:
- The animals were inspected several times on the day of administration, and twice daily during the following 14-day observation period (once on weekends and bank holidays). During inspections, the type, onset, duration, and intensity of clinical signs were recorded and dead animals were removed if necessary. The date of death was recorded.
The animals were individually weighed directly before administration, after one week and at the end of the 14-day observation period. The application volume for each individual animal was based on its body weight just before application.
Gross pathological examinations were done on all animals sacrificed under deep diethyl ether anesthesia at the end of study. Necropsy records were prepared for all animals.
Results and discussion
Effect levels
- Key result
- Sex:
- male/female
- Dose descriptor:
- discriminating dose
- Effect level:
- 2 000 mg/kg bw
- Based on:
- test mat.
- Mortality:
- None of the rats died.
- Clinical signs:
- other: No symptoms attributable to BAYSCRIPT Yellow CA 51069 occurred.
- Gross pathology:
- The animals sacrificed at the end of the study showed no gross pathological abnormalities.
Any other information on results incl. tables
No findings or symptoms appeared that could be attributed to the administration of BAYSCRIPT Yellow CA 51069. The LD50 values for male and female rats were greater than 2000 mg/kg body weight.
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- A single oral dose of 2000 mg/kg bw caused no deaths. The LD50 is greater than 2000 mg/kg bw (discriminating dose).
- Executive summary:
Acute toxicological investigations were conducted after oral administration of BAYSCRIPT Yellow CA 51069 to male and female Wistar rats.
The LD50 values for male and female rats were greater than 2000 mg/kg body weight.
No findings or symptoms appeared that could be attributed to the administration of BAYSCRIPT Yellow CA 51069.
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