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Reaction mass of sodium amino-bis{[4-(ethenylsubstituted)phenyl]diazenyl}-hydroxynaphthalenesulfonate and polysodium amino-{[4-(ethenylsubstituted)phenyl]diazenyl}-{[4-(ethenylsubstituted)-2-sulfonatophenyl]diazenyl}-hydroxynaphthalenesulfonate and polysodium amino-bis{[4-(ethenylsubstituted)-2-sulfonatophenyl]diazenyl}-hydroxynaphthalenesulfonate
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
Acute Toxicity: oral
Some information in this page has been claimed confidential.
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 24-07-2014 TO 24-10-2014
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- reference to same study
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 014
- Report date:
- 2014
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
- Deviations:
- no
- Principles of method if other than guideline:
- None
- GLP compliance:
- yes
- Test type:
- acute toxic class method
- Limit test:
- no
Test material
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- None
Constituent 1
- Specific details on test material used for the study:
- None
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source:Animal Breeding
RCC Laboratories India Private Limited
Genome Valley, Turkapally
Shameerpet (Mandal)
Ranga Reddy District
Hyderabad – 500 078
India
- Age at study initiation:9 - 11 weeks
- Weight at study initiation:Females: 140.2 to 178.3 g
- Fasting period before study:17 Hours
- Housing:Housed in groups of three animals each in Polycarbonate cages (approximate internal dimensions of 365 mm x 202 mm x 180 mm height) with paddy husk bedding. Results of analyses for contaminants will be archived at RCC Laboratories India Private Limited.
- Diet (e.g. ad libitum):Nutrilab rodent feed from Provimi Animal Nutrition India Pvt. Ltd., (Batch No. 0001887772 and 0001946849) was provided ad libitum. Results of analyses for contaminants will be archived at RCC Laboratories India Private Limited
- Water (e.g. ad libitum):Aquaguard filtered tap water was provided ad libitum. Results of bacteriological, chemical and contaminant analyses will be archived at RCC Laboratories India Private Limited.
- Acclimation period:Under laboratory conditions for 8 days for Step I, Step III and 13 days for Step II and Step IV animals, after veterinary examination. Only animals without any visible signs of illness were used for the study.
ENVIRONMENTAL CONDITIONSStandard Laboratory Conditions
- Temperature (°C):21.9 to 23.7o C
- Humidity (%):61 to 70%
- Air changes (per hr):adequate (above 10) air changes per hour
- Photoperiod (hrs dark / hrs light):12 hours light and 12 hours dark.
IN-LIFE DATES: From: July 31st 2014 To: September 9th 2014
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- water
- Details on oral exposure:
- VEHICLE
- Concentration in vehicle: 30mg/ml and 200mg/ml
- Amount of vehicle (if gavage): 10ml
- Justification for choice of vehicle: Universal Solvent
MAXIMUM DOSE VOLUME APPLIED: 10ml/Kg
- Rationale for the selection of the starting dose: Since no information on the toxicity available, the starting dose is selected as 300 mg/kg body weight. The test procedure was followed the attached scheme described in Annex 2c, OECD Guideline 423, adopted 17th December 2001 - Doses:
- Step I 300 mg/kg
Step II 300 mg/kg
Step III 2000 mg/kg
Step IV 2000 mg/kg - No. of animals per sex per dose:
- 3 females
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration:
14 days
- Frequency of observations and weighing:
Mortality / Viability
Daily during the acclimatization period, during the first 30 minutes and at approximately 1, 2, 3 and 4 hours after administration on test day 0 (in common with the clinical signs) and twice daily during days 1-14 (once on day of sacrifice).
Body weights
On test days 0 (prior to dose administration), day 7, and 14.
Clinical signs
Daily during the acclimatization period, during the first 30 minutes and at approximately 1, 2, 3 and 4 hours after administration on test day 0. Once daily during days 1-14.
- Necropsy of survivors performed:
yes
GROUPS / STEPS Dose
( mg/kg) NUMBER OF ANIMALS
PER STEP
(Female) ANIMAL NUMBER
First Step 300 3 01 - 03
Second Step 300 3 04 - 06
Third Step 2000 3 07 - 09
Fourth Step 2000 3 10 - 12 - Statistics:
- No statistical analysis was done
Results and discussion
- Preliminary study:
- No
Effect levels
- Key result
- Sex:
- female
- Dose descriptor:
- LD50
- Effect level:
- > 2 000 mg/kg bw
- Based on:
- test mat.
- Mortality:
- Step I 3 females treated at 300 mg/kg Mortality ‘0 out of 3’
Step II 3 females treated at 300 mg/kg Mortality ‘0 out of 3’
Step III 3 females treated at 2000 mg/kg Mortality ‘0 out of 3’
Step IV 3 females treated at 2000 mg/kg Mortality ‘0 out of 3’ - Clinical signs:
- All the animals of Step I (Animal No. 01, 02 and 03) and Step II (Animal No. 04, 05 and 06) treated at 300 mg/kg body weight appeared normal at first 30 minutes, 1, 2 , 3 and 4 hour observation on day 0 after treatment and throughout the experiment period ( up to day 14).
All the animals of Step III (Animal No. 07, 08 and 09) and Step IV (Animal No. 10, 11 and 12) treated at 2000 mg/kg body weight showed dullness at first 30 minutes, 1, 2, 3 and 4 hour observation on day 0 after treatment and appeared normal from day 1 of observation period to the last day of observation period (day 14) - Body weight:
- All the animals gained body weight by days 7 and 14 as compared to day 0
- Gross pathology:
- No abnormalities were observed in any of the treated animals at terminal sacrifice
Any other information on results incl. tables
None
Applicant's summary and conclusion
- Interpretation of results:
- practically nontoxic
- Remarks:
- Migrated information Criteria used for interpretation of results: OECD GHS
- Conclusions:
- Based on the results, the median lethal dose (LD50) of FAT 40865/A TE after single oral administration to female rats, observed over a period of 14 days was greater than 2000 mg/kg body weight.
- Executive summary:
An OECD 423 guideline study was performed in accordance to GLP to assess the oral toxicity of test item FAT 40865/A over a period of 14 days. The test item FAT 40865/A TE was administered to Wistar rats by oral gavage at a dose level of 300 mg/kg body weight and 2000 mg/kg body weight to 2 dose groups in 4 steps. The former two steps (Step I & II) represents the dose group of 300 mg/kg body weight and later two steps (Step III & IV) represents the dose group of 2000 mg/kg body weight. Three animals were allocated to each step. The test item was formulated in vehicle (distilled water) at a concentration of 30 mg/mL for Step I and Step II and 200 mg/mL for Step III and Step IV, administered at a dose volume of 10 mL/kg body weight.
The animals were observed daily during the acclimatization period and, mortality/viability, and clinical signs were recorded. All the animals were observed for clinical signs during first 30 minutes and at approximately 1, 2, 3 and 4 hours after administration on test day 0 and once daily during test days 1‑14. Mortality/viability was recorded during first 30 minutes and at approximately 1, 2, 3 and 4 hours after administration on test day 0 (in common with the clinical signs) and twice daily during days 1-14 (once on day of sacrifice). Body weights were recorded on test day 0 (prior to administration), and on day 7 and 14. All the animals were necropsied and examined macroscopically at the end of observation period.
All the animals appeared normal throughout the acclimatization period.
The animals were treated as follows:
Step I 3 females treated at 300 mg/kg Mortality ‘0 out of 3’
Step II 3 females treated at 300 mg/kg Mortality ‘0 out of 3’
Step III 3 females treated at 2000 mg/kg Mortality ‘0 out of 3’
Step IV 3 females treated at 2000 mg/kg Mortality ‘0 out of 3’
All the animals of Step I (Animal No. 01, 02 and 03) and Step II (Animal No. 04, 05 and 06) treated at 300 mg/kg body weight appeared normal at first 30 minutes, 1, 2 , 3 and 4 hour observation on day 0 after treatment and throughout the experiment period ( up to day 14).
All the animals of Step III (Animal No. 07, 08 and 09) and Step IV (Animal No. 10, 11 and 12) treated at 2000 mg/kg body weight showed dullness at first 30 minutes, 1, 2, 3 and 4 hour observation on day 0 after treatment and appeared normal from day 1 of observation period to the last day of observation period (day 14).
All the survived animals gained body weight by days 7 and 14 as compared to day 0.
No abnormalities were observed in any of the treated animals at terminal sacrifice.
Based on the results, the median lethal dose (LD50) of FAT 40865/A TE after single oral administration to female rats, observed over a period of 14 days was greater than 2000 mg/kg body weight.
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