Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
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: 419-710-0 | CAS number: 42774-15-2 NYLOSTAB S-EED; NYSEED
- 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
Additional information
Fish, acute
Freshwater fish (Brachydanio rerio) were exposed to the test article for 96 hours at nominal concentrations of 1, 10, 50, 100 and 250 mg of test article per liter of test medium. Ten fish were used per treated group, in comparison with an untreated group. A static system was used, and each group of 10 fish was kept in 4 litres of test medium. No auxiliary substance was used
The following results were obtained from the study for the test item: LC 50 > 250 mg/l, LC0 = 100 mg/l and LC100 > 250 mg/l.
A second study was conducted as a limit test to confirm that the test item has no effects on the test organisms around maximum concentration on applied test guidelines. No effect was observed on test organisms. Therefore, it was judged that the test item had no adverse acute effect on test organisms around maximum concentration on applied test guidelines. The test item concentrations in the test solution was maintained within ±20 % of measured concentration at the preparation and the environmental conditions were within the suitable range, therefore, it was concluded that this study complied with the applied test guidelines.
As a result of the study, both the 48-hour and 96-hour LC50 to Medaka were > 110 mg/L
Daphnia, acute
A study (CERI, 2010) was conducted according to OECD Guideline 202 in order to confirm the effect of the test item on the test organisms below the solubility of the test item in dilution water. As a result, pH unadjusted 48 -hourEC50 was 15 mg/L.In the highest concentration level, since pH exceeded 9, the test concentration division which performed pH adjusted levels prepared separately. As a result, pH adjusted 48 -hour EC50 was 16 mg/L. From this result, it is guessed that pH is not participating in the toxicity over the Daphnia magna of a test item. The concentration of the test item in the test solution during exposure was maintained at that of the start of the exposure. The environmental conditions were within the suitable range; therefore, it is concluded that this study complied with the applied test guidelines.
In a second study Daphnia magna were exposed to the test article for 48 hours at the nominal concentrations of 1, 10, 50, 100 and 250 mg of test article per liter of test medium. Measurements of pH, dissolved oxygen and temperature were performed at the beginning and at the end of the test for each test medium. Each test medium was sampled at the start and at the end of the test.
The following results were obtained from the study for the test item: EC50 (24 h) > 250 mg/l, EC50 (48 h) = 250 mg/l, EC0 < 1 mg/l and EC100 > 250 mg/l.
Daphnia, chronic
A Daphnia magna (Crustacea, Cladocera) reproduction test was performed according to the OECD Guideline No 211 (adopted September 21, 1998) and Principles of Good Laboratory Practice (GLP, OECD 1997).
The aim of the study was the determination of the reproductive output of Daphnia magna exposed to a range of concentrations of the test substance (determination of NOEC after 21-day exposure). 5 concentrations in the range from 1.00 to 100 mg/L with separation factor of 3.2 were used. The NOEC (21-day in mg/I) is 10 mg/I while LOEC is 32 mg/L.
Algae
The study (CERI, 2010) was conducted in order to estimate the effect on the test organisms under the solubility of the test item in medium. As a result, in pH unadjusted test, the EC50 and NOEC of the test item were 27 mg/L and 1.0 mg/L, respectively. The pH of the test solution at the start of exposure in the higher test item concentration tended to be higher (pH was 9.4 in 98 mg/L exposure level which was the highest exposure level at the start of exposure). Therefore the pH of test solution was adjusted to around that of medium, and this study was conducted. As a result, the EC50 and NOEC of the test item were 52 mg/L and 3.2 mg/L, respectively. The effect on the test organism was eased somewhat. Therefore, it was considered that the effect of the test item on the test organism was the total effect of pH and toxicity of the test item and the results from experiments with adjusted pH were used for the assessment (EC50 and NOEC: 52 mg/L and 3.2 mg/L).
In pH unadjusted test, the EC50 and NOEC of the test item were 27 mg/L and 1.0 mg/L, respectively. In pH adjusted test, the EC50 and NOEC of the test item were 52 mg/L and 3.2 mg/L, respectively.
In a second study (Pharmakon, 1997), the following results were obtained:
- EC50, for freshwater green algae (actual concentration of test article): Growth curves (IA) EC50 > 250 mg/l, Growth rates (Iµ) > 250 mg/l
- NOEC, for freshwater green algae (actual concentration of test article): Growth curves (IA) NOEC > 250 mg/l, Growth rates (Iµ) > 250 mg/l
Microorganisms
The inhibitory effect of the test item on the respiration rate of aerobic wastewater microorganisms of activated sludge was investigated in a 3-hour respiration inhibition test according to OECO Guideline for Testing of Chemicals, No. 209.The following nominal concentrations were tested: 10, 32, 100, 320, and 1000 mg/l.
Up to and including the concentration of nominal 100 mg/L l the test item had no significant («15%) inhibitory effect on the respiration rate of activated sludge after the incubation period of three hours. At the higher test item concentrations of nominal 320 and 1000 mg/L the inhibitory effect increased to 24% and to 45%, respectively.
The calculated 3-hour EC-values were as follows:
NOEC (EC15): 148 mg/L:
EC20: 220 mg/L
EC50: 1250 mg/L
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.