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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 425-560-7 | 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
Endpoint summary
Administrative data
Description of key information
Biodegradation
Key, CO2-evolution test, OECD 301B, GLP: not ready biodegradable
Bioaccumulation
Key, Bioconcentration, Cyprinus carpio, 28 d, OECD 305, GLP: BCF = 31, not bioaccumulative
Additional information
Biodegradation
CO2-evolution test, OECD 301B
The registered substance was tested for ready biodegradation in a CO2-evolution test according to OECD Guideline 301B following GLP.
Purpose
The purpose of this assay
was to provide information on the biodegradability of the test item in
aqueous environment and thus serve as a rational basis for risk
assessment for environmental fate in aqueous compartments.
Study Design
The test item was investigated for its ready biodegradability
in a dioxide evolution test (former Sturm test) over a period of 28
days. The biodegradation was followed measuring the production of carbon
dioxide (CO2) which is a clear indication of biodegradation.
The measured amount of carbon dioxide at the end of the test is compared
with the calculated maximal theoretical production (ThCO2) and indicated
as biodegradation degree in per cent. As the microorganisms oxidize only
a part of the test substance and incorporate the rest into biomass, a
degradation level >60 % is considered as sufficient biodegradation.
Result
Biodegradation
Under the test conditions the percentage biodegradation
amounts to 3 % (mean value) after 28 days of incubation.
The test item can therefore be considered not to be readily
biodegradable.
Biodegradation of Aniline
The reference item Aniline was sufficiently degraded to 95 %
after 14 days and 96 % after 28 days of incubation thus confirming the
suitability of the used activated sludge inoculum.
Biodegradation in the Toxicity
Control
In the toxicity control containing both, the test item and
the reference item Aniline, 42 % biodegradation was noted within 14 days
and 49 % biodegradation was determined after 28 days of incubation.
Thus, the test item can be assumed to be not inhibitory on the activated
sludge micro organisms.
Conclusion
The percentage biodegradation did not exceed 60 % within the
10-day window or after 28 days of incubation. The test item can
therefore be considered not to be readily biodegradable.
Bioaccumulation
OECD 305
The study was conducted in compliance with GLP regulations and in accordance with the OECD Test Guideline No.305 "Bioconcentration : Flow-through Fish test” (before 2ndOctober 2012).
10 fishes ofDanio rerio(Zebra fish) were used for acute toxicity test and 100 mg/L of Tween 80 was used as solubilising agent. LC50(96hr) was defined as >31 mg/L (limit test).
115 fishes (50 fishes for each test concentration, 15 fishes for control) ofCyprinus carpiowere used for the bioaccumulation test. Based on 96 hours LC 50 value the tests were performed in each 0.05 mg/L (1stconcentration), 0.005mg/L (2ndconcentration) of the test substance concentration and 0.15 mg/L (1stconcentration) 0.015 mg/L (2ndconcentration) of Tween 80 was used as solubiliging agent. Analysis of fish was done on 7th, 14th, 21st, 26thand 28thdays after the start of exposure.
Result
Concentration test result
|
Uptake period |
7 day |
14 day |
21 day |
26day |
28 day |
1stconcentration |
Test substance concentration in water (mg/L) |
0.0457 |
0.0495 |
0.0520 |
0.0506 |
0.0476 |
Concentration rate |
8 |
9 |
8 |
20 |
6 |
|
10 |
8 |
12 |
7 |
3 |
||
2ndconcentration |
Test substance concentration in water (mg/L) |
0.00477 |
0.00502 |
0.00494 |
0.00494 |
0.00468 |
Concentration rate |
<11 |
<11 |
31 |
27 |
<12 |
|
<11 |
25 |
<12 |
25 |
<12 |
Average recovery rate from water was determined as 94.5% (1stconcentration) and 94.2% (2ndconcentration) and average recovery rate from fish was determined as 86.2%.
Theoretical detection limit of BCF value was determined as≧1 (1stconcentration) and≧12 (2ndconcentration).
During 28 days exposure period BCF values showed less than 50fold through 28 days’ exposure period. Therefore 28 days after the start of exposure the concentration rate was regarded to reach steady state and the test was finished.
Bioconcentration factors (BCF) of the test substance in carp were 3 to 20 fold for the1stconcentration and 25 to 31 fold for the 2ndconcentration.
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.