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EC number: 249-720-9 | CAS number: 29598-76-3
- 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
Short-term toxicity to fish
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 14 August 2017 to 18 August 2017
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Version / remarks:
- OECD Guideline for Testing of Chemicals, No. 203, "Fish, Acute Toxicity Test", adopted July 17, 1992
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- Version / remarks:
- Commission Regulation (EU) 2017/735 of 14 February 2017 amending, for the purpose of its adaptation to technical progress, the Annex to Regulation (EC) No 440/2008 laying down test methods pursuant to Regulation (EC) No 1907/2006 of the European Parliament and of the Council on the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), Annex Part C, C.1.
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 850.1075 (Freshwater and Saltwater Fish Acute Toxicity Test)
- Version / remarks:
- EPA Health Effects Test Guidelines, OCSPP 850.1075
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- No further details specified in the study report.
- Analytical monitoring:
- yes
- Details on sampling:
- Duplicate samples were taken (40-40 mL) in plastic tubes at the test concentration at the beginning and at the end of the first and at the last renewal periods.
After sampling, samples were frozen and kept approximately at -20°C at the Test Facility. One set of the samples was sent to the Test Site for analysis and one set wasretained as a back-up at the Test Facility, if required for any confirmatory analyses (discarded after satisfactory results were obtained on the first set of). - Vehicle:
- no
- Details on test solutions:
- Because the test item is poorly soluble in water, a test solution, a test solution was
prepared using a saturated solution method (water accommodated fraction, WAF)
according to the Guidance Document on Aquatic Toxicity Testing of Difficult Substances and Mixtures, OECD No. 23.
Saturated test item solution (100 mg/L nominal loading rate WAF) was prepared by dispersing/dissolving the amount of test item into the test medium (aquarium water) two days before the start of the study. This solution was shaken for about 24 hours at approximately 30°C and then equilibrated for about 24 hours at approximately 20°C. The non-dissolved test material was removed by filtration through a fine (0.22 μm) filter to give appropriate 100 mg/L nominal loading rate WAF.
Since the test was performed under semi-static conditions, prior to the treatment, at each of the renewal periods, test item solution was prepared by the method described above.
Test solutions renewals were performed at 24-hour intervals during the experiment. - Test organisms (species):
- other: Zebrafish (Brachydanio rerio)
- Details on test organisms:
- Species: Zebrafish (Brachydanio rerio)
Source: István Szent University, 2100 Gödöllő, Páter Károly u. 1, Hungary
Justification of species: Zebrafish (Brachydanio rerio) is one of the convenient species for acute fish toxicity test.
Number of animals: seven fish per test group
Body length of animals: 2.6 – 2.9 cm
Food and Feeding: The fish were not fed during the test
Acclimatisation: more than 12 days
Animal health: Fish were bred in a well-known fish farm, under disease and parasite-controlled conditions. Fish were observed during the acclimatisation and test periods, the fish were healthy. There was no mortality of the population for seven days before the test. - Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- No post exposure observation period specified in the study report.
- Hardness:
- The hardness of the dilution water was determined as 194 mg/L (as CaCO3).
- Test temperature:
- The test temperature was between 20.3 and 21.7 °C.
- pH:
- The pH was in the range of 8.01 – 8.25.
- Dissolved oxygen:
- The dissolved oxygen concentration was in the range of 84 – 99 % of the air saturation value at the temperature used.
- Salinity:
- Not specified
- Conductivity:
- Not specified
- Nominal and measured concentrations:
- Test item concentration could not be detected and therefore measured concentration was below the Limit of Detection (LOD = 0.53 mg/L) at each measurement during the experiment, consequently biological results were based on the nominal loading rate WAF.
- Details on test conditions:
- ENVIRONMENTAL TEST CONDITIONS
The water temperature, oxygen concentration and pH were measured at the beginning and at the end of the renewal periods during the experiment in each test aquarium.
The test temperature was between 20.3 and 21.7 °C.
The dissolved oxygen concentration was in the range of 84 – 99 % of the air saturation value at the temperature used.
Test solutions were aerated during the test to avoid decreasing of dissolved oxygen concentration below the accepted level.
The pH was in the range of 8.01 – 8.25.
The hardness of the dilution water was determined as 194 mg/L (as CaCO3).
The light-dark cycle during the test was 16 hours light and 8 hours darkness.
DESCRIPTION OF THE TEST PROCEDURE
The test duration was 96 hours. One aquarium was used for test group and for the control group, respectively. Each aquarium comprised 7 fish and 5 L test solution. The animals were not fed during the test. The loading of the test aquaria was less than 1.0 g fish/L test solution at the start of the experiment.
The choice of the test concentrations was made on the basis of the results of the preliminary range-finding test.
Preliminary Range-Finding Test
A preliminary concentration range-finding test was conducted to determine the approximate toxicity of the test item so that appropriate test concentrations could be selected for use in the definitive test. Four fish were exposed to each concentration of the test item plus a control, for 96 hours under semi-static conditions (with 24-hour renewal in absence of stability data).
During the formulation procedure the test item stock solution was prepared individually by method described.
Test item concentrations in the Definitive Test
Because no toxic response was observed during the preliminary range-finding test, only one test concentration at 100 mg/L nominal loading rate WAF and one control group was tested in the definitive study in a semi-static system.
OBSERVATIONS
The observations of fish were carried out in the following intervals: at 3, 6, 24, 48, 72 and 96 hours. Mortality or any sub-lethal effects were not observed during the experiment.
The test conditions (pH, temperature, oxygen saturation) were measured at the beginning and at the end of the renewal periods during the test.
The body weights of the fish were recorded before the introduction of fish. The body weight of 7 fish per aquarium was registered. The loading of the aquaria was calculated on the basis of these body weights (1.0 g fish/litre testing liquid).
ANIMAL WELFARE
After the experiment, all fish were humanely killed. Euthanasia for all animals was applied by an overdose of an aqueous solution of 250 mg/L Tricaine Methanesulphonate (MS 222; CAS No.: 886-86-2). This technique is considered to provide a humane euthanasia by direct depression of the brain and vital centres. - Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 100 other: mg/L nominal loading rate WAF
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Key result
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 100 other: mg/L nominal loading rate WAF
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Details on results:
- MORTALITY DATA
No sub-lethal effect was observed.
BODY WEIGHT
There was no considerable difference observed concerning body weights between the groups. - Results with reference substance (positive control):
- None
- Reported statistics and error estimates:
- No statistical analysis was performed because of the lack of toxic effects.
- Sublethal observations / clinical signs:
Results of the Preliminary Range-Finding Test
Nominal loading rate WAF [mg/L]
Untreated control
0.1
1
10
100
Number of treated animals
4
4
4
4
4
Number of dead animals
0
0
0
0
0
Cumulative mortality data in the Limit Test
Test Group
Cumulative Mortality (number of dead fish)
[initial population = 7 fish]
3 h
6 h
24 h
48 h
72 h
96 h
Control
0
0
0
0
0
0
100 mg/L nominal loading rate WAF
0
0
0
0
0
0
Measured and calculated data of bodyweight
Test Group
Measured weight of 7 fish (g)
Calculated mean weight of 1 fish (g)
Loading of testing aquarium
(g fish/L testing liquid)
Control
1.73
0.25
0.35
100 mg/L nominal loading rate WAF
1.67
0.24
0.33
Temperature
Test Group
Temperature (°C)
Measuring
0h1)
24h2)
241)
482)
481)
722)
721)
962)
Control
21.7
20.4
21.6
20.3
21.5
20.5
21.3
20.4
100 mg/L nominal loading rate WAF
20.4
20.5
20.3
20.5
20.4
20.4
20.3
20.5
Dissolved oxygen concentration
Test Group
Dissolved oxygen concentration (%)
Measuring
0h1)
24h2)
241)
482)
481)
722)
721)
962)
Control
98
95
99
93
98
91
99
92
100 mg/L nominal loading rate WAF
87
92
85
91
85
98
85
88
pH
Test Group
pH
Measuring
0h1)
24h2)
241)
482)
481)
722)
721)
962)
Control
8.09
8.04
8.08
8.09
8.18
8.01
8.04
8.07
100 mg/L nominal loading rate WAF
8.18
8.15
8.24
8.25
8.24
8.14
8.15
8.18
1): measurement at the start of the renewal period in the fish test medium
2): measurement at the end of the renewal period in the old test medium
Body length of test fish at the end of the test
Test Group
Body length [cm]
1
2
3
4
5
6
7
Control
2.8
2.7
2.9
2.6
2.8
2.7
2.7
100 mg/L nominal loading rate WAF
2.7
2.6
2.8
2.7
2.9
2.8
2.7
Remark: At the end of the test, body length of test fish were measured in order to check their compliance with the size range recommended for the species by the test guideline [Commission Regulation (EC) No 440/2008; Annex Part C, C.1]
- Validity criteria fulfilled:
- yes
- Conclusions:
- The acute toxicity of 2,2-Bis[[3-(dodecylthio)-1-oxopropoxy]methyl]propane-1,3-diyl
bis[3-(dodecylthio)propionate]was assessed with acute fish toxicity test on Zebrafish
(Brachydanio rerio), over an exposure period of 96 hours in a semi-static system.
Under the conditions of the acute fish toxicity study on Zebrafish (Brachydanio rerio) the observed and calculated endpoints for the effect of 2,2-Bis[[3-(dodecylthio)-1-oxopropoxy]methyl]propane-1,3-diylbis[3-(dodecylthio)propionate] were the following:
The 24h, 48h, 72h and 96h LC50 value: > 100 mg/L nominal loading rate WAF
The 96h LC100 value: > 100 mg/L nominal loading rate WAF
The 96h No-Observed Effect Concentration (NOEC): 100 mg/L nominal loading rate WAF
The 96h Lowest Observed Effect Concentration (LOEC): > 100 mg/L nominal loading rate WAF - Executive summary:
The acute toxicity of the test item was assessed with acute fish toxicity test on Zebrafish (Brachydanio rerio), over an exposure period of 96 hours in a semi-static system.
Because no toxic response was observed during the preliminary range-finding test, only a Limit test was carried out using only one test concentration at 100 mg/L nominal loading rate WAF and one control group in the definitive study under static conditions.
The test concentration was analytically determined at the start and at the end of the first and at the last renewal periods. Test item concentration could not be detected and therefore measured concentration was below the Limit of Detection (LOD = 0.53 mg/L) for all WAF samples (freshly prepared and at renewal) during the experiment. The biological results are based on the nominal loading rate WAF.
One aquarium was used in the test group and one in the control group. Each aquarium comprised seven fish and five litre test solution.
All achievable validity criteria were met during this study.
Under the conditions of this acute fish toxicity study on Zebrafish (Brachydanio rerio) the observed and calculated endpoints for the effect of 2,2-Bis[[3-(dodecylthio)-1-oxopropoxy]methyl]propane-1,3-diylbis[3-(dodecylthio)propionate] were the following:
The 24h, 48h, 72h and 96h LC50 value: > 100 mg/L nominal loading rate WAF
The 96h LC100 value: > 100 mg/L nominal loading rate WAF
The 96h No-Observed Effect Concentration (NOEC): 100 mg/L nominal loading rate WAF
The 96h Lowest Observed Effect Concentration (LOEC): > 100 mg/L nominal loading rate WAF
Reference
Description of key information
The 24h, 48h, 72h and 96h LC50 value: > 100 mg/L nominal loading rate WAF
The 96h LC100 value: > 100 mg/L nominal loading rate WAF
The 96h No-Observed Effect Concentration (NOEC): 100 mg/L nominal loading rate WAF
The 96h Lowest Observed Effect Concentration (LOEC): > 100 mg/L nominal loading rate WAF
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Effect concentration:
- 100 mg/L
Additional information
The acute toxicity of the test item was assessed with acute fish toxicity test on Zebrafish (Brachydanio rerio), over an exposure period of 96 hours in a semi-static system.
Because no toxic response was observed during the preliminary range-finding test, only a Limit test was carried out using only one test concentration at 100 mg/L nominal loading rate WAF and one control group in the definitive study under static conditions.
The test concentration was analytically determined at the start and at the end of the first and at the last renewal periods. Test item concentration could not be detected and therefore measured concentration was below the Limit of Detection (LOD = 0.53 mg/L) for all WAF samples (freshly prepared and at renewal) during the experiment. The biological results are based on the nominal loading rate WAF.
One aquarium was used in the test group and one in the control group. Each aquarium comprised seven fish and five litre test solution.
Under the conditions of the acute fish toxicity study on Zebrafish (Brachydanio rerio) the observed and calculated endpoints for the effect of 2,2-Bis[[3-(dodecylthio)-1-oxopropoxy]methyl]propane-1,3-diylbis[3-(dodecylthio)propionate] were the following:
The 24h, 48h, 72h and 96h LC50 value: > 100 mg/L nominal loading rate WAF
The 96h LC100 value: > 100 mg/L nominal loading rate WAF
The 96h No-Observed Effect Concentration (NOEC): 100 mg/L nominal loading rate WAF
The 96h Lowest Observed Effect Concentration (LOEC): > 100 mg/L nominal loading rate WAF
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.
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