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EC number: 203-004-2 | CAS number: 102-08-9
- 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 aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2012 - 2013
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- Storage of samples: No
Samples treatment: Dilution with acetonitrile - Details on test solutions:
- For the range finding test and for the definitive test, a stock solution at 100 mg/L of the test item was prepared the day of the starting test by mixing 100 mg of the test item N,N’-DIPHENYL THIOUREA in 1 liter of dilution water. This solution was stirred during 5 h and was filtered through ester cellulose Millipore filter 0.45µm (HAWP 04700) to obtain limpid solution.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Daphnia magna Straus (Cladocera, Crustacea), clone 5 or clone A. Animals come from a stock breeding in the laboratory reared in VOLVIC® water added with vitamin B12, Na2SeO3, 5H2O, calcium and magnesium salts and fed with unicellular green fresh-water algae Pseudokirchneriella subcapitata and Chlorella Vulgaris. Selection of test organisms less than 24 hours-old is made by filtration.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- Not specified
- Test temperature:
- The temperature, continuously recorded in one test flask, remained between 20.1 and 20.6°C and was constant w ithin ± 1°C
- pH:
- see "Any other information on results incl. tables"
- Dissolved oxygen:
- see "Any other information on results incl. tables"
- Salinity:
- NC
- Nominal and measured concentrations:
- Preliminary test, range of nominal concentrations: 100, 50, 10, 5, 1 and 0.1 mg/L.
Definitive test, range of nominal concentrations: 100, 54.8, 30.0, 16.8, 9.2 and 5 mg/L. - Details on test conditions:
- The study was performed in a temperature-controlled room using 30 mL glass bottles stoppered with PTFE bungs and sealed with aluminium caps. The temperature, continuously recorded in one test flask, remained between 20.1 and 20.6°C and was constant w ithin ± 1°C according to OECD 202 Guideline.
Physical-chemical parameters were measured using a METTLER TOLEDO 345 pH-meter for measurement of pH and with a WTW OXI 538 oxymeter for dissolved oxygen measurement.
Water: ultra-pure water was used for the preparation of dilution water (resistivity > 18M).
Definitive and preliminary test: approximately 90% of the final volume of the test solution was added into test flasks. Five Daphnia magna aged from 6 to 24 hours were added into each test flask, which were then totally filled with the test solution (30 mL)
In the preliminary test, daphnids were exposed under static conditions to a series of 6 concentrations (100, 50, 10, 5, 1, 0.1 mg/L) of N,N’-DIPHENYL THIOUREA in dilution water.. Two replicates were prepared for each concentration. Two control flasks were prepared under the same conditions, with no test item. Test flasks were incubated in darkness at a temperature of 20 °C.
After 48 hours of incubation, mobile Daphnia magna were counted.
Dissolved O2 and pH were measured at the highest tested concentration and in the control.
Based on the results of preliminary test, the concentrations tested were: 100, 54.8, 30, 16.8, 9.2 and 5 mg/L. Volumetric flasks were filled with the required volumes of the test item stock solution and dilution water in order to obtain the test solutions at concentrations varying from 100 mg/L to 5 mg/L.
The definitive test was performed with a concentration range forming a geometric progression with a factor of 1.82. Four replicates were prepared for each concentration. Four control flasks were prepared under the same conditions, with no test item. Test flasks were incubated in darkness at a temperature of 20.3 ± 0.3°C.
Dissolved O2 and pH were measured at the highest concentration and in the control at the beginning and at all concentration and in the control the end of the test - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
- Duration:
- 48 h
- Dose descriptor:
- EC10
- Effect conc.:
- 2.3 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 95% CL (1.7-3.5)
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 10.2 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 95% CL (7.9-15)
- Details on results:
- The appearance of the test solutions was visually checked at the beginning and at the end of the test. Solutions were found to be clear, colourless over the period of the test. No precipitation was observed at the end of the test.
EC10 and EC50 calculated by Probit analysis have been recalculated using the software ToxRat. - Results with reference substance (positive control):
- The sensitivity of the test system and the methodology are evaluated every month by performing an inhibition test on potassium dichromate. The nearest value of EC50 obtained on May 2012 was 0.76 mg/L For reference, ISO 6341 has a validity criteria specifying that EC50 must be in the range 0.6 to 2.1 mg/L.
- Reported statistics and error estimates:
- Originally, the inhibition of mobility data were analyzed using an Excel program. It was designed to calculate the EC50 and the EC10 values and the 95% confidence intervals.
EC10 and EC50 have been recalculated using the software ToxRat (v.3.3.0) - Validity criteria fulfilled:
- yes
- Remarks:
- see conclusions
- Conclusions:
- The acute toxicity (inhibition of mobility) of the test item N,N’-DIPHENYL THIOUREA for a duration of 48 hours was assessed according to the OECD Guideline 202 under GLP.
The study was performed in compliance with the following quality criteria:
· The immobilisation in the control did not exceed 10 per cent at the end of the test;
· Daphnids in the control were not trapped at the surface of the water;
· The dissolved oxygen concentration remained above 3 mg/L over the test period. - Executive summary:
The acute toxicity (inhibition of mobility) of the test item N,N’-DIPHENYL THIOUREA for a duration of 48 hours was assessed according to the OECD Guideline 202 under GLP. Daphnia magna were exposed under static conditions to a range of concentrations of N,N’-DIPHENYL THIOUREA dissolved in dilution water. The toxic effect measured during the assay was the inhibition of mobility over time periods of 24 and 48 hours.
The concentration of test item causing a 50% reduction in mobility (EC50) was estimated as follows (geometric mean of measured concentration):
EC50-48h = 10.2 mg/L
Reference
Definitive test - Percentage of Daphnia magna immobilisation
Concentration (extrapolated) mg/L | Immobilisation (%) | |
24 h | 48 h | |
32.2 | 0 | 80 |
15.3 | 0 | 65 |
8.9 | 0 | 50 |
5.0 | 0 | 25 |
2.5 | 0 | 15 |
1.1 | 0 | 0 |
< DL | 0 | 0 |
Dissolved O2 and pH measured at the beginning and at the end (48h) of the exposition
Nominal concentration mg/L | pH | Dissolved O2 (mg/L) | ||
T0 | T48h | T0 | T48h | |
0 (T) | 8.12 | 7.66 | 9.0 | 8.4 |
5 | 7.96 | 7.70 | 8.3 | |
9.2 | 7.96 | 7.77 | 8.4 | |
16.8 | 7.99 | 7.76 | 8.4 | |
30 | 7.98 | 7.77 | 8.4 | |
54.8 | 7.98 | 7.78 | 8.5 | |
100 | 7.99 | 7.85 | 8.6 |
Nominal and measured concentrations of the test item at the beginning and at the end of the exposure period
Nominal (mg/L) | Measured in solutions | Extrapolated* Initial (mg/l) | ||
Initial (mg/l) | Final (mg/l) | Final/Initial % | ||
100 | 33.6 | 30.9 | 92 | 32.2 |
54.8 | 17.8 | 13.1 | 73 | 15.3 |
30 | 9.57 | 8.35 | 87 | 8.9 |
16.8 | 5.57 | 4.55 | 82 | 5.0 |
9.2 | 3.02 | 2.12 | 70 | 2.5 |
5 | 1.71 | 0.72 | 42 | 1.1 |
0 | < DL | < DL | - | < DL |
< QL: concentration lower than the Quantification Limit of the analytical method (0.15mg/L).
< DL: concentration lower than the Quantification Limit of the analytical method (0.045mg/L).
* Concentrations calculated using geometric mean
According to OECD guidance document on aquatic toxicity testing of difficult substances and mixtures
(n°23):
- For static tests, where the concentrations remain within 80-120% of nominal, the effect concentrations can be expressed relative to nominal or measured concentrations;
- For static tests, where the concentrations do not remain within 80-120% of nominal, the effect concentrations could be determined and expressed relative to the geometric mean of the measured concentrations.
As the ratio is lower than 80% for some final concentrations, extrapolated concentrations are used for the calculation of effective concentrations
Description of key information
The acute toxicity was assessed according to the OECD Guideline 202.
48h-EC50 = 10.2 mg/L
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 10.2 mg/L
Additional information
The acute toxicity (inhibition of mobility) of the test item N,N’-DIPHENYL THIOUREA for a duration of 48 hours was assessed according to the OECD Guideline 202 under GLP. Daphnia magna were exposed under static conditions to a range of concentrations of N,N’-DIPHENYL THIOUREA dissolved in dilution water. The toxic effect measured during the assay was the inhibition of mobility over time periods of 24 and 48 hours.
The concentration of test item causing a 50% reduction in mobility (EC50) was estimated as follows (geometric mean of measured concentration):
48h-EC50 = 10.2 mg/L
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