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Ecotoxicological information

Long-term toxicity to aquatic invertebrates

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Administrative data

Link to relevant study record(s)

Reference
Endpoint:
long-term toxicity to aquatic invertebrates
Type of information:
experimental study
Adequacy of study:
key study
Study period:
May-June 1995
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Remarks:
GLP
Qualifier:
according to guideline
Guideline:
other: OECD Test Guideline 202 (1984)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Specific details on test material used for the study:
The test material was supplied by the study Sponsor as follows:
- Common name: TCPP
- Product name: TCPP = Fyrol PCF
- Purity >99.5%
- Description: clear colourless liquid
Analytical monitoring:
yes
Details on sampling:
Determinations on test concentrations at 0, 2, 5, 7, 9, 12, 14, 16, 19, and 21 days. Samples were taken from the control and each surviving test group (replicates pooled).

Vehicle:
no
Test organisms (species):
Daphnia magna
Details on test organisms:
Daphnia magna (Straus) were maintained in a laboratory culture originating from a strain supplied by the Institut National de Recherche Chimique
Appliquee (I .R.CH.A.) France.
Adult Daphnia were maintained in polypropylene vessels containing approximately 2 litres of reconstituted water at a temperature of 21°C.
The lighting cycle was controlled to give a 16 hours light and 8 hours darkness cycle. Fed daily with a suspension of mixed algae.
Test type:
semi-static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
21 d
Hardness:
approximately 270 mg/L
Test temperature:
21.0
pH:
7.6 - 7.9
Dissolved oxygen:
7.9 - 8.6
Nominal and measured concentrations:
nominal test concentrations of : 10, 18, 32, 56 and 100 mg/L
Measured test concentrations were all in excess of the required 80% of nominal values with the exception of the 32 mg/L test group on days 2, 9, 16, 19 and 21 which showed measured concentrations of 75, 75, 75, 76 and 79 percent of nominal respectively. These low values were considered to be due to analytical and /or sampling variation given that the measured concentrations on all other sampling occasions were near nominal.
Reference substance (positive control):
no
Key result
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
32 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality
Remarks:
parent
Key result
Duration:
21 d
Dose descriptor:
NOEC
Effect conc.:
32 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
reproduction
Duration:
21 d
Dose descriptor:
EC50
Effect conc.:
40 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
immobilisation
Remarks:
parent
Details on results:
The overall mean measured concentrations were shown to range from 85 - 102% of nominal therefore it was considered justifiable to
calculate EC50 values in terms of nominal test concentrations only.
Reported statistics and error estimates:
The EC50 (immobilisation) values and associated confidence limit were calculated by the moving average method of Thompson (1947). The numbers of young produced per adult for the control and each test group were compared using one way analysis of variance (ANOVA) incorporating an Fmax test for homogeneity of variance and the Williams test for differences between treatment means when several dose levels are compared with a zero dose control.

Table - Surviving Adults During the Test














































































































































































































DayNominal Concentration (mg/L)
010183256100
1404040404040
2404040404040
3404040404040
4404040403938
5404040403017
640404040277
740404040233
84040404071
94040404060
104040404040
114040404010
124040404000
134040404000
144040404000
154040404000
164040404000
174040404000
184040404000
194040403800
204040403700
214040403700

Table - Total Cumulative Production of Young



































































































Nominal Concentration (mg/L)Day
025791214161921
000054282715973132416841973
10000352427101018139017752137
1800036234667941127116321927
3200041257672921119915141862
5600000A/D----
1000000A/D-----

 

Validity criteria fulfilled:
yes
Remarks:
Control mortality /= 60 %; First young produced within 9 days; cumulative young per female >/= 20 after 14 days and >/= 40 after 21 days; Number of broods per control>/= 3
Conclusions:
No impairment of reproduction was observed at the lower test concentrations of 10, 18 and 32 mg/l TCPP. The "No Observed Effect Concentration" (NOEC) of TCPP is therefore given as 32 mg/l.
Executive summary:

The chronic toxicity of TCPP to aquatic invertebrates (Dapnia magna) was conducted in a semistatic reproduction test according OECD Guideline for Testing of Chemicals 202 (1984). After 21 days of exposure a NOEC-reporduction of 32 mg/l and EC50-reproduction of 40 mg/l were determined. The results relate to nominal concentration, as the exposure concentrations were confirmed by chemical analysis. The analytical monitoring was performed via gaschromatography with external standard calibration. All validity criteria like control mortality, dissolved oxygen, pH, first young, cumulative young per female and number of broods per control group were fulfilled.

Description of key information

Chronic toxicity of TCPP to aquatic invertebrates (Daphnia magna) was assessed in a reproduction test, performed according the OECD Guideline for Testing of Chemicals 202, (1984). After 21 days of exposure a NOEC for reproduction of 32 mg/l was determined. 

Key value for chemical safety assessment

Fresh water invertebrates

Fresh water invertebrates
Effect concentration:
32 mg/L

Additional information

The chronic toxicity of TCPP to aquatic invertebrates (Daphnia magna) was conducted in a semistatic reproduction test according OECD Guideline for Testing of Chemicals 202 (1984). After 21 days of exposure a NOEC-reporduction of 32 mg/l and EC50-reproduction of 40 mg/l were determined. The results relate to nominal concentration, as the exposure concentrations were confirmed by chemical analysis. The analytical monitoring was performed via gaschromatography with external standard calibration. All validity criteria like control mortality, dissolved oxygen, pH, first young, cumulative young per female and number of broods per control group were fulfilled.