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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Ecotoxicological information

Short-term toxicity to fish

Currently viewing:

Administrative data

Link to relevant study record(s)

Referenceopen allclose all

Endpoint:
short-term toxicity to fish
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
test procedure in accordance with national standard methods with acceptable restrictions
Qualifier:
according to guideline
Guideline:
other: US EPA 1975, Methods for acute toxicity tests with fish, macroinvertebrates and amphibians.
Deviations:
no
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 203 (Fish, Acute Toxicity Test)
Deviations:
not applicable
GLP compliance:
no
Analytical monitoring:
no
Vehicle:
no
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION

- Method: an appropriate amount of CP65184 was added directly to the sea water in each test vessel to obtain the desired concentrations.

- Controls: sea water only
Test organisms (species):
Cyprinodon variegatus
Details on test organisms:
TEST ORGANISM

- Common name: sheepshead minnow

- Source: stocked ponds at BMRL

- Length at study initiation (range): 15-20 mm

- Method of breeding: not reported

- Feeding during test: animals were not fed during test



ACCLIMATION

- Acclimation period: min. 7 days

- Acclimation conditions (same as test or not): not reported

- Health during acclimation (any mortality observed): <1%
Test type:
static
Water media type:
saltwater
Limit test:
no
Total exposure duration:
96 h
Test temperature:
20 +/- 1 degC
pH:
Initial pH ranged from 5.4 in the highest concentration to 7.0 in the lowest concentration, controls were 8.3. Final pH ranged from 5.5 in the highest concentration to 7.1 in the lowest concentration, controls were 8.2.
Dissolved oxygen:
≥ 60% saturation
Salinity:
25 parts per thousand
Nominal and measured concentrations:
Nominal test concentrations were 1000, 10000, 18000, 32000 and 56000 ppm (ul/L)
Details on test conditions:
TEST SYSTEM

- Test vessel: jars

- Type (delete if not applicable): open

- Material, size, fill volume: 19 L uncovered glass jars with 15L test medium.

- Aeration: no

- No. of organisms per vessel: 10

- No. of vessels per concentration (replicates): 1

- No. of vessels per control (replicates): 1


TEST MEDIUM / WATER PARAMETERS

- Source/preparation of dilution water: natural filtered (5 um filters) sea water

- Culture medium different from test medium: no

- Intervals of water quality measurement: pH was measured at the beginning and end of the test; salinity, temperature and DO intervals of measurements are not reported.


OTHER TEST CONDITIONS

- Adjustment of pH: no

- Photoperiod: not reported

- Light intensity: not reported


EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : mortality was observed at 0, 24, 48 and 96 h.


TEST CONCENTRATIONS

- Spacing factor for test concentrations: 1.8-2

- Range finding study: not reported
Reference substance (positive control):
no
Duration:
96 h
Dose descriptor:
NOEC
Effect conc.:
104 mg/L
Nominal / measured:
nominal
Conc. based on:
act. ingr.
Basis for effect:
mortality (fish)
Remarks on result:
other: results corrected for active acid and density of TS
Duration:
96 h
Dose descriptor:
LC50
Effect conc.:
2 180 mg/L
Nominal / measured:
nominal
Conc. based on:
act. ingr.
Basis for effect:
mortality (fish)
Remarks on result:
other: results are corrected for active acid and density of TS
Details on results:
- Mortality of control: 0%
Reported statistics and error estimates:
LC50 values were calculated by linear regression.
Sublethal observations / clinical signs:

Table 1. Summary of findings.

  Nominal concentraions (ul/L/ppm)    Mortalities (%)       
 24 h  48 h  96 h
 Control  0  0  0
 1,000  0  0  0
 10,000  0  0  0
 18,000  30  50  50
 32,000  50  80  90
 56,000  100  100  100

Result expressed as nominal concentration. Properties of the test substance and evidence from other studies (where
concentrations were measured) indicate that nominal and measured concentrations are likely to be in good agreement.

LC50 corrected for density (1.1) and % active acid (9.42%),


24 hr LC50: 2455 mg/L active acid and 48 hr LC50: 2240 mg/L active acid (corrected), uncorrected values were 24 hr LC50: 23644, 48 hr LC50: 21573 and 96 hr LC50: 20997 all in uL/L (reported as ppm).

Validity criteria fulfilled:
no
Remarks:
the pH of the test medium lowered with increasing concentration
Conclusions:
A 96 h LC50 value of 2180 mg/L (active acid) has been determined for the effects of HEDP acid (CAS 2809-21-4) on mortality of saltwater water fish C. variegatus.
Endpoint:
short-term toxicity to fish
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1979-03-14 to 1979-03-28
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
test procedure in accordance with national standard methods with acceptable restrictions
Qualifier:
according to guideline
Guideline:
other: methods based on  Methods for Acute Toxicity Tests with Fish, Macroinvertebrates, and Amphibians, USEPA, 1975
Deviations:
not applicable
Qualifier:
according to guideline
Guideline:
other: study carried out based on ABC protocol 7807
Deviations:
yes
Remarks:
lower flow rate
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 204 (Fish, Prolonged Toxicity Test: 14-day Study)
Deviations:
not applicable
GLP compliance:
yes
Analytical monitoring:
yes
Details on sampling:
- Concentrations: All

- Sampling method: samples were taken on days 0, 1, 5, 10 and 14
Vehicle:
no
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)

- Method: a stock solution of 256.5 g/L (method of dispersion not stated) was diluted according to achieve the required concentrations. The nominal concentrations of D2010 were determined by measuring predetermined dilutions of a stock Rhodamine B dye.
Test organisms (species):
Oncorhynchus mykiss (previous name: Salmo gairdneri)
Details on test organisms:
TEST ORGANISM

- Common name: rainbow trout

- Source: Fish obtained from Spring Creek Hatchery, Lewiston, Montana. 

- Length at study initiation (mean): 33.2 mm

- Weight at study initiation (mean): 0.75 g

- Method of breeding: fish culture techniques were basically those described by Brauhn et al.

- Feeding during test

- Food type: standard commercial fish food (Rangen's)

- Amount: 3% body weight

- Frequency: daily


ACCLIMATION

- Acclimation period: at least 14 days, fish acclimatised to test temperature for 48 h.

- Acclimation conditions (same as test or not): similar holding conditions, but pH and ionic strength of the test solution 262 mg/L were significantly different from holding water (author's note).

- Type and amount of food: commercial fish food (Rangen's), 3% of body weight

- Feeding frequency: daily

- Health during acclimation (any mortality observed): some mortalities observed, mostly on the first day of stock arrival


QUARANTINE (wild caught)
- Duration:
- Health/mortality:
Test type:
flow-through
Water media type:
freshwater
Limit test:
no
Total exposure duration:
14 d
Hardness:
240 mg/L as CaCO3 (dilution water)
Test temperature:
Temperature maintained at 12 +/- 1 degree C.
pH:
The pH of the test media ranged between 6.3-6.6 in the high concentration to 7.1-7.2 in the low concentration. Control: 7.8-7.9
Dissolved oxygen:
>7.3 mg/L
Nominal and measured concentrations:
Nominal concentrations (mg/L active acid) were 30, 65, 125, 255, and 500 mg/L (active acid)
Actual concentrations determined on days 0, 1, 5, 10 and 14 and were 32, 60, 124, 270, and 529 mg/L (mean measures as active acid). See table 2 for details.
Details on test conditions:
TEST SYSTEM

- Test vessel: aquaria

- Material, size, headspace, fill volume: glass aquaria, filled with 30 L test solution

- Type of flow-through (e.g. peristaltic or proportional diluter): Mount & Brung proportional diluter

- Renewal rate of test solution (flow rate): 200 ml/min, the ABC protocol suggests a 300 ml/min flow rate

- No. of organisms per vessel: 30

- No. of vessels per concentration (replicates): 1

- No. of vessels per control (replicates): 1



TEST MEDIUM / WATER PARAMETERS

- Source/preparation of dilution water: well water

- Alkalinity: 300 mg/L as CaCO3

- Culture medium different from test medium: no

- Intervals of water quality measurement: Temperature, DO, and ammonia were measured on days 0, 1, 5, 10, and 14 in control, low concentration, and high concentration samples.


OTHER TEST CONDITIONS

- Adjustment of pH: not reported

- Photoperiod: 16 h light, 8 h dark


EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : the fish were observed for mortality and abnormal behaviour every 24 h.


TEST CONCENTRATIONS

- Spacing factor for test concentrations: 1.9-2.1

- Range finding study: not conducted
Reference substance (positive control):
yes
Remarks:
Antimycin A
Duration:
24 h
Dose descriptor:
LC50
Effect conc.:
310 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
act. ingr.
Basis for effect:
mortality (fish)
Duration:
48 h
Dose descriptor:
LC50
Effect conc.:
279 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
act. ingr.
Basis for effect:
mortality (fish)
Duration:
72 h
Dose descriptor:
LC50
Effect conc.:
200 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
act. ingr.
Basis for effect:
mortality (fish)
Duration:
14 d
Dose descriptor:
LC50
Effect conc.:
180 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
act. ingr.
Basis for effect:
mortality (fish)
Duration:
14 d
Dose descriptor:
NOEC
Effect conc.:
60 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
act. ingr.
Basis for effect:
behaviour
Remarks:
loss of equilibrium
Duration:
96 h
Dose descriptor:
LC50
Effect conc.:
195 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
act. ingr.
Basis for effect:
mobility
Details on results:
- Observations on body length and weight: (14 day) weight measurements of the surviving fish yielded the following weight percentages of the control group mean weight: 79% - 32 mg/L, 79% - 60 mg/L, 85% - 124 mg/L

- Other biological observations: backbone curvature was noticed on day 1 at higher concentrations, this has been explained by the author to be attributable to the different pH and ionic strength between holding water and exposure test water. Symptoms typically disappeared after 24 h.

- Mortality of control: 0%
Results with reference substance (positive control):
- Results with reference substance valid? yes

- LC50: not reported

- Results with reference substance valid? yes

- Mortality: 100% after 24 h at conc. 0.000042 mg/L

- LC50: 0.000032 mg/L
Reported statistics and error estimates:
LC50 and 95% confidence intervals determined by the method of Litchfield and Wilcoxon.
Sublethal observations / clinical signs:

Table 1. Recorded mortalities.

                                                           

 Measured concentrations (mg/L active acid)    Mortalities (%)                 
day 1  day 2  day 3  day 4  day 6 day 10  day 14
Control   0
 32  0  0  0  0  0  0  0
 60  0  0  0  0  0  0  0
 124  0  0  0  0  0  0  0
 270  33 53  90  93  93  100  100
 529  97  100  100  100  100  100  100

8h

Determined LC50 (other than the ones transcribed above):

24 h: 310 mg/L active acid

48 h: 270 mg/L active acid

day 4-6: 200 mg/L active acid

day 7 -14: 180 mg/L active acid

Table 2. Nominal and measured concentrations of D2010 as active acid.

Nominal Concentrations (mg/L active acid)     Measured concentrations (mg/L active acid)                               
Day 0   Day 1     Day 5     Day 10     Day 14     Mean   
 P  D2010  P  D2010  P  D2010  P  D2010  P  D2010  P  D2010
0  0.05  -  0.05  -  0.2  -  0  -  0  -  -  -
30  9.9  33  4.5*  15*  10.5  35  9.1  30  8.7  29  9.6  32
65  19.75  66  1.2*  4*  19  63  15  50  18.5  62  18  60
125  30  100  5.0*  17*  40  133  38.5  128  40  133  37  124
 255  74  246  31*  103*  85  283  80  266  85  283  81  270
 500  157.5  524  150  499  165  549  155  516  167.5  558  159  529

* author's note: Day 1 phosphorous values were much lower than expected and were not used in the calculations for mean Dequest 2010 levels. It was not determined why these samples did not correspond to phosphorous concentrations measured previously (day 0) and later (day 5). However, it was observed that sample aliquots during the analytical process were cloudy; indicating an interfering complex or incomplete sample digestion. An acceptable day 1 high concentration indicated that no malfunctions had occurred in the test system.


In order to achieve D2010 from P values the following equation was followed:

Total P (mg/L) * 5.54 (conversion factor for converting P to 2010 ) * 0.601 (correction factor for percent purity) = D2010 (mg/L active acid)


Validity criteria fulfilled:
yes
Conclusions:
A 96 h LC50 value of 195 mg/L (as active acid) and a 14 day LC50 of 180 mg/L (as active acid) have been determined for the effects of HEDP acid (CAS 2809-21-4) on mortality of the freshwater fish Salmo Gairdneri (now known as Onychorhynchus mykiss).
Endpoint:
short-term toxicity to fish
Type of information:
read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Justification for type of information:
Please refer to Annex 3 of the CSR and IUCLID Section 13 for justification of read-across between members of the HEDP category.
Reason / purpose for cross-reference:
read-across source
Reason / purpose for cross-reference:
read-across source
Duration:
96 h
Dose descriptor:
LC50
Effect conc.:
195 mg/L
Nominal / measured:
nominal
Conc. based on:
act. ingr.
Basis for effect:
mortality (fish)
Remarks on result:
other: ABC 1979
Duration:
96 h
Dose descriptor:
LC50
Effect conc.:
2 180 mg/L
Nominal / measured:
nominal
Conc. based on:
act. ingr.
Basis for effect:
mortality (fish)
Remarks on result:
other: EG&G 1976
Duration:
96 h
Dose descriptor:
NOEC
Effect conc.:
104 mg/L
Nominal / measured:
nominal
Conc. based on:
act. ingr.
Basis for effect:
mortality (fish)
Remarks on result:
other: EG&G 1976

Description of key information

96-hour LC50 195 mg active acid/L, Oncorhynchus mykiss,

96-hour LC50 2180 mg active acid/L, Cyprinodon variegatus.

Key value for chemical safety assessment

Fresh water fish

Fresh water fish
Dose descriptor:
LC50
Effect concentration:
195 mg/L

Marine water fish

Marine water fish
Dose descriptor:
LC50
Effect concentration:
2 180 mg/L

Additional information

Freshwater

The lowest result in terms of HEDP active acid is for a study with HEDP-H, therefore this study has been chosen as key. A reliable 96-hour LC50 value of 195 mg active acid/L has been determined for the effects of HEDP-H on the mortality of Salmo gairdneri (now known as O. mykiss) (ABC, 1979). This value is taken from a 14-day study, where the 96-hour LC50 has been reported. The same study determined a 14-day NOEC of 60 mg active acid/L and a 14-day LC50 of 180 mg active acid/L. Additional data on short term toxicity of HEDP-H and HEDP (2-3Na) to freshwater fish are available indicating low short-term toxicity to fish with LC50 values ranging between 207-2440 mg active acid/L (some values were only reported in terms of test substance concentration) (Industrial Bio-Test, 1972; Henkel, 1972; EG&G, 1976a-c; Henkel, 1979a and b; Kastner and Gode, 1983; Schmaland, 1987a and undated; Schoberl & Huber 1988a and b). Some supporting studies were assigned reliability 4 due to coming from secondary literature or due to insufficient documentation (Henkel, 1972; Henkel, 1979a and b; Kastner and Gode, 1983; Schoberl and Huber 1988a and b).

Marine

A reliable 96-hour LC50 value of 2180 mg active acid/L has been determined for the effects of HEDP-H on mortality of Cyprinodon variegatus (EG&G, 1976).

The acid, sodium and potassium salts in the HEDP category are freely soluble in water and, therefore, the HEDP anion is fully dissociated from its sodium or potassium cations when in solution. Under any given conditions, the degree of ionisation of the HEDP species is determined by the pH of the solution. At a specific pH, the degree of ionisation is the same regardless of whether the starting material was HEDP-H, HEDP (1-2Na), HEDP (2-3Na), HEDP-4Na, HEDP-xK or another salt of HEDP.

 

Therefore, when a salt of HEDP is introduced into test media or the environment, the following is present (separately):

  1. HEDP is present as HEDP-H or one of its ionised forms. The degree of ionisation depends upon the pH of the system and not whether HEDP (1-2Na), HEDP (2-3Na), HEDP-4Na, HEDP-xK salts, HEDP-H or another salt was added.
  2. Disassociated sodium/potassium cations. The amount of sodium/potassium present depends on which salt was added.
  3. Divalent and trivalent cations have much higher stability constants for binding with HEDP than the sodium or potassium ions, so would preferentially replace them. These ions include calcium (Ca2+), magnesium (Mg2+) and iron (Fe3+). Therefore, the presence of these in the environment or in biological fluids or from dietary sources would result in the formation of HEDP-dication (e.g. HEDP-Ca, HEDP-Mg) and HEDP-trication (e.g. HEDP-Fe) complexes in solution, irrespective of the starting substance/test material.

In this context, for the purpose of this assessment, read-across of data within the HEDP Category is considered to be valid.