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EC number: 248-953-3 | CAS number: 28305-25-1
- 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
Toxicity to aquatic algae and cyanobacteria
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Justification for type of information:
- For details and justification of read-across please refer to the read-across report attached to IUCLID section 13.
- Reason / purpose for cross-reference:
- read-across source
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 2 900 mg/L
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- EC20
- Effect conc.:
- 1 000 mg/L
- Basis for effect:
- biomass
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 4 000 mg/L
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC20
- Effect conc.:
- 2 700 mg/L
- Basis for effect:
- growth rate
- Conclusions:
- The 72-hour EC50 and EC20 for calcium chloride obtained on the basis of growth rate were >4000 (higher than the highest test dose) and 2700 mg/L, respectively.
- Executive summary:
This information is used in a read-across approach in the assessment of the target substance. For details and justification of read-across please refer to the read-across report attached to IUCLID section 13.
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Justification for type of information:
- For details and justification of read-across please refer to the read-across report attached to IUCLID section 13.
- Reason / purpose for cross-reference:
- read-across source
- Post exposure observation period:
- None
- pH:
- Buffered solutions
- Salinity:
- Not applicable, freshwater species
- Key result
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- > 533 mg/L
- Nominal / measured:
- meas. (TWA)
- Conc. based on:
- act. ingr.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 1.9 g/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- ca. 3.5 g/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Remarks on result:
- other: 95 % CI = 2.8–4.4
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 2.8 g/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Details on results:
- By visual comparison of the measured and the calculated growth curves of algal suspensions exposed to the test substance with those of the algal controls the no-observed-effect-concentration (NOEC) of the 80 % aqueous solution of L(+)-lactic acid was estimated to be 1.9 g/L. Microscopic examination of the cells at the start and end of the incubation period revealed no abnormalities, however many bacteria were found in the cultures exposed to test substance concentrations of 1.0, 1.9 and 2.8 g/L.
The pH of the algal medium containing different test substance concentrations was adjusted to the range pH 7.5-8.0 at the start of the test. It was found to remain constant (pH 8.0-8.1) during the test. In the presence of algae the pH was found to slightly increase with algal cell density (pH 8.2-8.7). - Validity criteria fulfilled:
- yes
- Conclusions:
- The NOEC of lactic acid (pH adjusted to approximately 8) to green algae is higher than 533 mg/L actual concentration of lactate (TWA).
- Executive summary:
In a 72 hour acute toxicity study, cultures of Selenastrum capricornutum (ATCC 22662) were exposed to L(+) lactic acid (80 %) at nominal concentrations of 0, 0.10, 0.33, 0.56, 1.0, 1.9 and 2.8 g/L under static conditions in accordance with the OECD 201 guideline. The NOEC and EC50 values based on growth rate were 1.9 g/L and 3.5 g/L, respectively. There were no compound-related phytotoxic effects. This toxicity study is classified as acceptable and satisfies the guideline requirements for alga growth inhibition study with S. capricornutum.
Results synopsis
Test organism: Selenastrum capricornutum
Test type: Static
72-hr EbC50: > 2.8 g/L (95% C.I.: 2.24–3.52 g/L), in terms of lactic acid
72-hr NOEC: > 533 mg/L, in terms of lactic acid
Endpoint(s) effected: Growth, abnormalities of the cells
This information is used in a read-across approach in the assessment of the target substance. For details and justification of read-across please refer to the read-across report attached to IUCLID section 13.
An effect on the inoculum viability, as found in this test, may be expected when a substance loses its toxicity during the test, in this case probably due to biodegradation. The concentrations quoted in this report are the nominal concentrations of the test substance (a solution of about 80 % L(+) lactic acid) as supplied by sponsor. At the start of the test 65–82 % of the nominal test substance concentrations were found by chemical analysis. At the end of the test the concentrations were considerably lower: 15, 57 and 73 % at the three concentrations analysed. The actual concentrations of lactic acid tested at the start of the test were < 0.005, 0.020–0.065, 0.44–0.62, 1.45–1.74 g/L. According to the calculated time-weighted mean (see formula below from the OECD guideline 211: TWM = (conc0 – conc1)/(LN(conc0) – (LN(conc1))) the concentrations which should be used for effect calculations are 31 mg/L, 533 mg/L, and 1620 mg/L. The EC50 and the NOEC from the test report have to be regarded as invalid, as they were calculated on the basis of nominal values. Concerning the NOEC of 1.9 g/L, the replicates with the test concentration of 1.9 g/L were not verified analytically. Therefore, no conclusion on the actual concentration can be drawn. However, the next lower concentration was assessed analytically, revealing that the NOEC is above 533 mg/L (time-weighted mean of the measured lactic acid concentration).
Referenceopen allclose all
Table: Measured algal cell densities
--------------------------------------------------
Nominal test Cell density x 10^4 (cells/ml)
concentration
--------------------------------------------------
(mg/l) Day 1 Day 2 Day 3
--------------------------------------------------
0 2.494 15.24 77.62
0 2.324 13.05 61.49
0 2.282 14.10 68.88
0 2.409 15.44 74.73
0 2.536 16.15 81.91
0 2.367 13.62 63.51
1000 1.859 9.106 39.74
1000 2.240 13.43 70.85
1000 2.071 12.02 60.09
1400 1.902 10.99 48.54
1400 1.859 10.19 46.84
1400 1.817 10.86 48.29
2000 1.859 17.49 33.98
2000 2.113 15.82 43.79
2000 1.902 12.52 32.03
2800 1.986 12.52 44.04
2800 2.155 8.389 30.73
2800 1.732 9.645 26.78
4000 1.775 8.299 19.88
4000 1.563 6.336 19.26
4000 1.732 11.93 18.35
----------------------------------------------------
Table: Percent biomass inhibition per concentration
----------------------------------------------------
Nominal test Percent growth inhibition
concentration
----------------------------------------------------
(mg/l) Area under the growth curve
----------------------------------------------------
0 0
1000 21.2
1400 33.6
2000 35.6
2800 47.1
4000 64.9
----------------------------------------------------
Table: Water parameters of test solutions
----------------------------------------------------
concentration Temperature pH
CaCl2 (mg/l) (°C)
----------------------------------------------------
0 22.2 8.5
1000 22.2 7.5
1400 22.4 7.8
2000 22.2 7.9
2800 22.3 7.9
4000 22.3 7.8
----------------------------------------------------
Table: EC50 and EC20
----------------------------------------------------
Hours of EC50 EC20
exposure (mg/l) (mg/l)
----------------------------------------------------
72 2900 1000
----------------------------------------------------
Table: Percent growth rate inhibition per concentration
-------------------------------------------------------
Nominal test Percent growth inhibition
concentration
(mg/l) Growth rate
-------------------------------------------------------
0 0
1000 4.9
1400 9.9
2000 15.5
2800 17.6
4000 31.0
-------------------------------------------------------
Table: EC50 and EC20
---------------------------------------
Hours of EC50 EC20
exposure (mg/l) (mg/l)
---------------------------------------
72 > 4000 2700
---------------------------------------
Description of key information
By way of read-across from lactic acid and calcium chloride, it is concluded that Calcium (S)-lactate is non-toxic to algae. No effects occurred up to the highest test concentration.
Key value for chemical safety assessment
- EC10 or NOEC for freshwater algae:
- 533 mg/L
Additional information
Calcium (S)-lactate fully dissociates into Ca2+ ions and lactate. The ecotoxicology of Calcium (S)-lactate can thus be understood in terms of the ecotoxicology of calcium chloride and lactic acid.
The NOEC (72 h) > 533 mg lactate/L (measured TWA; Hanstveit, 1992)
Experiments were performed in buffered solutions; i.e., the adjusted pH of the algal medium containing different test substance concentrations (pH 7.5–8.0 at the start of the test) remained largely constant (pH 8.0–8.1, pH 8.2–8.7 in the presence of algae) during the tests. Effects can be therefore assigned to lactate since lowering pH as a result of administration of lactic acid was compensated.
For calcium chloride, the ErC50 (72 h, Pseudokirchneriella subcapitata) is > 4000 mg/L (> 36.0 M).
Based on the derived threshold values from both studies, the substance would neither be classified as acutely nor chronically toxic to algae and cyanobacteria in accordance with the EU CLP Regulation.
This information is used in a read-across approach in the assessment of the target substance. For details and justification of read-across please refer to the read-across report attached to IUCLID section 13.
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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