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EC number: 232-350-7 | CAS number: 8006-64-2 Any of the volatile predominately terpenic fractions or distillates resulting from the solvent extraction of, gum collection from, or pulping of softwoods. Composed primarily of the C10H16 terpene hydrocarbons: α-pinene, β-pinene, limonene, 3-carene, camphene. May contain other acyclic, monocyclic, or bicyclic terpenes, oxygenated terpenes, and anethole. Exact composition varies with refining methods and the age, location, and species of the softwood source.
- 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:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2010-07-09 to 2010-08-09
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Loading rates: 0 (Control), 5.0, 25 and 100 mg/L
- Sampling method: Samples of the control and WAFs were taken for TOC analysis (TOC = Total Organic Carbon) and GC-MS analysis (GC-MS = Gas Chromatography - Mass Spectrometry) from separate vessels at 0 h and 72 h to assess the stability of exposure concentrations. - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: The test item Crude Sulfate Turpentine (S: 0.02 %) is a complex mixture with a low water solubility. To avoid adverse physical effects of undissolved or emulsified test material on the algae, the Alga Test with Crude Sulfate Turpentine (S: 0.02 %) was carried out with aqueous extracts (WAF = Water Accommo-dated Fraction) at various loading rates of the test item in culture medium.
In a preliminary study with a test item of comparably low water solubility (Sylva-blend TM PF 40, STZ No. 01-05-001; study sponsor Arizona Chemical), the durations of the stirring and phase separation phases of WAF preparation were investigated. Water Accommodated Fractions were prepared and analysed following a range of mixing and settling periods to ensure optimal equilibrium and phase separation of the test item in the WAFs. Quantitation of dissolved component concentrations was achieved by TOC analysis (TOC = Total Organic Carbon).
Taking into account the results of this preliminary WAF-study, the WAFs for the Alga Test Test with Crude Sulfate Turpentine (S: 0.02 %) were prepared by stirring various amounts of the test item in culture medium for 24 h with magnetic stirrers. The WAFs were prepared in closed glass vessels. The test load-ing rates of Crude Sulfate Turpentine (S: 0.02 %) were weighed on weighing scoops, that afterwards were placed into the glass vessels. The vessels were then filled with culture medium and closed immediately. The mixing was carried out at a speed that was slow enough not to cause dispersion or emulsification of the undissolved fraction of the test item. To ensure this, the vortex developed at the surface by stirring was set at approximately 10 % of the water depth. After stirring for 24 h the WAFs were allowed to stand for 1 h before use to facilitate phase separation. The extracts gained with this method were clear.
The Control (culture medium) for the Alga Test was treated in the same way as the WAFs.
The vessels used for Exposure Concentration Analysis, including the Control and WAFs, were kept under the same conditions as the test vessels.
- Controls: algal growth medium - Test organisms (species):
- Desmodesmus subspicatus (previous name: Scenedesmus subspicatus)
- Details on test organisms:
- TEST ORGANISM
- Common name: Green algae.
- Strain: SAG 86.81
- Source: Albrecht von Haller Institut für Pflanzenwissenschaften der Universität Göttingen.
- Age of inoculum: 72 h.
- Method of cultivation: on agar tubes (OECD Medium, 0.8% Agar), transferred to a new agar tube every 2 months.
ACCLIMATION
- Acclimation period: 72 h.
- Culturing media and conditions: same as test. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 72 h
- Post exposure observation period:
- None
- Hardness:
- Not applicable
- Test temperature:
- 25 ± 2°C
- pH:
- 7.8 - 7.9 at time 0 h, in the range of 8.0–10.4 at time 72 h.
The increase of pH is caused by the algal growth in the test vessels. In common with other species of freshwater algae, Desmodesmus subspicatus gains CO2 from HCO3-, leading to a release of hydroxide ions that raise the alkalinity of the medium.
The shift in pH of >1 unit is indicative of good algal growth and is not considered to invalidate the test result. - Dissolved oxygen:
- Not applicable
- Salinity:
- Not applicable
- Nominal and measured concentrations:
- Nominal loading rates: 0 (Control), 5, 10, 25, 50 and 100 mg/L as WAFs.
TOC-values of the Alga Test (Table 3) confirmed the low water solubility of the test item. The deviations of the TOC-values in the control and at test loading rates of 5.0 mg/L and 25 mg/L lie within or very close to the confidence-limits (± 0.3 mg C/L) of these measurements. The TOC-value at test loading rate of 100 mg/L decreased to 80 % of the initial value. Therefore the WAFs were considered to remain approximately stable over the 72-h test period.
GC-MS analysis of the Control medium and the WAFs in the Alga Test (Table 4) revealed that the total concentrations of fingerprint components decreased to 19 % of initial values at test loading rate 5.0 mg/L, to 24 % of initial values at test loading rate 25 mg/L and to 25 % of initial values at test loading rate 100 mg/L over 72 h. This finding is probably caused by biodegradation of these components during 72 h.
Quantitative GC-MS-values were definitely lower compared to TOC-values. This is caused by the fact that only fingerprints of the sample were detected by GC-MS analysis whilst TOC analysis detected Total Organic Carbon as a sum parameter.
The results of the test were reported and interpreted with reference to nominal loading rates. - Details on test conditions:
- TEST SYSTEM
- Test vessel: Erlenmeyer flasks with ground-in glass stoppers
- Material, size, headspace, fill volume: glass 250 ml with 200 mL of test medium.
- Aeration: None
- Renewal rate of test solution: none
- Initial cells density: ca. 2500 cells/mL
- Control end cells density: average over 3 vessels was 570,000 cells/mL
- No. of vessels per concentration: 3
- No. of vessels per control: 3
GROWTH MEDIUM
- Standard medium used: yes
The following stock solutions were prepared in deionised water according to OECD-Guideline 201 (final concentrations in the test solutions in brackets):
Solution 1:
NH4Cl: 1.5 g/L (15 mg/L)
MgCl2 x 6 H2O: 1.2 g/L (12 mg/L)
CaCl2 x 2 H2O: 1.8 g/L (18 mg/L)
MgSO4 x 7 H2O: 1.5 g/L (15 mg/L)
KH2PO4: 0.16 g/L (1.6 mg/L)
Solution 2:
FeCl3 x 6 H2O: 0.08 g/L (0.08 mg/L)
Na2 EDTA x 2 H2O: 0.1 g/L (0.01 mg/L)
Solution 3:
H3BO3: 0.185 g/L (0.185 mg/L)
MnCl2 x 4 H2O: 0.415 g/L (0.415 mg/L)
Na2MoO4 x 2 H2O: 0.0007 g/L (7 x 10-3 mg/L)
ZnCl2: 3.0 mg/L (3 x 10-3 mg/L)
CoCl2 x 6 H2O: 1.5 mg/L (1,5 x 10-3 mg/L)
CuCl2 x 2 H2O: 0.01 mg/L (10-5 mg/L)
Solution 4:
NaHCO3: 50.0 g/L (50 mg/L)
The culture medium was prepared by adding 10 mL of stock solution 1 and 1 mL of stock solution 3 per litre of deionised water. The mixture was then autoclaved at 121 °C for 15 minutes. Solution 2 + 4 (1 mL/L) were added after autoclaving by sterile filtration (0.45 µm pore size). The pH-value of the culture medium was 7.7 - 8.0.
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: culture medium and deionised water.
- Total organic carbon: See Table 3.
- Culture medium different from test medium: no
- Intervals of water quality measurement: beginning and end of experiment (0h and 72 h).
OTHER TEST CONDITIONS
- Sterile test conditions: yes
- Adjustment of pH: no
- Photoperiod: continuous
- Light intensity and quality: 8000 to 8200 Lux using cool-white light and maximum ± 15 % variation within the testing area, permanent illumination
EFFECT PARAMETERS MEASURED:
- Determination of cell concentrations: microscopy with counting chambers at time 24 h, 48 h and 72 h.
TEST CONCENTRATIONS
- Range finding study: None - Reference substance (positive control):
- no
- Duration:
- 72 h
- Dose descriptor:
- EL50
- Effect conc.:
- 17.1 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- Water Accommodated Fractions (WAFs)
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EL50
- Effect conc.:
- 16.4 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- Water Accommodated Fractions (WAFs)
- Basis for effect:
- biomass
- Remarks:
- (yield)
- Duration:
- 72 h
- Dose descriptor:
- NOELR
- Effect conc.:
- 10 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- Water Accommodated Fractions (WAFs)
- Basis for effect:
- other: growth rate and biomass (yield)
- Details on results:
- - Exponential growth in the control: yes, the cell concentration in the control cultures increased by a factor of 230 in 72 h.
- Effect concentrations exceeding solubility of substance in test medium: the loading rates at which the water-accommodated fractions were prepared exceeded the solubility of the test substance. - Reported statistics and error estimates:
- The results of the Alga Test were analysed statistically with reference to the specific growth rate [µ] and biomass (yield).
Normality of the data was tested using a Kolmogorov-Smirnov-test (α = 0.05).
Homogeneity of variances was tested by Bartlett`s test (α = 0.05).
For all measured end values, statistical differences among treatment groups were determined using a one-way analysis of variance (ANOVA).
Two-sided Dunnet's procedure for multiple comparison was used to determine, which concentration of the test item differed significantly from the control (p = 0.05).
The results of the two-sided Dunnet's test (p = 0.05) were used to determine the NOELR (No Observable Effect Loading Rate) of the specific growth rate [µ] and of the biomass (yield).
The NOELR (No Observable Effect Loading Rate) is defined as the highest test loading rate, where inhibition of the specific growth rate [µ] and of the biomass was statistically not significantly different when compared to the control. - Validity criteria fulfilled:
- yes
- Conclusions:
- A 72h EL50 of 17.1 mg/L and NOELR of 10 mg/L have been determined for the effect of the test substance on growth rate of Desmodesmus subspicatus.
Reference
Table 1. Test results – average specific growth rates (µ) over the test period 0-72 hours
Loading rate [mg/L] |
Cells / mL |
Average Specific growth rate [µ] |
Average Specific growth rate [µ] Mean value |
Standard deviation |
Coefficient of variation Vc [%] |
Inhibition of Average Specific growth rate [%] |
Inhibition of Average Specific growth rate Mean value [%] |
Control 1 |
576000 |
1.81 |
1.81 |
0.00 |
0.15 |
|
|
Control 2 |
568000 |
1.81 |
|||||
Control 3 |
576000 |
1.81 |
|||||
5.0 |
584000 |
1.82 |
1.81 |
0.01 |
0.45 |
-0.34 |
-0.08 |
5.0 |
560000 |
1.80 |
0.43 |
||||
5.0 |
584000 |
1.82 |
-0.34 |
||||
10 |
568000 |
1.81 |
1.80 |
0.01 |
0.68 |
0.17 |
0.79 |
10 |
528000 |
1.78 |
1.52 |
||||
10 |
552000 |
1.80 |
0.70 |
||||
25 |
5000 |
0.23 |
0.15 |
0.09 |
57.1 |
87.3 |
91.8 |
25 |
3000 |
0.06 |
96.7 |
||||
25 |
4000 |
0.16 |
91.4 |
||||
50 |
4500 |
0.20 |
0.10 |
0.10 |
95.7 |
89.2 |
94.3 |
50 |
2500 |
0.00 |
100 |
||||
50 |
3500 |
0.11 |
93.8 |
||||
100 |
3000 |
0.06 |
0.09 |
0.06 |
59.7 |
96.7 |
94.9 |
100 |
3000 |
0.06 |
96.7 |
||||
100 |
4000 |
0.16 |
91.4 |
Remark: A negative inhibition value means an enhancement of the parameter.
Table 2. Test results – biomass (yield) over the whole test period 0-72 hours
Loading rate [mg/L] |
Cells/mL |
Yield Cells/mL |
Yield Cells/mL Mean value |
Standard deviation |
Coefficient of variation Vc [%] |
Inhibition of Yield [%] |
Inhibition of Yield [%] Average |
Control 1 |
576000 |
573500 |
570833 |
4619 |
0.81 |
|
|
Control 2 |
568000 |
565500 |
|||||
Control 3 |
576000 |
573500 |
|||||
5.0 |
584000 |
581500 |
573500 |
13856 |
2.42 |
-1.87 |
-0.47 |
5.0 |
560000 |
557500 |
2.34 |
||||
5.0 |
584000 |
581500 |
-1.87 |
||||
10 |
568000 |
565500 |
546833 |
20133 |
3.68 |
0.93 |
4.20 |
10 |
528000 |
525500 |
7.94 |
||||
10 |
552000 |
549500 |
3.74 |
||||
25 |
5000 |
2500 |
1500 |
1000 |
66.7 |
99.6 |
99.7 |
25 |
3000 |
500 |
99.9 |
||||
25 |
4000 |
1500 |
99.7 |
||||
50 |
4500 |
2000 |
1000 |
1000 |
100 |
99.7 |
99.8 |
50 |
2500 |
0 |
100 |
||||
50 |
3500 |
1000 |
99.8 |
||||
100 |
3000 |
500 |
833 |
577 |
69.3 |
99.9 |
99.9 |
100 |
3000 |
500 |
99.9 |
||||
100 |
4000 |
1500 |
99.7 |
Remark: A negative inhibition value means an enhancement of the parameter.
Table 3. Results of TOC analysis of the test media
Time [h] |
Control |
5.0 mg/L |
25 mg/L |
100 mg/L |
0 |
0.3 |
0.3 |
1.7 |
4.7 |
72 |
≤0.3 |
0.1 |
1.2 |
3.8 |
Table 4. Results of GC-MS analysis of test media
Vessel |
Time [h] |
a-Terpineol |
a-Pinene |
b-Pinene |
3-Carene |
Limonene |
Total [µg/L] |
Control |
0 |
0.214** |
< 0.367* |
0.227** |
< 0.151* |
0.212** |
< 1.17 |
Control |
72 |
0.214** |
< 0.367* |
0.227** |
< 0.151* |
0.212** |
< 1.17 |
5.0 mg/L |
0 |
5.81 |
94.1 |
10.1 |
23.2 |
9.12 |
142 |
5.0 mg/L |
72 |
3.76 |
11.1 |
2.32 |
7.12 |
2.82 |
27.1 |
25 mg/L |
0 |
37.6 |
735 |
75.3 |
222 |
96.1 |
1166 |
25 mg/L |
72 |
22.5 |
116 |
22.8 |
84.5 |
38.4 |
285 |
100 mg/L |
0 |
125 |
1111 |
116 |
243 |
113 |
1708 |
100 mg/L |
72 |
104 |
173 |
32.7 |
81.6 |
41.5 |
432 |
Remarks:
* Limit of detection
** derived from equation of the calibration line (axis intercept); no signal was measured in the controls for α-Terpineol, β-Pinene and Limonene
Quantitative GC-MS-values are based on results and/or limits of detection
Description of key information
A 72h-EL50 of 17.1 mg/l and NOELR of 10 mg/l have been determined for the effect of the test substance on growth rate of Desmodesmus subspicatus. The substance had a sulfur content of 0.02%. A 72h-EL50 of 22.5 mg/l and NOELR of 5 mg/l have been determined for the same endpoint in a second test conducted on a sample of the substance with a sulfur content of 3.6%. It is therefore concluded that the two samples were equally toxic to aquatic algae.
Short-term toxicity data are also available for alpha- and beta-pinene, which are both constituents of block 1 of TOPP. The 48h-LOEC for alpha-pinene was determined as 0.494 mg/l (and the NOEC was estimated to be around 0.25 mg/l) and the 48h-EC50 and 48h-EC10 for beta-pinene was determined to be 0.83 mg/l and 0.38 mg/l respectively. However, significant loss of test substance was observed in both tests (presumably a result of biodegradation in and/or volatilisation from the static test system) and so these values may not represent the true toxicity of alpha- and beta-pinene.
Key value for chemical safety assessment
- EC50 for freshwater algae:
- 17.1 mg/L
- EC10 or NOEC for freshwater algae:
- 5 mg/L
Additional information
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