Registration Dossier
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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 205-288-3 | CAS number: 137-30-4
- 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
Adsorption / desorption
Administrative data
Link to relevant study record(s)
- Endpoint:
- adsorption / desorption: screening
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 05 Feb - 14 Oct 2014
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 106 (Adsorption - Desorption Using a Batch Equilibrium Method)
- Version / remarks:
- 2000
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- Swiss federal office of public health, consumer protection directorate, notification authority form chemicals, Bern, Switzerland
- Type of method:
- batch equilibrium method
- Media:
- soil
- Radiolabelling:
- yes
- Test temperature:
- 20 ± 2°C
- Analytical monitoring:
- yes
- Remarks:
- LSC and HPLC
- Details on sampling:
- FOR BOTH LSC and HPLC MEASUREMENTS
- Concentrations: screening test: control (without soil) and 0.1 µg/mL (nominal), advance test: control (without soil) and five concentrations of 0.110, 0.037, 0.010, 0.003 and 0.001 mg/L (nominal)
- Sampling interval:
- Screening test: after one and two hours of shaking
- Advanced test: Samples were taken after 1 h of shaking (based on results of preliminary test).
- Sample storage before analysis: no. due to degradation of test item - Matrix no.:
- #1
- Matrix type:
- sand
- % Clay:
- >= 2.7 - <= 2.9
- % Silt:
- >= 8.6 - <= 12.4
- % Sand:
- >= 85.4 - <= 88
- % Org. carbon:
- 0.66
- pH:
- 5.2
- CEC:
- >= 3.5 - <= 4.7 other: mmol/100 g soil
- Matrix no.:
- #2
- Matrix type:
- clay loam
- % Clay:
- 27
- % Silt:
- 52
- % Sand:
- 21
- % Org. carbon:
- 3.85
- pH:
- 5.64
- CEC:
- 13.6 other: mmol/100 g soil
- Matrix no.:
- #3
- Matrix type:
- silt loam
- % Clay:
- 15
- % Silt:
- 84
- % Sand:
- 2
- % Org. carbon:
- 1.3
- pH:
- 6.63
- CEC:
- 13.3 other: mmol/100 g soil
- Matrix no.:
- #4
- Matrix type:
- clay
- % Clay:
- >= 38.6 - <= 42.8
- % Silt:
- >= 31.9 - <= 37.1
- % Sand:
- >= 21.4 - <= 28.2
- % Org. carbon:
- 1.66
- pH:
- 7.1
- CEC:
- >= 25.8 - <= 28 other: mmol/100 g soil
- Matrix no.:
- #5
- Matrix type:
- sandy loam
- % Clay:
- >= 10.5 - <= 12.5
- % Silt:
- >= 29.2 - <= 32.2
- % Sand:
- >= 56.4 - <= 59.2
- % Org. carbon:
- 0.95
- pH:
- 7.3
- CEC:
- >= 13.8 - <= 20.4 other: mmol/100 g soil
- Details on matrix:
- COLLECTION AND STORAGE
- Geographic location: Soils were collected from different agricultural areas. Sampling and handling was performed under consideration of ISO 10381-6.
- Soil 1: Speyer 2.1 (Sand) sampled in Dudenhofen, Rhineland-Palatinate, Germany
- Soil 2: RefeSol 03-G (Clay loam/Silt loam) sampled in Schmallenberg, NorthrheineWestphalia, Germany
- Soil 3 RefeSol 02-A (Silt loam) sampled in Schmallenberg, Northrheine-Westphalia, Germany
- Soil 4: Speyer 6S (Clay) sampled in Siebeldingen, Rhineland-Palatinate, Germany
- Soil 5 Speyer 5M (Sandy loam) sampled in Mechtersheim Rhineland-Palatinate, Germany
- Collection procedures: Plant cover of the soil was removed and the soil was sampled from the top soil layer.
- Sampling depth (cm): 20-30 cm
- Storage conditions: in closed container, at room temperature
- Soil preparation: Air-dried at ambient temperature and sieved through a 2-mm sieve. The soil samples were pre-equilibrated with about 90% of the targeted volume of the aqueous phase (0.01 M CaCl2) by shaking for at least over night at 20 ± 2 °C prior to application of the test item. Soil was sterilized for the screening and the advanced test.
PROPERTIES
- Moisture (in g/100 d dry soil): Soil 1: Speyer 2.1 (Sand): 0.43, Soil 2: RefeSol 03-G (Clay loam/Silt loam): 2.38, Soil 3 RefeSol 02-A (Silt loam): 1.70, Soil 4: Speyer 6S (Clay): 3.78, Soil 5 Speyer 5M (Sandy loam): 1.26 - Details on test conditions:
- TEST SYSTEM
- Type, size and further details on reaction vessel: sealed Teflon centrifuge tubes
- Water filtered (i.e. yes/no; type of size of filter used, if any):
- Amount of soil and water per treatment (if simulation test): see Section "any other information on material and methods incl. tables"
- Soil-solution ratio (if simulation test):
- Preliminary test: 1:2, 1:10, 1:100
- Screening test: 1:100
- Advanced test: A soil-to-solution ratio of 1:100 was used for soils II, III, IV and V (1 g/100 mL) and a ratio of 1:20 for soil I (5 g/100 mL).
- Number of reaction vessels/concentration: Two (screening and advanced test was performed using one soil per day due to the instability of [14C]Ziram).
- Test performed in open system: no
- Method of preparation of application solutions:
- Preliminary test: A stock solution was prepared by dissolving an aliquot of the radiolabeled test item in 10 mL acetone. The radioactivity content (determined by triplicate LSC measurements of 20 µL stock solution diluted in 20 mL acetone) was 117'330'000 dpm/mL, corresponding to a concentration of 379 µg [14C]Ziram/mL. An aliquot of 1.3 mL of the stock solution was diluted with 3.7 mL acetone corresponding to a radioactivity of 31'424 dpm/µL and a concentration of 102 µg [14C]Ziram/mL.
- Screening test: Soil IV: An aliquot of 270 µL of the stock solution was diluted with 730 µL acetone (radioactivity of 31'818 dpm/µL, corresp. to 103 µg [14C]Ziram/mL). Remaining soils: A stock solution was prepared by dissolving an aliquot of the test item in 3 mL acetone (radioactivity of 75'530 dpm/µL, corresp. to 225 µg [14C]Ziram/mL). An aliquot of 450 µL of the stock solution was diluted with 550 µL acetone (radioactivity content of 39'545 dpm/µL, corresp. to 118 µg [14C]Ziram/mL). Radioactivity content was always determined by triplicate LSC measurements.
- Advanced test: An aliquot of the radioactive test item was dissolved in 3 mL acetone (radioactivity content: 58'780 dpm/µL, corresp. to 175 µg [14C]Ziram/mL). The application solutions with final nominal concentrations of 0.001, 0.003, 0.01, 0.032, 0.101 µg/mL were prepared by dilutions of the stock solution in acetone. The application solutions were stored at -20 °C and used for all soils in the advanced test. The actual concentration of each application solution was re-determined by LSC measurements prior each sample preparation day.
- Are the residues from the adsorption phase used for desorption: No desorption test was performed due to the instability of the test item in the test system.
- Other: Tubes were shaken in the dark to keep the soil in homogeneous suspension.
- Control samples: test item in 0.01 M CaCl2 solution (without soil)
- Blank samples: Soil I and IV were subjected to the same test procedure as the preliminary test (soil-to-solution ratio 1:10) using the same amount of soil and the same total volume of aqueous solution (without test item). These samples served as background control during analysis to detect any contamination. - Computational methods:
- - Other: All calculations were performed with Excel in Microsoft Office Professional 2010.
- Sample No.:
- #1
- Type:
- Koc
- Value:
- 775 L/kg
- pH:
- 5.2
- Temp.:
- 20 °C
- Matrix:
- sand
- % Org. carbon:
- 0.66
- Sample No.:
- #2
- Type:
- Koc
- Value:
- 1 147 L/kg
- pH:
- 5.64
- Temp.:
- 20 °C
- Matrix:
- clay loam
- % Org. carbon:
- 3.85
- Sample No.:
- #3
- Type:
- Koc
- Value:
- 3 261 L/kg
- pH:
- 6.63
- Temp.:
- 20 °C
- Matrix:
- silt loam
- % Org. carbon:
- 1.3
- Sample No.:
- #4
- Type:
- Koc
- Value:
- 34 779 L/kg
- pH:
- 7.1
- Temp.:
- 20 °C
- Matrix:
- clay
- % Org. carbon:
- 1.66
- Sample No.:
- #5
- Type:
- Koc
- Value:
- 12 501 L/kg
- pH:
- 7.3
- Temp.:
- 20 °C
- Matrix:
- sandy loam
- % Org. carbon:
- 0.95
- Adsorption and desorption constants:
- No desorption test was performed due to the instability of the test item in the test system.
- Recovery of test material:
- - Screening test: The recoveries ranged between 97.4% and 101.7%.
- Concentration of test substance at end of adsorption equilibration period:
- For results see Section "any other information on results incl. tables".
- Concentration of test substance at end of desorption equilibration period:
- No desorption test was performed due to the instability of the test item in the test system.
- Transformation products:
- not measured
- Details on results (Batch equilibrium method):
- PRELIMINARY TEST
- Sample purity: > 95% purity in all application solutions (HPLC). Degradation of [14C]Ziram after one hour of agitation was observed and considered for evaluation.
- Soil to solution ratios: 1:2, 1:10 and 1:100 were tested. In soil to solution ratios of 1:2 and 1:10 no test substance could be detected and therefore excluded from further testing.
- Weighed soil: 1 g
- Volume of aqueous solution: 100 mL
- Test substance concentration in final solution: 0.1 µg/mL (nominal)
- Adsorption times: 2, 6 and 24 h were tested. Short adsorption time was needed to avoid complete degradation of Ziram.
- Soil sterility: Sterile and non sterile soil were tested. The test item was not stable despite the use of sterilised soil.
MAIN TEST: PERFORMANCE
- Test material stability during adsorption phase: The results showed acceptable degradation in both phases for soils I to III. In soil extracts of soil IV (clay) and V (sandy loam), [14C]Ziram was below 40% of applied and in a few samples even not detectable. For more details see table 1 in Section "any other information on results incl. tables".
- Experimental conditions maintained throughout the study: yes
- Buffer/test substance interactions affecting sorption: no
- Further chemical interactions: no
- Buffer-catalyzed degradation of test substance: not observed
- Anomalies or problems encountered (if yes): no
- Other observations: No adsorption on test tubes observed.
RESIDUES
- Non-extractable residues (% of applied amount at end of study period): <10.7%
- Endpoint:
- adsorption / desorption: screening
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 14 June 1995 - 5 December 1995
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- other: 40 CFR 158 Environmental Fate, USEPA Pesticide Assessment Guidelines Subdivision N; Series 163-1.
- Deviations:
- no
- GLP compliance:
- yes
- Type of method:
- batch equilibrium method
- Media:
- soil
- Radiolabelling:
- yes
- Test temperature:
- 25 +/- 1°C
- Details on study design: HPLC method:
- EQUIPMENT
- Apparatus: Shimadzu HPLC System
- Detection system: 220 nm UV; RAM 14C
- Loop: 500 uL (nominal)
- Column: Zorbax RXC8 25 x 0.46 cm
- Solvent System: A = 0.002M zinc chloride/acetonitrile (80:20 v:v)
B = acetonitrile
Gradient: Time A B
0 100 0
19 15 85
24 15 85
30 100 0
30 STOP
- Run Time: 30 Minutes
- Flow Rate: 1.5 mL/min
- Sensitivity: 0.002 Absorbance
- Chart Speed: 5 mm/min
- Temperature: Ambient, room temperature
- Approximate Retention Times: 22 minutes ziram
12 minutes CS2
- Detection limits
Soil Combustions 0.0005 ppm
Preliminary Solutions 0.0008 ppm
Adsorption Solutions 0.0008 ppm
Desorption Solutions 0.00008 ppm - Analytical monitoring:
- yes
- Details on sampling:
- Radiocarbon analysis
- All solutions were analyzed by direct LSC in Scint-A (Packard Inst. Co.) scintillation cocktail. During the preliminary phase, duplicate 0.1 mL aliquots of each solution were removed for analysis at each sampling interval. For the definitive study, duplicate 0.1 mL aliquots of adsorption solutions and
1.0 mL of desorption solutions were analyzed
TLC analysis
- Samples of the radioactive test substance and definitive dose solutions were analyzed by one dimensional thin layer chromatography (TLC) using 10 x 20 cm glass plates pre-coated with silica gel 60 F—254 at a thickness of 0.25 mm. circled.
HPLC analysis
- Samples for the radiochemical purity check prior to definitive testing, definitive stock solutions, and one replicate per soil type of the highest concentration for the adsorption and desorption phases of the definitive study were chromatographed by HPLC - Details on matrix:
- - Four types of soil (clay, sand, silt loam, sandy loam) were used in the study. Three of the four soils (clay, sand, and silt loam) were obtained by Agrisearch Incorporated and were dug from a depth of 0 to 6 inches. The California sandy loam was provided to Agrisearch Incorporated by XenoBiotic Laboratories, Inc., Plainsboro, NJ. Soils were air dried at room temperature (20 to 30°C), sieved (2 mm mesh), and stored at ambient room temperature prior to use in the study. Soils were characterized under GLPS by AGVISE Laboratories, Northwood, NO. The soil clay fraction mineralogy was obtained by AGVISE, NO from the North Dakota State University at Fargo, North Dakota
- Details on test conditions:
- TEST SYSTEM
- Test containers: 50 mL centrifuge tubes
- Water filtered: the drinking water was filtered, deionized, boiled, and distilled prior to use
- Amount of soil and water per treatment: 0.5 g clay soil, 18 g sand soil, 8 g silt loam soil, 8 g sandy loam soil were added to each test tube and the corresponding volume of calcium ion solution
- Number of reaction vessels/concentration: 2 per test concentration
- Method of preparation of test solution: 3.1 mg of 14C-ziram was prepared in acetone at 0.31 mg/mL. Dilutions of this stock were prepared in acetone to yield definitive dosing solutions. The final test concentrations were: 4 ug/mL, 2 ug/L, 1 ug/mL, 0.6 ug/mL, and 0.2 ug/mL - Type:
- Koc
- Value:
- 314
- Remarks on result:
- other: Sandy Loam
- Type:
- Koc
- Value:
- 759
- Remarks on result:
- other: Silt Loam
- Type:
- Koc
- Value:
- 1 232
- Remarks on result:
- other: Sand
- Type:
- Koc
- Value:
- 3 732
- Remarks on result:
- other: Clay
- Type:
- log Koc
- Value:
- 2.5
- Remarks on result:
- other: Sandy Loam
- Type:
- log Koc
- Value:
- 2.8
- Remarks on result:
- other: Silt Loam
- Type:
- log Koc
- Value:
- 3.1
- Remarks on result:
- other: Sand
- Type:
- log Koc
- Value:
- 3.6
- Remarks on result:
- other: Clay
- Adsorption and desorption constants:
- Adsorption: 68.1 (clay), 2.9 (sand) , 7.6 (silt loam) and 5.7 (sandy loam)
Desorption: 450.6 (clay), 81.1 (sand), 4092.7 (silt loam) and 40.2 (sandy loam) - Endpoint:
- adsorption / desorption
- Remarks:
- adsorption/desorption
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 19 July 1985- 26 September 1985
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: GLP Guideline study with acceptable restrictions (only two soil types tested (sandy loam and loamy sand))
- Qualifier:
- according to guideline
- Guideline:
- other: 40 CFR 158 Environmental Fate, USEPA Pesticide Assessment Guidelines Subdivision N; Series 163-1.
- GLP compliance:
- yes
- Type of method:
- batch equilibrium method
- Media:
- soil
- Radiolabelling:
- yes
- Test temperature:
- 25 +/- 1°C
- Analytical monitoring:
- yes
- Details on matrix:
- - Sandy loam (2) and loamy sand (2) soils were supplied by Prochimie International and ABC labs. These soils were sieved through a 10 mesh screen and autoclaved at 121°C and 15 psi. Thereafter, the soils were oven-dried at 150°C in order to remove the moisture
- Details on test conditions:
- - Soil samples (1 g for the Hanford loamy sand; 2 g soil for the other soils) in suspension with 10 mL [14C]ziram-treated solution (0, 0.472, 0.868, 3.94, and 7.08 μg [14C]ziram/mL 0.01 N calcium sulfate solution) were shaken during 48 hours at 25°C in the dark. For desorption the suspensions were shaken in the dark at 25°C for 72 hours with 0.01N calcium sulfate solution.
- Type:
- Koc
- Value:
- 559
- Remarks on result:
- other: Sandy loam I
- Type:
- Koc
- Value:
- 987
- Remarks on result:
- other: Sandy loam II
- Type:
- Koc
- Value:
- 4 470
- Remarks on result:
- other: Loamy sand I
- Type:
- Koc
- Value:
- 12 010
- Remarks on result:
- other: Loamy sand II
- Type:
- log Koc
- Value:
- 2.7
- Remarks on result:
- other: Sandy loam I
- Type:
- log Koc
- Value:
- 3
- Remarks on result:
- other: Sandy loam II
- Type:
- log Koc
- Value:
- 3.6
- Remarks on result:
- other: Loamy sand I
- Type:
- log Koc
- Value:
- 4
- Remarks on result:
- other: Loamy sand II
- Adsorption and desorption constants:
- Adsorption:
Sandy loam I: 8.0
Sandy loam II: 9.87
Loamy sand I: 13.6
Loamy sand II: 57.4
Desorption:
Sandy loam I: 22.4
Sandy loam II: 33.2
Loamy sand I: 88
Loamy sand II: 11299
Referenceopen allclose all
PRELIMINARY TEST:
For the samples of the soil-to-solution ratio of 1:100 and 2 h of adsorption time, a complete mass balance was performed. Total recovery of the radioactivity was between 97.7 and 106.8% of the applied radioactivity for sterile and non-sterile samples. It was decided to perform the screening test with all five soils, sterilised and at a soil-to-solution ratio of 1g/100 mL and adsorption times of one and two hours.
Table 1: Preliminary test – Mass balance of test item between aqueous phase and soil after 2 hours of adsorption at a soil-to-solution ratio 1:100. Mean values are given in percent of applied radioactivity (AR).
Soil |
(ads)aq [%] |
(ads)extract [%] |
(ads)res [%] |
Recovery [%] |
Soil I Sand |
87.8 |
8.3 |
1.6 |
97.7 |
Soil IV Clay |
40.1 |
50.1 |
13.9 |
104.0 |
Soil I Sand |
88.4 |
11.5 |
1.6 |
101.5 |
Soil IV Clay |
34.1 |
59.9 |
12.8 |
106.8 |
(ads)aq = % of the amount applied remaining in the aqueous phase
(ads)extract = % of the amount applied extracted after adsorption
(ads)res = % of the amount applied irreversibly bound to the soil matrix
SCREENING TEST
Table 1: Screening test: % of [14C]Ziram (parent compound) in the aqueous phase (supernatant) and soil extract determined by HPLC.
Soil |
% of [14C] Ziram Adsorption time (hours)
|
|||
1 |
2 |
|||
I |
Supernatant |
Sample A |
80.3 |
73.2 |
|
Sample B |
n.a. |
n.a. |
|
Soil Extract |
Sample A |
86.3 |
85.1 |
|
|
Sample B |
n.a. |
n.a. |
|
II |
Supernatant |
Sample A |
100.0 |
85.8 |
|
Sample B |
n.a. |
n.a. |
|
Soil Extract |
Sample A |
84.7 |
82.8 |
|
|
Sample B |
n.a. |
n.a. |
|
III |
Supernatant |
Sample A |
85.4 |
94.2 |
|
Sample B |
n.a. |
n.a. |
|
Soil Extract |
Sample A |
90.7 |
56.9 |
|
|
Sample B |
n.a. |
n.a. |
|
IV |
Supernatant |
Sample A |
100.0 |
74.4 |
|
Sample B |
100.0 |
55.6 |
|
Soil Extract |
Sample A |
100.0 |
55.6 |
|
|
Sample B |
0.0 |
0.0 |
|
V |
Supernatant |
Sample A |
100.0 |
82.9 |
|
Sample B |
n.a. |
n.a. |
|
Soil Extract |
Sample A |
31.6 |
24.5 |
|
|
Sample B |
n.a. |
n.a. |
n.a.= not analysed
0.0 = not detected
Depending on the soil texture, the radioactivity recovered in the supernatant solutions, ranged between 17.7% and 93.9%. The amounts recovered in the soil extracts ranged from 6.2 % to 71.9%. The non-extracted amounts remained low, not exceeding 10.7%.
Table 2: Screening test – Mass balance of test item between aqueous phase and soil after 1 and 2 hours of adsorption at a soil-to-solution ratio 1:100. Values are given in percent of applied radioactivity (AR).
Soil |
Adsorption time point |
(ads)aq [%] |
(ads)extract [%] |
(ads)res [%] |
Recovery [%] |
Soil I Sand |
1 h |
93.9 |
6.2 |
1.6 |
101.7 |
|
2 h |
92.2 |
6.9 |
1.8 |
100.9 |
Soil II Clay loam |
1 h |
63.8 |
32.5 |
7.1 |
103.4 |
|
2 h |
59.3 |
32.9 |
10.1 |
102.3 |
Soil III Silt loam |
1 h |
64.5 |
31.2 |
3.7 |
99.4 |
|
2 h |
65.2 |
30.7 |
4.8 |
100.7 |
Soil IV Clay |
1 h |
17.7 |
71.0 |
9.3 |
98.1 |
|
2 h |
19.0 |
68.7 |
10.7 |
98.4 |
Soil V Sandy loam |
1 h |
20.4 |
70.1 |
6.8 |
97.4 |
|
2 h |
18.7 |
71.9 |
8.0 |
98.5 |
(ads)aq = % of the amount applied remaining in the aqueous phase
(ads)extract = % of the amount applied extracted after adsorption
(ads)res = % of the amount applied irreversibly bound to the soil matrix
Table 3: Screening test – Distribution of the test item between aqueous phase and soil after one and two hours of adsorption at a soil-to-solution ratio 1:100 including the calculated Kd and KOC values.
Soil |
Adsorption time point |
m [g] |
V0 [mL] |
m(ads)s [µg] |
m(ads)aq [µg] |
Kd [mL/g] |
Kd*Ratio [mL/g] |
KOC [mL/g] |
Soil I Sand |
1 h |
1 |
100 |
0.57 |
8.03 |
7.1 |
0.07 |
1093 |
2 h |
1 |
100 |
0.62 |
7.19 |
8.6 |
0.09 |
1327 |
|
Soil II Clay loam |
1 h |
1 |
100 |
3.18 |
7.36 |
43.1 |
0.43 |
1121 |
2 h |
1 |
100 |
3.14 |
5.87 |
53.6 |
0.54 |
1392 |
|
Soil III Silt loam |
1 h |
1 |
100 |
3.21 |
6.24 |
51.5 |
0.51 |
3958 |
2 h |
1 |
100 |
1.98 |
6.96 |
28.5 |
0.28 |
2189 |
|
Soil IV Clay |
1 h |
1 |
100 |
n.a. |
1.82 |
n.a. |
n.a. |
n.a. |
2 h |
1 |
100 |
1.40 |
1.27 |
95.3 |
0.95 |
5812 |
|
Soil V Sandy loam |
1 h |
1 |
100 |
2.62 |
2.42 |
108.7 |
1.09 |
10865 |
2 h |
1 |
100 |
2.08 |
2.02 |
103.9 |
1.04 |
10389 |
m = Mass of soil (g)
Vo = Volume of aqueous phase (mL)
m(ads)s = Mass of test item adsorbed to soil at adsorption equilibrium (µg)
m(ads)aq = Mass of test item in aqueous phase at adsorption equilibrium (µg)
Kd = Distribution coefficient (mL/g)
Kd *Ratio = Kd*m/V0 (mL/g)
Koc = Distribution coefficient (mL/g)
ADVANCED TEST
Table 1: Advanced test: Freundlich isotherm parameters after 1 hour of adsorption.
Parameter |
Soil I Sand |
Soil II Clay loam |
Soil III Silt loam |
Soil IV Clay |
Soil V Sandy loam |
Mean |
Standard deviation |
log(KF) |
0.709 |
1.645 |
1.627 |
2.761 |
2.075 |
|
|
KF |
5.1 |
44.2 |
42.4 |
577.3 |
118.8 |
|
|
KFoc |
775 |
1147 |
3261 |
34779 |
12501 |
10493 |
14387 |
KFom |
449 |
666 |
1892 |
20173 |
7251 |
6086 |
8345 |
1/n |
0.86 |
0.93 |
0.89 |
1.34 |
1.23 |
1.05 |
0.22 |
R² |
0.973 |
0.961 |
0.979 |
0.980 |
0.949 |
|
|
KF= Freundlich adsorption coefficient
KFoc= Freundlich adsorption coefficient related to organic carbon content of soil
KFom= Freundlich adsorption coefficient related to organic matter content of soil
1/n = Regression constant
r2= Regression coefficient
Table 2: Advanced test: Amount of radioactivity in the control samples. Values are given in percent of applied radioactivity.
Soil |
Initial test item concentration [µg/mL] |
||||
|
C1 |
C2 |
C3 |
C4 |
C5 |
Soil I Sand |
96.7 |
101.5 |
86.6 |
106.0 |
100.0 |
Soil II Clay loam |
99.9
|
- |
- |
- |
- |
Soil III Silt loam |
112.1
|
- |
- |
- |
- |
Soil IV Clay |
97.5
|
- |
- |
- |
- |
Soil V Sandy loam |
98.7
|
- |
- |
- |
- |
C1-C5 = Initial test concentration as applied
Using the McCall Classification scale* to assess a chemical’s potential mobility in soil (based on its KFoc), the tested substance can be classified as having a low mobility in soil or being even immobile.
No desorption test was performed due to the instability of
the test item in the test system.
*McCall P.J., Laskowski D.A., Swann R.L., and Dishburger H.J., (1981): Measurement of sorption coefficients of organic chemicals and their use in environmental fate analysis. In Test Protocols for Environmental Fate and Movement of Toxicants. Proceedings of AOAC Symposium, AOAC, Washington DC.
Observation:
However, the role of organic matter in adsorption and hence use of Koc is questionable when considering the Koc range obtained. Therefore it has to be considered also the stability of ziram.
Description of key information
KFocvalues between 775 and 34779 (corresponding to log KFocvalues of 2.89 – 4.54).
Key value for chemical safety assessment
Additional information
The adsorption potential of zinc bis dimethyldithiocarbamate (CAS No. 137-30-4) was investigated in three studies.
The key study was conducted according to the OECD Guideline No. 106 and under GLP conditions (2014). A radiolabeled test substance was used for the test. The screening test was performed with 5 soils, a soil-to-solution ratio of 1g/100 mL and adsorption times of one and two hours. The advanced test (standard batch equilibrium method) was performed with five soils, five different concentrations of the test item and a soil-to-solution ratio of 1 g/100 mL for four soils and 5 g / 100 mL for one soil in order to obtain higher adsorption. The adsorption was quantified after 1 hour. The adsorption times studied were short since the test substance is unstable (investigated in preliminary test). The concentrations of the tested substance in soil extracts and aqueous phases, were analysed by HPLC. The recoveries of the radiolabeled substance in the screening test ranged from 97.4% to 103.4% (mean values). The Koc values ranged between 1093 and 11'624 mL/g depending on the soil properties. The desorption study was not performed due to the fast degradation of the test item. The batch equilibrium method resulted Freundlich isotherm coefficients for adsorption KFoc between 775 and 34779 depending on the soil. Based on this study the substance was characterized as poorly mobile in soil.
Two supporting studies are available, which were conducted according to the US EPA Pesticide Assessment Guideline, Subdivision N163-1: Leaching and Adsorption/Desorption studies (1988) and GLP. In the first supporting study (1995) 14C-labeled test substance was tested in four different soil types at 25°C, obtaining log Koc values of 2.5 (sandy loam), 2.8 (silt loam), 3.1 (sand) and 3.6 (clay). In the second supporting study (1985) radiolabeled test material was tested in sandy loam and loamy sand soil at 25°C. The resulting log Koc values were between 2.7 and 4.0.
The studies show that the adsorption potential of the substance strongly depends on the soil properties. However the data show a moderate to high adsorption potential of the substance in soil.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.