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EC number: 700-991-6 | CAS number: 8007-24-7
- 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

Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- test procedure in accordance with national standard methods with acceptable restrictions
- Remarks:
- The study was conducted to an internationally recognised method (OECD 301D). There were deviations from this guideline, but these were implemented to address the poor water solubility of the test substance.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 D (Ready Biodegradability: Closed Bottle Test)
- Deviations:
- yes
- Remarks:
- Modifications to the concentrations of suspended solids and test material have been made to account for the poor water solubility of the test substance
- Principles of method if other than guideline:
- The OECD guideline specifies a suspended solids concentration of 20 mg/l, whereas the study used a concentration of 30 mg/l. The guideline specifies a test material concentration of 5-10 mg ThOD/l, whereas the study used a concentration of approximately 20 mg ThOD/l. The guideline specifies that at least 10 replicates should be used for each of the test substance, positive control and control blank as well as 6 replicates for a toxicity control, whereas this study used three replicates for the test substance and positive control and an unknown number of control blanks. No details of toxicity controls were reported.
- GLP compliance:
- yes
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic (adaptation not specified)
- Details on inoculum:
- Mixed bacterial inoculum (30 mg suspended solids/l), stabilised under laboratory conditions for one week prior to the study.
- Duration of test (contact time):
- 28 d
- Initial conc.:
- 18.6 - 19.8 other: mg ThOD/flask
- Based on:
- other: ThOD
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- TEST CONDITIONS
- Composition of medium: Defined mineral medium (according to OECD tests) inoculated with mixed bacterial inoculum, stabilised under laboratory conditions for one week
- Test temperature: Not reported
- pH: Not reported
- CEC (meq/100 g): Not reported
- Aeration of dilution water: Not reported
- Suspended solids concentration: 30 mg/l
TEST SYSTEM
- Number of culture flasks/concentration: Three
- Method used to create aerobic conditions: Test vessels were shaken continuously to assure steady state oxygen partitioning between liquid and gass phase
- Test performed in open system: No, test vessels were closed glass bottles
- Volume of test vessels: Approximately 300 ml, two thirds test mixture, one third air
SAMPLING
- Sampling frequency: Sampling conducted on days 7, 14, 21 and 28
- Sampling method: Total oxygen uptake was calculated from the measured dissolved oxygen
- Sterility check if applicable: Not reported
- Sample storage before analysis: Not reported
- Reference substance:
- acetic acid, sodium salt
- Remarks:
- >99.5% a.i.; Batch number 0137A
- Parameter:
- % degradation (O2 consumption)
- Value:
- 46
- Sampling time:
- 7 d
- Parameter:
- % degradation (O2 consumption)
- Value:
- 72
- Sampling time:
- 14 d
- Parameter:
- % degradation (O2 consumption)
- Value:
- 86
- Sampling time:
- 21 d
- Parameter:
- % degradation (O2 consumption)
- Value:
- 96
- Sampling time:
- 28 d
- Details on results:
- Refer to Table 3.
- Results with reference substance:
- Sodium acetate was 97% degraded after 28 days. Refer to Table 4.
- Interpretation of results:
- readily biodegradable
- Conclusions:
- Based on these results, Cardolite NC-511 (a distilled grade CNSL sample) can be regarded as very highly biodegradable.
- Executive summary:
A 28 day aerobic ready biodegradability study (to OECD Guideline No. 301D – Closed Bottle Test) was carried out using Cardolite NC-511(a distilled grade CNSL sample). The effects of the test substance on ready biodegradability were assessed based on the measurement of chemical oxygen demand (COD) using an activated sludge inoculum (from a domestic wastewater plant). Test performance was evaluated using the reference substances sodium acetate.
This toxicity study is classified as not reliable (Klimisch Code 2) on the basis that there were some deviations from the test guideline.
Results Synopsis
There was 96% degradation of the test substance (Cashew Nutshell Extract, Decarboxylated, Distilled (Distilled Grade))after 28 days.
There was 97% degradation of the reference substance after 28 days meaning the test was considered valid.
Reference
Table 3: Biodegradation of Cardolite NC-511 (a distilled grade CNSL sample)
Measurement |
Replicate |
Incubation time (days) |
|||
7 |
14 |
21 |
28 |
||
Oxygen concentration (mg O2/l) |
1 |
6.35 |
7.58 |
8.14 |
8.29 |
2 |
5.31 |
7.83 |
8.20 |
8.29 |
|
3 |
7.03 |
7.01 |
8.28 |
8.15 |
|
Oxygen saturation value (mg O2/l) |
- |
9.20 |
9.20 |
9.20 |
9.20 |
Relative oxygen uptake |
1 |
0.29 |
0.15 |
0.10 |
0.06 |
2 |
0.40 |
0.13 |
0.09 |
0.06 |
|
3 |
0.22 |
0.22 |
0.08 |
0.08 |
|
Total oxygen uptake |
1 |
0.29 |
0.44 |
0.54 |
0.60 |
2 |
0.40 |
0.53 |
0.62 |
0.68 |
|
3 |
0.22 |
0.43 |
0.51 |
0.59 |
|
Total oxygen uptake x oxygen capacity of flasks |
1 |
8.49 |
12.98 |
15.87 |
17.62 |
2 |
11.80 |
15.50 |
18.19 |
19.95 |
|
3 |
6.32 |
12.63 |
15.07 |
17.27 |
|
% oxidation |
1 |
46 |
70 |
85 |
95 |
2 |
60 |
78 |
92 |
101 |
|
3 |
34 |
67 |
80 |
92 |
|
Average |
46 |
72 |
86 |
96 |
Table 4: Biodegradation of sodium acetate
Measurement |
Replicate |
Incubation time (days) |
|||
7 |
14 |
21 |
28 |
||
Oxygen concentration (mg O2/l) |
1 |
4.27 |
8.34 |
8.79 |
8.57 |
2 |
4.26 |
8.35 |
8.65 |
8.52 |
|
3 |
4.47 |
8.34 |
8.67 |
8.39 |
|
Oxygen saturation value (mg O2/l) |
- |
9.20 |
9.20 |
9.20 |
9.20 |
Relative oxygen uptake |
1 |
0.52 |
0.07 |
0.03 |
0.03 |
2 |
0.52 |
0.07 |
0.04 |
0.03 |
|
3 |
0.49 |
0.07 |
0.04 |
0.05 |
|
Total oxygen uptake |
1 |
0.52 |
0.59 |
0.61 |
0.64 |
2 |
0.52 |
0.59 |
0.63 |
0.66 |
|
3 |
0.49 |
0.56 |
0.60 |
0.65 |
|
Total oxygen uptake x oxygen capacity of flasks |
1 |
15.04 |
17.10 |
17.90 |
18.78 |
2 |
15.07 |
17.10 |
18.35 |
19.36 |
|
3 |
14.40 |
16.48 |
17.65 |
19.08 |
|
% oxidation |
1 |
76 |
87 |
91 |
95 |
2 |
76 |
87 |
93 |
96 |
|
3 |
73 |
83 |
89 |
97 |
|
Average |
75 |
86 |
91 |
97 |
Description of key information
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
Additional information
A 28 day aerobic ready biodegradability study (to OECD Guideline No. 301D – Closed Bottle Test) was carried out using Cardolite NC-511 (a Distilled Grade sample). The effects of the test substance on ready biodegradability were assessed based on the measurement of chemical oxygen demand (COD) using an activated sludge inoculum (from a domestic wastewater plant). Test performance was evaluated using the reference substances sodium acetate.
This toxicity study is classified as not reliable (Klimisch Code 2) on the basis that there were some deviations from the test guideline.
Cardolite NC-511 (a Distilled Grade sample) was classified as readily biodegradable as there was 96% degradation of the test substance after 28 days.
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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