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EC number: 695-930-2 | CAS number: 13676-53-4
- 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
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- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
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- Nanomaterial crystalline phase
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- Nanomaterial pour density
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- Endpoint summary
- Stability
- Biodegradation
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- Transport and distribution
- Environmental data
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- 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
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- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
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- Toxicological Summary
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- Additional toxicological data

Water solubility
Administrative data
Link to relevant study record(s)
- Endpoint:
- water solubility
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2018-01-29 to 2018-04-18
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 105 (Water Solubility)
- Version / remarks:
- 1995
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.6 (Water Solubility)
- Version / remarks:
- 2008
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- flask method
- Key result
- Water solubility:
- 37.6 mg/L
- Conc. based on:
- test mat.
- Incubation duration:
- >= 48 - <= 72 h
- Temp.:
- 20 °C
- pH:
- 5.3
- Conclusions:
- In the present study conducted according to OECD guideline 105 (1995) the water solubility of m-Xylylenebismaleimide was determined by the flask method. The water solubility of the test item is 37.6 mg/L at 20°C and a pH of 5.3.
Reference
Table 2: Results of the preliminary test
phase separation procedure |
Meass. Conc. [mg/L] |
||
Replicate 1 |
Replicate 2 |
||
centrifugation |
10000 x g for 10 min |
72.2 |
76.9 |
20000 x g for 20 min |
69.3 |
74.0 |
|
filtration |
0.2 µm pore-size |
69.1 |
73.5 |
Table 3: Procedural Control for the Filtration Procedure (preliminary test)
Procedural control |
Meas. Conc. [mg/L] |
Mean |
RR [%] |
from calibration |
10.24872 |
10.22 |
- |
10.19639 |
|||
filtrated |
10.1841 |
- |
99.6 |
Table 4: Recovery rates of the fortified samples (HPLC analysis):
Replicate No |
1 x LOQ |
10 x LOQ |
||
Calc. conc. [mg/L] |
RR [%] |
Calc. conc. [mg/L] |
RR [%] |
|
1 |
5.07 |
101 |
49.3 |
99 |
2 |
5.07 |
101 |
49.7 |
99 |
3 |
5.08 |
102 |
50.2 |
100 |
4 |
5.11 |
102 |
50.3 |
101 |
5 |
5.09 |
102 |
49.9 |
100 |
Mean |
5.08 |
102 |
49.9 |
100 |
SD |
0.02 |
0.4 |
||
CV [%] |
0.37 |
0.85 |
Calc. conc. = Calculated concentration, exact weight and dilution factor of 10 taken into account
RR = Recovery rate, related to the fortified concentration
SD = Standard deviation
CV = Coefficient of variation
Description of key information
-study according to OECD guideline 105, GLP, water solubility of m-Xylylenebismaleimide is 37.6 mg/L at 20°C and a pH of 5.3.
Key value for chemical safety assessment
- Water solubility:
- 37.6 mg/L
- at the temperature of:
- 20 °C
Additional information
In the present study conducted according to OECD guideline 105 (1995) the water solubility of m-Xylylenebismaleimide was determined by the flask method. A preliminary test was performed in order to verify the planned study design. For this purpose 50 mg of the test item were mixed with 50 mL double distilled water in duplicate and stirred for 2 weeks. after this incubation aliquots of each mixture were centrifuged at 20 °C and 10000 x g for 10 min as well as at 20000 x g for 20 min and filtrated via syringe filters with a pore-size of 0.2 um, respectively. For each sample, 0.5 mL of the aqueous phase was transferred into a clear glass vial and checked for Tyndall-effects. For each sample, and thus for each used phase separation procedure, a Tyndall effect was observed. The least visible Tyndall effect was observed for the filtrated samples. The solubility was determined to be in the range of 70 mg/L for the filtrated samples, no significant loss of the test item was observed for the procedural control. For the definitive testing, filtration was used for the phase separation and slight Tyndall effects are deemed to be acceptable.
In the definitive test HPLC analysis after a preincubation time of 48 and 72 h revealed a water solubility of 37.6 mg/L at 20°C and a pH of 5.3.
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