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EC number: 472-110-0 | CAS number: 71868-15-0
- 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
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:
- 2019-01-07 - 2019-01-24 (experimental phase)
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 105 (Water Solubility)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.6 (Water Solubility)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- column elution method
- Key result
- Water solubility:
- 23.12 mg/L
- Conc. based on:
- test mat.
- Temp.:
- 20 °C
- pH:
- >= 5.72 - <= 5.96
- Conclusions:
- water solubility (at 20 °C): 23.12 mg/L [RSD = 3.44%]
- Executive summary:
According to the column elution method of OECD Test Guideline 105 (and EU Method A.6) the water solubility of the test item
2-Hydroxy-1-[4-(4-(2-hydroxy-2-methylpropionyl)phenoxy)phenyl]-2-methylpropan-1-one was determined to be 23.12 mg/L at 20 °C (RSD = 3.44 %).
- Endpoint:
- water solubility
- Type of information:
- (Q)SAR
- Adequacy of study:
- supporting study
- Study period:
- 2019-01-15
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- results derived from a valid (Q)SAR model and falling into its applicability domain, with adequate and reliable documentation / justification
- Justification for type of information:
- 1. SOFTWARE
EPIWIN v4.1
2. MODEL (incl. version number)
WSKOWWIN v1.42
3. SMILES OR OTHER IDENTIFIERS USED AS INPUT FOR THE MODEL
CC(C)(O)C(=O)c1ccc(Oc2ccc(cc2)C(=O)C(C)(C)O)cc1
4. SCIENTIFIC VALIDITY OF THE (Q)SAR MODEL
please refer to attached QMRF
5. APPLICABILITY DOMAIN
Please refer to attached QPRF
- Guideline:
- other: REACH Guidance R.6
- Principles of method if other than guideline:
- - Software tool(s) used including version:
EPIWIN 4.1
- Model(s) used: WSKOWWIN v1.42
- Model description: see field 'Justification for non-standard information' and 'Attached justification'
- Justification of QSAR prediction: see field 'Justification for type of information' and 'Attached justification' - Specific details on test material used for the study:
- CC(C)(O)C(=O)c1ccc(Oc2ccc(cc2)C(=O)C(C)(C)O)cc1
- Key result
- Water solubility:
- 85.44 mg/L
- Conc. based on:
- test mat.
- Temp.:
- 25 °C
- Remarks on result:
- other: pH not specified in the model
- Conclusions:
- water solubility: 85.44 mg/L
- Executive summary:
The water solubility of the test substance, 2-Hydroxy-1-[4-(4-(2-hydroxy-2-methylpropionyl)phenoxy)phenyl]-2-methylpropan-1-one was predicted by the model WSKOWWIN v1.42 implemented in the QSAR software EPIWIN v4.1. The experimental melting point of 100.7°C was entered for this prediction. The water solubility was determined to be 85.44 mg/L. The prediction falls within the applicability domain of this model.
Referenceopen allclose all
Preliminary Test:
The preliminary test at room temperature showed, that the water solubility of the test item was below 9.9 mg/L. The observations of the preliminary test are summarized in Table 3.
Table 3: Preliminary test for the water solubility
Amount of test item [mg] |
Total volume of added water [mL] |
Stirring time at RT |
Remark |
105.66 |
0.1 |
-- |
not dissolved |
0.6 |
-- |
not dissolved |
|
1.6 |
-- |
not dissolved |
|
3.6 |
3 min1) |
not dissolved |
|
13.6 |
3 min1) |
not dissolved |
|
100 |
7 min1) |
not dissolved |
|
9.43 |
100 |
approx. 2 days |
not dissolved |
4.97 |
250 |
approx. 2 days |
not dissolved |
4.95 |
500 |
approx. 2 days |
not dissolved |
1)The mixtures were treated in an ultrasonic bath.
The solubility of the test item in water at room temperature was estimated to be < 9.9 mg/L. Therefore, the column elution method was performed.
Main Test:
The mean value and its standard deviation from five consecutive samples taken from the saturation plateau, each measured twice, were calculated for each run. The mean concentrations calculated on two tests using different flows were compared and the repeatability was calculated, which should be better than 30 %. The measured concentrations which are shown in the following tables are rounded values. The calculation was performed with not rounded values.
Table 4: Results of column 1 (flow rate 12.5 mL/h)
Fraction |
pH value |
Measured concentration [mg/L] |
Mean measured concentration [mg/L] |
Mean concentration [mg/L] |
Relative standard deviation (RSD) [%] |
29 |
5.72 (23.4 °C) |
22.71 |
22.42 |
23.69 |
5.27 |
30 |
5.74 (23.4 °C) |
22.96 |
23.11 |
||
31 |
5.72 (23.3 °C) |
22.92 |
22.91 |
||
32 |
5.79 (23.3 °C) |
24.64 |
24.64 |
||
33 |
5.82 (23.2 °C) |
25.66 |
25.35 |
The first column showed a value of the water solubility of 23.69 mg/L.
Table 5: Results of column 2 (flow rate 25.0 mL/h)
Fraction |
pH value |
Measured concentration [mg/L] |
Mean measured concentration [mg/L] |
Mean concentration [mg/L] |
Relative standard deviation (RSD) [%] |
56 |
5.73 (23.3 °C) |
21.73 |
21.58 |
22.56 |
2.70 |
57 |
5.80 (23.2 °C) |
22.30 22.57 |
22.44 |
||
58 |
5.75 (23.2 °C) |
22.92 |
22.91 |
||
59 |
5.84 (23.2 °C) |
22.77 |
22.73 |
||
60 |
5.93 (23.2 °C) |
23.33 |
23.15 |
The second column showed a value of the water solubility of 22.56 mg/L.
Table 6: Results of column 3 (flow rate 25.0 mL/h, blank)
Fraction |
pH value |
Measured concentration [mg/L] |
Mean measured concentration [mg/L] |
Mean concentration [mg/L] |
Relative standard deviation (RSD) [%] |
56 |
5.96 (23.2 °C) |
-- |
-- |
-- |
-- |
57 |
5.86 (23.2 °C) |
-- |
-- |
||
58 |
5.85 (23.2 °C) |
-- |
-- |
||
59 |
5.94 (23.1 °C) |
-- |
-- |
||
60 |
5.90 (23.1 °C) |
-- |
-- |
The third column showed no test item in the water or any signals in the HPLC chromatograms.
The mean measured concentration in water was determined to be 23.12 mg/L (RSD = 3.44%; the calculation was carried out with the original not rounded values).
To verify the accuracy of the analytical method freshly prepared standard solutions (prepared with the test item) were measured in between the samples of the column elution method. The results of these measurements are shown in Table 7. The recovery rates should lie between 90 and 110 %.
Table 7: Measurement of standard solutions
Standard solution (nominal value [mg/L]) |
Measured value [mg/L] |
Recovery rate [%] |
Standard-Ü1 (20.84)
|
20.75 |
100.4 |
20.96 |
99.4 |
|
20.56 |
101.4 |
|
20.99 |
99.3 |
|
20.8 |
100.2 |
|
20.75 |
100.4 |
|
Standard-Ü2 (22.28) |
22.38 |
99.5 |
22.20 |
100.4 |
|
21.89 |
101.8 |
|
22.40 |
99.5 |
|
22.42 |
99.4 |
|
22.18 |
100.5 |
|
Standard-Ü3 (5.41) |
5.63 |
96.1 |
5.67 |
95.4 |
|
Standard-Ü4 (6.88) |
7.28 |
94.5 |
7.23 |
95.1 |
The recovery rate of the measured standard solutions was in the range from 94.5 % to 101.8 %, which shows a good accuracy of the analytical method.
Following the measurements, the amount of the test item in the columns was checked. For this purpose, columns 1 and 2 were each purged with 50 mL acetone. 0.5 mL of the acetone solutions were diluted to 100 mL with acetone and measured by HPLC.
These measurements showed that 75.02 mg of the test item was found in column 1 after the main test, which corresponds to 59.9 % of the starting amount. 44.32 mg of the test item could be found in column 2 after the main test, which corresponds to 35.42 % of the starting amount. In both columns enough test item was found after the main tests to ensure correct performance of the test.
The water solubility was determined to be 85.44 mg/L.
Description of key information
The water solubility of the test substance was determined using the column elution method according to OECD Guideline 105 and EU Method A.6 (Schiewer, 2019).
Water solubility was also predicted using the WSKOWWIN v1.42 model of EPIWIN v4.1. The experimental melting point of 100.7°C was entered for this prediction. The water solubility was determined to be 85.44 mg/L. The prediction falls within the applicability domain of this model.
Key value for chemical safety assessment
- Water solubility:
- 23.12 mg/L
- at the temperature of:
- 20 °C
Additional information
The column elution method results were retained as key data.
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