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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
water solubility
Type of information:
experimental study
Adequacy of study:
key study
Study period:
29 April - 25 July, 2008
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: The study has been performed according to OECD and/or EC guidelines and according to GLP principles.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2008
Report date:
2008

Materials and methods

Test guidelineopen allclose all
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:
flask method

Test material

Constituent 1
Chemical structure
Reference substance name:
1-Propanone, 2-hydroxy-2-methyl-, 1-(4-C10-13-alkylphenyl) derivs.
Cas Number:
1001416-18-7
Molecular formula:
Not applicable - UVCB
IUPAC Name:
1-Propanone, 2-hydroxy-2-methyl-, 1-(4-C10-13-alkylphenyl) derivs.

Results and discussion

Water solubility
Water solubility:
0.764 - 1.53 mg/L
Temp.:
20 °C
pH:
ca. 7.8
Details on results:
The maximum difference (MD) of the mean concentrations determined in the 24, 48 and 72 hour test samples was > 15%. This may be explained by the variation in data for each individual sampling point. Despite the fact that the sample solutions were visually clear after the alternative sample treatment procedure, undissolved test substance may still be present. Since centrifugation was not successful, this treatment procedure was considered the best possible alternative to determine the water solubility of the test substance. It will be reported as a range, i.e. 0.764 – 1.53 mg/l.

Any other information on results incl. tables

Since the test substance was not detected in any of the aqueous solutions after three- and four-times centrifugation, this was not considered to be a suitable sample treatment. It was suspected that the test substance adsorbed to the wall of the centrifugation vials and was lost in the first two centrifugation steps.

No test substance was detected in the pre-treated samples from the blank water mixture.

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information): slightly soluble (0.1-100 mg/L)
The flask method was chosen for the determination of the water solubility of LE 5288. The water solubility of the test substance at 20.0°C +/- 0.5°C was 0.764 – 1.53 x 10-3 g/l. The pH of the aqueous sample after 72 hours stirring was 7.8.
Executive summary:

The water solubilty of the substance wasd determined according to OECD Guidelline 105. The flask method was chosen for the determination of the water solubility of LE 5288. The water solubility of the test substance at 20.0°C +/- 0.5°C was 0.764 – 1.53 x 10-3 g/l. The pH of the aqueous sample after 72 hours stirring was 7.8.