Registration Dossier

Administrative data

Endpoint:
water solubility
Type of information:
experimental study
Adequacy of study:
key study
Study period:
19 August 2008 - 09 October 2008
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Test performed in accordance with OECD guidelines.

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:
OECD Guideline 105 (Water Solubility)
Qualifier:
according to
Guideline:
EU Method A.6 (Water Solubility)
GLP compliance:
yes (incl. certificate)
Type of method:
column elution method

Test material

Reference
Name:
Unnamed
Type:
Constituent
Test material form:
solid: crystalline
Details on test material:
- Substance type: white powder
- Physical state: solid
- Analytical purity: 99.80%
- Expiration date of the lot/batch: 31 Jan 2009
- Storage condition of test material: At room temperature in the dark

Results and discussion

Water solubility
Water solubility:
0.115 mg/L
Temp.:
20 °C
pH:
> 7.1 - < 7.4

Applicant's summary and conclusion

Conclusions:
The water solubility of the test substance at 20.0C+/-0.6C was 0.115mg/l.
Executive summary:

The column elution was selected for the determination of the water solubility of the test substance. The water solubility of the test substance at 20.0C+/-0.6C was 0.115mg/l. The pH of the aqueous sample was 7.1 and 7.4