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Physical & Chemical properties

Water solubility

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Reference
Endpoint:
water solubility
Type of information:
experimental study
Adequacy of study:
key study
Study period:
17 Jun - 5 Sep 2013
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP guideline study with acceptable restrictions
Qualifier:
according to guideline
Guideline:
OECD Guideline 105 (Water Solubility)
Deviations:
yes
Remarks:
: To obtain a more accurate value for water solubility, it was decided to perform an additional test based on the flask method in which evaporation was excluded as much as possible.
Qualifier:
according to guideline
Guideline:
EU Method A.6 (Water Solubility)
Deviations:
yes
Remarks:
: To obtain a more accurate value for water solubility, it was decided to perform an additional test based on the flask method in which evaporation was excluded as much as possible.
Qualifier:
according to guideline
Guideline:
EPA OPPTS 830.7840 (Water Solubility)
Deviations:
yes
Remarks:
: To obtain a more accurate value for water solubility, it was decided to perform an additional test based on the flask method in which evaporation was excluded as much as possible.
Principles of method if other than guideline:
Deviation from the protocol: As the maximum difference (MD) in the water solubility test according to column elution method was >30% between the two flow rates (12 mL/h and 24 mL/h), the test substance was most likely volatile. To obtain a more accurate value for water solubility, it was decided to perform an additional test based on the flask method in which evaporation was excluded as much as possible.
GLP compliance:
yes (incl. QA statement)
Remarks:
Ministerie van Volksgezondheid, Welzijn en Sport, Den Haag
Type of method:
column elution method
Remarks:
additionally: flask method
Key result
Water solubility:
< 0.6 mg/L
Temp.:
20 °C
pH:
7.3 - 8.4

Preliminary test:

The content of test substance dissolved in the water sample was after two centrifugation steps 0.0076 mg/L and after three centrifugation steps 0.00148 mg/L.

Main column elution test:

Flow rate [mL/h]

Sample no.

Concentration analysed

pH

Individual [mg/L]

Mean [mg/L]

CV [%]

24-I

1

0.496

0.564

8.2

8.4

2

0.582

3

0.7922

4

1.0002

5

1.1342

6

0.547

7

0.539

8

0.546

9

0.598

10

0.638

12

1

0.009

0.009

51

8.0

2

0.007

3

0.006

4

0.005

5

0.008

6

0.012

7

0.017

8

0.017

9

0.007

10

0.004

24-II

1

0.037

0.034

13

7.3

2

0.034

3

0.029

4

0.032

5

0.028

6

0.031

7

0.036

8

0.040

9

0.029

10

0.039

The turbidity of the eluates was < 0.2 NTU. According to this, no undissolved particles were detected in the eluates. No test substance was detected in the samples from the blank column.

A large variability was observed in the water solubility results obtained by the column elution test (0.6, 0.009 and 0.03 mg/L). To obtain a more accurate value for water solubility, it was decided to perform an additional test based on the flask method.

Additional test (flask method):

Stirring time [h]

Analysed concentration [mg/L]

Mean [mg/L]

pH

3

0.383

0.278

7.9

6

0.201

24

0.250

29

0.279

Based on all results, an accurate value could not be obtained. Water solubility was estimated to be < 0.6 mg/L.

Exact temperatures: 19.7 ± 0.3 °C (column elution); 19.8 ± 0.3 °C (flask method).

Description of key information

< 0.6 mg/L at 20 °C

Key value for chemical safety assessment

Water solubility:
0.6 mg/L
at the temperature of:
20 °C

Additional information

The water solubility of the substance was measured using column elution method according to EU method A.6 and guidelines OECD 105 and OPPTS 830.7840, with the following restriction: since the substance was difficult to test, and the results were inconsistent, the additional test using flask method was performed. The final result summarizes the two approaches.