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Density

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Reference
Endpoint:
relative density
Type of information:
experimental study
Adequacy of study:
key study
Study period:
6-10 August 2010
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
guideline study without detailed documentation
Remarks:
The study was conducted according to an internationally recognised method, and under GLP. The substance is adequately identified, but details on composition are missing. Therefore validation applies with restrictions.
Qualifier:
according to guideline
Guideline:
EU Method A.3 (Relative Density)
Deviations:
no
Principles of method if other than guideline:
Not applicable
GLP compliance:
yes (incl. QA statement)
Remarks:
effective 24 July 2009 (validity 18 months)
Type of method:
pycnometer method
Specific details on test material used for the study:
Storage conditions of test material: Stored at room temperature protected from direct sun light.
Key result
Type:
relative density
Density:
0.849 other: dimensionless
Temp.:
20 °C

Table 4.4/1: Density results

 

Replicate

Certified volume

Empty weight

Test with water

Test with test item

Relative density D20/4

Temperature

Total weight

Temperature

Total weight

1

50.007

35.6274 g

4.4 °C

85.5621 g

20.3 °C

78.0114 g

0.849

2

51.841

31.4314 g

4.4 °C

83.1954 g

20.3 °C

75.3741 g

0.849

 

Relative density D20/4 = 0.849 ± 0.000

Density = 0.848 g/mL

Conclusions:
The substance is much less dense than water.
Executive summary:

The density of the test substance was measured under GLP according EU A3 guideline, pycnometer method.

 

Experiment was performed at 20 °C in duplicate, and compared to water at 4.4°C.

 

The relative density (D20/4) of the test substance was calculated to be 0.849.

Description of key information

The substance is much less dense than water.

Key value for chemical safety assessment

Relative density at 20C:
0.849

Additional information

A reliable experimental study, conducted according to a recognized EC method and under GLP, is available.

Despite minor restrictions due to incomplete test item identification, it is considered as a key study, and the result is retained as key data.