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Diss Factsheets

Physical & Chemical properties

Density

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Reference
Endpoint:
relative density
Type of information:
experimental study
Adequacy of study:
key study
Study period:
11 December 2017 to 01 June 2018
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 109 (Density of Liquids and Solids)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method A.3 (Relative Density)
Deviations:
no
GLP compliance:
yes
Type of method:
pycnometer method
Key result
Type:
relative density
Density:
1 other: unitless
Temp.:
20 °C

Table 1: Results of relative density study

 Parameter  Replicate 1  Replicate 2
 w1

 24.82370

 24.60316

 w2

 49.40051

 49.68507

 w3

 27.86420

 27.65666

 w4

 49.43535

49.66750 

 W1

 24.57681

 25.08191

 W2

 3.04050

 3.05350

 W3

 21.57115

 22.01084

 Vs

 3.01

 3.08

 Dt4

 1.01

 0.99

 Mean Dt4

1.00 

Where:

w1= weight of empty pycnometer (g)

w2= weight of pycnometer and water (g)

w3= weight of pycnometer and test item (g)

w4= weight of pycnometer, test item and water (g)

Dt4= relative density of test item at test temperature compared to water at 4°C

Conclusions:
The relative density of the test item was determined to be 1.00 at 20°C.
Executive summary:

The relative density of the test item was determined in a study following OECD 109 and EC Method A.3 guidelines, using the pycnometer method. The relative density of the test item was determined to be 1.00 at 20°C.

The study is a GLP-compliant, guideline experimental study and is fully acceptable for assessment of this endpoint.

Description of key information

The relative density of the test item was determined to be 1.00 at 20°C.

Key value for chemical safety assessment

Relative density at 20C:
1

Additional information

The relative density of the test item was determined in a study following OECD 109 and EC Method A.3 guidelines, using the pycnometer method (Dunning 2018).

The study is a GLP-compliant, guideline experimental study and is fully acceptable for assessment of this endpoint.