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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Physical & Chemical properties

Density

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Administrative data

Link to relevant study record(s)

Reference
Endpoint:
relative density
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2004
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Justification for type of information:
The study was conducted according to an internationally recognised method, and under GLP. No deviation was reported. Substance ID is adequately specified with purity. Therefore full validation applies.
Reason / purpose for cross-reference:
reference to other study
Qualifier:
according to guideline
Guideline:
EU Method A.3 (Relative Density)
Deviations:
not specified
Qualifier:
according to guideline
Guideline:
OECD Guideline 109 (Density of Liquids and Solids)
Version / remarks:
1995
Deviations:
not specified
GLP compliance:
yes (incl. QA statement)
Remarks:
Swiss Federal Office of Public Health (inspected on September 09 and 30, 2002 / signed on December 2002
Type of method:
oscillating densitimeter
Dynamic viscosity of test material:
52 mPa.s
Key result
Type:
relative density
Density:
0.915
Temp.:
20 °C
Conclusions:
The relative density of the test substance was determined to be 0.915 at 20°C
Executive summary:

The relative density of the test substance was measured under GLP according to OECD 109 / EU A3 guideline, oscillating densitimeter method.

The relative density of test substance has been determined to be 0.915 at 20°C.

Description of key information

The substance is less dense than water.

Key value for chemical safety assessment

Relative density at 20C:
0.915

Additional information

A fully reliable experimental study, conducted under GLP according to a recognized OECD/EU method, is available. It is considered as a key study, and the result is retained as key data.