Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Appearance / physical state / colour

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Administrative data

Link to relevant study record(s)

Reference
Endpoint:
appearance / physical state / colour
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Data available from the test item section and associated certificate of analysis of a GLP, guideline study scored Klimisch 1
Reason / purpose for cross-reference:
other: Data available from the test item section, and associated certificate of analysis, of a GLP, guideline study
Principles of method if other than guideline:
Data available from the test item section and associated certificate of analysis of a GLP, guideline study scored Klimisch 1
GLP compliance:
no
Physical state at 20°C and 1013 hPa:
liquid
Key result
Form:
liquid
Colour:
Colourless clear
Odour:
other: Not stated
Substance type:
organic
Conclusions:
The test item is a colourless clear liquid at room temperature.
Executive summary:

The test item is a colourless, clear liquid at room temperature as reported in the test item section, and associated certificate of analysis, in a GLP-compliant experimental study. This is considered to be acceptable for assessment of this endpoint.

Description of key information

The test item is a colourless, clear liquid at room temperature.

Key value for chemical safety assessment

Physical state at 20°C and 1013 hPa:
liquid

Additional information

The test item is a colourless, clear liquid at room temperature as reported in the test item section, and associated certificate of analysis, in a GLP-compliant experimental study (2017). This is considered to be acceptable for assessment of this endpoint.