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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Study period:
From 14 to 15 April 2016
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
test procedure in accordance with generally accepted scientific standards and described in sufficient detail
Justification for type of information:
Data comes from the description of the test substance in the GLP reports on other physico-chemical properties. No guideline is required according to REACh TGD. The substance is considered to be adequately characterised. Therefore full validation applies.
Reason / purpose for cross-reference:
reference to same study
Qualifier:
no guideline required
Principles of method if other than guideline:
Visual observation
GLP compliance:
yes (incl. QA statement)
Remarks:
Date of inspection: 13-14/10/2014; Signature Date: 8/4/2015
Physical state at 20°C and 1013 hPa:
liquid
Form:
liquid
Colour:
Clear yellow
Substance type:
organic
Conclusions:
The substance is a clear yellow liquid
Executive summary:

The substance was tested for physico-chemical properties. A description of the sample is provided in the report as a clear yellow liquid.

Description of key information

Clear yellow liquid

Key value for chemical safety assessment

Physical state at 20°C and 1013 hPa:
liquid

Additional information

Data comes from the description of the test substance in the GLP reports on other physico-chemical properties. No guideline is required according to REACh TGD. The substance is considered to be adequately characterised. Therefore full validation applies.