Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
surface tension
Data waiving:
study technically not feasible
Justification for data waiving:
the study does not need to be conducted because water solubility is below 1 mg/L at 20°C
Justification for type of information:
A test was carried out in accordance to EU Regulation (EC) 440/2008, Annex Part A test A5 and OECD Test Guideline 115. The endpoint has been exempted under Column 2 of Annex VII (EC 440/2008) as the water solubiliy is <1 mg per litre.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2017
Report date:
2017

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
EU Method A.5 (Surface Tension)
GLP compliance:
yes

Test material

Constituent 1
Reference substance name:
Hop, Humulus lupulus, ext.
EC Number:
232-504-3
EC Name:
Hop, Humulus lupulus, ext.
Cas Number:
8060-28-4
Molecular formula:
No simple molecular formula for UVCB
IUPAC Name:
Hop, Humulus lupulus, ext.
Test material form:
liquid: viscous
Remarks:
Depending on the extraction conditions and on the hop variety, the colour of the extract can vary from yellow to dark green. It is a semi-fluid paste at room temperature. The product becomes more fluid when heated.
Specific details on test material used for the study:
Hop extract batch number 160025. This is a liquid carbon dioxide extract of hops variety 'Cascade'.

Results and discussion

Any other information on results incl. tables

Two solutions were made up of the following dilutions: 10 mg per 10 ml and 1 mg per 1 litre. They were shaken and left for approximately 3 hours. After 30 minutes of sonication of the 1 mg per 1 litre solution the sample remained visible, therefore the sample's solubility is <1 mg per litre. This endpoint has been exempted under Column 2 of Annex VII (EC 440/2008) as the water solubility is <1 mg/L.

Applicant's summary and conclusion

Conclusions:
This endpoint has been exempted under Column 2 of Annex VII (EC 440/2008) as the water solubility is <1 mg/L.