Registration Dossier
Registration Dossier
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EC number: 201-244-2 | CAS number: 80-04-6
Vapour pressure
Administrative data
Link to relevant study record(s)
- Endpoint:
- vapour pressure
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 18 January 2011 to 01 June 2012
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.4 (Vapour Pressure)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 104 (Vapour Pressure Curve)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- effusion method: vapour pressure balance
- Temp.:
- 25 °C
- Vapour pressure:
- 0.001 Pa
- Transition / decomposition:
- no
- Transition temp.:
- 25 °C
- Conclusions:
- Rikabinol HB was found to have a vapour pressure of 9 x 10^-4 Pa at 25°C.
Reference
Description of key information
The determination of vapour pressure of HBPA was carried out using the vapour pressure balance method (Huntingdon Life Sciences, 2012, Study MOG0004). The procedure was designed to be compatible the EC Method A.4 and the OECD test guidelines 104, and was conducted in compliance with GLP.
HBPA was found to have a vapour pressure of 9 x 10-4 Pa at 25°C.
Key value for chemical safety assessment
- Vapour pressure:
- 0.001 Pa
- at the temperature of:
- 25 °C
Additional information
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