Registration Dossier
Registration Dossier
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EC number: 241-010-7 | CAS number: 16941-12-1
Particle size distribution (Granulometry)
Administrative data
Link to relevant study record(s)
- Endpoint:
- particle size distribution (granulometry)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP compliant, guideline study, available as unpublished report acceptable without restrictions
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 110 (Particle Size Distribution / Fibre Length and Diameter Distributions)
- Version / remarks:
- Screening Test
- Principles of method if other than guideline:
- The method used is based on a procedure designed to comply with that given in 'Particle size distribution, fibre length and diameter distribution', June 1996 European Commission technical guidance document, which satisfies the requirements of OECD Guideline 110
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- sieving
- No.:
- #1
- Size:
- < 100 µm
- Distribution:
- 0.1 %
- Conclusions:
- The proportion of hexachloroplatinic acid <100 μm was 0.1 %.
- Executive summary:
This is a GLP compliant study following OECD guideline 110 (screening test) and is considered to be reliable and suitable for use as the key study for this endpoint. The proportion of hexachloroplatinic acid <100 μm was 0.1 %.
Reference
The results of the sieving procedure are shown below:
Measurement |
Result |
Mass of test item transferred to sieve |
10.13g |
Mass of test item passed through sieve |
0.01g |
Proportion of test item <100µm |
0.1% |
Description of key information
The proportion of hexachloroplatinic acid <100 μm was 0.1 %.
Additional information
Walker and White (2011) is a GLP compliant study following OECD guideline 110 (screening test) and is considered reliable and suitable for use as the key study for this endpoint. The proportion of Hexachloroplatinic acid <100 μm was 0.1 %.
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