Registration Dossier
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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 241-527-8 | CAS number: 17527-29-6
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Endpoint summary
Administrative data
Description of key information
OECD 231 (See Section 6.1.8. for study summary. No endpoint summary functionality is available in Section 6.1.8 for this endpoint, therefore the summary is provided here): At 107 mg test item/L (the top dose; day 21): a statistically significant increase compared to the control was observed in normalised hind limb length and developmental stage (advanced development observed).
At 1.07 mg test item/L, no statistically significant difference compared to the control was observed for any endpoint. At 10.7 mg test item/L, wet weight and snout vent length were statistically significantly increased compared to the control on day 7, whereas on day 21 no statistically significant difference compared to the control was observed for any endpoint. At 107 mg test item/L on day 7, no statistically significant difference regarding developmental stage was detected; however, statistically significant advanced development on day 21 was observed. Body wet weight and snout vent length were statistically significantly increased on day 7 of exposure, but not on day 21. Under the conditions of this study, there were no changes in the thyroid glands that could be attributed to treatment with the test item.
OECD 234: Please see Section 6.1.2 for the Endpoint Summary for the Fish Sexual Development Test.
Additional information
Endocrine disruptor testing in aquatic vertebrates - in vivo - Endpoint Summary - IUCLID Section 6.1.8 - OECD 231 (Amphibian Metamorphosis Assay)
Summary
A test in accordance with OECD 231 (2009) was performed on PFHxA in order to assess the thyroid activity potential of the test item. See Section 6.1.8 for the OECD 231 robust study summary.
Fertilised Xenopus laevis (African clawed frog) eggs were hatched and the tadpoles reared until they reached NF (Nieuwkoop & Faber, 1994) developmental stage 51. The organisms were then exposed in a flow-through test for 21 days. There were 4 treatment groups (3 concentrations of test item and 1 negative control), with 4 replicates each containing 20 organisms. The test concentrations used were 1.07, 10.7 and 107 mg test item/L and a control, corresponding to 1.0, 10 and 100 mg perfluorohexanoate/L. Analytical verification of the test item concentration in test medium was performed (the overall mean recovery value was 99 %).
The endpoints assessed in the study were developmental stage (day 7 and 21); body weight (day 7 and 21); snout to vent length (SVL; day 7 and 21); hind limb length (HLL; day 7 and 21) thyroid histology (day 21) as indicators of thyroidal activity of the test item. Furthermore, survival and behaviour were monitored daily.
Key results: At 107 mg test item/L, statistically significant advanced development on day 21 was observed compared to the control. A statistically significant increase of HLL (normalised by SVL) at 107 mg test item/L on day 7 and 21 were observed compared to the control.
At 1.07 mg test item/L, no statistically significant difference compared to the control was observed for any endpoint. At 10.7 mg test item/L, wet weight and snout vent length were statistically significantly increased compared to the control on day 7, whereas on day 21 no statistically significant difference compared to the control was observed for any endpoint. At 107 mg test item/L on day 7, no statistically significant difference regarding developmental stage was detected; however, statistically significant advanced development on day 21 was observed. Body wet weight and snout vent length were statistically significantly increased on day 7 of exposure, but not on day 21. Under the conditions of this study, there were no changes in the thyroid glands that could be attributed to treatment with the test item.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.