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Diss Factsheets
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EC number: 810-258-3 | CAS number: -
- 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
Key value for chemical safety assessment
Skin sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
A skin sensitization study of the test item, HF-1000 Solvent, in guinea pigs was carried out by Nucro-Technics according to Study Plan No. INT/296962. Three groups of Hartley guinea pigs were used. Twenty animals were in the test group, ten animals in the solvent control group and five animals were in the positive control group. The test item, HF-1000 Solvent, was applied “as is” to 2.5 x 2.5 cm gauze patches. The gauze patches were then topically applied for a 6-hour exposure period to the shaved left flanks of 20 guinea pigs on Days 0, 7 and 13. The applications on Days 0, 7 and 13 represented the induction phase of the study. 14 Days after the final induction application (Day 27), a 2.5 x 2.5 cm gauze patch loaded with the test item, HF-1000 Solvent, was applied to the shaved right flank of each animal in the Test Group for a 6-hour exposure period. This application represented the challenge application. A naïve control group, consisting of 10 animals was used. During the induction phase (Days 0, 7, and 13) the left flank of each control animal was shaved and a blank 2.5 x 2.5 cm gauze patch was applied on each animal. On Day 27 (Challenge Phase), the test item, HF-1000 Solvent, was applied to the shaved right flank of each control animal for a 6-hour exposure period. A group of 5 positive control animals was subjected to identical procedures as outlined above for the test group of animals (induction phase), with the exception that the positive control item, 0.3% 1-chloro-2, 4-dinitrobenzene (DNCB), was substituted as a reference substance. During the challenge phase, the positive control item (0.1% DNCB) was applied to the shaved right flank of each positive control animal. An evaluation of skin reaction was carried out and recorded at 24 hours and 48 hours after completion of each application. None of the guinea pigs administered the test item had any signs of local skin irritation after the induction applications or after the challenge period. All 5 of the positive control animals showed a positive response. Based on these findings, the test item, HF-1000 Solvent, was found to be non-sensitizing in a Buehler Skin Sensitization Study in guinea pigs
Migrated from Short description of key information:
he test item, HF-1000 Solvent, was found to be non-sensitizing in a Buehler Skin Sensitization Study in guinea pigs
Justification for classification or non-classification
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.
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