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EC number: 203-808-3 | CAS number: 110-85-0
- 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
Piperazine has been found corrosive to the skin in animal tests. Thus, serious eye damage can also be expected.
Based on the EpiDermTM prediction model for corrosion, piperazine at a 34% concentration was classified as corrosive while all the other dilutions <= 30% were classified as non-corrosive.
No effects were noted on human skin at concentrations below 2.2 %.
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (corrosive)
Additional information
Skin corrosion/irritation
There are no in vitro data on skin corrosion/irritation because sufficient in vivo data were available.
In a skin irritation/corrosion test performed according to OECD404, rabbits were exposed for 4 hours to 50% piperazine solution under semi-occlusive dressing (BASF, 1984). After 4 h exposure washing with Lutrol was performed. Full thickness necrosis was observed after 24 hours and thus, the study was terminated after 72 h. Piperazine is corrosive to rabbit skin. In supporting, in a Primary skin irritation test, rabbits were exposed for 3 min and 1 h to piperazine under occlusive dressing (Myers, 1990). Skin reactions were observed for 14 days. Full thickness necrosis, scab formation and alopecia were observed after the 1 h exposure.
Before OECD404 was established in 1982, skin irritation of piperazine was tested using an internal method in rabbits, exposing 2.5 x 2.5 cm2 for 1, 5, 15 min or 20 h under occlusinve dressing (BASF, 1964). After 20 h exposure mean erythema score for 24/48/27 h was 1.55, mean edema score was 0.83; both findings were fully reversible within the observation period of 14 days. Superficial necrosis was observed, indicating strong skin irritation.
Eye irritation
An eye irritation study is scientifically not needed as the substance is classified as skin corrosive, leading to classification of serious eye damage (Category 1).
Other data:
No effects were noted on human skin at concentrations below 2,2 %.
Justification for classification or non-classification
Based on the available data, piperazine is corrosive to the skin. According to Annex VI of Regulation (EC) No 1272/2008 (CLP Regulation), piperazine [solid] is classified as Skin Corr. Cat. 1B (H314).
The classification for skin corrosion also leads to a classification of serious eye damage (Eye Dam. 1; H318) according to Regulation (EC) No 1272/2008 (CLP Regulation).
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