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EC number: 202-509-5 | CAS number: 96-48-0
- 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
Skin irritation: negative
Eye Irritation: causes irreversible effects
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Additional information
γ-butyrolactone (GBL) has been adequately tested for skin and eye irritation and found to not be a skin irritant but is capable of causing irreversible effects in the eye. When applied to clipped Vienna White rabbits and occluded, mean Erythema and Edema scores were 0 out of 4 after 24, 48, and 72 hours (BASF AG, 1960). When applied to an eye of a single New Zealand White rabbit in an OECD 405 guideline study under GLP conditions, effects on the cornea were observed (BASF AG, 2005). The mean cornea score was 1.3 out of 4 after 24, 48, and 72 hours, and were not fully reversible after 28 days. Similar results were observed in an earlier study of similar design (BASF, 1960) and are further supported by several in vitro tests. However, another OECD 405 guideline study, under GLP conditions, reported in the European Centre for Ecotoxicology and Toxicology of Chemicals (ECETOC) Technical Report No. 48 (Version 2), indicated that effects observed in the cornea were reversible within 14 days (ECETOC, 1998), but some details of the study design were not available for review. GBL should be regarded as an eye irritant capable of causing irreversible effects.
Effects on eye irritation: irritating
Justification for classification or non-classification
Skin irritation
Based on the results of the key study (Draize score = 0 after 24, 48 and 72 hours under occlusive conditions), gamma-butyrolactone would not be classified as a primary dermal irritant under the EU DSD criteria (EU Directive 67/548/EEC) or under the EU CLP criteria (EU Regulation 1272/2008).
Eye irritation
When applied to the eye of a rabbit, effects on the cornea were observed. The mean cornea score was 1.3 out of 4 after 24, 48, and 72 hours and was not fully reversible after 28 days. Based on the results of the key study gamma-butyrolactone would be classified as Xi; R41 (Risk of serious damage to eyes) under the EU DSD criteria (EU Directive 67/548/EEC). Gamma-butyrolactone also meets the criteria for classification as a Category 1 eye irritant (Causes serious eye damage) under the EU CLP criteria (EU Regulation 1272/2008) because the effects were not fully reversible after 28 days.
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