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Diss Factsheets
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EC number: 203-742-5 | CAS number: 110-16-7
- 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
Acute oral toxicity, rat:
Eastman 1969: LD50 = 708 mg per kg body weight
Löser 1978 (maleic anhydride): LD50 = 1030 mg/kg body weight
Mürmann 1984 (maleic anhydride): LD50 = 1090 mg/kg body weight
Acute dermal toxicity, rabbit:
Vernot 1977 (maleic anhydride): LD50 = 2620 mg/kg body weight
Sax 1989: LD50 = 1560 mg/kg body weight
Younger Labs 1976 (maleic anhydride): 298 <LD50<1000 mg/kg body weight
Acute toxicity, inhalation:
Existing data are inadequate to determine the acute toxicity by inhalation.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 708 mg/kg bw
Acute toxicity: via dermal route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 1 560 mg/kg bw
Additional information
Acute oral toxicity:
LD50 data for maleic acid as well as for maleic anhydride are in the same range: 708, 1030, 1090 mg per kg body weight and result in the same classification. Therefore the data for maleic acid are used for classification (LD50 = 708 mg/kg bw). These data are also flagged "critical study for SIDS endpoint" in the SIDS dossier.
Acute dermal toxicity:
LD50 data for maleic acid are 1560 mg per kg body weight, whereas the LD50 data for maleic anhydride are between (practically) 400 and 100 mg/kg or above 2000 mg/kg (2620 mg/kg). For safety reasons, the data on maleic acid are taken for classification (1560 mg/kg bw). These data are also flagged "critical study for SIDS endpoint in the SIDS dossier.
Acute inhalation toxicity: Inhalation is not relevant, as the size particles are to large to inhale.
The derivation of the relevant toxicity descriptors and the calculation of the DNELs and their justifications was the task of DSM Netherlands. DSM Netherlands requested to use their data and justifications in the IUCLID.
Justification for classification or non-classification
Based on the LD50 of 708 mg per kg body weight for oral toxicity the test substance is classified as "R22 Harmful if swallowed" and as "Acutely toxic Category 4".
Based on the LD50 of 1560 mg per kg body weight for dermal toxicity the test substance is classified as "R21 Harmful in contact with skin" and as "Acutely toxic Category 4".
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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