lexiara

ANNEX III

INFORMATION REFERRED TO IN ARTICLE 3 1. General information 1.1. Name of substance 1.2. Einecs No 1.3. CAS No 1.4. Synonyms 1.5. Purity 1.6. Impurities 1.7. Molecular formula 1.8. Structural formula 1.9. Type of substance 1.10. Physical state 1.11. Please indicate who is submitting the data set 1.12. Quantity produced or imported, greater than 1 000 tonnes per year 1.13. Indicate if the substance has been produced during the last 12 months 1.14. Indicate if the substance has been imported during the last 12 months 1.15. Classification and labelling 1.16. Use pattern 1.17. Has the complete data set already been submitted by another manufacturer or importer? 1.18. Specify if you are acting on behalf of another concerned manufacturer or importer 1.19. Other remarks: (e. g. options for disposal) 2. Physical-chemical data 2.1. Melting point 2.2. Boiling point 2.3. Density 2.4. Vapour pressure 2.5. Partition coefficient (log10 POW) 2.6. Water solubility 2.7. Flash point 2.8. Auto flammability 2.9. Flammability 2.10. Explosive properties 2.11. Oxidizing properties 2.12. Other data and remarks 3. Environmental fate and pathways 3.1. Stability 3.1.1. Photodegradation 3.1.2. Stability in water 3.1.3. Stability in soil 3.2. Monitoring data (environment) 3.3. Transport and distribution between environmental compartments including estimated environmental concentrations and distribution pathways 3.3.1. Transport 3.3.2. Distribution among environmental compartments 3.4. Biodegradation 3.5. Bioaccumulation 3.6. Other remarks 4. Ecotoxicity 4.1. Toxicity to fish 4.2. Toxicity to daphnia and other aquatic invertebrates 4.3. Toxicity to algae 4.4. Toxicity to bacteria 4.5. Toxicity to terrestrial organisms 4.6. Toxicity to soil dwelling organisms 4.7. Other remarks 5. Toxicity 5.1. Acute toxicity 5.1.1. Acute oral toxicity 5.1.2. Acute inhalation toxicity 5.1.3. Acute dermal toxicity 5.1.4. Acute toxicity (other routes of administration) 5.2. Corrosiveness and irritation 5.2.1. Skin irritation 5.2.2. Eye irritation 5.3. Sensitization 5.4. Repeated dose toxicity 5.5. Genetic toxicity in vitro 5.6. Genetic toxicity in vivo 5.7. Carcinogenicity 5.8. Toxicity to reproduction 5.9. Other relevant information 5.10. Experience with human exposure 6. List of references

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Source: EUR-Lex (Cellar) · retrieved 2026-10-29 · Text as adopted (Official Journal); later amendments are not incorporated in this text.