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EC number: 276-481-8 | CAS number: 72214-18-7
- 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
Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: inherent biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1992
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 302 B (Inherent biodegradability: Zahn-Wellens/EMPA Test)
- Version / remarks:
- Method A-37
- Deviations:
- no
- GLP compliance:
- no
- Specific details on test material used for the study:
- Name: FAT 41001/F
Purity: >90 % - Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge (adaptation not specified)
- Duration of test (contact time):
- 28 d
- Initial conc.:
- 153 mg/L
- Based on:
- DOC
- Parameter followed for biodegradation estimation:
- DOC removal
- Reference substance:
- not specified
- Parameter:
- % degradation (DOC removal)
- Value:
- 19
- Sampling time:
- 28 d
- Results with reference substance:
- 100% degradation was observed in 14 days.
- Validity criteria fulfilled:
- no
- Interpretation of results:
- not inherently biodegradable
- Conclusions:
- The inherent biodegradation of FAT 41001/F was observed to be 19 % in 28 days.
- Executive summary:
Inherent biodegradablity of FAT 41001/F was determined according to OECD TG 302B (Zahn Wellens test) in DOC removal test. The test concentration was 153 mg/L DOC and test duration was 28 days. The bio-elimination of FAT 41001/F was determined to be 19 % after 28 days. Hence, FAT 41001/F is not inherently biodegradable under the conditions of this test.
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1992
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- other: Method A-22
- Version / remarks:
- Comparable to internationally accepted guidelines.
- Deviations:
- no
- GLP compliance:
- no
- Specific details on test material used for the study:
- Name: FAT 41001/F
Purity: >90 % - Oxygen conditions:
- not specified
- Inoculum or test system:
- not specified
- Remarks on result:
- not measured/tested
- Details on results:
- Not available
- Parameter:
- COD
- Value:
- 905 mg O2/g test mat.
- Validity criteria fulfilled:
- no
- Interpretation of results:
- not readily biodegradable
- Conclusions:
- COD of FAT 41001/F was found to be 905 mg O2/g test mat.
- Executive summary:
COD of FAT 41001/F was determined according to in house Ciba Geigy Method A22. Based on the findings of the study, the COD of test substance was found to be 905 mg O2/g. Considering the BOD5 value determined with the test substance 12 mg O2/g, the resulting BOD5/COD quotient is also 0.01, indicating that the test substance is unlikely to be biodegradable.
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1992
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- other: Method A-15
- Version / remarks:
- Comparable to international accepted guidelines.
- GLP compliance:
- no
- Specific details on test material used for the study:
- Name: FAT 41001/F
Purity: >90 % - Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge (adaptation not specified)
- Duration of test (contact time):
- 5 d
- Parameter followed for biodegradation estimation:
- O2 consumption
- Remarks on result:
- not measured/tested
- Parameter:
- BOD5
- Value:
- 12 mg O2/g test mat.
- Validity criteria fulfilled:
- no
- Interpretation of results:
- not readily biodegradable
- Conclusions:
- BOD5 of FAT 41001/F is 12 mg O2/g.
- Executive summary:
BOD5 of FAT 41001/F was determined according to in house Ciba Geigy Methode A.15, which is comparable to internationally accepted guidelines. Based on these investigations, the BOD5 of test substance was found to be 12 mg O2/g. Considering the COD value determined with the test substance which is 905 mg O2/g, the resulting BOD5/COD quotient is 0.01, indicating that the test substance is not biodegradable.
Referenceopen allclose all
Description of key information
The substance is a reactive dye and as such the substance should not be considered to be biodegradable. Key studies describe experimental techniques and results obtained in inherent biodegradation studies of FAT 41001/F. The most reliable study was performed according to OECD Guideline for testing chemicals No.302B, and biodegradation of FAT 41001/F after 28 d was 19 %, confirming that the substance should not be considered as readily biodegradable under the conditions of this test. In addition, determination of BOD and COD values and calculation of the BOD5/COD quotient resulted in a value close to zero. In additional supporting studies, the BOD/COD ratio was found to be value close to zero. Based on this estimation the substance is regarded to be not biodegradable.
Key value for chemical safety assessment
- Biodegradation in water:
- under test conditions no biodegradation observed
Additional information
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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