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EC number: 212-728-8 | CAS number: 860-22-0
- 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
Acute oral toxicity:
The acute oral LD50 value of substance Indigocarmine is considered to be >2000 mg/kg ddY mice.
Key value for chemical safety assessment
Acute toxicity: via oral route
Link to relevant study records
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Qualifier:
- according to guideline
- Guideline:
- other: as mentioned below
- Principles of method if other than guideline:
- Acute oral toxicity of substance Indigo carmine in ddY mice.
- GLP compliance:
- no
- Test type:
- other: No data available
- Species:
- mouse
- Strain:
- other: ddy
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS- Source: Tokyo Kasei Kogyo Industry Ltd- Age at study initiation: 7 weeks old- Weight at study initiation: No data available- Fasting period before study: No data available- Housing: No data available- Diet (e.g. ad libitum): commercial pellets MF (Oriental Yeast Industries Co., Tokyo, Japan)- Water (e.g. ad libitum): tap water ad libitum- Acclimation period: 1 weekENVIRONMENTAL CONDITIONS- Temperature (°C): 20–24 °C- Humidity (%):No data available- Air changes (per hr): No data available- Photoperiod (hrs dark / hrs light): 12 h light–dark cycle.IN-LIFE DATES: From: To: No data available
- Route of administration:
- oral: unspecified
- Vehicle:
- physiological saline
- Details on oral exposure:
- No data available
- Doses:
- 2000 mg/kg
- No. of animals per sex per dose:
- 4 male
- Control animals:
- not specified
- Details on study design:
- No data available
- Statistics:
- No data available
- Preliminary study:
- No data available
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- > 2 000 mg/kg bw
- Based on:
- test mat.
- Mortality:
- No data available
- Clinical signs:
- other: No data available
- Gross pathology:
- No data available
- Other findings:
- No data available
- Interpretation of results:
- practically nontoxic
- Remarks:
- Migrated informationCriteria used for interpretation of results: EU
- Conclusions:
- The acute oral LD50 value of substance Indigocarmine is considered to be >2000 mg/kg ddY mice.
- Executive summary:
Acute oral toxicity test of Indigocarmine was carried out with ddY mice. Test substance was administered orally to group of four male mice at 2000 mg/kg dose. The acute oral LD50 value of substanceIndigo carmineis considered to be >2000 mg/kgin ddY mice.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- LD50
- Value:
- 2 000 mg/kg bw
- Quality of whole database:
- Data is from peer reveiw journal.
Additional information
Acute Oral Toxicity:
Peer reviewed articles were viewed to determine the acute oral toxicity of the test compound C.I. Acid blue 74 (CAS no 860-22-0). The studies are summarized as below:
Acute oral toxicity testwas performed by Yu F. Sasaki et al, 2002 forIndigo carminewas carried out withddY mice. Test substance was administered orally to group of four male mice at 2000 mg/kg dose. The acute oral LD50 value of substanceIndigo carmineis considered to be>2000 mg/kg in ddY mice.
From review article (Richard J. Lewis, Sr., 2012) acute oral toxicity test was conducted on rat administered indigo carmine by oral route.LD50 value was found to be 2000 mg/kg. In acute oral toxicity test of chemical indigo carmine administered orally to rat.
From Danish (Q)SAR Database predicted data, The acute oral LD50 value of substance Indigo carmine is considered to be 3500 mg/kg in rat and 5200 mg/kg in mouse.
From review article of Acute oral toxicity of chemical Indigo carmine (Food additives handbook, 1989)test was conducted on rat administered indigo carmine by oral route.LD50 value was found to be >3000 mg/kg. In acute oral toxicity test of chemical indigo carmine administered orally to rat
From EFSA Journal (2014) Scientific Opinion on the re-evaluation of Indigo Carmine (E 132) as a food additive,The acute oral median lethal dose (LD50) of indigo carmine in rat was found to be 2000mg/kg and mice was found to be 2500mg/kg. Acute oral toxicity of indigo carmine to rat and mouse by oral route indicates that indigo carmine does not exhibits acute toxicity by the oral route.
From RTECS handbook (2015), theAcute oral toxicity test of(delta(sup 2,2')Biindoline) 5,5' disulfonic acid, 3,3'dioxo, disodium salt(Indigo Carmine) was conducted in rat. The acute oral LD50 value of substance(delta(sup 2,2')Biindoline) 5,5' disulfonic acid, 3,3'dioxo, disodium salt is considered to be 2000 mg/kg in rat and 2500 mg/kg in mouse..Acute oral toxicity of indigo carmine to rat and mouse by oral route indicates that indigo carmine does not exhibits acute toxicity by the oral route.
Based on the key study used, its relative supporting data and as per the CLP classification, the test material does not classify as an acute oral toxicant.
Justification for selection of acute toxicity – oral endpoint
The acute oral LD50 value of substance Indigocarmine is considered to be >2000 mg/kg ddY mice.
Justification for classification or non-classification
Acute oral toxicity:
Based on the key study used, its relative supporting data and as per the CLP classification, the test material does not classify as an acute oral toxicant.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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