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EC number: 255-288-2 | CAS number: 41272-40-6
- 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
Key value for chemical safety assessment
Additional information
Ames tests are negative for Malachite Green (MG). In Fessard et al. (1999) study results show an higher cytotoxicity of MG: it had no mutagenic activity in any bacterial strains, with and without metabolic activation, for doses at or lower than 10 µg per plate. In Clemmensen at al (1984) cell toxicity was usually encountered at 1.28 µg/plate unless S-9 was added. In TA 98 there was no increase without metabolic activation, but a significant increase was seen in the three highest doses after addition of S-9, nevertheless these doses are well above the citotoxicity level and the consideration is of doubtful relevance.
In the study of Fessard et al. (1999) MG was found to be extremely cytotoxic to mammalian cells (CHO) in culture and study confirmed also that MG induced DNA alterations only at cytotoxic doses.
In another study on chromosomal aberration (Au et al., 1979) MG did not show a relevant number of brakes for metaphase.
In the in vivo study of Clemmensen (1984) no significant increase in the number of micronuclei in bone marrow smears of mice treated by gavage with a single dose of 37.5 mg/kg bw was observed.
In the study of Mittelstaedt (2004), gene mutations in transgenic Big Blue B6C3F1 mice was investigated. In female Big Blue mice fed up to 408 ppm Leucomalachite Green (LG) or 450 ppm MG chloride for 16 weeks, the ceII mutant frequency was significantly increased in the liver of mice exposed to LG, but not MG chloride. In the same study, neither MG nor LG increased the peripheral blood micronucleus frequency or Hprt lymphocyte mutant frequency in female mice. The results of this study suggest a correlation between the mutagenicity of LG and its tumorigenicy in mice and rats.
In conclusion MG was found to be cytotoxic. Tests in vitro and in vivo on genetic toxicity of MG are in general negative up to the cytotoxicity level.
Despite some results are not conclusive, there is not enough evidence to consider MG genetoxic according to CLP classification.
Short description of key information:
Not mutagen
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
According to CLP regulation (EC1272/2008) Malachite Green Acetate is not classified as mutagen
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