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EC number: 268-612-2 | CAS number: 68131-30-6 A solution obtained by dissolving the chemicals recovered in the alkaline pulping process in water.
- 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
Key value for chemical safety assessment
Skin sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
Migrated from Short description of key information:
Skin sensitisation studies are not available for green liquor. Therefore assessment of this endpoint shall comprise an assessment of the available other information, human, animal and alternative data of the known constituents of GL. All constituents of green liquor have been used extensively for many decades by the industry and by consumers. However, apart from skin irritation or burns skin sensitization has normally not been described as secondary effects. Most GL constituents are ions, which are naturally present in the body and for this reason it is unlikely that they were strong skin sensitizers. Some information exists that Na2S has skin sensitizing properties (Deralenko and Hollinger, 2002), even if it has a harmonized classification for corrosivity only. Based on the data available, it is concluded that GL is not currently classifiable as a skin sensitiser, but potential for skin sensitisation effect cannot be completely ruled out.
Respiratory sensitisation
Endpoint conclusion
- Additional information:
Migrated from Short description of key information:
All constituents of green liquor have been used extensively for many decades by the industry and by consumers. Long-lasting respiratory exposure for sulfides and sulfites may enhance symptoms of asthma in sensitive individuals. However, these human case reports are inplausible and NOAEL or LOAEL values cannot be evaluated. Based on the data available, it can be concluded that respiratory sensitisation of green liquor cannot be excluded.
Justification for classification or non-classification
According to CLP regulation, substances shall be classified as respiratory sensitisers (Category 1) in accordance with the following criteria: (a) if there is evidence in humans that the substance can lead to specific respiratory hypersensitivity and/or (b) if there are positive results from an appropriate animal test.
Test results from animal studies for green liquor are not available. Instead, data is available on the known inorganic constituents (hydroxides, sulfides, sulfites, sulfates, carbonates). Irritating and corrosive effects have been reported for skin and pulmonary track for these inorganic ions. However, no allergic response in skin or hypersensitivity of the airways has been reported in such extent that would lead to classification.
When considering the human evidence, the evidence could be referred to a chemical structure related to substances known to cause respiratory hypersensitivity. Mixtures should be classified as a respiratory or skin sensitiser when at least one ingredient has been classified as a respiratory or skin sensitiser and is present at or above the appropriate generic concentration limit (as shown in Table 3.4.3 of the CLP). Evidence from analogous substances, can contribute to the procedure for classification.
Regarding GL none of the known > 0.1% constituent is classified as respiratory sensitiser in the CLP List of harmonised classification and labelling of hazardous substances. Trace < 0.1% constituents Cr(VI) and Ni(SO4) are classified as sensitisers. The analysed concentrations of these metals in GL remain at 0.1 mg/l level (as Ni) which is 0,00001 %. Chromium was not detected in reference sample (see 1.2 Composition) (VTT 2010) and therefore highly sensitizing Cr(VI) is not an issue in GL. In addition if Cr were present in GL, the reducing conditions of GL would favor the Cr(III) oxidation state.
Based on information available, it can be concluded that GL cannot be classified as skin or respiratory sensitising substance.
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