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EC number: 700-751-0 | CAS number: -
- 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 toxicity was tested according to OECD TG 423 and GLP. 2 x3 female Wistar rats were given 2000 mg/kg bw by gavage. No mortality occurred and no clinical signs or effects on weight gain were observed. Thus, the LD50 cut-off of Ca-/Mg-salt of fumarated tall oil rosin is > 5000 mg/kg bw.
Acute dermal toxicity was tested according to OECD TG 402 and GLP by applying 2000 mg/kg bw on the back of male and female rats for 24 hours and a 14 day post exposure observation period. The resulding LD50 is >2000 mg/kg bw.
Key value for chemical safety assessment
Additional information
ORAL APPLICATION
According to OECD TG 423 3 female Wistar rats were given 2000 mg/kg bw by gavage. No mortality occurred and no clinical signs or effects on weight gain were observed . Therefore the test was repeated with further 3 female Wistar rats. Again, the dose of 2000 mg/kg bw was tolerated by female rats without mortalities, or effects on weight gain. No gross pathological findings were noted from both groups of female Wistar rats.. Thus, the LD50 cut-off of Ca-/Mg-salt of fumarated tall oil rosin is > 5000 mg/kg bw (Bayer Pharma AG 2011).
DERMAL APPLICATION
Acute dermal toxicity was tested according to OECD TG 402 and GLP. 2000 mg/ kg bw test substance was applied to the back of male and female Wistar rats for 24 hours covered by a semi occlusive dressing. After removal of the dressing and the test substance the animals were observed for further 14 days. No mortality occurred and no clinical signs or effects on body weight development were observed. Gross pathological examination revealed no findings. Thus, the LD50 (dermal, rat) is > 2000 mg/kg bw under the condition of this test (Bayer Pharma AG 2011).
Justification for classification or non-classification
Based on the available data no classlification or labelling is required.
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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