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Diss Factsheets
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EC number: 209-167-6 | CAS number: 557-28-8
- 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
No acute toxicity study with zinc dipropionate is available, thus the acute toxicity will be addressed with existing data on its two individual moieties zinc and propionate, respectively propionic acid.
Based on in vivo acute toxicity data on the moieties, it can safely be assumed, that zinc dipropionate has no pronounced acute toxicity.
Please refer to the section for the respective assessment entity for data on the moieties.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
Acute toxicity: via inhalation route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
Acute toxicity: via dermal route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
Additional information
An acute toxicity leading to clasification is not expected for zinc dipropionate, since the two moieties zinc and propionate, respectively propionic acid are not classified for acute toxicity. Under the assumption that the moieties of zinc dipropionate show their toxicological profile individually upon dissolution, acute toxicity estimates (ATE) for the acute oral and inhalative (systemic) toxicity of zinc dipropionate can be calculated using the equation given in regulation (EC) 1272/2008, Annex I, Section 3.1.3.6.1.
Because of lacking of a dose descriptor for the acute dermal toxicity of the zinc moiety, an acute toxicity estimates (ATE) for the acute dermal (systemic) toxicity of zinc dipropionate can not be calculated. However, the dose descriptors for the acute toxicity of the moieties via the oral route are very high (substantially > 2000 mg/kg bw). Thus, it can safely be assumed, that zinc dipropionate has no pronounced acute dermal toxicity.
There are no indications on narcotic effects.
For further information on the toxicity of the individual moieties, please refer to the relevant sections in the IUCLID and CSR.
Justification for classification or non-classification
Based on in vivo acute toxicity data on the moieties, it can safely be assumed, that zinc dipropionate has no pronounced acute toxicity. There are no indications on narcotic effects.
According to the criteria of REGULATION (EC) No 1272/2008 and its subsequent adaptions, Zinc dipropionate does neither have to be classified and has neither obligatory labelling requirement for acute oral, inhalative or dermal toxicity nor for specific target organ toxicity after single exposure (STOT SE narcotic effects).
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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