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EC number: 264-727-7 | CAS number: 64194-22-5
- 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
Link to relevant study record(s)
Description of key information
No experimental toxicokinetic study is available on 3-methyl-1,5-pentanediyl diacrylate. However, as per REACH guidance document R7.C (May 2008), information on absorption, distribution, metabolism and excretion may be deduced from the physicochemical properties.
Based on the toxicological data and the physicochemical properties, the absorption of 3-methyl-1,5-pentanediyl diacrylate is expected to be low by oral route, dermal route and inhalation.
Key value for chemical safety assessment
- Bioaccumulation potential:
- no bioaccumulation potential
- Absorption rate - oral (%):
- 100
- Absorption rate - dermal (%):
- 10
- Absorption rate - inhalation (%):
- 100
Additional information
No experimental toxicokinetic study is available on 3-methyl-1,5-pentanediyl diacrylate. However, as per REACH guidance document R7.C (2012), information on absorption, distribution, metabolism and excretion may be deduced from the physical-chemical properties, including:
-Mean molecular weight: 226 g/mol
-Water solubility: 541 mg/L (20°C) (moderately soluble)
-Partition coefficient Log Kow: 2,76
-Vapour pressure: 0,105 Pa (20°C)
ABSORPTION
The moderate value of log Kow (between -1 and 4) and the moderate solubility of 3-methyl-1,5-pentanediyl diacrylate are favorable for an oral absorption. Indeed clinical effects as hunched posture were observed one or two days after one single (2000 mg/kg) of 3-methyl-1,5-pentanediyl diacrylate by gavage (oral route) in rats.
An oral absorption is expected for 3-methyl-1,5-pentanediyl diacrylate.
With a solubility of 541 mg/L, dermal absorption is anticipated to be moderate to high. A Log Kow of 2,76 and a molecular weight lower than 500 g/mol are optimal for a dermal absorption. Howerver, the acrylates are known to bind to skin components, and this binding decreases their dermal absorption. Indeed, the dermal absorption of 3-methyl-1,5-pentanediyl diacrylate is anticipated to be low.
According to the IH skin perm (QSAR), the dermal absorption of 3-methyl-1.5-pentanediyl diacrylate is 0.1%.
The low dermal absorption can be confirmed in the dermal acute toxicity study, where no systemic effect or mortality were observed in rats treated with 2000 mg/kg bw. However, 3-methyl-1,5-pentanediyl diacrylate showed allergic reaction in the LLNA: it is evidence that some uptake must have occurred although it may only have been a small fraction of the applied dose. For the risk assessment, 10% of dermal absorption is taken into account.
Based on the low value of the vapour pressure (<1 Pa), 3-methyl-1,5-pentanediyl diacrylate is not a volatile substance. Moreover, the absorption by inhalation can be expected for 3-methyl-1,5-pentanediyl diacrylate based on the moderate values of water solubility and log kow. The absorption is confirmed by the acute inhalation study in which mortalities were observed at the dose of 5.14 mg/L.
DISTRIBUTION and METABOLISM
No specific data is available on the distribution or metabolism of 3-methyl-1,5-pentanediyl diacrylate. No organ toxicity was showed in the repeated studies.
ELIMINATION
Due to the moderate water solubility and the low molecular mass (226 g/mol), the excretion of 3-methyl-1,5-pentanediyl diacrylate in the urines is expected. An excretion via bile and faeces is also possible.
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