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Diss Factsheets
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EC number: 219-909-0 | CAS number: 2568-90-3
- 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
Low potential of bioaccumulation as log Kow <3.
Data related to metabolism of methylal (Dahl & Hadley, 1983; Tomilina et al., 1984; Poon et al., 2000; Virtue, 1951; Heilman J. & Duggan A., 2014), general metabolism of acetals (EFSA, 2011) and metabolism of degradation products (Ecetoc Publications, 2004) are provided in this section. Aim is to support the similarity of toxicokinetic behaviour between source and target of the read-across approach (Redebel, 2016).
Key value for chemical safety assessment
- Bioaccumulation potential:
- low bioaccumulation potential
- Absorption rate - oral (%):
- 100
- Absorption rate - dermal (%):
- 100
- Absorption rate - inhalation (%):
- 100
Additional information
ABSORPTION
Oral / gastrointestinal absorption
With a low molecular weight (160.26 g/mol), moderate water solubility (222.5 mg/L) and log Kow of 2.75, oral/gastrointestinal absorption of butylal is favoured subsequent to oral ingestion. Log Kow values between -1 and 4 are favourable for absorption by passive diffusion.
Oral absorption of butylal is set to 100% for risk assessment.
Inhalation absorption
Butylal low vapour pressure (0.079 kPa) indicates that the substance will unlikely be available for inhalation as a vapour. However, it will depend on the use. Its moderate log Kow value is favourable for absorption directly across the respiratory tract epithelium by passive diffusion. Solubility level of butylal in water indicates that it may be retained within the mucus.
Inhalation absorption of butylal is set to 100% for risk assessment.
Dermal absorption
As a liquid with a molecular weight close to 100 g/mol, butylal dermal uptake is favoured.
Based on molecular weight < 500 and log Kow in the (-1, 4) range, default dermal absorption of butylal is set to 100% for risk assessment.
Dermal absorption of butylal is set to 100% for risk assessment.
DISTRIBUTION
A wide distribution is expected due to the low molecular weight. As a small water-soluble molecule, butylal is going to diffuse through aqueous channels and pores.
METABOLISM and EXCRETION
Butylalis not considered as substance with a potential to accumulate within the body. The read across report for the toxicity super endpoint showed a NOAEC > 2000 which indicates a very low risk of chronic toxicity.
The following values for absorption assessment were taken into account according to butylal behaviour (absorption, metabolism, distribution and elimination):
oral absorption of butylal is set to 100% for risk assessment;
inhalation absorption of butylal is set to 100% for risk assessment;
dermal absorption of butylal is set to 100% for risk assessment.
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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