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EC number: 212-133-3 | CAS number: 764-99-8
- 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
Link to relevant study record(s)
Description of key information
Absorption by the oral, dermal and inhalation routes is expected. Moreover, distribution through extracellular body fluids is likely. Excretion will most likely occur via the urine. No bioaccumulation is expected.
Key value for chemical safety assessment
- Bioaccumulation potential:
- no bioaccumulation potential
Additional information
Toxicokinetic analysis of 1,1'-[oxybis(ethyleneoxy)]diethylene (Diethyleneglycol divinyl ether)
Diethyleneglycol divinyl ether is liquid at room temperature with a molecular weight of 158.19 g/mol and an absolute density of 0.968 g/cm³ at 20 °C. The substance has a melting point of – 21 °C and a boiling point of 191 °C. A water solubility for Diethylene glycol divinylether of 16 g/L (20 °C) and a log Pow of 0.23 (25 °C) were determined.The vapour pressure was estimated to be 0.3 mbar (20 °C).
Absorption:
Based on the low molecular weight, the moderate log Pow and a high water solubility, Diethyleneglycol divinyl ether is likely to be absorbed in the GI tract. As it is a non-ionisable substance, absorption is independent of the pH value which is present in the different GI sections. The vast amount of Diethyleneglycol divinyl ether will be absorbed in the small intestine due to the much larger surface area when compared to stomach.The log Pow between -1 an 4 indicates that it will diffuse well across plasma membranes. In addition, gastro-intestinal absorption of Diethyleneglycol divinyl ether is triggered by passage via passive diffusion through aqueous pores or carriage with the bulk passage of water, which is favoured for small (molecular weight < 200 g/mol), water soluble substances. It is unclear whether an active transport for Diethyleneglycol divinyl ether exists. Overall, extensive gastrointestinal absorption is expected for Diethyleneglycol divinyl ether based on its physicochemical properties. Moreover, numerous systemic effects seen in acute and repeated dose toxicity studies after oral administration demonstrate and support that Diethyleneglycol divinyl ether is well absorbed in the gastrointestinal tract.
As Diethyleneglycol divinyl ether is a liquid with relative high water solubility (16 g/L), a molecular weight well below 500 and a log Pow of 0.23, dermal absorption is likely, but lower than oral absorption as Diethyleneglycol divinyl ether showed only mild effects when tested for acute dermal toxicity.
Diethyleneglycol divinyl ether exhibits a low volatility (vapour pressure of 0.3 hPa) and a high boiling point (> 190 °). Therefore, only a minimal amount of the substance is available for inhalation. However, when vapour or particles reach the alveolar region of the lung they are assumed to be absorbed directly across the respiratory tract epithelium of the alveolar and capillary membranes due to the log Pow > 0.
Distribution and metabolism:
Based on the physicochemical properties (molecular weight: 158.19 g/mol, log Pow: 0.23, water solubility: 16 g/L), Diethyleneglycol divinyl ether is likely to be widely distributed systemically throughout the extracellular compartments of the body after absorption.
Particularly due to the high water solubility and the moderate log Pow value below 3, a long biological half-life in tissues can not be expected. Thus, Diethyleneglycol divinyl ether has no bioaccumulation potential.
The metabolism is determined by physicochemical factors like electronic and steric effects within the molecule and/or by the presence of functional groups. Phase II conjugation reactions like glucuronidation or sulfatation might occur subsequent to Phase I reaction,e.g.after introduction of a OH-group via Cytochrome P450 mediated oxidation. Generally, metabolism will render the molecule more polar and harmless, leading to faster excretion. No conversion into a metabolite that is more toxic than the partent is expected as no increases in toxicity where noted in the presence of metabolic activation during the in vitro tests. Therefore, a clear indication is given that the formation of reactive metabolites is unlikely.
Excretion:
The relatively high water solubility and the low molecular weight (< 200) indicate that renal excretion is the most relevant route of systemically available Diethyleneglycol divinyl ether.
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