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Diss Factsheets
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EC number: 203-961-6 | CAS number: 112-34-5
- 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
Description of key information
ORAL:
Mouse, male: LD50=2410mg/kg (fasted animals), 5530mg/kg (fed animals)
Rat, male: LD50=7291mg/kg (fasted animals), 9633mg/kg (fed animals)
Rat, male: LD50=6560mg/kg
Guinea pig, male/female: LD50=2000mg/kg
Rat: LD50=3305, 5560mg/kg
Rat: LD50>5080mg/kg
Rabbit: LD50=2200mg/kg
INHALATION:
LD50 greater than saturated vapour pressure
DERMAL
Rabbit, male: LD50=2764mg/kg
Rat: LD50>2000ml/kg (4 hour exposure only)
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- LD50
- Value:
- 2 410 mg/kg bw
Acute toxicity: via inhalation route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
Acute toxicity: via dermal route
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- LD50
- Value:
- 2 764 mg/kg bw
Additional information
A number of reliable key studies plus supporting information are available in multiple species for the acute oral toxicity of 2 -(2 -butoxyethoxy)ethanol. A well documented study which looked at both fasted and unfasted animals showed that mice were more sensitive than rats with fasted animals (not surprisingly) more sensitive than fed animals. The lowest value seen was 2410mg/kg as the LD50 for fasted mice. The full results are shown in the key information field. Four studies showed the rat LD50 to be in the range 3305 to 9623mg/kg. Single values for the guinea pig and rabbit were in the range 2000 -2200mg/kg.
There are two reliable studies plus supporting information which shows that acute toxicity by the dermal route is low. The available information covers toxicity in rabbits and rats. The key study showed a dermal LD50 of 2764mg/kg in the rabbit. The supporting studies showed dermal LD50's of 4000 -4120mg/kg and a limit study in the rat which shows an LD0>2000mg/kg .
In an acute inhalation risk assessment assay that followed the basic principles as described in OECD test guideline 403, both rats and mice were exposed to an atmosphere saturated with vapors of the substance 2 -(2 -butoxyethoxy)ethanol for a period of 2 hours. Documentation of clinical signs was performed over the 8-day study period. No mortality was seen with the rats but 3 out of 20 mice died within the observation period. There were no other adverse clinical signs in either species apart from evidence for some eye irritation were observed. This could have been due to aerosol exposure as the vapour generation method did not exclude this possibility. On the basis of this result, the substance does not warrant classification for an acute inhalation hazard.
Justification for classification or non-classification
The rat and mouse are the two species normally used for acute oral toxicity classification. The values obtained for these species are greater than the threshold for classification. Values for other species also fall outside the range for classification under either directive 67/548 or regulation 1272/2008
Acute toxicity data by the dermal route clearly shows that the LD50 is greater than the threshold for classification under either directive 67/548 or regulation 1272/2008.
The LC50 cannot be reached by inhalation exposure up to the saturated vapour concentration and therefore classification for this route is not warranted.
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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