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EC number: 271-264-4 | CAS number: 68527-23-1 A complex combination of hydrocarbons produced by distillation of products from a steam-cracking process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C9 and boiling in the range of approximately 110°C to 165°C (230°F to 329°F).
- 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
Developmental toxicity / teratogenicity
Administrative data
- Endpoint:
- developmental toxicity
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: GLP status unknown, non-guideline study, published in peer reviewed literature, no restrictions, fully adequate for assessment
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- publication
- Title:
- Inhalation developmental neurotoxicity study of ethylbenzene in Crl-CD rats
- Author:
- Faber WD, Roberts LSG, Stump DG, Beck M, Kirkpatrick D, Regan KS, Tort M, Moran E and Banton M
- Year:
- 2 007
- Bibliographic source:
- Birth Defects Res (Part B) 80:34-48
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- other: EPA OPPTS 870.3800 (Reproduction and Fertility Effects)
- Deviations:
- yes
- Remarks:
- inclusion of developmental neurotoxicity assessment
- Principles of method if other than guideline:
- 2-generation reproduction study with evaluation of F2 offspring for nervous system functional and morphological end points
- GLP compliance:
- not specified
- Limit test:
- no
Test material
- Reference substance name:
- Ethylbenzene
- EC Number:
- 202-849-4
- EC Name:
- Ethylbenzene
- Cas Number:
- 100-41-4
- Molecular formula:
- C8H10
- IUPAC Name:
- ethylbenzene
- Details on test material:
- - CAS number: 100-41-4
- Source: The Dow Chemical (Midland, MI) via Ashland Chemical (Morrisville, PA, USA)
- Storage: under refrigeration
- Analytical purity: at least 99.9%
Constituent 1
Test animals
- Species:
- rat
- Strain:
- other: Crl:CD(SD)IGS BR
- Details on test animals or test system and environmental conditions:
- - Source: Charles River Laboratories (Raleigh, NC, USA) on 8 April 2003
Details on acclimation, husbandry and welfare published in Faber et al., 2006
Administration / exposure
- Route of administration:
- inhalation: vapour
- Vehicle:
- other: air
- Details on exposure:
- Not described in this publication but in earlier publication by Faber, 2006.
- Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- Exposure chambers, gas chromatography with flame ionization detection. Analysed concentrations were very close to nominal.
Dosing solutions, gas chromatography with mass spectroscopy. - Details on mating procedure:
- 1 male:1 female for 14 days or until confirmation of mating observed
- Duration of treatment / exposure:
- Inhalation: 6 hours daily, 7 days per week. F0 and F1 animals exposed for at least 70 consecutive days prior to mating. Males continued on the same regime whilst on study. The females were similarly exposed throughout mating and gestation, through to day GD 20; exposure recommenced on day 5 of lactation (LD5) and continued through to weaning (LD21).
Oral gavage: females only days 1-4 of lactation. Ethylbenzene administered in corn oil at dose levels of 0, 26, 90, and 342 mg/kg/day (dose levels selected to result in similar internal maternal exposure based on PBPK modelling). Each dose was divided into 3 equal amounts and administered approximately two hours apart. - Frequency of treatment:
- Daily
- Duration of test:
- Approximately 42 weeks
- No. of animals per sex per dose:
- 30 F0, 25 F1
- Control animals:
- yes, concurrent vehicle
Examinations
- Maternal examinations:
- Parental animals observed twice daily for mortality and clinical signs.
FOB: F1 dams GD6 and 12 and on LD 10 and 21 - Statistics:
- Analyses were conducted using two-tailed tests for a minimum significance level of 5%, comparing each test group to the control group. The litter was used as the unit of analysis where appropriate as was analysis by gender.
Results and discussion
Results: maternal animals
Effect levels (maternal animals)
- Dose descriptor:
- NOAEC
- Remarks:
- ethyl benzene
- Effect level:
- >= 500 ppm
- Basis for effect level:
- other: other:
Results (fetuses)
Effect levels (fetuses)
- Dose descriptor:
- NOAEC
- Remarks:
- Ethylbenzene
- Effect level:
- >= 500 ppm
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: Developmental toxicity
Fetal abnormalities
- Abnormalities:
- not specified
Overall developmental toxicity
- Developmental effects observed:
- not specified
Applicant's summary and conclusion
- Conclusions:
- The NOAEC for physical and neurobehavioural development of the F2 offspring from a 2-generation study was 500 ppm ethylbenzene (equivalent to 2171 mg/m3).
- Executive summary:
Male and female Crl:CD(SD)IGS BR rats were exposed by inhalation to 0, 25, 100 or 500 ppm ethylbenzene for 6 hr/day throughout a 2-generation study except for females between lactation days 1 and 4 when the dose was administered in corn oil by oral gavage at dose levels of 26, 90 or 342 mg/kg/day (to provide similar maternal blood (AUC) as provided by inhalation). The physical and neurobehavioural development of the F2-generation was evaluated using a number of developmental landmarks, a functional observational battery, a motor activity assessment, an acoustic startle response and a learning and memory task. Evaluations of whole-brain measurements and brain morphometric and histological assessments were also included.
Parental exposure to ethylbenzene at concentrations up to and including 500 ppm did not adversely affect the survival of the F2 offspring, their clinical condition or body weight or their acquisition of several developmental landmarks. No treatment-related alterations were detected in the FOB tests, the motor activity counts, acoustic startle endpoints or the performance in the Biel water maze. Furthermore, no exposure-related differences were evident from the neuropathology assessments. The NOAEC for physical and neurobehavioural development was 500 ppm ethylbenzene.
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