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EC number: 204-111-7 | CAS number: 115-84-4
- 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
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Endpoint summary
Administrative data
Key value for chemical safety assessment
Genetic toxicity in vivo
Description of key information
Link to relevant study records
- Endpoint:
- in vivo mammalian somatic cell study: cytogenicity / erythrocyte micronucleus
- Remarks:
- Type of genotoxicity: other:
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 10 September to 16 October 2003
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline and GLP-compliant study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 474 (Mammalian Erythrocyte Micronucleus Test)
- Deviations:
- yes
- Remarks:
- : Relative humidity ranged between 30 - 80% (and not between 30 - 70%). 5 animals per sex and group were used in the current study instead of 5 animals per group.
- GLP compliance:
- yes (incl. QA statement)
- Type of assay:
- micronucleus assay
- Species:
- mouse
- Strain:
- NMRI
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- Mice obtained from RCC Ltd., Biotechnology and Animal Breeding Division, CH-4414 Füllinsdorf. They were 8-10 weeks old with a mean bodyweight of 33.9 g (SD ±2.7 g) males and 27.3 g (SD ±2.3 g) females at the start of treatment. The animals were under quarantine for a minimum of five days after arrival. The animal room temperature was at 22 ± 3°C with a relative humidity of 30 - 80%. Artificial light was controlled to be switched on between 6:00 - 18:00.
- Route of administration:
- oral: gavage
- Vehicle:
- PEG 400
- Details on exposure:
- A preliminary study on acute toxicity was performed with two animals/sex under identical conditions as in the mutagenicity study. The animals were treated orally with the test material and examined for acute toxicity symptoms at intervals of 1, 2-4, 6, 24, 30 and 48 hours after administration.
Single dose at 312.5, 625 and 1250 mg BEPD/kg bw formulated in PEG 400. The volume administered was 10 mL/kg bw. - Duration of treatment / exposure:
- The mutagenicity study was conducted on six male and six female mice per dose group and sampling time, but only 5/group were evaluated.
- Frequency of treatment:
- Once
- Post exposure period:
- Toxicity symptoms were examined at 1, 2-4, 6 and 24 hours after administration of the test material.
Sampling of bone marrow was done 24 and 48 hours after treatment. - Remarks:
- Doses / Concentrations:
312.5, 625 and 1250 mg/kg
Basis:
other: achieved doses - No. of animals per sex per dose:
- 6 males and 6 females per dose. The high dose group was conducted twice, also with 6 males and 6 females.
- Control animals:
- yes, concurrent vehicle
- Positive control(s):
- CPA (cyclophosphamide)
- Tissues and cell types examined:
- Bone marrow smears were prepared from the shafts of both femurs. After staining, slides of 5 animals/sex/dose were scored (2000 polychromatic erythrocytes per animal).
- Details of tissue and slide preparation:
- Bone marrow smears were prepared from the shafts of both femurs. After staining, slides of 5 animals/sex/dose were scored (2000 polychromatic erythrocytes per animal).
- Evaluation criteria:
- Negative controls in the range of 0.01 - 0.15% (mean = 0.066 ± 0.32 PCEs with micronuclei).
Positive controls in the range of 0.91 - 2.975% (mean = 1.644 ± 0.446 PCEs with micronuclei).
At least 80% of animals are evaluable.
PCE to erythrocyte ratio should not be less than 20% of the negative control. - Statistics:
- Nonparametric Mann-Whitney test
- Sex:
- male/female
- Genotoxicity:
- negative
- Toxicity:
- yes
- Vehicle controls validity:
- valid
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Additional information on results:
- RESULTS OF RANGE-FINDING STUDY
- Dose range: 1000, 1250, 1500 and 2000 mg/kg bw
- Clinical signs of toxicity in test animals: 2 males and 2 females showed signs of reduced spontaneous activity, abdominal position and apathy for up to 6 hours when dosed at 1000 mg/kg bw.
All 4 animals (2 males, 2 females) dosed at 1250 mg/kg bw showed reduced spontaneous activity up to 6 hours after dosing. All male mice had ruffled fur during the 48-hour period of observation. Both female mice had ruffled fur up to 6 hours after dosing, but this was not observed at 24 hours. One male and one female had closed eyelids one hour after dosing but this was not observed at 2-4 hours. One male mouse showed apathy one hour after dosing.
Death of one male dosed at 1500 mg/kg bw after 4 hours and one female after 6 hours. Reduced spontaneous activity and ruffled fur were observed in all 4 mice up to 4 hours after dosing. This observation was reduced to one male and one female mouse between 6 and 30 hours after dosing. Abdominal position was observed in one male and one female mouse up to 4 hours after dosing. One male and one female mousee had their eyelids closed up to one hour after dosing. One male mouse showed apathy one hour after dosing and one female mouse up to 4 hours after dosing.
Death of two females dosed at 2000 mg/kg bw after 4 hours and one male after 6 hours. All four mice showed a reduction of spontaneous activity, ruffled fur and apathy one hour after dosing.
On the basis of these data, 1250 mg/mg bw was chosen to be the highest dose level.
RESULTS OF DEFINITIVE STUDY
- Dose range: 312.5, 625 and 1250 mg/kg bw
- Clinical signs of toxicity in test animals:
No deaths were observed at 312.5 mg/kg bw. All signs of reduced spontaneous activity, eyelid closure and ruffled fur had disappeared by 24 hours after dosing.
No deaths were observed at 625 mg/kg bw. 3 males and 3 females had ruffled fur one hour after dosing but this was not observed by the end of the experiment at 24 hours. Eyelid closure was observed in 4 females at 4 hours after dosing but it was gone by hour 6. Reduction of spontaneous activity was observed in 3 males and 2 females one hour after dosing, 2 males and 4 females 4 hours after dosing and 2 males and 3 females 6 hours after dosing. No reduction in spontaneous activity was observed at 24 hours after dosing.
2/12 males died 4 hours after being dosed at 1250 mg/kg bw. No deaths were observed in the females. All 24 animals (12 males, 12 females) had ruffled hair one hour after dosing and this dropped to being only observed in 2 female mice by 24 hours after dosing. 12 females and 11 males had reduced spontaneous activity one hour after dosing, which dropped to being only observed in 3 females 24 hours after dosing. - Conclusions:
- Interpretation of results (migrated information): negative
Preliminary tests showed 1250 mg BEPD /kg bw was suitable as the highest dose level. In the main study, 2 males died after treatment with 1250 mg/kg bw 4 hours after dosing. The mean number of polychromatic erythrocytes did not increase after treatment with the test material when compared to the mean number of PCEs of the vehicle control, indicating that BEPD had no cytotoxic properties in the bone marrow. There were no statistically significant or biologically relevent enhancement on the frequency of the detected micronuclei at any preparation intercal and dose level after administration of the test material when compared with the corresponding vehicle controls. The mean values of micronuclei observed after treatment with BEPD were below or near the value of the vehicle control group. 40 mg cyclophosphamide/kg bw (positive control) was administered orally and showed a statistically significant increase of induced micronucleus frequency. Under the experimental conditions of this test, BEPD did not induce micronuclei. - Executive summary:
In a standard mouse in vivo micronucleus test, dose levels of 312.5, 625 and 1250 mg/kg bw were orally administered to NMRI mice (5/sex/group). Bone marrow smears were prepared from each femur. After staining the smear slides from 5 mice/sex/dose were scored for 2000 polychromatic erythrocytes per animal. The number of micronuclei was assessed. Under the conditions of this test, there was no evidence of genotoxicity. Appropriate responses to the positive control substance (cyclophosphamide) confirmed the sensitivity of the assay.
Reference
To describe a cytotoxic effect due to the treatment with the test material, the ratio between polychromatic and total erythrocytes was determined in the same sample and reported as the number of PCEs per 2000 erythrocytes.
Test group |
Dose (mg/kg bw) |
Sampling time (h) |
PCEs with micronuclei (%) |
Range |
PCE per 2000 erythocytes |
Significance |
p |
Vehicle |
0 |
24 |
0.055 |
0-3 |
1125 |
|
|
Test item (BEPD) |
312.5 |
24 |
0.075 |
0-3 |
1046 |
- |
0.2610 |
Test item (BEPD) |
625 |
24 |
0.090 |
0-3 |
1051 |
- |
0.1224 |
Test item (BEPD) |
1250 |
24 |
0.100 |
0-4 |
1063 |
- |
0.0820 |
Positive control |
40 |
24 |
1.860 |
21-64 |
1052 |
+ |
< 0.0001 |
Test item (BEPD) |
1250 |
48 |
0.060 |
0-4 |
980 |
- |
0.5000 |
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Additional information
2-butyl-2-ethylpropanediol (BEPD) was found to be negative for mutagenicity in an Ames test and a mouse lymphoma assay. No study of clastogenicity in vitro has been performed; however a negative higher tier study (micronucleus assay) is available.
Ames test
The mutagenicity of BEPD was investigated in an Ames test (plate incorporated method) using Salmonella typhimurium strains TA 1535, TA 1537, TA 98 and TA 100. Triplicate plates were exposed to the test substance (dissolved in ethanol) at 0, 50, 150, 500, 1500 and 5000 µg/plate in the presence and absence of exogenous metabolic activation system (Aroclor 1254 -induced male Sprague-Dawley rat liver S9 fraction). The assay was repeated using the same concentrations of BEPD. No evidence for mutagenicity was seen in the absence or presence of a metabolic activation system. Results were confirmed in an independently repeated assay. Appropriate positive control compounds confirmed the sensitivity of the assay.
Mouse lymphoma assay
BEPD was examined for its potential to induce gene mutations at the TK-locus of cultured mouse lymphoma L5178Y cells, in both the absence and the presence of a metabolic activation system (S9-mix). Two assays were conducted; in the first assay 13 single cultures were treated for 24 hours and 4 hours in the absence and presence of S9-mix, respectively, and in the second assay cultures were treated for 4 hours in both the absence and presence of a different S9-mix. The test substance was dissolved in culture medium without serum prior to testing. In the first assay, the highest concentration BEPD evaluated for mutagenicity was 5.0 mmol/l and 10 mmol/l in the absence and presence of S9-mix, respectively. In the second assay the highest concentration evaluated for mutagenicity was 7.2 mmol/l in both the absence and presence of S9-mix. The maximum concentrations were limited by cytotoxicity. BEPD was cytotoxic in both the absence and presence of S9-mix. In the absence of S9-mix resulting in a reduction in initial cell yield and suspension growth at and above 2.6 mmol/l. The relative total growth (RTG) values at the highest concentrations evaluated for mutagenicity (7.2 and 5.0 mmol/l) were 1% and 20% after 4 and 24 hours treatment. In the presence of S9-mix the RTG at the highest concentration (10 mmol/l and 7.2 mmol/l) was 4% in the presence of S9-mix in both the first and second assay. In both the absence and presence of S9-mix no increase in mutant frequency was observed at any test substance concentration evaluated. All data were within the range of the negative control and the historical background. Methyl methanesulphonate (MMS) and 3-methylcholanthrene (MCA) were used as positive control substances in the absence and presence of the S9-mix, respectively; Culture medium without serum served as negative control. The negative controls were within historical background ranges and treatment with the positive control yielded the expected significant increase in mutant frequency compared to the negative controls. It is concluded that under the conditions used in this study, the test substance BEPD is not mutagenic at the TK-locus of mouse lymphoma L5178Y cells.
Mouse micronucleus assay
In a standard mouse in vivo micronucleus test, dose levels of 312.5, 625 and 1250 mg/kg bw were orally administered to NMRI mice (5/sex/group). Bone marrow smears were prepared from each femur. After staining the smear slides from 5 mice/sex/dose were scored for 2000 polychromatic erythrocytes per animal. The number of micronuclei was assessed. Under the conditions of this test, there was no evidence of genotoxicity. Appropriate responses to the positive control substance (cyclophosphamide) confirmed the sensitivity of the assay.
Justification for selection of genetic toxicity endpoint
Higher tier study, confirming negative results seen in vitro
Justification for classification or non-classification
There is no evidence from the available data that 2-butyl-2-ethylpropanediol is mutagenic or clastogenic. No classification is therefore proposed according to the CLP Regulation.
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