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EC number: 201-245-8 | CAS number: 80-05-7
- 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

Endocrine disrupter testing in aquatic vertebrates – in vivo
Administrative data
- Endpoint:
- fish adult: (sub)lethal effects
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study
- Remarks:
- OECD 234 with minimal modifications
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 2 019
- Report date:
- 2019
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD TG 234 (Fish Sexual Development Test)
- GLP compliance:
- no
Test material
- Reference substance name:
- 4,4'-isopropylidenediphenol
- EC Number:
- 201-245-8
- EC Name:
- 4,4'-isopropylidenediphenol
- Cas Number:
- 80-05-7
- Molecular formula:
- C15H16O2
- IUPAC Name:
- 4-[2-(4-hydroxyphenyl)propan-2-yl]phenol
Constituent 1
- Specific details on test material used for the study:
- BPA obtained from Tokyo Chemical Industry Co., Ltd, Tokyo, Japan,
purity >99.0%
Sampling and analysis
- Analytical monitoring:
- yes
Test solutions
- Vehicle:
- no
- Details on test solutions:
- PREPARATION OF STOCK SOLUTIONS
14.4, 45, 144, 450 and 1440 mg of BPA were placed separately, each into 5-L glass media bottles (body diameter, 182 mm) and dissolved in 4.5 L of Milli-Q water with sonication for 120-180 minutes in an ultrasonic bath.
PREPARATION OF TEST SOLUTIONS
The stock solutions were diluted with dechlorinated tap water to the nominal concentrations for each group at a dilution ratio of 1 (aqueous stock solution) to 100 (dechlorinated tap water) by using a flow-through exposure system (SIS-1F; Shibata Scientific Technology (Tokyo, Japan). The water exchange rate was 5 volumes/day, and the stock solution was renewed every 3-4 days.
Test organisms
- Aquatic vertebrate type:
- fish
- Test organisms (species):
- Oryzias latipes
Study design
- Test type:
- flow-through
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 60 d
Test conditions
- Test temperature:
- 25 +/- 2 °C
- pH:
- 7.5 +/- 1
- Nominal and measured concentrations:
- nominal concentrations: control, 32, 100, 320, 1000 and 3200 μg/L
measured concentrations: 45, 92, 326, 1030 and 3406 μg/L - Details on test conditions:
- FERTILIZATION AND HATCHING
Eggs were checked under a stereomicroscope, and the unfertilized, damaged or developmentally abnormal eggs were removed. After this selection process, fertilized eggs were exposed to BPA within 2 hours postfertilization (2hpf).
20 fertilized eggs from each concentration were distributed into 100-mL glass vessels. Observations were performed every 24 hours vira microscopic examination. Test solutions were exchanged once every 24 hours. Eight replicate 100-mL glass vessels were used for each concentration, for a total of 48 vessels.
0 - 30 DAYS POST HATCHING
After hatching, four replicate 5-L glass tanks were used for each concentration, for a total of 24 tanks. Thirty larvae were moved to each 5-L cubic glass tank (in total, 120 larvae per concentration) and cultured until 30 days posthatching (dph) using a flow-through system (water exchange rate, 5 volumes/day).
30 - 60 DAYS POST HATCHING
At 30 dph, 15 fish per tank (in total, 60 fish per treatment) were dissected. Thereafter, each 5-L cubic glass tank contained 15 fish (in total, 60 fish per treatment),which were cultured until 60 dph using the same flow-through system (water exchange rate, 5 volumes/day). A separate set of BPA exposure and control groups for the expression analysis of gonadal sex differentiation-related genes at stage 38 (n = 4) and 30 dph (n = 4) was set up additionally.
Dead individuals were removed as soon as they were observed. - Reference substance (positive control):
- no
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 60 d
- Dose descriptor:
- LOEC
- Effect conc.:
- 1.03 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- genetic/phenotypic sex ratio
- Remarks:
- sex reversal
- Duration:
- 60 d
- Dose descriptor:
- NOEC
- Effect conc.:
- 326 µg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- secondary sexual characteristics
- Remarks:
- or gonadal sex differentiation
- Reported statistics and error estimates:
- Test on homogeneity of variance of the data was performed with Bartlett's test (significance level, 5%) by using the open source statistical software R (http://www.R-project.org/) and the package Rcmdr (Fox & Bouchet-Valat, 2018). If homogeneity of variance was not rejected, differences in test results among treatments were performed using Dunnett's test. Otherwise Steel's test was performed.
Any other information on results incl. tables
Effect of BPA on gonadal sex differentiation
|
Measured concentration |
Genetic sex |
|
Gonadal sex |
|
|
Ratio of sex |
Genetic sex |
Gonadal sex |
Ratio of sex |
|||||||||
Age (dph) |
μg/L |
|
n |
|
XX |
|
Ovary |
Testis-ova |
Testis |
reversal (%) |
XY |
Ovary |
Testis-ova |
Testis |
reversal (%) |
||||
30 |
Control |
|
40 |
|
21 |
|
21 |
|
0 |
|
|
0 |
|
0 |
19 |
0 |
0 |
19 |
0 |
|
45 |
|
40 |
|
21 |
|
21 |
|
0 |
|
|
0 |
|
0 |
19 |
0 |
0 |
19 |
0 |
|
92 |
|
40 |
|
22 |
|
22 |
|
0 |
|
|
0 |
|
0 |
18 |
0 |
0 |
18 |
0 |
|
326 |
|
40 |
|
20 |
|
20 |
|
0 |
|
|
0 |
|
0 |
20 |
0 |
0 |
20 |
0 |
|
1030 |
|
40 |
|
19 |
|
19 |
|
0 |
|
|
0 |
|
0 |
21 |
1 |
0 |
20 |
4.7 |
|
3406 |
|
40 |
|
17 |
|
17 |
|
0 |
|
|
0 |
|
0 |
23 |
22 |
1 |
0 |
95.6 |
60 |
Control |
|
60 |
|
32 |
|
32 |
|
0 |
|
|
0 |
|
0 |
28 |
0 |
0 |
28 |
0 |
|
45 |
|
60 |
|
29 |
|
29 |
|
0 |
|
|
0 |
|
0 |
31 |
0 |
0 |
31 |
0 |
|
92 |
|
60 |
|
22 |
|
22 |
|
0 |
|
|
0 |
|
0 |
38 |
0 |
0 |
38 |
0 |
|
326 |
|
58 |
|
29 |
|
29 |
|
0 |
|
|
0 |
|
0 |
29 |
0 |
0 |
29 |
0 |
|
1030 |
|
59 |
|
28 |
|
28 |
|
0 |
|
|
0 |
|
0 |
31 |
4 |
23 |
4 |
12.9 |
|
3406 |
|
60 |
|
33 |
|
33 |
|
0 |
|
|
0 |
|
0 |
27 |
27 |
0 |
0 |
100 |
dph = days post hatching
Applicant's summary and conclusion
- Validity criteria fulfilled:
- not specified
- Conclusions:
- The effect of BPA on Japanese medaka using OECD TG234 with minor modifications, including analysis of the expression of gonadal sex differentiation and sex-determining genes at early developmental stages was studied by Horie et al. Testis-ova and sex reversal in XY males were observed in response to 1030 and 3406 μg/L BPA exposure at 30 and 60 dph from 2 hours postfertilization. Longer and higher concentrations of BPA exposure induced a greater rate of testis-ova and sex reversal.
- Executive summary:
The effect of BPA on Japanese medaka using OECD TG234 with minor modifications, including analysis of the expression of gonadal sex differentiation and sex-determining genes at early developmental stages was studied by Horie et al. Testis-ova and sex reversal in XY males were observed in response to 1030 and 3406 μg/L BPA exposure at 30 and 60 dph from 2 hours postfertilization. Longer and higher concentrations of BPA exposure induced a greater rate of testis-ova and sex reversal.
The lowest observed effect concentration of BPA in the present study is LOEC < 3406 μg/L for mortality, embryo hatching and growth in O. latipes. In addition the no observed effect concentration of BPA on secondary sex characteristics or gonadal sex differentiation is NOEC = 326 μg/L
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