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EC number: 216-823-5 | CAS number: 1675-54-3
- 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
Genetic toxicity: in vivo
Administrative data
- Endpoint:
- in vivo mammalian germ cell study: cytogenicity / chromosome aberration
- Remarks:
- Type of genotoxicity: chromosome aberration
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- not stated
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study was not conducted according to guideline/s and GLP but the report contains sufficient data for interpretation of study results
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- reference to same study
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 982
- Report date:
- 1982
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Dominant lethal study in which male mice were orally gavaged with test material and subsequently mated with untreated female mice over a period of six weeks. The number of females pregnant and number of offspring in each litter was determined.
- GLP compliance:
- no
- Type of assay:
- rodent dominant lethal assay
Test material
- Reference substance name:
- 4,4'-Isopropylidenediphenol, oligomeric reaction products with 1-chloro-2,3-epoxypropane
- EC Number:
- 500-033-5
- EC Name:
- 4,4'-Isopropylidenediphenol, oligomeric reaction products with 1-chloro-2,3-epoxypropane
- Cas Number:
- 25068-38-6
- Molecular formula:
- (C15 H16 O2 . C3 H5 Cl O)x
- IUPAC Name:
- 4,4'-Isopropylidenediphenol, oligomeric reaction products with 1-chloro-2,3-epoxypropane
- Reference substance name:
- 2,2'-[(1-methylethylidene)bis(4,1-phenyleneoxymethylene)]bisoxirane
- EC Number:
- 216-823-5
- EC Name:
- 2,2'-[(1-methylethylidene)bis(4,1-phenyleneoxymethylene)]bisoxirane
- Cas Number:
- 1675-54-3
- Molecular formula:
- C21H24O4
- IUPAC Name:
- 2,2'-[propane-2,2-diylbis(4,1-phenyleneoxymethylene)]dioxirane
- Details on test material:
- TK 12386 (25068-38-6)
Constituent 1
Constituent 2
Test animals
- Species:
- mouse
- Strain:
- other: Tif: MAG f (SPF)
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- Animals were 3-4 months of age at the time of test, were fed a standard rodent diet and water ad libitum, and were kept in environmentally-adequate housing facilities.
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- polyethylene glycol (PEG 400)
- Details on exposure:
- The test material was administered orally in single doses to 20 male albino mice per group, which were then mated to untreated females from the same strain over a period of 6 weeks. At the end of each week, the 2 females per male were replaced by new ones, repeated for 6 weeks to cover the stages of the maturation of the germ cell from the A-spermatogonia to the mature spermatozoon. Doses of 3333 mg/kg and 10,000 mg/kg were given in polyethylene glycol (PEG 400). A control group was given only the vehicle.
- Duration of treatment / exposure:
- One dose. Test material was dissolved in polyethylene glycol 400.
- Frequency of treatment:
- once
- Post exposure period:
- Each male mouse was allowed to mate with two untreated females beginning six hours after receiving a single oral dose of test material. Each group of two untreated females remained with the treated male mouse for a week. After one week the females were removed and replace by another group of two untreated females.
Doses / concentrations
- Remarks:
- Doses / Concentrations:
Doses of 3333 mg/kg and 10,000 mg/kg
Basis:
nominal conc.
- No. of animals per sex per dose:
- 20 male mice/group
- Control animals:
- yes, concurrent vehicle
Examinations
- Tissues and cell types examined:
- Females were necropsied on the 14 day of gestation. The number of live embryos and embryonic deaths were listed. In addition, the uteri were placed in a solution of ammonium sulphide in order to detect sites of early embryonic resorptions.
- Statistics:
- To compare the total number of implantations indicating pre-implantation loss, the t-test or Mann-Whitney's U-test was used. The total numbers of mated and pregnant dams or embryonic deaths were compared with the aid of the X2-test or Fisher's exact test.
Results and discussion
Test results
- Sex:
- male
- Genotoxicity:
- negative
- Toxicity:
- yes
- Remarks:
- In-life observations included diarrhea in males of the high dose group two days after treatment.
- Vehicle controls validity:
- valid
- Additional information on results:
- In-life observations included diarrhea in males of the high dose group two days after treatment. There were no adverse effects on females associated with any of the groups.
The data on mating ratio, numbers of implantations, and embryonic deaths are comparable for all groups.
Any other information on results incl. tables
The data on mating ratio, on the numbers of implantations and embryonic deaths were comparable for all groups.
The diarrhea observed two days after dosing male mice was most likely the result of the vehicle rather than the test material.
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information): negative
The test material was negative in the dominant lethal assay. - Executive summary:
A mouse dominant lethal study was conducted with DGEBPA. There was no evidence of an effect on male fertility or number of offspring/litter.
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