Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 413-750-2 | CAS number: 171090-93-0 ANOX 1315; ANOX BF; DURAD AX 38
- 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
![](https://echa.europa.eu/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_toxicological-information.png)
Genetic toxicity: in vivo
Administrative data
- Endpoint:
- in vivo mammalian somatic cell study: cytogenicity / erythrocyte micronucleus
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- November 11, 1991 to December 18, 1991
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 991
- Report date:
- 1991
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 474 (Mammalian Erythrocyte Micronucleus Test)
- Version / remarks:
- Organization for Economic Cooperation and Development Guidelines, Section 4, Subpart 474, Paris 1981 and subsequent revisions.
- Deviations:
- not specified
- GLP compliance:
- yes
- Type of assay:
- mammalian erythrocyte micronucleus test
Test material
- Test material form:
- liquid
Constituent 1
- Specific details on test material used for the study:
- No further details specified to the study report.
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Details on species / strain selection:
- Sprague dawley rats used in accordance with the specified guidelines.
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- Test system: Sprague Dawley Charles River Crl:CD (SD) BR rat.
Number of animals: Seventy rates (35M + 35F) supplied by the Charkes River Company of Calco (Como), Italy, were used (shipping slip no. 08564, dated November 8, 1991). The animals, 5-weeks old, weighed from 113 to 150g at the time of use.
Accommodation: The rats were housed in a room having the following ambient conditions: temperature 22 °C ±2, relative humidity 55% ±10, about 20 air changes per hour filtered on HEPA 99.97%, artificial lighting with a circadian cycle of 12 hours of light (7 a.m. – 7 p.m.). An automatic standby power supply was brought into operation should the main supply fail.
The rats were kept for the entire duration of the study in wire cages (cm 40.5x38.5x18h) with a stainless steel feeder.
The waste that drops through the wire bottom on a removable paper was periodically disposed of.
Identification system for animals and groups: Five animals were allocated to each cage and were individually identified by colour mark. Each cage bore a tag with indelible identification of experiment number, dosage group, cage number and progressive number of the animals.
Diet and water supply: The animals were fed a diet coded 4RF21GLP, produced by Charles River Italia’s feed licensee Mucedole S.r.l., Settimo Milanese.
The declared contents, on the label, on dry matter basis (moisture 12%). Were
Crude protein 18.5%
Crude fat 3 %
Crude fiber 6%
Ash 7%
The diet was supplemented by the Producer with vitamins and trace elements. According to the analytical certificates provided by the Supplier, the contents of the batch of diet used in this study were within ± 5% of the declared values and contaminants were within the limits proposed by EPA-TSCA 44FR:44053-44093, July 26, 1979).
The animal feed, in compliance with RBM SOPs is analysed twice a year for bacterial contamination.
The diet was available to the animals “ad libitum”.
Filtered water was distributed by means of an automatic watering valve system. The drinking water offered to the animals came from the municipal water main.
The water is periodically analysed for microbiological count, heavy metals, other contaminants (e.g. solvents, pesticides) and chemical and physical characteristics.
The acceptance limits of quality of the drinking water are those defined in EEC Directive 80/778.
Contaminants that might interfere with the objectives of the study were not expected to be present either in the diet or the water.
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- methylcellulose
- Details on exposure:
- Of the test article [ANOX BF] about 21 grams (d=0.93) were suspended omogeneously in 0.5% methylcellulose in order to obtain a concentration of 250 mg/ml.
- Duration of treatment / exposure:
- Single exposure
- Frequency of treatment:
- Single dose
- Post exposure period:
- 66 hours
Doses / concentrations
- Dose / conc.:
- 5 000 mg/kg bw (total dose)
- Remarks:
- 20 ml/kg
- No. of animals per sex per dose:
- Test group: 30 animals (15M/15F)
Negative control: 30 animals (15M/15F)
Poitive control: 10 animals (5M/5F) - Control animals:
- yes, concurrent vehicle
- other: concurrent positive control (Mitomycin C)
- Positive control(s):
- Mitomycin C: 8 mg/kkg (10 ml/kg) administered by intraperitoneal route.
Examinations
- Tissues and cell types examined:
- Bone marrow from femurs taken from test animals.
- Details of tissue and slide preparation:
- Animals were sacrificed at three intervals after treatment: 18th, 42nd, 66th hours.
At each time, 10 animals (5M + 5F) treated with [ANOX BF] and 10 of the negative controls were sacrificed by cervical dislocation under i.p. anaesthesia with penobarbital.
The animals treated with Mitomycin C were sacrificed after about 42 hours.
The femurs were immediately removed and the bone marrow taken, suspended, and carefully washed in 3 ml of fetal bovine serum.
The suspension was centrifuged at 1,000xg for 10’. The supernatant was carefully taken off and the cell sediment smeared on microscope slides.
Two slides/animal were prepared.
At least 20 hours later, the smears were stained as follows:
1. immersion in May-Gruenwald (Merck, batch no. 08943240, expiry date April 30, 1992) solution for 3 min;
2. washing in 1.779 g/l NaNH4HPO4.4H2O (buffer) (Merck, batch no. 938A194382)
3. immersion in May Gruenwald solution diluted 1:1 with buffer for 2 min., then rinsed twice with buffer.
4. immersion in Giesma (Merck, batch no. 98498177, expiry date October 31, 1992) solution diluted 1:6 with buffer for 7.5 min;
5. rinsing with buffer and carefully dried with filter paper.
The stained slides were coded and read at the microscope (1250 X). For each animal, 2000 polychromatic erythrocytes were counted and scored for micronucleated cells.
Furthermore, the ratio of polychromatic to normochromatic erythrocytes (P/N) was calculated on one slide/animal by counting a total of 1000 polychromatic erythrocytes. - Evaluation criteria:
- Not detailed in the study report.
- Statistics:
- Comparison of the frequency among groups was perfomed with a non-parametric method (Mann Whitney).
Significances are expressed in the following manner:
* p < 0.05
** p < 0.01
*** p < 0.001
Results and discussion
Test results
- Key result
- Sex:
- male/female
- Genotoxicity:
- negative
- Toxicity:
- not specified
- Vehicle controls validity:
- valid
- Negative controls validity:
- not examined
- Positive controls validity:
- valid
- Additional information on results:
- No cytotoxic effects on bone marrow cells were evidenced.
On the basis of the results and the statistical analysis there is no significant difference between the micronucleus frequency in the treated group in comparison with the control group, at any sampling time.
The group of animals treated with Mitomycin C showed a statistically different frequency of micronucleated cells in comparison to the control group.
Applicant's summary and conclusion
- Conclusions:
- The results of the study indicate that the test article [ANOX BF] administered to Charles River rats by oral route at the dose of 5000 mg/kg, did not induce any statistically significant increase in the frequency of micronucleated cells in the bone marrow, 18, 42 and 66 hours from the administration.
On the basis of the results described, [ANOX BF] is not mutagenic in the micronucleus test. - Executive summary:
Appraisal of the possible genotoxic activity exercised by the test article [ANOX BF] by the micronucleus in the rat.
The animals were divided into the following experimental groups:
Negative control (vehicle treated animals): 30 (15M + 15F)
Treated with [ANOX BF]: 30 (15M + 15F)
Positive control (Mitomycin C): 10 (5M + 5F)
The negative control and the test article were administered by oral route (by gavage), while Mitomycin C was administered by intraperitoneal route.
Animals were sacrificed at three intervals after treatment: 18th, 42nd, 66th hours.
At each time, 10 animals (5M + 5F) treated with [ANOX BF] and 10 of the negative controls were sacrificed by cervical dislocation under i.p. anaesthesia with penobarbital.
The animals treated with Mitomycin C were sacrificed after about 42 hours.
The femurs were immediately removed and the bone marrow taken, suspended, and carefully washed in 3 ml of fetal bovine serum. Cell sediment was smeared on microscope slides.
Two slides/animal were prepared.
No cytotoxic effects on bone marrow cells were evidenced.
On the basis of the results and the statistical analysis there is no significant difference between the micronucleus frequency in the treated group in comparison with the control group, at any sampling time.
The group of animals treated with Mitomycin C showed a statistically different frequency of micronucleated cells in comparison to the control group.
The results of the study indicate that the test article [ANOX BF] administered to Charles River rats by oral route at the dose of 5000 mg/kg, did not induce any statistically significant increase in the frequency of micronucleated cells in the bone marrow, 18, 42 and 66 hours from the administration.
On the basis of the results described, [ANOX BF] is not mutagenic in the micronucleus test.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
![ECHA](/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/echa_logo.png)
ECHA har meget materiale online på dit sprog, men en del af det er kun på engelsk. Læs mere om ECHA’s flersprogspolitik.
Velkommen til ECHA's websted. Webstedet understøtter ikke fuldt ud Internet Explorer 7 (og tidligere udgaver). Du skal opgradere din Internet Explorer til en nyere udgave.
Dette websted anvender cookies for at sikre dig den bedste brugeroplevelse.
Få mere at vide om, hvordan vi anvender cookies.