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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 279-505-5 | CAS number: 80584-91-4
- 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
Endpoint summary
Administrative data
Key value for chemical safety assessment
Genetic toxicity in vitro
Link to relevant study records
- Endpoint:
- in vitro cytogenicity / micronucleus study
- Remarks:
- Type of genotoxicity: genome mutation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2012-06-01 to 2012-12-06
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study, detailed documentation
- Qualifier:
- according to guideline
- Guideline:
- other: OECD 487
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of assay:
- in vitro mammalian cell micronucleus test
- Target gene:
- Formation of micronuclei in human peripheral blood lymphocytes
- Species / strain / cell type:
- lymphocytes:
- Metabolic activation:
- with and without
- Metabolic activation system:
- Mammalian liver post-mitochondrial fraction (S9), prepared from Sprague Dawley male rats
- Test concentrations with justification for top dose:
- Range-finding: 0, 9.375, 18.75, 37.5, 75, 150, 300 µg/mL (final concentrations)
Definitive test. experiment 1, -S9: 75, 150, 300 µg/mL + vehicle (1% DMSO v/v ) + Cytosine arabinoside (pos. control)
Definitive test. experiment 1, +S9: 75, 150, 300 µg/mL + vehicle (1% DMSO v/v ) + Cytosine arabinoside (pos. control)
Definitive test. experiment 2, -S9: 7.5, 15, 30, 60, 120, 240, 480 µg/mL + vehicle (1% DMSO v/v ) + DMBA (pos. control)
Definitive test. experiment 2, +S9: 7.5, 15, 30, 60, 120, 240, 480 µg/mL + vehicle (1% DMSO v/v ) + DMBA (pos. control)
Appropriate amount of test item was weighted and diluted in DMSO not earlier than 30 min prior to test start. For dilution of final doses, sterile DMSO was used. - Vehicle / solvent:
- - Vehicle/solvent used: DMSO+ culture medium
- Untreated negative controls:
- yes
- Remarks:
- culture medium
- Negative solvent / vehicle controls:
- yes
- Remarks:
- DMSO
- Positive controls:
- yes
- Positive control substance:
- cyclophosphamide
- Remarks:
- Cytosine arabinoside was used as positive control without S9mix, Cyclophosphamide monohydrate was used as positive control with S9mix.
- Details on test system and experimental conditions:
- METHOD OF APPLICATION:
10exp5 cells in 75 µl
DURATION
- Exposure duration: 20 hr
METHOD OF APPLICATION: in medium;
DURATION
- Preincubation period: 24 hours
- Exposure duration: 20 hours
- Time with Cytochalasin B: 28 hours:
- Fixation time (start of exposure up to fixation or harvest of cells): 72 hours
SPINDLE INHIBITOR (cytogenetic assays): Cytochalasin B
STAIN (for cytogenetic assays): 2% Giemsa-Romanowski for 10 minutes
NUMBER OF CELLS EVALUATED: 10exp5 cells
DETERMINATION OF CYTOTOXICITY
- Method: other: replication index (Number of binucleated cells, mulinucleated cells and toatal number) - Evaluation criteria:
- For the untreated controls and solvent controls, the measured average number of micronuclei is related to the spontanous occurence of micronuclei. A two tailed Student's t-test revealed if the test substance can be considered as positive, negative or equivocal.
- Statistics:
- Student's t-test
- Species / strain:
- lymphocytes: human
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Conclusions:
- Interpretation of results (migrated information):
negative
TC, dried did not induce micronuclei neither with nor without metabolic activation by S-9 mix in human lymphocytes. TC, dried was considered to be non-mutagenic. - Executive summary:
TC, dried was dissolved in DMSO in concentrations of 9.375 to 300 µg/ml in an in vitro micronucleus test with human lymphocytes according to OECD 487.
Up to and including the highest possible concentrations TC, dried, did not induce micronuclei neither with nor without metabolic activation by S-9 mix.
Therefore TC, dried was considered to be non-mutagenic.
- Endpoint:
- in vitro gene mutation study in bacteria
- Remarks:
- Type of genotoxicity: gene mutation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2012
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study, detailed documentation
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 471 (Bacterial Reverse Mutation Assay)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of assay:
- bacterial reverse mutation assay
- Target gene:
- TA100: his G46
TA98: his D3052
TA97: his D6610
TA102: his G428 (pAQ1)
TA1535: his G46 - Species / strain / cell type:
- S. typhimurium TA 100
- Additional strain / cell type characteristics:
- other: Strain is histidine-dependent
- Species / strain / cell type:
- S. typhimurium TA 98
- Additional strain / cell type characteristics:
- other: Strain is histidine-dependent
- Species / strain / cell type:
- S. typhimurium TA 97
- Additional strain / cell type characteristics:
- other: Strain is histidine-dependent
- Species / strain / cell type:
- S. typhimurium TA 102
- Additional strain / cell type characteristics:
- other: Strain is histidine-dependent
- Species / strain / cell type:
- S. typhimurium TA 1535
- Additional strain / cell type characteristics:
- other: Strain is histidine-dependent
- Metabolic activation:
- with and without
- Metabolic activation system:
- Mammalian liver post-mitochondrial fraction (S9), prepared from Sprague Dawley male rats.
- Test concentrations with justification for top dose:
- Range-Finding: 7 concentrations in the range of 0.0001-5.0 mg/plate
Confirmatory assay with preincubation: 0.00001-0.5 mg/plate
Appropriate amount of test item was weighted and diluted in DMSO not earlier than 30 min prior to test start. For dilution of final doses, sterile DMSO was used. - Vehicle / solvent:
- - Vehicle/solvent used: DMSO
- Untreated negative controls:
- yes
- Negative solvent / vehicle controls:
- yes
- Positive controls:
- yes
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: in agar (plate incorporation)
DURATION
- Exposure duration: 48-72 hr
NUMBER OF REPLICATIONS: 3 - Evaluation criteria:
- - concentration-related increase over the tested range and reproducible increase at one or more concentrations in the number of revertant colonies per plate in at least one strain with or without metabolic activation
- mutation factor >2 - Statistics:
- Student's t-test was used
- Species / strain:
- S. typhimurium TA 100
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not specified
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Species / strain:
- S. typhimurium TA 1535
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not specified
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Species / strain:
- S. typhimurium TA 97
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not specified
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Species / strain:
- S. typhimurium TA 102
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not specified
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Species / strain:
- S. typhimurium TA 98
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not specified
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Conclusions:
- Interpretation of results (migrated information):
negative
TC, dried is considered to be non-mutagenic in bacterial gene mutation test system. - Executive summary:
TC, dried was dissolved in DMSO and tested in the in vitro gene mutation test according to OECD 471 (Ames-Test).
5 strains of Salmonella typhimurium were used: TA100, TA98, TA97, TA102, and TA1535.
The test was performed with and without metabolic activation with S-9 mix.
The test article did not induce mutagenicity up to and including concentrations of 5 mg/plate.
Therefore TC, dried is considered to be non-mutagenic.
- Endpoint:
- in vitro gene mutation study in mammalian cells
- Remarks:
- Type of genotoxicity: gene mutation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2012
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study, detailed documentation
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 476 (In Vitro Mammalian Cell Gene Mutation Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of assay:
- mammalian cell gene mutation assay
- Target gene:
- hprt locus of V79 Chinese Hamster lung cells
- Species / strain / cell type:
- Chinese hamster lung fibroblasts (V79)
- Metabolic activation:
- with and without
- Metabolic activation system:
- Mammalian liver post-mitochondrial fraction (S9), prepared from Sprague Dawley male rats
- Test concentrations with justification for top dose:
- Range-finding: 0, 0.75, 7.5, 15, 30, 60, 120, 240, 480 µg/mL (final concentrations)
Definitive test. experiment 1, -S9: 3.75, 7.5, 15, 30, 60, 120 µg/mL + vehicle (1% DMSO v/v ) + EMS (pos. control)
Definitive test. experiment 1, +S9: 7.5, 15, 30, 60, 120, 240, 480 µg/mL + vehicle (1% DMSO v/v ) + EMS (pos. control)
Definitive test. experiment 2, -S9: 7.5, 15, 30, 60, 120, 240, 480 µg/mL + vehicle (1% DMSO v/v ) + DMBA (pos. control)
Definitive test. experiment 2, +S9: 7.5, 15, 30, 60, 120, 240, 480 µg/mL + vehicle (1% DMSO v/v ) + DMBA (pos. control)
Appropriate amount of test item was weighted and diluted in DMSO not earlier than 30 min prior to test start. For dilution of final doses, sterile DMSO was used. - Vehicle / solvent:
- - Vehicle/solvent used: DMSO
- Untreated negative controls:
- yes
- Positive controls:
- yes
- Positive control substance:
- other: Ethyl methanesulphonate 600 µg/mL, 7,12-dimethyl-benz[a]anthracene 3 µg/mL
- Details on test system and experimental conditions:
- METHOD OF APPLICATION:
10exp6 cells in 5 mL Dulbecco's Modified Eagle's medium, with 4.5 g/L glucose supplemented with L-glutamine seeded in Petri dishes
DURATION
- Exposure duration: 3 hr
NUMBER OF REPLICATIONS: 2 - Evaluation criteria:
- - mutant frequency at one or more concentrations at least 3-fold greater than that of negative control
- concentration-related increase in mutant frequency
- effects described above were reproducible - Statistics:
- Kruskat-Wallis test, p<0.01
- Species / strain:
- Chinese hamster lung fibroblasts (V79)
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Conclusions:
- Interpretation of results (migrated information):
negative
TC, dried did not induce mutation at the hprt locus of V79 Chinese Hamster lung cells in concentrations up to and including 480 µg/mL (limit of solubility). - Executive summary:
TC, dried was dissolved in DMSO in concentrations up to the limit of solubility at 480 µg/ml and tested in an in vitro mammalian cell gene mutation test according to OECD 476. The ability to induce mutagenicity was tested in this cytogenetic test at the hprt locus.
Up to and including the highest possible concentrations TC, dried did not induce mutagenic activity neither with nor without metabolic activation by S-9 mix. The maximum tested concentration was limited by solubility.
Therefore TC, dried was considered to be non-mutagenic.
Referenceopen allclose all
Experiment 1: range-finding test without metabolic activation
Experiment 2:definitive test with and without metabolic activation
The results indicate that TC, dried neither produce statistically significant dose-related increase in the number of revertants nor a statistically significant and reproducible positive response at any of the test points.
Experiment 1:
RPE was ca. 115.2% in absence of S-9 at 120 µg/mL and 72.6% in presence of S-9 (480 µg/mL.
Experiment 2:
at 480 µg/mL RPE was ca. 102.0% in absence of S-9 and ca. 82.6% in presence of S-9.
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Genetic toxicity in vivo
Description of key information
6,6',6''-(1,3,5-Triazine-2,4,6-triyltriimino)trihexanoic acid has no potential to cause chromosomal damage in vivo.
Link to relevant study records
- Endpoint:
- in vivo mammalian somatic cell study: cytogenicity / erythrocyte micronucleus
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2002
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 474 (Mammalian Erythrocyte Micronucleus Test)
- Version / remarks:
- (adopted 1997)
- Deviations:
- no
- GLP compliance:
- yes
- Type of assay:
- micronucleus assay
- Species:
- mouse
- Strain:
- other: Hsd:ICR (CD-1)
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Harlan Italy S.r.l., San Pietro al Natisone (UD)
- Age at study initiation: 5-6 weeks
- Weight at arrival: 22-30 g
- Housing: 5 animals per cage in clear polycarbonate cages
- Diet: commercially available laboratory rodent diet (Altromin MT, Altromin, D-32770 Lage, Postfach 1120, Germany), ad libitum
- Water: ad libitum
- Acclimation period: 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 ± 2
- Humidity (%): 55 ± 10
- Photoperiod: 12 hrs dark / 12 hrs light - Route of administration:
- oral: gavage
- Vehicle:
- - Vehicle used: CMC (carboxymethyl cellulose, 0.5%)
- Concentration of test material in vehicle: 200 mg/mL; 100 mg/mL; 50 mg/mL
- Amount of vehicle: 10 mL/kg
- Batch No. (from BDH): 1072067 - Details on exposure:
- PREPARATION OF DOSING SOLUTIONS:
Solutions of the test item, as received, were prepared immediately before use in carboxymethylcellulose 0.5%. Solutions were prepared on a weight/volume basis without connection for the displacement due to the volume of the test item. - Duration of treatment / exposure:
- Not applicable.
- Frequency of treatment:
- Single treatment.
- Post exposure period:
- Control group: 24 and 48 h
500 mg/kg bw: 24 h
1000 mg/kg bw: 24 h
2000 mg/kg bw: 24 and 48 h
Positive control: 24 h - Dose / conc.:
- 500 mg/kg bw/day (actual dose received)
- Dose / conc.:
- 1 000 mg/kg bw/day (actual dose received)
- Dose / conc.:
- 2 000 mg/kg bw/day (actual dose received)
- No. of animals per sex per dose:
- Control group: 10 per sex
500 mg/kg bw: 5 per sex
1000 mg/kg bw: 5 per sex
2000 mg/kg bw: 10 per sex
Positive control: 5 per sex - Control animals:
- yes, concurrent vehicle
- Positive control(s):
- Mitomycin-C (batch no. 31K2504; SIGMA)
- Route of administration: oral, gavage
- Doses / concentrations: 3 mg/kg bw - Tissues and cell types examined:
- Erythrocytes of femur bone marrow
- Details of tissue and slide preparation:
- CRITERIA FOR DOSE SELECTION:
A toxicity test was performed to aid in the selection of dose-levels. Groups of two male and two female mice were dosed by oral gavage with the test item at 2000, 1000 and 500 mg/kg bodyweight. The animals were observed for 48 hours and sacrificed. Scoring was performed on slides prepared from the femurs of animals.
DETAILS OF SLIDE PREPARATION:
Animals were sacrificed at appropriate sampling times and the femurs of animals were removed and bone marrow cells obtained by flushing with fetal calf serum. The cells were centrifuged and a concentrated suspension was prepared to make smears on slides. These slides were air-dried and then stained with May-Gruenwald and Giemsa, and mounted with Eukitt. Three slides were made from each animal.
METHOD OF ANALYSIS:
The slides were randomly coded by a person not involved in the subsequent microscope scoring. The slides were examined under low power (x 16 objective) and one slide from each animal was selected according to staining and quality of smears. Where no depression of polychromatic erythrocytes was observed at least 2000 polychromatic cells per animal were examined for the presence of micronuclei at high power (x 100 objective, oil immersion). At the same time the numbers of normal and micronucleated normochromatic erythrocytes were also recorded. - Evaluation criteria:
- The test item is considered to induce micronuclei if a statistically significant increase in the micronucleus incidence in polychromatic erythrocytes (at P<0.05) is observed in any treatment group, in the pooled data for both sexes, or for either sex considered separately. Where increases in the incidence of micronucleated PCE's are observed which are statistically significant, but fall within the range of negative control values within this laboratory, then concurrent and historical control data are used to demonstrate that these increases do not have biological significance.
- Statistics:
- Only counts obtained from polychromatic cells were subjected to statistical analysis. Using the original observations (and not the micronucleus frequencies per 1000 cells), a modified Chi-squared calculation was employed to compare treated and control groups.
The degree of heterogeneity within each group was first calculated and where this was significant it was taken into account in the comparison between groups. Variance ratios or Chi-squared values are taken to show the significance of any difference between each treated group and the controls. - Sex:
- male/female
- Genotoxicity:
- negative
- Toxicity:
- no effects
- Vehicle controls validity:
- valid
- Negative controls validity:
- not applicable
- Positive controls validity:
- valid
- Additional information on results:
- RESULTS OF RANGE-FINDING STUDY
Reduced activity was observed in female animals on the day of the treatment and the day after. No other adverse reactions to treatment were noted. Treatment with the test item had no adverse effect on the proliferation of bone-marrow erythropoietic cells. Based on the above results, dose-levels of 500, 1000 and 2000 mg/kg bodyweight were selected for the Main assay.
RESULTS OF DEFINITIVE STUDY
No increases in the numbers of micronucleated PCE's were observed in any treatment group at any sampling time. Pronounced increases in the frequency of micronucleated PCE's were observed in the positive control group, indicating the correct functioning of the test system.
The ratio of mature to immature erythrocytes and the proportion of immature erythrocytes among total erythrocytes were analyzed to evaluate the bone marrow cell toxicity. Based on these results, no inhibitory effect on erythropoietic cell division was observed in male or female animals at any sampling time. - Conclusions:
- On the basis of the results obtained, it is concluded that the test article administered by oral gavage, does not induce micronuclei in the polychromatic erythrocytes of treated mice, under the reported experimental conditions.
- Executive summary:
The test article's potential to cause chromosomal damage in vivo was investigated in a micronucleus test. Based on results obtained in a preliminary toxicity trial, dose-levels selected were 500, 1000 and 2000 mg/kg bodyweight for male and female animals. Hsd:ICR (CD-I) mice were dosed once by gavage with the vehicle alone (carboxymethylcellulose 0.5%), the test material in the vehicle at the selected dose-levels or with the positive control substance Mitomycin-C. Each group consisted of five male and five female animals with the exception of the control and high-dose group, which included an additional five animals of each sex per group. Five animals per sex from each group were sacrificed at the 24 hour sampling time. The additional animals were sacrificed at the 48 hour sampling time. Bone-marrow smear slides were made and stained with May-Gruenwald and Giemsa stains. At least 2000 polychromatic cells per animal were examined for the presence of micronuclei. The slides were coded prior to scoring. The results obtained at each sampling time were subjected to statistical analysis using a modified chi-squared test. Following treatment with the test substance, no statistically significant increase in the incidence of micronucleated PCE's over the control value was observed at any dose level, at any sampling time. Following treatment with the positive control Mitomycin-C, statistically significant increases in the incidence of micronucleated PCE's over the control values were observed, indicating the correct functioning of the test system. No clinical signs or depression of bone marrow erythropoietic cell division, were observed at any dose-level, at any sampling time. It is concluded that, under the reported experimental conditions, the test item administered by oral gavage at the selected dose-levels to male and female mice, does not induce micronuclei in the polychromatic erythrocytes.
Reference
Table 1: Incidence of micronucleated PCEs and ratio of PCE/NCE of the in-vivo bone marrow micronucleus study.
Treatment |
Dose level (mg/kg bw) |
Incidence of micronucleated PCEs |
PCE/(PCE+NCE) % over the mean negative control value |
|||
|
male/female |
Mean |
SE |
range |
|
|
24 hr sampling time |
||||||
Vehicle |
10 mL/kg |
0.6 |
0.2 |
0 |
1.5 |
100 |
Test item |
500 |
0.9 |
0.3 |
0 |
3.0 |
99 |
Test item |
1000 |
0.5 |
0.2 |
0 |
1.5 |
101 |
Test item |
2000 |
0.8 |
0.3 |
0 |
2.5 |
98 |
Mitomycin C |
3 |
10.6*** |
1.4 |
6.0 |
17.0 |
102 |
48 hr sampling time |
||||||
Vehicle |
10 mL/kg |
0.6 |
0.2 |
0 |
1.5 |
100 |
Test item |
2000 |
0.8 |
0.3 |
0 |
3.0 |
98 |
***: Incidence significantly greater than control value at p < 0.001
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Additional information
Potential mutagenicity of 6,6',6''-(1,3,5-Triazine-2,4,6-triyltriimino)trihexanoic acid was tested:
- Twice according to OECD 471 with negative results
- Once according to OECD 487 with negative result
- Once according to OECD 473 with positive result
- Once according to OECD 476 with negative result
- Once according to OECD 474 with negative result
All tests together enable thorough assessment for gene mutations and effects on chromosome structure and number.
6,6',6''-(1,3,5-Triazine-2,4,6-triyltriimino)trihexanoic acid has no potential to cause chromosomal damage in vivo.
According to Annexes VII, VIII, IX & X no further tests are required.
It can be concluded that 6,6',6''-(1,3,5-Triazine-2,4,6-triyltriimino)trihexanoic acid is not genotoxic.
Justification for classification or non-classification
All tests together enable thorough assessment for gene mutations and effects on chromosome structure and number.
6,6',6''-(1,3,5-Triazine-2,4,6-triyltriimino)trihexanoic acid has no potential to cause chromosomal damage in vivo.
It can be concluded that 6,6',6''-(1,3,5-Triazine-2,4,6-triyltriimino)trihexanoic acid is not genotoxic.
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.