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EC number: 500-057-6 | CAS number: 27104-30-9
- 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
Additional toxicological data
Administrative data
- Endpoint:
- additional toxicological information
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 1980
- Reliability:
- 3 (not reliable)
- Rationale for reliability incl. deficiencies:
- other: Scientific paper. Refers to other scientific papers for method descriptions. May be in accordance with the later OECD or EU guidelines, but it is uncertain.
Cross-reference
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 980
Materials and methods
- Type of study / information:
- Extracts tested in three assays:
-V79 Cell Mutagenesis Assay
-Agar Suspension Transformation Assay
-3T3 Cell Transformation Assay
Only data relevant for Proban CC is cited.
Test guideline
- Qualifier:
- no guideline followed
- Deviations:
- not applicable
- Principles of method if other than guideline:
- V79 cell mutation assay was performed accorcing to Kuroki et al. (1977) and Langenbach et al. (1978).
BHK 21/Cl 13 agar suspension transformation assay was performed according to MacPherson et al. (1966) and Styles (1977).
3T3 cell transformation assay was performed according to Kakunaga (1973). - GLP compliance:
- no
Test material
- Details on test material:
- Extracts from cotton textile treated with THPC-urea precondensate (condensation product between tetrakis(hydroxymethyl)phosphonium chloride and urea, not further characterised) and subsequently cured with ammonia gas.
Constituent 1
Results and discussion
Any other information on results incl. tables
Effect on mutagenesis in V79 cells of DMSO extracts of cotton fabrics treated with THPC-urea precondensate.
|
Survival (% of control) |
Ouabain-resistant mutants per 10" survivors |
|||||
- S9 |
- S9 |
- S9 |
- S9 |
||||
Treatment |
Concentration |
Exp. I |
Exp. 2 |
+ S9 |
Exp. I |
Exp.2 |
+ S9 |
DMSO |
0.5% |
100 |
100 |
100 |
0 |
0 |
0 |
Extract unconcentrated |
0.5% |
98 |
108 |
83 |
22 |
0 |
44 |
Extract 10-fold concentrated |
0.5% |
35 |
21 |
88 |
113 |
71 |
24 |
Effect on colony-forming ability of BHK cells in agar of DMSO extracts of cotton fabrics treated with THPC-urea precondenate.
Survival (% of control) In experimenta |
Average number of colonies per plate in experiment |
Estimated number of colonies per 106 survivors in experiment |
|||||
Treatment |
Concentration |
1 |
2 |
1 |
2 |
1 |
2 |
DMSO |
0.5% |
102 |
100 |
27 |
35 |
31 |
35 |
Extract unconcentrated |
0.5% |
85 |
107 |
37 |
106 |
43 |
102 |
Extract 10 -fold concentrated |
0.5% |
0 |
0 |
4 |
23 |
> 660 |
>2230 |
a) Experiment 1 was performed without S9 and experiment 2 with S9
3T3 Cell Transformation Assay of Extracts of Flame Retardant-treated Cotton Fabricsa
Transformed foci per 8 plates |
Transformed foci per 105 surviving cellsb |
||||||||||
3T3 (ATTC) |
3T3 (A31-714) |
3T3 (ATTC) |
3T3 (A31-714) |
||||||||
Treatment |
Concentration |
3T3 (ATTC) |
3T3 (A31-714) |
Exp. 1 |
Exp. 2 |
Exp. 3 |
Exp. 4 |
Exp. 1 |
Exp. 2 |
Exp. 3 |
Exp. 4 |
DMSO |
0.5% |
31 |
13 |
0 |
4 |
1 |
0 |
0 |
16 |
10 |
0 |
Extract unconcentrated |
0.5% |
31 |
13 |
13 |
2 |
7 |
NT |
21 |
8 |
67 |
NT |
Extract 10-fold concentrated |
0.5% |
2.5 |
0.5 |
12 |
7 |
4 |
NT |
240 |
350 |
1000 |
NT |
a) in experiment 1 - 2.5x104 cells were treated per plate; in experiments 2 and 3 - 1x104 cells; in experiment 4 - 5x104 cells. In experiment 4 only samples that showed no evidence of precipitation were used.
b) survival measured by cloning efficiency; actual values may be lower if survival increases with number of cells planted.
NT=not tested
Applicant's summary and conclusion
- Conclusions:
- The results show that components in the concentrated extracts are quite toxic to BHK and 3T3 cells, but less toxic to V79 cells. The unconcentrated extracts, which are almost not cytotoxic, are mutagenic and transforming. The data do not relate the mutagenic and transforming effects to actual components; thus the response cannot be quantified. It has been not determined whether the toxic components were formed during the concentration or storage of the samples. All tested samples are extracts from dyed fabrics treated with THPC-urea precondensate and subsequently cured with ammonia gas. Therefore, the samples may also contain dyes extracted from the fabrics. No precise conclusion can be drawn from present study about the transforming or mutagenic potential of THPC-urea precondensates.
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.
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