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EC number: 240-539-0 | CAS number: 16484-77-8
- 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

Oxidising properties
Administrative data
Link to relevant study record(s)
- Endpoint:
- oxidising solids
- Remarks:
- Solids
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 11 February 1999 to 16 April 1999
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.17 (Oxidising Properties (Solids))
- Deviations:
- no
- GLP compliance:
- yes
- Contact with:
- powdered cellulose
- Key result
- Sample tested:
- test mixture as specified
- Parameter:
- burning rate
- Remarks on result:
- mixture does not ignite and burn
- Interpretation of results:
- other: Not classified according to EU criteria.
- Conclusions:
- Under the conditions of the study the test material is not oxidising.
- Executive summary:
The oxidising properties of the test material were assessed according to EU Method A.17 and in compliance with GLP.
The test material, cellulose and barium nitrate used as a reference were dried and sieved (125 μm) prior to use. The dried test material (2 parts) was thoroughly mixed with dried cellulose (1 part) and formed into a cone shaped pile of dimensions 3.5 cm (diameter of base) x 2.5 cm (height). The cone, on a non-combustible, non-porous surface was ignited with a gas burner. The vigour and duration of the combustion were observed, recorded and compared with that of a similarly prepared cone consisting of 3 parts of barium nitrate to 2 parts of cellulose.
As the sample cone failed to burn to completion, cones consisting of the test material (technical grade) (1 part) and cellulose (1 and 2 parts) were prepared and tested.
As neither mixture of 2:1, 1:1 or 1:2 test substance/cellulose burned to completion, the test material (technical grade) is considered to be non-oxidising. By comparison, the reference mixture burned vigorously to completion in 64 seconds.
Under the conditions of the study the test material is not oxidising.
- Endpoint:
- oxidising solids
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 11 April 1990 to 20 August 1990
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.17 (Oxidising Properties (Solids))
- Deviations:
- no
- GLP compliance:
- yes
- Contact with:
- other: Dried cellulose
- Duration of test (contact time):
- >= 5 min
- Key result
- Sample tested:
- test mixture as specified
- Parameter:
- burning rate
- Result:
- ca. 5 min
- Remarks on result:
- other: The outside of the pile burned but extinguished itself in approximately 5 minutes.
- Interpretation of results:
- other: Not classified according to EU criteria.
- Conclusions:
- Under the conditions of the study the test material is non-oxidising.
- Executive summary:
Oxidising properties was assessed according to EEC Method A17 and in compliance with GLP.
The test mixture was prepared by mixing the test material thoroughly with dried cellulose (2:1 w/w). Also subjected to the test was dried cellulose alone and, as a reference, a mixture of barium nitrate and dried cellulose (2:1 w/w). The test samples were formed into conical piles by filling a plugged 35 nm glass funnel and inverting onto an asbestos board. The top of each pile was subsequently ignited with a gas burner flame, and burning times observed.
The burning rate for the test material/cellulose (2:1 w/w) mix was considerably slower than for barium nitrate/cellulose (2:1 w/w) or cellulose alone. The outside of the pile burned but extinguished itself in approximately 5 minutes. The test material melted forming a brown, viscous liquid and a large amount of unburned sample remained within this charred outer shell.
Under the conditions of the study the test material is non-oxidising.
Referenceopen allclose all
As neither mixture of 2:1, 1:1 or 1:2 test material/cellulose burned to completion, the test material is considered to be non-oxidising.
By comparison, the reference mixture burned vigorously to completion in 64 seconds. No further testing was therefore necessary.
Sample |
Observation |
Cellulose
|
The outside of the pile burned slowly (approx 2 minutes), with some unburned cellulose remaining within the charred outer shell. |
Barium nitrate/cellulose (2:1 w/w)
|
A rapid reaction occurred with the whole pile burning in less than 1 minute. |
Test material/cellulose (2:1 w/w)
|
Burning rate was considerably slower than for barium nitrate/cellulose (2:1 w/w) or cellulose alone. The outside of the pile burned but extinguished itself in approximately 5 minutes. The test material melted forming a brown, viscous liquid and a large amount of unburned sample remained within this charred outer shell. |
The test material is non-oxidising.
Description of key information
Comb (2000)
Under the conditions of the study the test material is not oxidising.
O'Connor (1990)
Under the conditions of the study the test material is non-oxidising.
Key value for chemical safety assessment
- Oxidising properties:
- non oxidising
Additional information
O'Connor (1990)
Oxidising properties was assessed according to EEC Method A17 and in compliance with GLP. The study was awarded a reliability score of 1 in accordance with the criteria set forth by Klimisch et al. (1997).
The test mixture was prepared by mixing the test material thoroughly with dried cellulose (2:1 w/w). Also subjected to the test was dried cellulose alone and, as a reference, a mixture of barium nitrate and dried cellulose (2:1 w/w). The test samples were formed into conical piles by filling a plugged 35 nm glass funnel and inverting onto an asbestos board. The top of each pile was subsequently ignited with a gas burner flame, and burning times observed.
The burning rate for the test material/cellulose (2:1 w/w) mix was considerably slower than for barium nitrate/cellulose (2:1 w/w) or cellulose alone. The outside of the pile burned but extinguished itself in approximately 5 minutes. The test material melted forming a brown, viscous liquid and a large amount of unburned sample remained within this charred outer shell.
Under the conditions of the study the test material is non-oxidising.
Comb (2000)
The oxidising properties of the test material were assessed according to EU Method A.17 and in compliance with GLP. The study was awarded a reliability score of 1 in accordance with the criteria set forth by Klimisch et al. (1997).
The test material, cellulose and barium nitrate used as a reference were dried and sieved (125 μm) prior to use.The dried test material (2 parts) was thoroughly mixed with dried cellulose (1 part) and formed into a cone shaped pile of dimensions 3.5 cm (diameter of base) x 2.5 cm (height). The cone, on a non-combustible, non-porous surface was ignited with a gas burner. The vigour and duration of the combustion were observed, recorded and compared with that of a similarly prepared cone consisting of 3 parts of barium nitrate to 2 parts of cellulose.
As the sample cone failed to burn to completion, cones consisting of the test material (technical grade) (1 part) and cellulose (1 and 2 parts) were prepared and tested.
As neither mixture of 2:1, 1:1 or 1:2 test substance/cellulose burned to completion, the test material (technical grade) is considered to be non-oxidising.By comparison, the reference mixture burned vigorously to completion in 64 seconds.
Under the conditions of the study the test material is not oxidising.
Justification for classification or non-classification
In accordance with the criteria for classification as defined in Annex I, Regulation (EC) No 1272/2008, the material does not require classification with respect to oxidising properties.
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