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EC number: 232-417-0 | CAS number: 8017-16-1
- 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
Description of key information
Skin irritation / corrosion
0.5 mL of a 80% phosphoric acid solution was observed to be corrosive to rabbit skin after 24 hours of exposure.
Eye irritation:
No reliable data are available for the eye irritation endpoint. Nevertheless as the substance is skin corrosive and classified accordingly, the substance is as well considered as eye corrosive. This is as well in accordance with the results of the unreliable studies.
Key value for chemical safety assessment
Skin irritation / corrosion
Link to relevant study records
- Endpoint:
- skin irritation: in vivo
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study performed according to 1500.41 in the Federal Register Vol. 38, No. 187, S. 26019 from 1973-09-27 with limited documentation.
- Qualifier:
- according to guideline
- Guideline:
- other: 1500.41 in the Federal Register Vol. 38, No. 187, S. 26019 from 1973-09-27
- Deviations:
- not specified
- GLP compliance:
- not specified
- Species:
- rabbit
- Strain:
- Vienna White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: no data
- Age at study initiation: no data
- Weight at study initiation: 2.45-3.14 kg (mean: 2.79 kg)
- Housing: no data
- Diet: SSNIFF diet (Intermast), witheld during the contact period
- Water: withheld during the contact period
- Acclimation period: no data
ENVIRONMENTAL CONDITIONS
- Temperature (°C): no data
- Humidity (%): no data
- Air changes (per hr): no data
- Photoperiod (hrs dark / hrs light): no data
IN-LIFE DATES: From: 1979-07-03 To: 1979-07-06 - Type of coverage:
- not specified
- Preparation of test site:
- other: all test sites were shaved, half of the test sites were abraded
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 mL
- Concentration (if solution): 80 %
VEHICLE
- Amount(s) applied (volume or weight with unit): not applicable
- Concentration (if solution): not applicable
- Lot/batch no. (if required): not applicable
- Purity: not applicable - Duration of treatment / exposure:
- 24 hours
- Observation period:
- - Observations were performed at 24 and 72 hours and at 8 days post-dosing.
- Number of animals:
- 6 males
- Details on study design:
- TEST SITE
- Area of exposure: 2.5 x 2.5 cm
- % coverage: no data
- Type of wrap if used: the test sites were covered with a rubberized covering (5 x 5 cm), fixed with bandaid strips, and wrapped with gauze.
REMOVAL OF TEST SUBSTANCE
- Washing (if done): no data
- Time after start of exposure: no data
SCORING SYSTEM:
- The scoring system appears to be equivalent to the Draize scale. - Irritation parameter:
- erythema score
- Remarks:
- (intact and abraded)
- Basis:
- mean
- Time point:
- other: 24 and 72 hours
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Remarks:
- within 72 hours post-dosing
- Irritation parameter:
- edema score
- Remarks:
- (intact)
- Basis:
- mean
- Time point:
- other: 24 hours
- Score:
- 2.8
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 72 hours post-dosing
- Remarks on result:
- other: 1 score was 2, 5 scores were 3
- Irritation parameter:
- edema score
- Remarks:
- (intact)
- Basis:
- mean
- Time point:
- other: 72 hours
- Score:
- 2.3
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 72 hours post-dosing
- Remarks on result:
- other: 4 scores were 2, 2 scores were 3
- Irritation parameter:
- edema score
- Remarks:
- (abraded)
- Basis:
- mean
- Time point:
- other: 24 hours
- Score:
- 3
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 72 hours post-dosing
- Remarks on result:
- other: all scores were 3
- Irritation parameter:
- edema score
- Remarks:
- (abraded)
- Basis:
- mean
- Time point:
- other: 72 hours
- Score:
- 2.2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 72 hours post-dosing
- Remarks on result:
- other: 5 scores were 2, 1 score was 3
- Irritation parameter:
- primary dermal irritation index (PDII)
- Time point:
- other: 72 hours
- Score:
- 6.6
- Irritant / corrosive response data:
- Intact and Abraded Test Sites:
- In intact and abraded sites at 24 hours, edema and mild necrosis was observed in all animals.
- In intact sites at 72 hours, edema was observed in 3 animals and deep tissue necrosis was observed in the other 3 animals with gross pathological effects.
- In abraded sites at 72 hours, deep tissue necrosis was observed in all animals with accompanying edema in 1 animal. The necrosis was observed with gross pathological effects. - Other effects:
- - All animals were sacrificed at 72 hours for humane reasons.
- Interpretation of results:
- corrosive
- Remarks:
- Migrated information 80% phosphoric acid Criteria used for interpretation of results: not specified
- Conclusions:
- The test substance was corrosive to the rabbit skin.
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (corrosive)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Polyphosphoric acid is a mixture of the corresponding acids to phosphate anion and its condensed phosphates as follows:
- orthophosphoric acid or phosphoric acid (17 -76%),
- pyrophosphoric acid (23 -50%),
- triphosphoric acid (1.5 -25%),
- tetraphosphoric acid (0 -12%)
- and pentaphosphoric acid (0 -7%).
When the substance polyphosphoric acid is in contact of excess of water, a rapid hydrolysis is observed with the longer chains (tri, tetra or penta) while a very slow hydrolysis is observed for the dimer form to ortho phosphate. However, in biological media, the pyrophosphate ion is cleaved rapidly into two orthophosphate molecules by one of the different members of the alkaline phosphatase family which are present in all tissues. Thus a read across from phosphoric acid to pyrophosphoric acid is justified.
All the data discussed below were generated with phosphoric acid.
Skin irritation / corrosion:
BASF (1980) studied the skin irritant/corrosive properties of phosphoric acid on Vienna White rabbit skin (6 male rabbits tested according to guideline 1500.41 in the Federal Register Vol. 38, No. 187, S. 26019 from 1973 -09 -27). 0.5 mL of an 80% solution was applied to the shaved test sites (half of the test sites were abraded). After 24 hours of exposure, observations were done at 24 and 72 hours and at 8 days post dosing. The substance was observed to be corrosive to rabbit skin. These data were considered as key information for the skin irritation/corrosion endpoint. BASF (1980) studied as well the skin irritation properties of 0.5 mL 19% solution of phosphoric acid in 2 female Vienna White rabbit (4 hours of exposure). The test substance was considered as a non skin irritant substance.
Eye irritation:
Phosphoric acid is classified as a skin corrosive substance category 1B (concentration > or = 25%) and an eye irritant (10% < or = concentration < 25%) according to the CLP Regulation Annex VI, table 3.1 (EC Regulation 1272/2008 on classification, labelling and packaging of substances and mixtures). Therefore, according to the REACH Regulation, in vitro testing for eye irritation with this substance does not need to be conducted (column 2 adaptation, Annex VII, section 8.2). In vivo testing can be waived according to the REACH Regulation as phosphoric acid is classified as corrosive to the skin and as an eye irritant (column 2 adaptation, Annex VIII, section 8.2.1).
Justification for selection of skin irritation / corrosion endpoint:
Read-across justified from phosphoric acid to polyphosporic acid.
Effects on skin irritation/corrosion: corrosive
Effects on eye irritation: corrosive
Justification for classification or non-classification
According to the available data, phosphoric acid is considered as a skin corrosive substance (80% solution tested). This is in the line with the Harmonized CLP classification where phosphoric acid is classified as a Skin Corrosive substance category 1B. In addition, the harmonized classification (Table 3.1 of the CLP Regulation (EC) No 1272/2008 reports that phosphoric acid is a skin irrtant substance category 2 at following concentration limits: 10% < or = C <25% although the available data didn't show an irritant effect at a concentration of 19% phosphoric acid. The classification of the CLP Regulation will nevertheless be followed in this substance dossier.
According to the CLP Regulation (EC) 1272/2008, phosphoric acid is considered as an eye irritant substance category 2 with a concentration limit of 10% < or = C < 25% (Annex VI harmonized classification (Tabel 3.1))
In conclusion and based on the read across perfomed, pyrophosphoric acid will be classified as phosphoric acid.
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