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EC number: 291-905-1 | CAS number: 90506-43-7
- 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
There is no evidence for a skin sensitising potential of Phosphoric acid, C12-18-alkyl esters, potassium salts from information of related read-across substance Phosphoric acid, dodecyl ester, potassium salt.
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Justification for type of information:
- REPORTING FORMAT FOR THE ANALOGUE APPROACH
Refer to attached document - Reason / purpose for cross-reference:
- read-across source
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 10 %
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Clinical observations:
- no effects
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 10 %
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- no effects
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 10 %
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Clinical observations:
- no effects
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 10 %
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- no effects
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 0.1 %
- No. with + reactions:
- 5
- Total no. in group:
- 10
- Clinical observations:
- discrete/patchy erythema
- Remarks on result:
- positive indication of skin sensitisation
- Remarks:
- Positive control study performed from 2008-03-19 to 2008-04-25
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 0.1 %
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- no effects
- Remarks on result:
- no indication of skin sensitisation
- Remarks:
- Positive control study performed from 2008-03-19 to 2008-04-25
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 1 %
- No. with + reactions:
- 9
- Total no. in group:
- 10
- Clinical observations:
- Discrete/patchy to moderate/confluent erythema with or without scaling
- Remarks on result:
- positive indication of skin sensitisation
- Remarks:
- Positive control study performed from 2008-03-19 to 2008-04-25
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 1 %
- No. with + reactions:
- 9
- Total no. in group:
- 10
- Clinical observations:
- Discrete/patchy to moderate/confluent erythema with or without scaling
- Remarks on result:
- positive indication of skin sensitisation
- Remarks:
- Positive control study performed from 2008-03-19 to 2008-04-25
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 0.1 and 1 %
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Clinical observations:
- no effects
- Remarks on result:
- no indication of skin sensitisation
- Remarks:
- Positive control study performed from 2008-03-19 to 2008-04-25
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 0.1 and 1 %
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Clinical observations:
- no effects
- Remarks on result:
- no indication of skin sensitisation
- Remarks:
- Positive control study performed from 2008-03-19 to 2008-04-25
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Available data from Phosphoric acid, dodecyl ester, potassium salt were used to evaluate the skin sensitising potential of Phosphoric acid, C12-18-alkyl esters, potassium salts.
Phosphoric acid, dodecyl ester, potassium salt does not need to be classified and labelled as a skin sensitizer, based on results of a guinea pig maximization test according to OECD guideline 406.
Taken together there is no evidence for a skin sensitising potential of Phosphoric acid, C12-18-alkyl esters, potassium salts from information of related read-across substance Phosphoric acid, dodecyl ester, potassium salt.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
Available data from Phosphoric acid, dodecyl ester, potassium salt were used to evaluate the skin sensitising potential of Phosphoric acid, C12-18-alkyl esters, potassium salts.
Phosphoric acid, dodecyl ester, potassium salt does not need to be classified and labelled as a skin sensitizer, based on results of a guinea pig maximization test according to OECD guideline 406.In a dermal sensitisation study according to OECD TG 406, 1992) with Phosphoric acid, dodecyl ester, potassium salt, young adult Dunkin-Hartley guinea pigs were tested using the Maximization test method. The intradermal induction of sensitization in the test group was performed in the nuchal region with a 1 % dilution of the test item in purified water in an emulsion of Freund's Complete Adjuvant (FCA)/physiological saline. The epidermal induction of sensitization was conducted for 48 hours under occlusion with the test item at 75 % in purified water one week after the intradermal induction. The animals of the control group were intradermally induced with purified water and FCA/physiological saline and epidermally induced with purified water under occlusion.
Two weeks after epidermal induction the control and test animals were challenged by epidermal application of the test item at 10 % in purified water and purified water alone under occlusive dressing. Cutaneous reactions were evaluated at 24 and 48 hours after removal of the dressing.
No toxic signs were evident in the guinea pigs of the control or test group. No deaths occurred. No skin effect/reaction was observed in the control and test group after challenge treatment with the test item at 10 % in purified water.
Justification for read-across
Evaluation of structure-activity relationship is based on data from structural similar substances with the same basic structure, potassium salts of phosphoric acid alkyl ester, varying mainly in the chain length of fatty acid moiety. A detailed justification document for the read-across is attached in the respective target records of IUCID.
Taken together there is no evidence for a skin sensitising potential of Phosphoric acid, C12-18-alkyl esters, potassium salts from information of related read-across substance Phosphoric acid, dodecyl ester, potassium salt.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
Based on read-across data from a study according to OECD Guideline 406 on the read-across substance Phosphoric acid, dodecyl ester, potassium salt,of Phosphoric acid, C12-18-alkyl esters, potassium salts does not need to be classified as skin sensitizer according the criteria of CLP, EU GHS (Regulation (EC) No 1272/2008).
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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