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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 232-221-5 | CAS number: 7790-76-3
- 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
![](https://echa.europa.eu/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_toxicological-information.png)
Endpoint summary
Administrative data
Description of key information
There are currently no experimental data available to assess repeated dose toxicity for the test substance. A data waiver is set in place to justify that no further repeated dose toxicity testing is required.
Key value for chemical safety assessment
Repeated dose toxicity: via oral route - systemic effects
Link to relevant study records
- Endpoint:
- sub-chronic toxicity: oral
- Data waiving:
- other justification
- Justification for data waiving:
- other:
Reference
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: inhalation - systemic effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: inhalation - local effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: dermal - systemic effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: dermal - local effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
One subacute study is available for calcium hydrogenorthophosphate.
Subacute
For calcium hydrogenorthophosphate (CAS 7757 -93 -9) one short-term toxicity study is available. This study is not adequate for the risk assessment for the following reason:
A non-guideline repeated dose toxicity study was performed in 1970. Calcium hydrogenorthophosphate was administered at a limit dose of 214 mg/kg bw/day to male rats by means of a stomach tube daily for 14 days. 24 hours after the final dose animals were autopsied and observed for pathological changes. No adverse effects were noted at that dose level under the conditions of this study. Since the treatment lasted only for 14 days and only the limit dose of 214 mg/kg bw was used this study is not reliable to fulfil the endpoint because the treatment duration should have been at least 28 days and the limit dose 1000 mg/kg bw.
Subchronic
For the structural similar substance beta dicalcium pyrophosphate (CAS 7790 -76 -3) a 90 -day study is available (Lee, 2009). This study was performed similar to OECD 408. In this study 30 mg/kg bw/day of beta dicalcium pyrophosphate was administered to male and female Sprague Dawley rats (10 each) in diet for 90 days. There were no compound related effects in mortality, clinical signs, body weight, food consumption, hematology, clinical chemistry, urinalysis, organ weights, or gross and histologic pathology observed. The NOAEL is > 30mg/kg bw/day. Since only 30 mg/kg bw/day is tested and no effects were observed at that dose this study is not sufficient for classification because in a limit test 1000 mg/kg bw/day should have been tested.
A combined repeated dose and reproductive/developmental (OECD 422) study was conducted onpotassium dihydrogenorthophosphate (CAS 7758 -11 -4)in the rat on behalf of the National Institute of Environmental
Research, and reported publicly in the OECD SIDS (1). Since the phosphorus is considered to be the critical part in calcium phosphates (see discussion below) this study is reliable to be used as read across. No effects were observed at the highest dose resulting in a NOAEL of 1000 mg/kg bw/day. The lead registrant has sought to access this data however it has not been possible to agree data sharing terms for all co-registrants. As soon as this data is available it will be integrated in the dossier. Nonetheless, the lack of effects on repeated dose toxicity at dose levels well in excess of normal human exposure suggests that calcium and potassium orthophosphates are not a significant risk to repeated exposure in males and females. Further studies are unlikely to show any significant effects on repeated dose toxicity.
Calcium phosphates are used in the following human food and pharmaceutical applications: calcium bis(dihydrogenorthophosphate) is used as acidulant and mineral supplement. Calcium hydrogenorthophosphate is used as a dietary supplement in doses of 1g orally. Tricalcium bis(orthophosphate) is used as a gastric antacid in doses of 1g orally. The relatively high pharmaceutical doses taken orally by humans support the low toxicity of these salts. In addition other food additive uses also exist. As a consequence of their use patterns extensive review of the potential toxicity of calcium phosphates (as well as a number of other inorganic phosphate substances) has been undertaken by a number of regulatory authorities. In particular the Joint FAO/WHO Expert Committee on Food Additives (JEFCA) (which assesses and evaluates the biological data and toxicological data available for substances that are used as food additives) has published a monograph in which the aforementioned calcium phosphates have been evaluated for acceptable daily intake on the basis of the available toxicity data (2). An estimate of the maximum tolerable daily intake (MTDI) intake for man has been derived to be 70 mg/kg bw of phosphorus (2). This figure applies to the sum of phosphorus naturally present in the diet and from other sources, such as food additives. As the uses of calcium phosphates that fall under the scope of REACH are not considered to contribute a significant amount of phosphorus to the daily intake, it is not considered to be necessary or scientifically justified to conduct further testing for repeated dose oral toxicity. Reference values for the intake of calcium are considerably higher than that for phosphorus: Adequate intake (AI) value for calcium in male and female 19-30 years old is 1000 mg/day (3). It is also not considered to be appropriate to take into account the toxicity of calcium ions as these are indispensable nutrients that are very highly metabolically regulated systemically as well as intra-cellular. As such, the MTDI for phosphorus is considered to be the most appropriate and conservative value for risk assessment. In addition, as the phosphate moiety is not considered to differ from that of any other inorganic phosphate from a toxicological point of view for the purpose of risk assessment for the inhalation route and the derivation of appropriate DNELs it is considered to be appropriate to use the most reliable data available for phosphates and no further data was generated on calcium phosphates.
It is considered that the regulatory endpoint for repeated dose toxicity is fulfilled on the basis that the available information is both sufficient for characterisation of the hazard profile and the dose response of a substance upon repeated dose exposure and for the performance of a chemical safety assessment for repeated dose toxicity. It is not considered to be scientifically justified to conduct further in vivo testing for this endpoint and as such no testing is proposed. Furthermore, as body phosphate homeostasis in animals enables them to tolerate a wide range of dietary phosphate intakes providing an appropriate phosphate to calcium balance is maintained. Phosphate toxicity may be associated with metabolic disorders of calcium absorption and function and interactions of phosphate with other physiological cations such as calcium, magnesium and manganese (4). Therefore, animal studies to evaluate the safety of high levels of phosphate in the diets of animals are complicated by the need to separate the effect of the phosphate itself from the imbalance in the ratios of phosphate and other essential cations and therefore it is not appropriate to conduct a standard OECD 408 study (90 day repeated dose oral study in rodents) as this would not yield any meaningful data and as such would be an unnecessary in vivo study. It is therefore considered that the safety evaluation of inorganic phosphates as a class, including the various ionic forms, has been thoroughly completed by the use of animal studies and regulatory reviews. No additional animal studies are necessary to understand the calcium phosphate salts in this group. The effects of inorganic phosphate exposure are well known, as are those of calcium, all biological nutrients for life.
(1)http://webnet.oecd.org/Hpv/UI/SIDS_Details.aspx?id=545E2F43-CF57-4AED-8784-
C0391BCCC562
(2) Standing Committee on the Scientific Evaluation of Dietary Reference Intakes, Food and Nutrition Board,of. Dietary Reference Intakes for Calcium, Phosphorus, Magnesium, Vitamin D and Fluoride., Press, 1997.
(3) Evaluation of certain food additives and contaminants. Twenty-sixth report of the joint FAO/WHO expert committee of food additives. World Health Organisation. Technical Report Series 683. 1982. ISBN92 4 120683 7
(4) NRC, Mineral Tolerance of Animals. Second revised edition, 2005. The National Academies Press.www.nap.edu
Justification for classification or non-classification
The available data on repeated dose toxicity with the test substance do not meet the criteria for classification according to Regulation (EC) No 1272/2008, and are therefore conclusive but not sufficient for classification.
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.
![ECHA](/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/echa_logo.png)