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EC number: 237-059-9 | CAS number: 13597-86-9
- 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
Toxicity to aquatic algae and cyanobacteria
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 23 August 2000 - 13 December 2000
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Justification for type of information:
- REPORTING FORMAT FOR THE ANALOGUE APPROACH
1. HYPOTHESIS FOR THE ANALOGUE APPROACH
In accordance with REACH Annex XI, Section 1.5, of Regulation (EC) No. 1907/2006 (REACH) the standard testing regime may be adapted in cases where a grouping or read-across approach has been applied.
The similarities may be based on:
(1) a common functional group
(2) the common precursors and/or the likelihood of common breakdown products via physical or biological processes, which result in structurally similar chemicals; or
(3) a constant pattern in the changing of the potency of the properties across the category
The proposed source chemical (diammonium hydrogenorthophosphate) is highly soluble in water (> 10000 mg/L). In aqueous media soluble inorganic orthophosphates will dissociate to their ionic constituents; in this case ammonium and orthophosphate ions. Diammonium dihydrogenpyrophosphate will dissociate to ammonium cations and pyrophosphate anions. The pyrophosphate anions are unstable in aqueous solutions with the degree of instability varying according to pH. In distilled water they will hydrolyse slowly via abiotic mechanisms to orthophosphate. In natural waters a number of different processes can occur; abiotic hydrolysis, biotic degradation (as a result of the action of phosphatases which cleave pyrophosphates into orthophosphate subunits) and assimilation by organisms in the water. Thus the target substance (diammonium dihydrogenpyrophosphate) and the source substance (diammonium hydrogenorthophosphate) will be primarily absorbed as the same inorganic ions: ammonium and orthophosphate and are expected to behave in a similar manner under test conditions.
All (bio) transformation products of the source chemical are common to the target chemical and as such the data is considered to be adequate and reliable for use in the assessment of diammonium dihydrogenpyrophosphate for the ecotoxicity hazard assessment.
2. SOURCE AND TARGET CHEMICAL(S) (INCLUDING INFORMATION ON PURITY AND IMPURITIES)
See read-across justification report attached.
3. ANALOGUE APPROACH JUSTIFICATION
See read-across justification report attached.
4. DATA MATRIX
See read-across justification report attached. - Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- Deviations:
- yes
- Remarks:
- The purity, expiration date, and lot number of the test substance were not given.
- GLP compliance:
- yes
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material (migrated information):
PHYSICO-CHEMICAL PROPERTIES: DIAMMONIUM HYDROGENORTHOPHOSPHATE
- Melting point: 155°C (decomposition)
- Vapour pressure at 20°C: 7.62 x 10-2 Pa
: 5.71 x 10-4 mmHg
- Water solubility (under test conditions): 400 - 588 g/L
- Henry's law constant: not applicable
- log Pow: not applicable
OTHER PROPERTIES (if relevant for this endpoint)
- Results of test for ready biodegradability: not applicable - Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: Nominal: 0.0 (control), 1.56, 3.13, 6.25, 12.5, 25.0, 50.0, and 100 mg DAP/L
- Sampling method: At test initiation (0 hrs), 15-mL samples were collected from each parent solution. At test termination (72 hrs), 4-mL samples were removed from each individual replicate and composited by treatment into a 12-mL total sample.
- Sample storage conditions before analysis:no data. - Vehicle:
- no
- Details on test solutions:
- STOCK AND TEST SOLUTION AND THEIR PREPARATION
- Vehicle, solvent: no
- Concentration of vehicle/ solvent: 0 mL/L
- Other procedures: 100 and 50 mg/L were prepared by direct addition to freshwater algal nutrient medium (FWAM) followed by sonication and 50% serial dilutions were prepared from the 50 mg/L solution in FWAM to prepare subsequent test solutions.
DILUTION WATER
- Source: freshwater algal nutrient medium by addition of nutrients to ABC reagent water. After preparation, the algal medium
was pH-adjusted to 7.5 ± 0.1 (using 0.1 N HCl) and filtered through a 0.45-μm Millipore filter. - Test organisms (species):
- Raphidocelis subcapitata (previous names: Pseudokirchneriella subcapitata, Selenastrum capricornutum)
- Details on test organisms:
- TEST ORGANISM
- Common name: Selenastrum capricornutum
- Strain: Pseudokirchnerella subcapitata
- Source (laboratory, culture collection): Department of Botany, Culture Collection of Algae, University of Texas at Austin, Austin, Texas
- Age of inoculum (at test initiation): 6 days old culture
- Method of cultivation: In 250-mL Erlenmeyer flasks fitted with foam stoppers. Positioned on a rotary shaker set at 100 rpm and incubated for 72 hours at 24 ± 2°C under continuous cool-white fluorescent lighting. Light intensity was maintained at approximately 8600 ± 860 lux.
ACCLIMATION
- Acclimation period: No data.
- Culturing media and conditions (same as test or not): Freshwater algal nutrient medium (FWAM), same as test. The medium was prepared by the
addition of appropriate reagent grade nutrients to ABC reagent water. After preparation, the medium was pH-adjusted to 7.5 ± 0.1 (using 0.1 N HCl) and filtered through a 0.45-:m Millipore filter.
- Any deformed or abnormal cells observed: No data - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Remarks on exposure duration:
- Cell counts were performed every 24 ± 1 hour after inoculation
- Post exposure observation period:
- no data
- Hardness:
- No data
- Test temperature:
- 22.5-25.7 °C
- pH:
- ranged from 7.39 to 7.42 at test initiation and from 7.56 to 9.35 at test termination
- Dissolved oxygen:
- No data
- Salinity:
- No data
- Nominal and measured concentrations:
- - Nominal concentrations (mg/L): 0, 1.56, 3.13, 6.25, 12.5, 25.0, 50.0 and 100 mg/L DAP
- Calculated concentrations at initiation: 0, 1.65, 3.57, 6.41, 12.0, 24.1, 47.4 and 97.1mg/L (95-114% of nominal).
DAP concentrations decreased during the exposure period (43-86% of niminal) which was likely due to incorporation of the phosphate into the algal biomass rather than instability of the test substance. Therefore, effect values were determined based on initial calculated concentrations. - Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Type (delete if not applicable): closed
- Material, size, headspace, fill volume: 250 mL Erlenmeyer flask containing 100 mL solution, fitted with foam stoppers.
- Initial cells density: 1.05 x10*4 cells/mL
- Control end cells density: 103 x10*4 cells/mL
- No. of organisms per vessel: 103 x10*6 cells/vessel
- No. of vessels per concentration (replicates): 3
- No. of vessels per control (replicates):3
- No. of vessels per vehicle control (replicates): n/a (no vehicle)
GROWTH MEDIUM
- Standard medium used: yes
OTHER TEST CONDITIONS
Light intensity in the environmental chamber ranged from 8034 to 8788 lux.
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
- Determination of cell concentrations: Cell counts were performed every 24 ± 1 hour after inoculation on all replicates of the control and
each test concentration. The algal cell counts were accomplished utilizing a hemacytometer and an optical microscope.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2-fold
- Range finding study
- Test concentrations: nominal test concentrations of 0.10, 1.0, 10, 100, and 1000 mg DAP/L.
- Results used to determine the conditions for the definitive study:
Cell counts for the four lowest test concentrations ranged from 95.0 to 140x10*4 cells/mL. The control cell count was 103x10*4 cells/mL. The cell count in the 1000 mg DAP/L solution was 13.3x10*4 cells/mL. This test solution was cloudy and contained particulate matter throughout the test, indicating that the test substance was not soluble at this concentration. - Reference substance (positive control):
- no
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 97.1 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element
- Remarks:
- phosphate
- Basis for effect:
- growth rate
- Remarks on result:
- other: No inhibition of algal growth observed in study
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 97.1 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element
- Remarks:
- phosphate
- Basis for effect:
- biomass
- Remarks on result:
- other: No inhibition of algal growth observed
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 97.1 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- other: element phosphate
- Basis for effect:
- growth rate
- Remarks on result:
- other: Toxicity
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 3.57 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element
- Remarks:
- phosphate
- Basis for effect:
- growth rate
- Remarks on result:
- other: Stimulation of algal growth
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 3.57 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element
- Remarks:
- phosphate
- Basis for effect:
- biomass
- Remarks on result:
- other: Stimulation of algal growth
- Details on results:
- no data
- Results with reference substance (positive control):
- no data
- Reported statistics and error estimates:
- Statistical analysis to determine EbC50 and ErC50 values was not performed due to the lack of inhibition of growth during the definitive test.
The NOEC was calculated using Dunnett’s test as performed by SAS. - Validity criteria fulfilled:
- yes
- Remarks:
- Growth factor control: 98
- Conclusions:
- NOEC (toxicity) = 97.1 mg DAP/L (no inhibition of algal growth observed in study) / NOEC (stimulation) = 3.57 mg DAP/L
No adverse inhibitory effects were observed. There was some growth stimulation at 6.25 mg/L and above. This was consistent with the known stimulatory effect of phosphate compounds. The reported NOEC reflects this stimulatory response and is not considered to be an adverse effect. - Endpoint:
- toxicity to aquatic algae and cyanobacteria
- 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
1. HYPOTHESIS FOR THE ANALOGUE APPROACH
In accordance with REACH Annex XI, Section 1.5, of Regulation (EC) No. 1907/2006 (REACH) the standard testing regime may be adapted in cases where a grouping or read-across approach has been applied.
The similarities may be based on:
(1) a common functional group
(2) the common precursors and/or the likelihood of common breakdown products via physical or biological processes, which result in structurally similar chemicals; or
(3) a constant pattern in the changing of the potency of the properties across the category
The proposed source chemical (diammonium hydrogenorthophosphate) is highly soluble in water (> 10000 mg/L). In aqueous media soluble inorganic orthophosphates will dissociate to their ionic constituents; in this case ammonium and orthophosphate ions. Diammonium dihydrogenpyrophosphate will dissociate to ammonium cations and pyrophosphate anions. The pyrophosphate anions are unstable in aqueous solutions with the degree of instability varying according to pH. In distilled water they will hydrolyse slowly via abiotic mechanisms to orthophosphate. In natural waters a number of different processes can occur; abiotic hydrolysis, biotic degradation (as a result of the action of phosphatases which cleave pyrophosphates into orthophosphate subunits) and assimilation by organisms in the water. Thus the target substance (diammonium dihydrogenpyrophosphate) and the source substance (diammonium hydrogenorthophosphate) will be primarily absorbed as the same inorganic ions: ammonium and orthophosphate and are expected to behave in a similar manner under test conditions.
All (bio) transformation products of the source chemical are common to the target chemical and as such the data is considered to be adequate and reliable for use in the assessment of diammonium dihydrogenpyrophosphate for the ecotoxicity hazard assessment.
2. SOURCE AND TARGET CHEMICAL(S) (INCLUDING INFORMATION ON PURITY AND IMPURITIES)
See read-across justification report attached.
3. ANALOGUE APPROACH JUSTIFICATION
See read-across justification report attached.
4. DATA MATRIX
See read-across justification report attached. - Reason / purpose for cross-reference:
- read-across source
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 97.1 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element
- Remarks:
- phosphate
- Basis for effect:
- growth rate
- Remarks on result:
- other: No inhibition of algal growth observed in study
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 97.1 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element
- Remarks:
- phosphate
- Basis for effect:
- biomass
- Remarks on result:
- other: No inhibition of algal growth observed
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 97.1 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- other: element phosphate
- Basis for effect:
- growth rate
- Remarks on result:
- other: Toxicity
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 3.57 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element
- Remarks:
- phosphate
- Basis for effect:
- growth rate
- Remarks on result:
- other: Stimulation of algal growth
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 3.57 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- element
- Remarks:
- phosphate
- Basis for effect:
- biomass
- Remarks on result:
- other: Stimulation of algal growth
- Details on results:
- no data
- Results with reference substance (positive control):
- no data
- Reported statistics and error estimates:
- Statistical analysis to determine EbC50 and ErC50 values was not performed due to the lack of inhibition of growth during the definitive test.
The NOEC was calculated using Dunnett’s test as performed by SAS. - Validity criteria fulfilled:
- yes
- Remarks:
- Growth factor control: 98
- Conclusions:
- NOEC (toxicity) = 97.1 mg DAP/L (no inhibition of algal growth observed in study) / NOEC (stimulation) = 3.57 mg DAP/L
No adverse inhibitory effects were observed. There was some growth stimulation at 6.25 mg/L and above. This was consistent with the known stimulatory effect of phosphate compounds. The reported NOEC reflects this stimulatory response and is not considered to be an adverse effect.
Referenceopen allclose all
none
none
Description of key information
One key study exists on an analogous substance. This study had been conducted in accordance with a recommended guideline (OECD 201, EU Method C.3) and under the conditions of GLP. As such, no further testing is considered necessary.
Key value for chemical safety assessment
- EC50 for freshwater algae:
- 97.1 mg/L
- EC10 or NOEC for freshwater algae:
- 97.1 mg/L
Additional information
NOEC (toxicity) = 97.1 mg DAP/L (no inhibition of algal growth observed in study) / NOEC (stimulation) = 3.57 mg DAP/L
No adverse inhibitory effects were observed. There was some growth stimulation at 6.25 mg/L and above. This was consistent with the known stimulatory effect of phosphate compounds. The reported NOEC reflects this stimulatory response and is not considered to be an adverse effect.
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.