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EC number: 248-322-2 | CAS number: 27205-99-8
- 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
Endpoint summary
Administrative data
Link to relevant study record(s)
Description of key information
Key value for chemical safety assessment
- Bioaccumulation potential:
- no bioaccumulation potential
- Absorption rate - oral (%):
- 0
- Absorption rate - dermal (%):
- 0
- Absorption rate - inhalation (%):
- 0
Additional information
Toxicokinetic analysis of Sodium O, O-diisopropyldithiophosphate (IPP1-Na)
Summary
No toxicokinetic study for IPP1-Na itself is available. However the toxicokinetic behaviour can be predicted based on the available physico-chemical data and studies/information from structural similar substances also containing dialkyldithiophosphate moieties.
Based on physicochemical characteristics, particularly water solubility, octanol-water partition coefficient, and vapour pressure, no or only limited absorption by the dermal and inhalation routes is expected for the salt IPP1-Na. For the oral route, uptake will strongly depend on the pH value and is more likely for the acidic pH environment of the stomach at which the un- dissociated free acid is present. Even for the oral route limited absorption is expected, as the predominant effects in acute or repeated dose toxicity tests are disturbances of the gastro-intestinal tract due to the corrosive properties of the substances causing local tissue damage at high doses. Based on data from similar dialkyldithioester structures, the following metabolites after ester cleavage and/or oxidative desulfurization (conversion of thio to oxo) can be expected if the substance is not excreted unchanged: dithiophosphate, thiophosphate and phosphate, monoesters (with two, one or no thio being present), as well as the respective alcohol (isopropanol). For the substance itself as well as for the potential metabolites a fast distribution and excretion (mainly via urine) is expected. Based on the physico-chemical properties neither for IPP1-Na nor for its even more polar and high water soluble cleavage products bioaccumulation is expected. Respective experimental data for isopropanol also show that this metabolite is not expected to be bioaccumulative.
Physico-chemical characteristics
IPP1-Na is a white crystalline salt at room temperature with a molecular weight of 236 g/mol. The substance is highly soluble in water (>1000 g/l). The logPOWof the free acid IPP1 was measured and determined to be 0.6 at 22°C and pH 1. A 50% solution of the salt (IPP1-Na) has a pH of 13.8 due to the necessary excess of NaOH. IPP1-Na as expected for a salt has a very low vapour pressure of approximately 1.4x10-6Pa. The substance is expected to be stable in water at different pH values and not being surface active [1].
Absorption
Based on the low logPOWof 0.6 for the free acid at pH 1 (an even lower value can be expected for the salt) and the very high water solubility, no or only limited absorption by the dermal route is expected for the hydrophilic salt IPP1-Na, as long as the skin barrier is not compromised due to the corrosive properties of the substance.
Due to the very low vapour pressure (calculated a 1.4x10-6Pa) and the above described physico-chemical properties also no to very limited absorption is expected for the inhalation route.
Generally, oral absorption is favoured for molecular weights below 500 g/mol. However, the oral route, uptake will strongly depend on the pH value and is more likely for the acidic pH environment of the stomach at which the undissociated free acid is present. Even for the oral route limited absorption is expected, as the predominant effects in acute or repeated dose toxicity tests are disturbances of the gastro-intestinal tract due to the corrosive properties of the substances causing local tissue damage.
Distribution
Assuming that IPP1-Na is absorbed into the body following oral intake, it will be as such or potential bound to proteins well distributed extracellular with the body fluids due to its polarity and high water solubility. This also applies for potential hydrolysis products as monoalkyl esters, dithiophosphate, thiophosphate and phosphate (see metabolism). For isopropanol studies after inhalative or oral exposure also show a fast distribution [2,9]. Due its high polarity and ionic-character crossing membranes will be difficult but IPP1-Na may enter cells via direct transport through aqueous pores. Based on the results observed in reproduction and developmental studies (lack of any developmental/ reproductive toxicity) with a very similar structure analogue [1] indicate that the substance is not likely to cross the placenta. Based on its low logPOWvalue neither IPP1-Na nor the free acid (IPP1) are considered to get enriched in fatty tissues or being bioaccumulative (see also metabolism and excretion).
Metabolism
Based on data from similar dialkyldithiophosphate-ester structures (dithioorganophosphate insecticides), the following metabolites after enzyme-mediated ester cleavage and/or oxidative desulfurization (conversion of thio to oxo) can be expected if the substance is not excreted unchanged: dithiophosphate, thiophosphate and phosphate, monoesters (with two, one or no thio being present), as well as the respective alcohol isopropanol. For the inorganic salts, no further degradation is expected [3,4,5,6,7,8]. The metabolism of isopropanol is well investigated. Isopropanol is very fast metabolized by alcohol dehydrogenase to acetone (predominant metabolite) In addition, acetol and methylglyoxal, propylene glycol, acetate, and formiate are reported with conversion of these metabolites to glucose and other products of the intermediary metabolism [2,9].
Excretion
For the substance itself as well as for the potential inorganic metabolites a fast distribution and excretion (mainly via urine) is expected. Based on the physico-chemical properties of IPP1-Na and its even more polar and high water soluble cleavage products bioaccumulation is highly unlikely. Respective experimental data for the alcohol also show that this metabolite is quickly excreted (via exhaled air as such or acetone or via urine [2,9]) and is not expected to be bioaccumulative.
References
[1] IULICD CAS 27205-99-8
[2] IUCLID CAS 67-63-3
[3] Forth W., Henschler D., Rummel W.(Hrsg): Allgeimeine und spezielle Pharmakoligie und Toxikologie.Bibliographisches Institut, 1983.
[4] Metabolism of Chlorpyrofos, US EPA, 2008
http://npic.orst.edu/factsheets/archive/chlorptech.html
[5] Laveglia J,Dahm PA. Degradation of organophosphorus and carbamate insecticides in the soil and by soil microorganisms.Annu Rev Entomol.1977;22:483-513.
[6] Malathion Pathway Map,http://eawag-bbd.ethz.ch/mal/mal_map.html
[7] Franca M. Buratti,Alessandra D'Aniello,Maria Teresa Volpe,Annarita MeneguzandEmanuela Testai:Malathion bioactiviation in the human liver: the contribution of different cytochrome P450 isoforms.Drug Metabolism and Disposition March 2005, 33 (3) 295-30
[8] El-Oshar, M. A. and Dauterman, W. C. (1979), In-vitro metabolism ofO,O-diethylS-(N-methylcarbamoylmethyl) phosphorodithioate by mouse liver. Pestic. Sci., 10: 14–18.
[9] Slaughter RJ,Mason RW,Beasley DM,Vale JA,Schep LJ.: Isopropanol poisoning.Clin Toxicol (Phila).2014 Jun 52(5):470-8
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