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EC number: 820-225-5 | CAS number: 101747-77-7
- 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
Basic toxicokinetics
Administrative data
- Endpoint:
- basic toxicokinetics in vivo
- Type of information:
- other: expert statement
- Adequacy of study:
- key study
- Study period:
- 2018
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: An extensive assessment of the toxicokinetic behaviour of the registered substance was performed, taking into account the chemical structure, the available physico-chemical and toxicological data.
Data source
Reference
- Reference Type:
- other: expert statement
- Title:
- Toxicokinetic Statement for Phosphorodithioic acid, mixed O,O- bis(iso-Bu and iso-Pr and pentyl) esters, zinc salts (CAS 101747-77-7)
- Author:
- Chemservice GmbH
- Year:
- 2 018
- Report date:
- 2018
Materials and methods
- Objective of study:
- absorption
- distribution
- excretion
- metabolism
- toxicokinetics
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- An extensive assessment of the toxicokinetic behaviour of the registered substance was performed, taking into account the chemical structure, the available physico-chemical and toxicological data.
- GLP compliance:
- no
Test material
- Reference substance name:
- Zinc, O,O-mixed (iso-Bu), (iso-Pr), (pentyl) phosphorodithioate
- EC Number:
- 820-225-5
- Cas Number:
- 101747-77-7
- Molecular formula:
- C12-20H28-44O4P2S4Zn
- IUPAC Name:
- Zinc, O,O-mixed (iso-Bu), (iso-Pr), (pentyl) phosphorodithioate
- Test material form:
- liquid
Constituent 1
Administration / exposure
- Route of administration:
- other: all relevant routes of administration are discussed in the expert statement
Results and discussion
Main ADME resultsopen allclose all
- Type:
- absorption
- Results:
- The absorption rate of the substance is assumed to be 100 % via the oral, dermal and inhalation route
- Type:
- distribution
- Results:
- The substance is not expected to be distributed widely throughout the body.
- Type:
- metabolism
- Results:
- Transport between cells through cell membranes might be possible.
- Type:
- excretion
- Results:
- The substance is expected to be mainly excreted via the bile since it is amphipathic (containing both polar and nonpolar regions) and has a high molecular weight.
Applicant's summary and conclusion
- Executive summary:
The absorption rate of the substance is assumed to be 100 % via the oral, dermal and inhalation route. The substance is not expected to be distributed widely throughout the body. Transport between cells through cell membranes might be possible. The substance is expected to be mainly excreted via the bile since it is amphipathic (containing both polar and nonpolar regions) and has a high molecular weight. For more details please refer to attached expert statement in section 13.
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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