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Diss Factsheets
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EC number: 611-431-4 | CAS number: 569316-81-0
- 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, other
- Type of information:
- other: Expert review and assessment
- Adequacy of study:
- key study
- Reliability:
- other: Not assignable as result is from expert assessment
- Rationale for reliability incl. deficiencies:
- other: Not assignable as result is from expert assessment
Data source
Materials and methods
- Objective of study:
- toxicokinetics
- Principles of method if other than guideline:
- Assessment of toxicokinetic behaviour of the substance derived from available data as required by REACH Annex VIII section 8.8
Test material
- Reference substance name:
- 3-((3,4-dicyanophenyl)sulfonyl)-N-(2-hydroxypropyl)propane-1-sulfonamide
- EC Number:
- 611-431-4
- Cas Number:
- 569316-81-0
- Molecular formula:
- C14H17N3O5S2
- IUPAC Name:
- 3-((3,4-dicyanophenyl)sulfonyl)-N-(2-hydroxypropyl)propane-1-sulfonamide
- Test material form:
- solid
Constituent 1
Results and discussion
Applicant's summary and conclusion
- Conclusions:
- An assessment of the potential absorption of the susbtance, based on its physico-chemical properties, suggest that absorption across the gastrointestinal mucosa is likely to be slow and part of an oral dose may be excreted in the faeces. It is possible that a proportion of the substance may be systemically absorbed following oral administration.
The susbtance is likely to be subject to metabolism via a hydroxy group on its structure and this will also aid excretion via the kidneys. Although it is possible that the substance may be systemically absorbed, there is no expectation that it will preferentially distribute to particular organs or tissues in the body. - Executive summary:
INTRODUCTION
An expert assessmentof the toxicokinetic behaviour of the test substance was undertaken using data derived from an Annex VIII testing regime.
CONCLUSION
An assessment of the potential absorption of the susbstance, based on its physico-chemical properties, suggest that absorption across the gastrointestinal mucosa is likely to be slow and part of an oral dose may be excreted in the faeces. It is possible that a proportion of the substance may be systemically absorbed following oral administration. The substance is likely to be subject to metabolism via a hydroxy group on its structure and this will also aid excretion via the kidneys. Although it is possible that the substance may be systemically absorbed, there is no expectation that it will preferentially distribute to particular organs or tissues in the body.
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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