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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
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EC number: 910-404-7 | CAS number: -
- 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
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Short description of an in-vivo study performed similar to the OECD guideline. However several information details are missing in this summary.
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 974
- Report date:
- 1974
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- as only a summary report is available several information details were not given, e.g. controls, detailed application description, information on washing, individual results.
- GLP compliance:
- no
Test material
- Reference substance name:
- Sodium hydrogensulphide
- EC Number:
- 240-778-0
- EC Name:
- Sodium hydrogensulphide
- Cas Number:
- 16721-80-5
- Molecular formula:
- HNaS
- IUPAC Name:
- sodium hydrogensulphide
- Reference substance name:
- sodium hydrogensulfide
- IUPAC Name:
- sodium hydrogensulfide
- Reference substance name:
- sodium sulfhydrate
- IUPAC Name:
- sodium sulfhydrate
- Details on test material:
- - Name of test material (as cited in study report): Sulfhydrat F150, Natriumsulfhydratlauge
- Molecular formula (if other than submission substance): NaHS (aqueous solution)
- Molecular weight (if other than submission substance): 56.06 g/mol
- Substance type: technical product
- Physical state: yellow liquid
- Storage condition of test material: In tightly closed original container, in a cool, well-ventilated place; protect from sunlight; do not store with acids; do not store together with oxidizing agents
- Other: pH value: 12 - 13
Constituent 1
Constituent 2
Constituent 3
Test animals / tissue source
- Species:
- rabbit
- Strain:
- Himalayan
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS-albino
- Housing: in single cages
- Diet: mixed diet ERKA 8300 (Futtermittelwerke Robert Koch oHG/Hamm, Germany), ad libitum
- Water: tap water, ad libitum
Test system
- Vehicle:
- physiological saline
- Controls:
- not specified
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.1 mL
- Concentration (if solution): undiluted Sulfhydrat solution (ca. 31-32% NaHS), 10 % Sulfhydrat solution, 5 % Sulfhydrat solution, and 1 % Sulfhydrat solution - Duration of treatment / exposure:
- single treatment
- Observation period (in vivo):
- 144 hours
- Number of animals or in vitro replicates:
- 6
- Details on study design:
- - the test substance was placed in the conjunctival sac
- eyes were examined at 1, 3, 7, 24, 48, 72 and 144 hours after test substance application
-for the 24 hours examination, the eyes were further examined with the aid of fluorescein
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- other: no data
- Remarks on result:
- other: After 6 days the observation was stopped. The effect of the undiluted Sulfhydrat solution (31-32 % NaHS) was not reversible at this time. Even if the observation period should be up to 21 days this result is interpreted as a corrosive effect.
- Remarks on result:
- other: Short description of an in-vivo study performed similar to the OECD guideline. However several information details are missing in this summary.
- Irritant / corrosive response data:
- - the undiluted sample resulted in general to deep red colouring and an obvious lacteal swelling of the conjunctivae for 144 hours; furthermore a mild to severe opaque cornea was observed
- the 10 % solution resulted in a mild general red colouring of the conjunctivae for a little bit longer than 24 hours; in addition two rabbits showed a very mild redness of the conjuntivae for about three hours
- the 5 % solution resulted in a very mild redness of conjunctivae in 3 rabbits for approximately 3 hours
- the 1 % solution resulted in no irritating or corrosive effects
Any other information on results incl. tables
The authors considered the undiluted product as strongly irritant and the 5% and 10 % solutions as very slight to mildly irritant to eyes.
Applicant's summary and conclusion
- Interpretation of results:
- Category 1 (irreversible effects on the eye)
- Remarks:
- Migrated information Criteria used for interpretation of results: expert judgment
- Conclusions:
- After 6 days the observation was stopped. The effect of the undiluted Sulfhydrat solution (31-32 % NaHS) was not reversible at this time. Even if the observation period should be up to 21 days this result is interpreted as a corrosive effect. The 1 % solution can be judged as not corrosive and not irritant.
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