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EC number: 200-543-5 | CAS number: 62-56-6
- 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:
- experimental study
- Adequacy of study:
- key study
- Study period:
- no data
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- Überprüfung der Durchführbarkeit von Prüfungsvorschriften und der Aussagekraft der Grundprüfung des E.Chem.G. - Schleimhautverträglichkeit (OECD-Richtlinie)
- Author:
- Korte, F.; Greim, H.
- Year:
- 1 981
- Bibliographic source:
- Umweltbundesamt (UBA-FB 82-019) Forschungsbericht 107 04 006/01
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Qualifier:
- according to guideline
- Guideline:
- other: Entwurf der Prüfungsvorschrift der OECD "Short term toxicology group, Acute eye irritation/corrosivity" vom 31.12.1979
- GLP compliance:
- no
Test material
- Reference substance name:
- Thiourea
- EC Number:
- 200-543-5
- EC Name:
- Thiourea
- Cas Number:
- 62-56-6
- Molecular formula:
- CH4N2S
- IUPAC Name:
- thiourea
- Test material form:
- solid: particulate/powder
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- Himalayan
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: own breed
- Age at study initiation: no data
- Weight at study initiation: 2.5 to 2.8 kg
- Housing: individually
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: no data
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20°C +/- 3°C
- Humidity (%): 60% +/- 5%
- Air changes (per hr): no data
- Photoperiod (hrs dark / hrs light): 12/12
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: the right eye of the animals served as control
- Amount / concentration applied:
- TEST MATERIAL
- Amount applied: 100 mg or 0.1 mL (1 g equates to 1.5 mL)
- Concentration: n.a.
VEHICLE
- Amount applied: no vehicle
- Concentration: n.a.
- Lot/batch no.: n.a.
- Purity: n.a. - Duration of treatment / exposure:
- The substance is put into the left eye and kept close for 1 second. The substance was not washed out the eye. The exposure was throughout the observation period.
- Observation period (in vivo):
- An observation of the animals was done immediatetly after the application and 1, 24, and 72 hours after apllication of the test substance.
- Number of animals or in vitro replicates:
- 6 male Himalayan rabbits
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Time after start of exposure: n.a.
SCORING SYSTEM: The scoring was done after Draize et al. 1944
TOOL USED TO ASSESS SCORE: fluorescein
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- not specified
- Remarks on result:
- other: There were no individual animal data available.
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- not specified
- Remarks on result:
- other: There were no individual animal data available.
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- not specified
- Remarks on result:
- other: There were no individual animal data available.
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- not specified
- Remarks on result:
- not measured/tested
- Other effects:
- No other effects were reported.
Any other information on results incl. tables
No effects were reported after examination of the eyes following the fluorescein treatment.
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- In this study Thiourea is not considered to be irritation to the eye.
- Executive summary:
In a primary eye irritation study similar to the OECD guideline 405, 100 mg Thiourea were instilled undiluted without any vehicle into the conjunctival sac of the left eye of 6 male Himalayan rabbits. The eye lids were kept close for 1 second and the application lasted during the whole observation period for 72 hours as the eyes were not washed after application. Animals were observed immediately after application, and 1, 24 and 72 hours after the treatment. Irritation was scored according to Draize et al. (1944). Fluorescein was used to assess the score. The right eye in which 0.1 ml isotonic NaCl were instilled served as control.
A deficiency of the study is that there is no detailled documentation of individual animal data. Due to the fact that thiourea is not considered to be irritating in this eye irritation test and the detailled description of the procedure of the test this fact can be neglected.
The scores were reported as mean. Thiourea is reported to be not irritating to the eye. Nevertheless a with respect to the conjunctiva an irritation score of 1-2 has been reported for swelling and redness.
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