Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
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
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 213-030-6 | CAS number: 917-61-3
- 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
Description of key information
The substance sodium cyanate revealed only minimal skin irritating effects in rabbits (edema score 0.22, erythema score 0).
The substance Sodium cyanate revealed only very weak irritating effects to rabbit´s eye (cornea score 0.22, iris score 0.22, conjunctivae score 1.11, chemosis score 0) wich were reversible within at least 3 days.
Based on experience in handling and use sodium cyanate is not irritating to the respiratory system.
Key value for chemical safety assessment
Skin irritation / corrosion
Link to relevant study records
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1984-08-15 to 1984-08-29
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study
- Qualifier:
- according to guideline
- Guideline:
- other: see references below
- Deviations:
- not applicable
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
- Deviations:
- not applicable
- Principles of method if other than guideline:
- Test is perfomed according to the following references:
-Draize, J. H.; Woodward, G.; Calvery, H. O. : j. Pharmacol. Exp. Therap., 82, 377 -390, 1944
- Draize, J.H.: Appraisal of the safety of chemicals in foods, drugs and cosmetics, 46 -59, Assoc. of Food and drug officials of the united states, Topeka, Kansas, 1965
- OECD Guedline for testing of chemicals, OECD, ISBN-92 - 64 - 12221 -4, 1981 - GLP compliance:
- no
- Species:
- rabbit
- Strain:
- other: white Russian
- Details on test animals or test system and environmental conditions:
- body weight: 2.0 - 2.5 kg
age: 6-8 months - Type of coverage:
- occlusive
- Preparation of test site:
- shaved
- Vehicle:
- water
- Controls:
- no
- Amount / concentration applied:
- 500 mg of the test item was moistened with 0.15 mL water.
- Duration of treatment / exposure:
- The duration of exposure was 4 hours. The duration of treatment was 1, 24, 48 and 72 hours after application.
- Observation period:
- Observation period was 21 days after the application.
- Number of animals:
- 3
- Details on study design:
- NA
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0.66
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 h
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0.22
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 h
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritant / corrosive response data:
- NA
- Other effects:
- No other effects.
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The substance sodium cyanate revealed only minimal skin irritating effects in rabbits (edema score 0.22, erythema score 0).
- Executive summary:
In a primary dermal irritation study 6-8 months old White Russian rabbits (3 animals, sex not specified) were dermally exposed to 0.5 g of sodium cyanate (98 %) moistened in 0.15 mL water for 4 hours. Animals then were observed for 14 days. Irritation was scored by the method of Draize. The substance sodium cyanate revealed only minimal skin irritating effects in rabbits (mean edema score 0.22 - one of three animals score 0.66 , mean erythema score 0). Effects were reversible within 72 h. In this study, sodium cyanate is not a dermal irritant.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Eye irritation
Link to relevant study records
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1984-09-04 to 1984-09-25
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- non-GLP study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Version / remarks:
- OECD 1981
- Deviations:
- no
- Principles of method if other than guideline:
- NA
- GLP compliance:
- not specified
- Species:
- rabbit
- Strain:
- other: white Russian
- Details on test animals or tissues and environmental conditions:
- body weight: 2.4 - 2.75 kg
age: 6-7 months - Vehicle:
- unchanged (no vehicle)
- Controls:
- other: the untreated left eye served as negative control.
- Amount / concentration applied:
- 0.1 g test item was applied once in rabbit´s eye.
- Duration of treatment / exposure:
- The subsatnce was applied one to the rabbit's eye (without washing).
- Observation period (in vivo):
- Examinations: 1, 24, 48 and 72 hours after application and thereafter once per day.
The observation period was 21 days after application. - Number of animals or in vitro replicates:
- 3 ( female)
- Details on study design:
- NA
- Irritation parameter:
- cornea opacity score
- Remarks:
- (opacity)
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- cornea opacity score
- Remarks:
- (opacity)
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- cornea opacity score
- Remarks:
- (opacity)
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- cornea opacity score
- Remarks:
- (opacity)
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0.22
- Max. score:
- 4
- Irritation parameter:
- cornea opacity score
- Remarks:
- (extent of opacity area)
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.67
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 hours
- Irritation parameter:
- cornea opacity score
- Remarks:
- (extent of opacity area)
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0.67
- Max. score:
- 2
- Reversibility:
- fully reversible within: 24 h
- Irritation parameter:
- cornea opacity score
- Remarks:
- (extent of opacity area)
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- cornea opacity score
- Remarks:
- (extent of opacity area)
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0.44
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- iris score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 2
- Reversibility:
- fully reversible within: 48 hours
- Irritation parameter:
- iris score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 2
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- iris score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0.22
- Max. score:
- 2
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- conjunctivae score
- Remarks:
- (redness)
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 1.33
- Max. score:
- 3
- Reversibility:
- fully reversible within: 3 days
- Irritation parameter:
- conjunctivae score
- Remarks:
- (redness)
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 1.33
- Max. score:
- 3
- Reversibility:
- fully reversible within: 3 days
- Irritation parameter:
- conjunctivae score
- Remarks:
- (redness)
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0.67
- Max. score:
- 3
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- conjunctivae score
- Remarks:
- (redness)
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 1.11
- Max. score:
- 3
- Reversibility:
- fully reversible within: 3 days
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- chemosis score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- chemosis score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritant / corrosive response data:
- Not indicated.
- Other effects:
- No other effects.
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The substance Sodium cyanate revealed only very weak irritating effects to rabbit´s eye (mean 24/48/72 h scores: cornea score 0.22, iris score 0.22, conjunctivae score 1.11, chemosis score 0) wich were reversible within at least 3 days.
- Executive summary:
In a primary eye irritation study, 0.1 g of sodium cyanate (98 %) was instilled into the conjunctival sac of the right eye of 6-7 months old White Russian rabbits (3 females) for 72 h hours. Animals then were observed for 21 days. Irritation was scored by the method of Draize. The substance Sodium cyanate revealed only very weak irritating effects to rabbit´s eye (mean 24/48/72 h scores: cornea score 0.22, iris score 0.22, conjunctivae score 1.11, chemosis score 0) which were reversible within at least 3 days. None of the individual animals showed a mean score over 24/48/72 h treatment higher than the threshold values given in 67/548/EEC and Regulation (EC) No 1272/2008.
Reference
Additional results:
irriation parameter Basis Time point results Max. scroce Reversibility
conjunctivae score (secretion) animal #1 24/48/72 h 0.33 3 fully reversible within: 48 hours
conjunctivae score (secretion) animal #2 24/48/72 h 0 3
conjunctivae score (secretion) animal #3 24/48/72 h 0 3
conjunctivae score (secretion) mean 24/48/72 h 0.11 3 fully reversible within: 48 hours
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Additional information
Skin:
Key study:
In a primary dermal irritation study 6-8 months old White Russian rabbits (3 animals, sex not specified) were dermally exposed to 0.5 g of sodium cyanate (98 %) moistened in 0.15 mL water for 4 hours. Animals then were observed for 14 days. Irritation was scored by the method of Draize. The substance sodium cyanate revealed only minimal skin irritating effects in rabbits (mean edema score 0.22 - one of three animals score 0.66 , mean erythema score 0). Effects were reversible within 72 h. In this study, sodium cyanate is not a dermal irritant.
Supporting study:
In a primary dermal irritation study, 4-5 month old White Russian rabbits (3 animals, sex not specified) were dermally exposed to 0.5 g of sodium cyanate (90 %) moistened with 0.3 mL water for 4 hours. Animals then were observed for 14 days. Irritation was scored by the method of Draize.
Sodium cyanate showed no skin irritating effects (edema and erythema scores 0) In this study, sodium cyanate is not a dermal irritant.
Eye:
Key study:
This study was chosen as key study, as it was conducted with the purest sodium cyanate preparation available (98 %, instead of 90 %).
In a primary eye irritation study, 0.1 g of sodium cyanate (98 %) was instilled into the conjunctival sac of the right eye of 6-7 months old White Russian rabbits (3 females) for 72 h hours. Animals then were observed for 21 days. Irritation was scored by the method of Draize. The substance Sodium cyanate revealed only very weak irritating effects to rabbit´s eye (mean 24/48/72 h scores: cornea score 0.22, iris score 0.22, conjunctivae score 1.11, chemosis score 0) which were reversible within at least 3 days. None of the individual animals showed a mean score over 24/48/72 h treatment higher than the threshold values given in 67/548/EEC and Regulation (EC) No 1272/2008.
Supporting study:
In a primary eye irritation study, 0.1 g of sodium cyanate (90 %) was instilled into the conjunctival sac of the right eye of 5 months old White Russian rabbits (3 females) for 72 h hours. Animals then were observed for 21 days. Irritation was scored by the method of Draize. The substance Sodium cyanate revealed slightly irritating effects to rabbit´s eye (mean 24/48/72 h socres: cornea score 0.11, iris score 0.33, conjunctivae score 1.89, chemosis score 0.44) wich were reversible within at least 7 days. Two out of 3 animals showed a conjunctivae score of >= 2. In this study sodium cyanate with up to 10% sodium carbonate is an eye irritant according to 67/548/EEC and Regulation (EC) No 1272/2008.
Justification for selection of skin
irritation / corrosion endpoint:
Most reliable study was chosen.
Justification for selection of eye irritation endpoint:
Most reliable study was chosen.
Justification for classification or non-classification
The classification and labelling was made based on the results of the key studies (98% product).
Skin and eye irritation:
Based on the available experimental data, the test item is not considered to be classified for skin irritation or eye irritation under Regulation (EC) No 1272/2008, as amended for the tenth time in Regulation (EU) No 2017/776.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.