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EC number: 286-344-4 | CAS number: 85209-91-2
- 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
Skin irritation/corrosion: EPA OPP 81-5 (Acute Dermal Irritation)
Rabbit, 4h semiocclusive treatment of clipped intact skin with 0,5 g NA-11 moistened with 0,9% saline: no effects observed.
Eye irritation: EPA OPP 81-4 (Acute Eye Irritation)
0.03 g NA-11 instilled in rabbit eyes (6 animals), eyes kept unwashed. Observation time points: 1, 24, 48, 72 h after instillation. Slight irritation after application disappeared within 72 hours.
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
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Well documented and reported study fully adequate for assessment. The study was conducted according to internationally accepted technical guidelines and in compliance with GLP in a recognized contract research organization.
- Qualifier:
- according to guideline
- Guideline:
- EPA OPP 81-5 (Acute Dermal Irritation)
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- Adult albino rabbits, Hra:(NZW)SPF
- Source:Hazleton Research Products, Inc., Denver PA
- Weight at study initiation: 2032 - 2116 g
- Housing: individually in screen-bottom cages,
- husbandry and housing: addording to "Guide for the Care and Use of Laboratory Animals" (NIH Publication No. 86-23 (revised 1985)).
- Diet (e.g. ad libitum): measured, High Fiber Rabbit Chow® 5326, Purina Mills, Inc.
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 7 days
- Temperature (°C): 18.9-23.3
- Humidity (%):48 to 55 - Type of coverage:
- semiocclusive
- Preparation of test site:
- clipped
- Vehicle:
- physiological saline
- Controls:
- no
- Amount / concentration applied:
- - Amount(s) applied (volume or weight with unit): 0,5 g test material (moistened with 0,9% saline)
VEHICLE
- Concentration (if solution): 0,9% saline - Duration of treatment / exposure:
- 4 hours
- Observation period:
- 30 minutes = 4 hours; 24, 48, and 72 hours after patch removal
- Number of animals:
- 6 (3 male, 3 female)
- Details on study design:
- TEST SITE
- Area of exposure: 2,5 cm x 2,5 cm
- Type of wrap if used: gauze patch secured with paper tape, loosely overwrapped with Saran Wrap® and secured with Elastoplast® tape to provide a
semiocclusive dressing
REMOVAL OF TEST SUBSTANCE
- Washing (if done): lukewarm water
- Time after start of exposure: 4 h
SCORING SYSTEM:according to the Draize technique (Draize, J.H. 1975) - Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- over 6 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- over 6 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritant / corrosive response data:
- no erythema, no edema observed
- Interpretation of results:
- other: not 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
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Well documented and reported study fully adequate for assessment. The study was conducted according to an internationally accepted technical guideline and in compliance with GLP in a recognized contract research organization.
- Qualifier:
- according to guideline
- Guideline:
- EPA OPP 81-4 (Acute Eye Irritation)
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Species, Strain: albino rabbits, Hra:(NZW)SPF
- Source: Hazleton Research Products, Inc., Denver PA
- Weight prior to dosing (Day 1): 2006 - 2224 g
- Husbandry and housing: individually in screen-bottom cages; according to standards outlined in the "Guide for the Care and Use of Laboratory" (NIH Publication.86-23 (revised 1985)).
- Diet (ad libitum): measured amount of High Fiber Rabbit Chow® 5326, Purina Mills, Inc.,
- Water(ad libitum): ad libitum
- Acclimation period: 7 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 18.9 - 23.3
- Humidity (%): 48 - 70
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.1-ml dose, 0.03 g - Duration of treatment / exposure:
- Eyes kept unwashed.
- Observation period (in vivo):
- observations: 1, 24, 48, and 72 hours after treatment
- Number of animals or in vitro replicates:
- 3 male, 3 female rabbits
- Details on study design:
- SCORING SYSTEM: Irritation was graded and scored according to the Draize technique.
TOOL USED TO ASSESS SCORE: At the 72-hour reading, sodium fluorescein was used to aid in revealing possible corneal injury. - Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Remarks:
- over 6 animals and 4 time points
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 320
- Irritation parameter:
- iris score
- Basis:
- mean
- Remarks:
- over 6 animals
- Time point:
- 24 h
- Score:
- 1.7
- Max. score:
- 10
- Reversibility:
- fully reversible within: 48-72 h
- Remarks on result:
- other: 3 of 6 animals concerned
- Irritation parameter:
- iris score
- Basis:
- mean
- Remarks:
- over 6 animals
- Time point:
- 48 h
- Score:
- 0.8
- Max. score:
- 10
- Reversibility:
- fully reversible within: 72 h
- Remarks on result:
- other: 3 of 6 animals concerned
- Irritation parameter:
- iris score
- Basis:
- mean
- Remarks:
- over 6 animals
- Time point:
- 72 h
- Score:
- 0
- Max. score:
- 10
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Remarks:
- over 6 animals
- Time point:
- 24 h
- Score:
- 6.7
- Max. score:
- 20
- Reversibility:
- fully reversible within: 72 h
- Remarks on result:
- other: 2 animals: symptom "discharge" resolved
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Remarks:
- over 6 animals
- Time point:
- 48 h
- Score:
- 6
- Max. score:
- 20
- Reversibility:
- fully reversible within: 72 h
- Remarks on result:
- other: redness of conjunctivae remained in all animals, chemosis only in 1 animal
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Remarks:
- over 6 animals
- Time point:
- 72 h
- Score:
- 0
- Max. score:
- 20
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Remarks:
- over 6 animals
- Time point:
- 24 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- fully reversible within: 24 h
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Remarks:
- over 6 animals
- Time point:
- 48 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Remarks:
- over 6 animals
- Time point:
- 72 h
- Score:
- 0
- Max. score:
- 4
- Irritant / corrosive response data:
- The test material produced iridal involvement and moderate conjunctival irritation when instilled into the eyes of six albino rabbits.
All ocular irritation cleared within 72 hours after instillation of the test material. - Interpretation of results:
- other: not irritating
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Justification for classification or non-classification
In view of absence of any effects on clipped intact skin treated for 4 hours with NA-11 classification regarding skin irritation or corrosion according to EU classification rules [REGULATION (EC) 1272/2008] is not necessary.
The reversible mild irritation of neat NA-11 in rabbit eye does not necessitate classification for eye irritation [REGULATION (EC) 1272/2008].
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