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EC number: 208-796-3 | CAS number: 542-02-9
- 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:
- 1989-11-06 till 1989-11-20
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Reliable without restrictions; Guideline study (OECD 405) according to GLP
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 990
- Report date:
- 1990
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- GLP compliance:
- yes
Test material
- Reference substance name:
- 2,4-Diamino-6-methyl-1,3,5-triazine
- IUPAC Name:
- 2,4-Diamino-6-methyl-1,3,5-triazine
- Reference substance name:
- 6-methyl-1,3,5-triazine-2,4-diyldiamine
- EC Number:
- 208-796-3
- EC Name:
- 6-methyl-1,3,5-triazine-2,4-diyldiamine
- Cas Number:
- 542-02-9
- Molecular formula:
- C4H7N5
- IUPAC Name:
- 6-methyl-1,3,5-triazine-2,4-diamine
- Details on test material:
- - Name of test matereial (as cited in study report): Acetoguanamine
- Lot/batch No.: 10/08/89 AG
- Purity: 99.2 %
Constituent 1
Constituent 2
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Froxfield Farms (U.K.) Ltd., Petersfield, Hampshire, England.
- Age at study initiation: 12 to 13 weeks of age
- Weight at study initiation: 2.8 to 3.0 kg
- Housing: individually housed in metal cages with perforated floors
- Diet (e.g. ad libitum): free access to SDS Standard Rabbit Diet
- Water (e.g. ad libitum): free access to tap water
- Acclimation period: yes, but no period of time mentioned
ENVIRONMENTAL CONDITIONS
- Temperature (°C): approx. 19 °C
- Humidity (%): 30-70 %
- Air changes (per hr): 19 air changes per hour
- Photoperiod (hrs dark / hrs light): lightning was controlled to give 12 hours of artificial light (0700-1900 hours) in each 24 hour period.
Test system
- Vehicle:
- not specified
- Controls:
- not required
- Amount / concentration applied:
- Approx. 85 mg of Acetoguanamine, the weight occupying a volume of 0.1 ml.
- Duration of treatment / exposure:
- Acetoguanamine was placed into the lower everted lid of one eye of each animal. The eyelids were then gently held together for one second before releasing. The contralateral eye remained untreated and served as a control.
- Observation period (in vivo):
- Examination of the eyes was made after 1 hour and 1, 2, 3, 4 and 7 days after instillation.
- Number of animals or in vitro replicates:
- three
Results and discussion
In vivo
- Other effects:
- The numerical scores awarded to the ocular reactions elicited by Acetoguanamine, are given in Table 1.
A corneal opacity developed in one animal 24 h after instillation and was still visible 4 d following instillation. The opacity had resolved 7 days after instillation.
No iridial inflammation was seen throughtout oberservation period.
A diffuse crimson-red colouration of the conjunctivae was observed, 1 h after instillation only, in all three animals.
All conjuctival reactions had resolved 24 or 48 h after instillation.
Any other information on results incl. tables
TABLE 1: Ocular reactions elicited by Acetoguanamine.
Rabbit Number and Sex |
Bodyweight (Day 1) |
Region of Eye |
One hour |
Day after instillation |
||||||
1 |
2 |
3 |
4 |
7 |
||||||
812 female |
2980 g |
Corea |
Density |
0 |
0 |
0 |
0 |
0 |
0 |
|
Area |
0 |
0 |
0 |
0 |
0 |
0 |
||||
Iris |
0 |
0 |
0 |
0 |
0 |
0 |
||||
Conjunctivae |
Redness |
2 |
0 |
0 |
0 |
0 |
0 |
|||
Chemosis |
1 |
0 |
0 |
0 |
0 |
0 |
||||
838 female |
2870 g |
Corea |
Density |
0 |
0 |
0 |
0 |
0 |
0 |
|
Area |
0 |
0 |
0 |
0 |
0 |
0 |
||||
Iris |
0 |
0 |
0 |
0 |
0 |
0 |
||||
Conjunctivae |
Redness |
2 |
0 |
0 |
0 |
0 |
0 |
|||
Chemosis |
1 |
0 |
0 |
0 |
0 |
0 |
||||
839 female |
3000 g |
Corea |
Density |
0 |
2 |
1 |
1 |
1 |
0 |
|
Area |
0 |
1 |
1 |
1 |
1 |
0 |
||||
Iris |
0 |
0 |
0 |
0 |
0 |
0 |
||||
Conjunctivae |
Redness |
2 |
1 |
0 |
0 |
0 |
0 |
|||
Chemosis |
1 |
1 |
0 |
0 |
0 |
0 |
SCORING SYSTEM:
Cornea:
Opacity: degree of density (area most dense taken from reading)
0 No ulceration or opacity
1 Scattered or diffuse areas of opacity (other than slight dulling of normal lustre), details of iris clearly visible
2 Easily discernible translucent areas, details of iris slightly obscured
3 Nacrous areas, no details of iris visible, size of pupil barely discernible
4 Opaque cornea, iris not discernible through the opacity
Area of cornea involved:
1 One quarter (or less) but not zero
2 Greater than one quarter, but less then half
3 Greater than half, but less than three quarters
4 Greater than three quarters, up to whole area
Iris:
0 Normal
1 Markedly depened rugae, congestion, swelling, moderate circumcorneal hyperaemia or injection, any of these or combination of any thereof, iris still reacting to light (sluggish reaction is positive)
2 No reaction to light, haemorrhage, gross destruction (any or all of these)
Conjunctivae:
Redness (refers to palpebral and bulbar conjunctivae cornea and iris)
0 Blood vessels normal
1 Some blood vessels definitely hyperaemic (injected)
2 Diffuse, crimson colour, individual vessels not easily discernible
3 Diffuse, beefy red
Chemosis (lids and/or nictitating membranes)
0 No swelling
1 Any swelling above normal (includes nictitating membranes)
2 Obvious swelling with partial eversion of lids
3 Swelling with lids about half-closed
4 Swelling with lids more than half-closed
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Acetoguanamine elicites transient, corneal opacification and temporary well-defined conjuctival reactions. Nevertheless this effects do not lead to a classification of the test substance.
- Executive summary:
In an eye irritation study according to OECD 405 approx. 85 mg of Acetoguanamine, the weight occupying a volume of 0.1 mL was placed into the lower lid of one eye of each of the test animals (three adult New Zealand White rabbits). Examination of the eyes was made after 1 hour, and 1, 2, 3, 4 and 7 days after instillation. Irritation was scored and it was determined that Acetoguanamine elicites only transient, corneal opacification and temporary well-defined conjuctival reactions. Nevertheless this effects do not lead to a classification of the test substance.
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