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EC number: 216-823-5 | CAS number: 1675-54-3
- 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
Test material was slightly irritating to the skin and eye in the key studies. For the skin, mean erythema and edema scores were 0.8 and 0.5, respectively. The mean eye score was 0.4.
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:
- 14 Nov 2006 - 9 March 2007
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study conducted under GLP
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Medical University of Silesia, Katowice
- Age at study initiation: 3.5-4.5 months
- Weight at study initiation: 2.6-3.4 kg
- Housing: Individual metal cage
- Diet (e.g. ad libitum): standard granulated fodder "LSK" produced by Wytwórnia Koncentratów i Mieszanek Paszowych AGROPOL, Motycz
- Water (e.g. ad libitum): tap water
- Acclimation period: 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20-22
- Humidity (%): 35-70
- Air changes (per hr): not specified
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: Not stated - Type of coverage:
- occlusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- 0.5 mL
- Duration of treatment / exposure:
- 4 hours
- Observation period:
- Observations of skin were performed after 1, 24, 48 and 72 hours as well as 7 days since the end of exposure.
- Number of animals:
- 3
- Details on study design:
- The undiluted test material was applied in volume of 0.5 mL to multilayered gauze patch with dimensions of 2.5 x 2.5 cm and then laid on the prepared skin of one rabbit (rabbit No 1). The area of skin surface treated with the test material was about 6 cm2. The gauze patches were covered with PCV foil and fixed with sticking plaster. The rabbit’s trunk was covered with lignin and elastic bandage was used to make circular protecting band. After 4 hours exposure time, the band and gauze patches were taken off and the residual test material was removed using water.
Following evaluation of the exposed skin and to confirm the obtained results the test material was administered to skin of the next two rabbits (rabbit No 2 and No 3) for four hours. The procedure was the same as in case of rabbit No 1. - Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.7
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 h
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0.7
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 h
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- fully reversible within: 7 d
- Irritation parameter:
- edema score
- Basis:
- animal: #1, #2, #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Interpretation of results:
- slightly irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: OECD GHS
- Conclusions:
- Epidian 6 – epoxy resin with an average molecular mass <= 700 does not irritate skin of rabbits.
- Executive summary:
Acute skin irritation/skin corrosion study of Epidian 6 – epoxy resin with an average molecular mass <=700 to rabbits was performed according to the agreement with Zakłady Chemiczne ORGANIKA – SARZYNA S.A., Nowa Sarzyna. The study was coded OS-29/06.
The methodological basis was the OECD Guideline for Testing of Chemicals No 404/EU Method B.4 as well as Principles of Good Laboratory Practice (GLP, OECD 1997). The study was performed with white rabbits of New Zealand strain. The undiluted test material was administered in volume of 0.5 mL as a single dose to shaved skin of three rabbits and covered with appropriate band. The exposure time was 4 hours. After 1, 24, 48 and 72 hours as well as 7 and 14 days since the end of exposure time
skin condition was examined.
During observation all test rabbits showed changes on skin in a form of erythema. Classification of the test material was performed according to Annex to Decree of Ministry of Health of September 2nd, 2003 (Acts Daily No 171, Position 1666). Taking into account the obtained results, one may say that Epidian 6 – epoxy resin with an average molecular mass <=700 does not irritate skin of rabbits.
Reference
Rabbit
No
Observation
type 1 hour
24
hours
48
hours
72
hours
7 days
Average
after 24,
48 and 72
hours
erythema 1 1 1 0 - 0.7
1
edema 0 0 0 0 - 0
erythema 1 1 1 0 - 0.7
2
edema 0 0 0 0 - 0
erythema 1 1 1 1 0 1
3
edema 0 0 0 0 0 0
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (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: Guideline study conducted under GLP
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Institute of Occupational Medicine, Lodz
- Age at study initiation: 3.5 months
- Weight at study initiation: 3-3.1 kg
- Housing: Individual metal cages
- Diet (e.g. ad libitum): standard granulated fodder "LSK" produced by Wytwórnia Koncentratów i Mieszanek Paszowych AGROPOL, Motycz
- Water (e.g. ad libitum): tap water
- Acclimation period: 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20-21
- Humidity (%): 30-60
- Air changes (per hr): Not specified
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: From: 29.01.2007 To: 12.02.2007 - Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- 0.1 mL
- Duration of treatment / exposure:
- Single treatment
- Observation period (in vivo):
- After 1, 24, 48 and 72 hours, and 7 days since administration of the test material condition of cornea, iris and conjunctiva was evaluated.
- Number of animals or in vitro replicates:
- 3
- Irritation parameter:
- cornea opacity score
- Basis:
- animal: #1, #2, #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- iris score
- Basis:
- animal: #1, #2, #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 3
- Reversibility:
- fully reversible within: 7 d
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0.3
- Max. score:
- 3
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 1.7
- Max. score:
- 3
- Reversibility:
- fully reversible within: 7 d
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.7
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 h
- Irritation parameter:
- chemosis score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0.3
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- chemosis score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- fully reversible within: 7 d
- Irritant / corrosive response data:
- During observation after 24 hours since the test material administration the following changes in eye conjunctiva were stated: in rabbit No 1 and 2 – redness in form of some blood vessels hyperaemia (injection); in rabbit No 3 – diffuse crimson redness. The congestion of third eyelid in all test rabbits was stated whereas circumocorneal hyperaemia was noticed in rabbit No 1 and 3. The swelling of third eyelid was stated
in rabbit No 1. The rabbit No 3 showed swelling of conjunctiva and third eyelid. Additionally in rabbit No 1 the slight volume of excretion was stated while in rabbit No 3 the excretion on eyelids and eyelids hair was observed.
During observation after 48 hours since administration of the test material no pathological changes in rabbit No 2 were stated. In conjunctiva of rabbit No 1 the redness in form of some blood vessels hyperaemia (injection) was stated. In conjunctiva of rabbit No 3 the diffuse crimson redness and circumcorneal hyperaemia were observed. Furthermore, in rabbits No 1 and 3 the swelling of third eyelid and slight volume of excretion were stated.
During observation after 72 hours since administration of the test material in conjunctiva of rabbit No 1 and 3 the redness in form of some blood vessels hyperaemia (injection) and congestion of third eyelid were noticed. The rabbit No 3 showed also the swelling of third eyelid. - Other effects:
- During observation after 7 days since administration of the test material no pathological changes in test rabbits were stated.
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: OECD GHS
- Conclusions:
- Epidian 6 – epoxy resin with an average molecular mass <= 700 does not irritate eyes of the rabbits.
- Executive summary:
Acute eye irritation study of Epidian 6 – epoxy resin with an average molecular mass < 700 to rabbits was performed according to the agreement with Zakłady Chemiczne ORGANIKA – SARZYNA S.A., Nowa Sarzyna. The study was coded OS-
29/06.
The methodological basis was OECD Guideline for Testing of Chemicals No 405/ EU Method B.5 as well as Principles of Good Laboratory Practice (GLP, OECD 1997).
The study was performed with three white rabbits of New Zealand strain. The test material was administered in volume of 0.1 mL to conjunctival sac of one eye to each rabbit. After 1, 24, 48 and 72 hours and 7 days since administration of the test material, condition of cornea, iris and conjunctiva was evaluated.
After administration of the test material, during the observations, changes in conjunctival sac of rabbits eyes were noticed.
Classification of the test material was performed according to Annex to Decree of Ministry of Health of September 2, 2003 (Acts Daily No 171, Position 1666). Taking into account the obtained results, one may say that Epidian 6 – epoxy resin with an average molecular mass < 700 does not irritate eyes of rabbits.
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Test material was slightly irritating to the skin and eye in the key studies. For the skin, mean erythema and edema scores were 0.8 and 0.5, respectively. The mean eye score was 0.4.
One dermal study had slightly higher scores while the remainder were comparable or less than the key study.
Effects on skin irritation/corrosion: slightly irritating
Effects on eye irritation: slightly irritating
Justification for classification or non-classification
Because the tests on the substance resulted in irritation consistent with Category 2 for both eye and skin, the substance will be classified as irritant.
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.
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