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EC number: 216-940-1 | CAS number: 1704-62-7
- 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
DMEE is considered to be corrosive to skin based on skin irritation studies conducted in rabbits that reported severe irritation (erythema) and corrosion following a 4-hour exposure to DMEE.
DMEE is also considered to be corrosive to the eyes based on an eye irritation study conducted in rabbits indicating that DMEE is extremely irritating and the effects were not reversible within 15 days.
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:
- supporting study
- Study period:
- 1983-06-22 to 1983-08-15
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study did not include the initial test, but was similar to the confirmatory test in OECD 404; the study report lacks full animal information and method details. No GLP certificate or indication of compliance with GLP provided.
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- No initial test; confirmatory test ran with 6 animals instead of up to 3.
- Qualifier:
- according to guideline
- Guideline:
- other: U.S. Department of Transportation Skin Irritancy Test
- Deviations:
- not specified
- Principles of method if other than guideline:
- N/A
- GLP compliance:
- not specified
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
IN-LIFE DATES: From: 1983-06-22 (date of exposure) To: Not specified - Type of coverage:
- occlusive
- Preparation of test site:
- other: clipped
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- 0.5 mL
- Duration of treatment / exposure:
- 4 hrs
- Observation period:
- Skin reaction was scored at one hour, and 1, 2, 3, and 7 days after dosing.
- Number of animals:
- 3/sex
- Details on study design:
- TEST SITE
- Area of exposure: Trunk
- Type of wrap if used: Gauze patch and impervious sheeting
REMOVAL OF TEST SUBSTANCE
- Washing (if done): No, although the excess was wiped away to avoid ingestion.
- Time after start of exposure: 4 hours
SCORING SYSTEM: Draize - Irritation parameter:
- erythema score
- Remarks:
- and Eschar formation
- Basis:
- mean
- Time point:
- other: 5 hrs
- Score:
- 2.3
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Mean score of 6 animals (3/sex). irritation persisted through 7 days.
- Irritation parameter:
- erythema score
- Remarks:
- and Eschar formation
- Basis:
- mean
- Time point:
- other: 1 day
- Score:
- 2.8
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Mean score of 6 animals (3/sex). Irritation persisted through 7 days.
- Irritation parameter:
- erythema score
- Remarks:
- and Eschar formation
- Basis:
- mean
- Time point:
- other: 2 days
- Score:
- 3.2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Mean score of 6 animals (3/sex). Irritation persisted through 7 days.
- Irritation parameter:
- erythema score
- Remarks:
- and Eschar formation
- Basis:
- mean
- Time point:
- other: 3 days
- Score:
- 3.3
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Mean score of 6 animals (3/sex). Irritation persisted through 7 days.
- Irritation parameter:
- erythema score
- Remarks:
- and Eschar formation
- Basis:
- mean
- Time point:
- other: 7 days
- Score:
- 2.8
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Mean score of 6 animals (3/sex). Irritation persisted through 7 days.
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 5 hrs
- Score:
- 1.3
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Mean score of 6 animals (3/sex). Irritation persisted through 7 days.
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 1 day
- Score:
- 1.7
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Mean score of 6 animals (3/sex). Irritation persisted through 7 days.
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 2 days
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Mean score of 6 animals (3/sex). Irritation persisted through 7 days.
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 3 days
- Score:
- 2.2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Mean score of 6 animals (3/sex). Irritation persisted through 7 days.
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 7 days
- Score:
- 2.2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Mean score of 6 animals (3/sex). Irritation persisted through 7 days.
- Irritant / corrosive response data:
- Application of the test substance to covered rabbit skin resulted in moderate to severe erythema and moderate edema in all 6 rabbits. Ecchymosis and necrosis were also evident on each rabbit. Irritation (including erythema, edema, desquamation, necrosis, and scab formation) persisted through 7 days.
- Other effects:
- Ecchymosis: 6/6 at 5 hrs, 6/6 at 1 day, 5/6 at 2 days, 4/6 at 3 days, 0/6 at 7 days.
Necrosis: 4/6 at 5 hrs, 5/6 at 1 day, 6/6 at 2 days, 6/6 at 3 days, 6/6 at 7 days.
Desquamation: 0/6 at 5 hrs, 0/6 at 1 day, 0/6 at 2 days, 0/6 at 3 days, 6/6 at 7 days.
Scab formation: 0/6 at 5 hrs, 0/6 at 1 day, 0/6 at 2 days, 0/6 at 3 days, 6/6 at 7 days.
One animal was dead at 7 days; observations made immediately after death are included under the 7-day observation period above. - Interpretation of results:
- corrosive
- Conclusions:
- The test substance was classified as corrosive by the author according to D.O.T. standards. The results also meet the requirements for classification as corrosive to the skin according to OECD 404.
Reference
The author stated that the material classifed as "corrosive" by D.O.T. definition.
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (corrosive)
Eye irritation
Link to relevant study records
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: OECD guideline study with acceptable restrictions (no test substance purity given). Acceptable, well documented report which meets basic scientific principles.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Version / remarks:
- (adopted 1981)
- Deviations:
- no
- Remarks:
- (no deviations compared to QECD TG 405 , 1981 & 2002, except testing protocol was according to guideline version from 1981)
- GLP compliance:
- no
- Species:
- rabbit
- Strain:
- Vienna White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Gaukler, Offenbach, Germany
- Weight at study initiation: 3.03, 2.54 kg (males); 2.26 kg (female)
- Housing: 1 animal per cage
- Diet: KLIBA 341, 4 mm; Klingentalmuehle AG, CH, ad libitum
- Water: tap water ad libitum
- Acclimation period: at least 1 week
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 - 24 °C
- Humidity (%): 30 - 70 %
- Photoperiod (hrs dark / hrs light): 12/12 - Vehicle:
- unchanged (no vehicle)
- Controls:
- other: untreated eye of the same animal
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.1 mL - Duration of treatment / exposure:
- once, eyes were not washed after application
- Observation period (in vivo):
- 15 days
The study was discontinued after 15 days due to severe eye irritation. - Number of animals or in vitro replicates:
- 3 (2 males, 1 female)
- Details on study design:
- APPLICATION
Single application to the conjunctival sac of the right eyelid
REMOVAL OF TEST SUBSTANCE
- Washing (if done): the substance was not washed out
READINGS
1 h, 24 h, 48 h, 72 h, 15 d after application
SCORING SYSTEM: Draize Scoring System - Irritation parameter:
- cornea opacity score
- Basis:
- animal #1
- Time point:
- other: mean over 24, 48 and 72 h
- Score:
- 1.7
- Max. score:
- 4
- Reversibility:
- not reversible
- Remarks on result:
- other: Cornea score increased until study termination (3 out of 4).
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Remarks:
- of animal 2 and 3
- Time point:
- other: mean over 24, 48 and 72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- not reversible
- Remarks on result:
- other: Identical scores in both animals. Cornea score increased until study termination (4 out of 4); staphyloma observed in one animal.
- Irritation parameter:
- iris score
- Basis:
- mean
- Remarks:
- of all 3 animals
- Time point:
- other: mean over 24, 48 and 72 h
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- not reversible
- Remarks on result:
- other: Identical scores in all animals. At study termination: iris score: 1
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Remarks:
- of all 3 animals
- Time point:
- other: mean over 24, 48 and 72 h
- Score:
- 2
- Max. score:
- 3
- Reversibility:
- not reversible
- Remarks on result:
- other: Identical scores in all animals. At study termination: conjunctivae score: 2
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Remarks:
- of animal 1 and 2
- Time point:
- other: mean over 24, 48 and 72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- not reversible
- Remarks on result:
- other: Identical scores in both animals. At study termination: chemosis score: 2
- Irritation parameter:
- chemosis score
- Basis:
- animal #3
- Time point:
- other: mean over 24, 48 and 72 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- not reversible
- Remarks on result:
- other: At study termination: chemosis score: 1
- Other effects:
- Additional findings observed at study termination (after 15 days):
- animal 1: loss of corneal tissue, small retractions in the eyelids, marginal vascularization of the cornea, pannus, suppuration, loss of hair at margins of eyelids
- animal 2: loss of corneal tissue, small retractions in the eyelids, marginal vascularization of the cornea, pannus, suppuration, staphyloma
- animal 3: loss of corneal tissue, small retractions in the eyelids, pupil contracted, marginal vascularization of the cornea - Interpretation of results:
- Category 1 (irreversible effects on the eye) based on GHS criteria
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
In a semiocclusive skin irritation study in rabbits exposed to DMEE for 3 minutes or 1 hour, no corrosive effects were observed.
Justification for selection of skin irritation / corrosion
endpoint:
The key skin irritation study had a reliability score of 2 and was
conducted according to OECD 404. Three New Zealand White rabbits (2
males, 1 female) were dosed with 0.5 mL of DMEE for 4 hours under
semi-occlusive dressings. The animals were observed for 72 hours
post-exposure. After the 4 hour exposure, hemorrhages were seen and
after 24 hours necrosis occurred in all three animals. At the end of the
observation period at 72 hours, full thickness necrosis was observed in
all three animals. This finding was confirmed by gross-pathological
examination. The substances was reported to be corrosive (Category 1C)
to the skin of rabbits.
Justification for selection of eye irritation endpoint:
The key eye irritation study had a reliability score of 2 and was
performed in Vienna White rabbits according to the OECD 405 guideline.
Following exposure to 0.1 mL of DMEE (unwashed), ocular responses were
assessed using the Draize scoring system. Loss of corneal tissue, small
retractions in the eyelids and marginal vascularization of the cornea
were reported in all three animals. Pannus and suppuration were reported
in two of the animals and loss of hair at the margins of the eyelids and
staphyloma were reported in one animal each. Eye effects were not
reversible in the 15 day observation period. DMEE was reported to be a
Category 1 (irreversible effects on the eye) eye irritant.
Justification for classification or non-classification
Based on the available results, the suggested classification for DMEE according to EU Regulation 1272/2008 is skin corrosion category 1C and eye damage category 1.
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