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EC number: 202-845-2 | CAS number: 100-37-8
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1982
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Well documented guideline study (OECD 404), conducted under GLP-like conditions.In accordance to OECD Guideline 404 of 1981, "Acute Dermal Irritation/Corrosion", a 4 hour application time was used, but additional application times (3 min and 1 h) were also used.
Data source
Referenceopen allclose all
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 982
- Report date:
- 1982
- Reference Type:
- publication
- Title:
- Studies on the design of animal tests for the corrosiveness of industrial chemicals
- Author:
- Potokar, M. et al.
- Year:
- 1 985
- Bibliographic source:
- Food Chem. Toxicol. 23, 615-617.
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- in accordance to OECD Guideline 404 of 1981, "Acute Dermal Irritation/Corrosion", a 4 hour application time was used, but additional application times (3 min and 1 h) were also used.
- GLP compliance:
- no
Test material
- Reference substance name:
- 2-diethylaminoethanol
- EC Number:
- 202-845-2
- EC Name:
- 2-diethylaminoethanol
- Cas Number:
- 100-37-8
- Molecular formula:
- C6H15NO
- IUPAC Name:
- 2-(diethylamino)ethanol
- Details on test material:
- - Name of test material (as cited in study report): Diaethylaethanolamin
- Physical state: liquid
- Analytical purity: > 99 %
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Gaukler, Offenbach Germany
- Weight at study initiation: male: 2.91 kg; female: 2.74 kg
- Housing: single
- Diet: Ovator Solikanin 4 mm (MUSKATOR-WERKE, Düsseldorf, Germany, ad libitum
- Water: on week days, purified water ad libitum; on weekends, tap water ad libitum
- Acclimation period: 8 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 - 26 °C
- Humidity (%): 30 - 70 %
- Photoperiod (hrs dark / hrs light): 12/12
Test system
- Type of coverage:
- other: varied with exposure time, see below for details
- Preparation of test site:
- other: clipped
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: untreated skin area served as control
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 mL - Duration of treatment / exposure:
- 3 min, 1 h or 4 h
- Observation period:
- 7 days
- Number of animals:
- Two males and four females were used for the 3 min application time.
Three males and three females were used for 1hour and 4 hour application times. - Details on study design:
- Dorsal and lateral regions of the trunk were used as the application sites (3x3 cm per application site). 0.5 mL/patch of test item was used. Two males and four females were treated for 3 minutes whereas three males and three females were treated for 1 hour and 4 hours. Each animal had 4 sites of application (except for the 3 min application; in this case, each animal had 2 application sites, one treated occlusively and the other under semi-occlusive conditions), namely, a site for 1 hr application under occlusive conditions, a site for 4 hr application under occlusive conditions, a site for 1 hr application under semi-occlusive conditions and a site for 4 hr application, under semi-occlusive conditions. After treatment the patches were removed, and the treated area was rinsed with a polyethylene glycol 400 solution or a polyethylene glycol 400/water (1:1) solution and dried. Observations were made 1 hr after the removal of the patch, and at 24, 48 and 72 hr, as well as 7 days after start of application.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Remarks:
- 4 hours of treatment, semi-occlusive
- Basis:
- mean
- Remarks:
- out of 6 animals
- Time point:
- other: mean over 24, 48 and 72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Remarks on result:
- other: all animals displayed erythema grade 4 at day 7
- Irritation parameter:
- edema score
- Remarks:
- 4 hours of treatment, semi-occlusive
- Basis:
- mean
- Remarks:
- out of 6 animals
- Time point:
- other: 24 h - 48 h - 72 h
- Score:
- 1.5
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: at day 7, all animals still displayed edema graded 1
- Irritant / corrosive response data:
- Overview of findings following 1 and 4 hours of application:
After 1 hr and 4 hr occlusive and semi-occlusive exposure severe erythema, eschar formation and necrosis were observed. Very slight to slight edema was also observed. By day 7 after application the findings were not reversed. The score for erythema after the 4 hr occlusive exposure was always a 4 at all times, with the exception of one reading of 3 at 1 h. The scores for edema after the 4 hr occlusive exposure was 2 in all animals 1 hr after patch removal; 24 hr after the start scores of 2 were seen in 5 animals and a score of 3 was seen in 1 animal; 48 hr after the start scores of 1 were seen in 2 animals, and scores of 2 were seen in 4 animals; the same scores were seen at 72 hr after the start; and at 7 days 3 animals had a score of 1, and 3 had a score of 2. The scores for erythema after the 4 hr semi-occlusive exposure were reported to be: 2-3 at 1 hr after patch removal; 3-4 at 24 hr after the start; and thereafter it was observed to have a score of 4. The scores for edema after the 4 hr semi-occlusive exposure were reported to be: 1 in 1 animal and 2 in 5 animals one hr after patch removal; 1 in 3 animals and 2 in 3 animals 24 hr after the start; 1 in 2 animals and 2 in 4 animals 48 hr after the start; 1 in 4 animals and 2 in 2 animals 72 hr after the start; and 7 d after the start a score of 1 was reported in all 6 animals. Necrosis was confirmed histologically. In this regard, in the semi-occlusive 1 hr application group full thickness necrosis was seen in 2/6 animals; in the 4 hr application group full thickness necrosis was seen in 5/6 animals. In the occlusive 1 hr application group full thickness necrosis was seen in 3/6 animals; in the 4 hr application group full thickness necrosis was seen in all animals.
Findings considered for assessment of the skin irritating potential of the test item:
Only the findings obtained after 24, 48 and 72 h, referring to the 4 hour application under semi-occlusive conditions were considered for the purpose of assessment. The mean scores, the absence of reversibility, and the histologically-confirmed necrosis clearly indicate that the test item is corrosive. - Other effects:
- 3 min application:
After a 3 min occlusive exposure, as well as semi-occlusive exposure only slight erythema was observed. It was reversible by the end of the experiment. Some scaling was observed on day 7.
Any other information on results incl. tables
Mean erythema score:
occlusive:
Exposure time | 3 min | 1 h | 4 h | 24 h | 48 h | 72 h | day 7 |
3 min | 1/1/1/1/1/1 | - | - | 1/1/1/1/1/1 | 1/1/1/1/1/1 | 1/1/1/1/1/1 | 0/0/0/0/0/0 |
1 h | - | 3/2/2/3/3/4 | - | 4/2/2/4/3/4 | 4/4/4/4/4/4 | 4/4/4/4/4/4 | 4/4/4/4/4/4 |
4 h | - | 4/4/4/4/3/4 | - | 4/4/4/4/4/4 | 4/4/4/4/4/4 | 4/4/4/4/4/4 | 4/4/4/4/4/4 |
semiocclusive:
Exposure time | 3 min | 1 h | 4 h | 24 h | 48 h | 72 h | day 7 | ||
3 min | 1/1/1/1/1/1 | - | - | 1/1/1/1/1/1 | 1/1/1/1/1/1 | 1/1/1/1/1/1 | 0/0/0/0/0/0 | ||
1 h | - | 3/2/3/4/3/3 | - | 4/2/2/4/3/2 | 4/2/2/4/4/2 | 4/2/4/4/4/4 | 4/2/4/4/4/4 | ||
4 h | - | - | 3/3/3/3/2/3 | 4/4/4/4/3/4 | 4/4/4/4/4/4 | 4/4/4/4/4/4 | 4/4/4/4/4/4 |
Mean edema score:
occlusive:
Exposure time | 3 min | 1 h | 4 h | 24 h | 48 h | 72 h | day 7 | ||
3 min | 0/0/0/0/0/0 | - | - | 0/0/0/0/0/0 | 0/0/0/0/0/0 | 0/0/0/0/0/0 | 0/0/0/0/0/0 | ||
1 h | - | 1/2/2/2/2/2 | - | 1/2/2/1/2/2 | 1/2/2/1/1/1 | 1/2/2/2/1/1 | 1/1/1/1/1/1 | ||
4 h | - | - | 2/2/2/2/2/2 | 2/2/2/2/2/3 | 2/2/2/2/1/1 | 2/2/2/2/1/1 | 2/1/2/2/1/1 |
semiocclusive:
Exposure time | 3 min | 1 h | 4 h | 24 h | 48 h | 72 h | day 7 | ||
3 min | 0/0/0/0/0/0 | - | - | 0/0/0/0/0/0 | 0/0/0/0/0/0 | 0/0/0/0/0/0 | 0/0/0/0/0/0 | ||
1 h | - | - | 1/2/2/2/2/2 | 1/1/2/1/1/2 | 1/1/2/2/1/1 | 1/1/1/1/1/1 | |||
4 h | - | - | 2/2/2/2/1/2 | 2/1/2/1/1/2 | 2/2/2/2/1/1 | 1/2/2/1/1/1 | 1/1/1/1/1/1 |
Applicant's summary and conclusion
- Interpretation of results:
- corrosive
- Remarks:
- Migrated information
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