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EC number: 244-599-9 | CAS number: 21829-50-5
- 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 sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Basic data given. Data were obtained from a reliable secondary source (MAK. 33rd update, 2001).
Data source
Reference
- Reference Type:
- publication
- Title:
- Alkanolamines - sensitizing capacity, cross reactivity and review of patch test reactivity.
- Author:
- Wahlberg JE and Boman A
- Year:
- 1 996
- Bibliographic source:
- Dermatosen Beruf Umwelt 44: 222-224
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Guinea pig maximisation test
- GLP compliance:
- not specified
- Type of study:
- guinea pig maximisation test
Test material
- Reference substance name:
- 2-aminoethanol
- EC Number:
- 205-483-3
- EC Name:
- 2-aminoethanol
- Cas Number:
- 141-43-5
- IUPAC Name:
- 2-aminoethanol
- Details on test material:
- - Name of test material (as cited in study report): 2-aminoethanol
- Analytical purity: not specified
- Impurities (identity and concentrations): < 0.1 % di- and triethanolamine
- no further data
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- Dunkin-Hartley
- Sex:
- not specified
- Details on test animals and environmental conditions:
- Albino guinea pigs of the Dunkin-Hartley strain were obtained from SahIins Försöksdjursfarm Malmö, Sweden) and kept in groups of three in plastic cages.
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- intradermal and epicutaneous
- Vehicle:
- water
- Concentration / amount:
- 0.6 % (intradermal) and 10.3 % (epicutaneous) for induction
0.41, 2.05 and 4.1 % for challenge
Challengeopen allclose all
- Route:
- epicutaneous, open
- Vehicle:
- water
- Concentration / amount:
- 0.6 % (intradermal) and 10.3 % (epicutaneous) for induction
0.41, 2.05 and 4.1 % for challenge
- No. of animals per dose:
- 15 animals used for the test substance (5 animals per concentration)
12 animals used for controls - Details on study design:
- The GPMT protocol with the same experimental design as in a previous study on TEA (Boman et al., 1993) was followed. Groups of 15 animals were induced with either MEA, DEA or TEA and then challenged after three weeks with the inducing amine and the two others. Prior to the topical induction, pretreatment with 10% sodium dodecyl sulphate was carried out. The concentrations used for induction and challenge were based on previous experience with TEA and the concentrations of MEA and DEA were equimolar to those of TEA. The challenge reactions were read blindly 48 and 72 h after application or the patches (Finn chambers). Two separate experiments were carried out with MEA. Control groups of twelve animals were given the same treatment (Freund's Complete Adjuvant, vehicle, occlusion, etc.) except for the inducing amine.
- Challenge controls:
- no data
- Positive control substance(s):
- no
Results and discussion
In vivo (non-LLNA)
Resultsopen allclose all
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 4.1%
- No. with + reactions:
- 2
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 48.0. Group: test group. Dose level: 4.1%. No with. + reactions: 2.0. Total no. in groups: 15.0.
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 2.05%
- No. with + reactions:
- 1
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 48.0. Group: test group. Dose level: 2.05%. No with. + reactions: 1.0. Total no. in groups: 15.0.
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 0.41%
- No. with + reactions:
- 2
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 48.0. Group: test group. Dose level: 0.41%. No with. + reactions: 2.0. Total no. in groups: 15.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 72
- Group:
- test chemical
- Dose level:
- 4.1 %
- No. with + reactions:
- 3
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 72.0. Group: test group. Dose level: 4.1 %. No with. + reactions: 3.0. Total no. in groups: 15.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 72
- Group:
- test chemical
- Dose level:
- 2.05 %
- No. with + reactions:
- 2
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 72.0. Group: test group. Dose level: 2.05 %. No with. + reactions: 2.0. Total no. in groups: 15.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 72
- Group:
- test chemical
- Dose level:
- 0.41 %
- No. with + reactions:
- 3
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 72.0. Group: test group. Dose level: 0.41 %. No with. + reactions: 3.0. Total no. in groups: 15.0.
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- negative control
- No. with + reactions:
- 0
- Total no. in group:
- 12
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 48.0. Group: negative control. No with. + reactions: 0.0. Total no. in groups: 12.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 72
- Group:
- negative control
- No. with + reactions:
- 0
- Total no. in group:
- 12
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 72.0. Group: negative control. No with. + reactions: 0.0. Total no. in groups: 12.0.
- Reading:
- 1st reading
- Hours after challenge:
- 72
- Group:
- other: vehicle control
- No. with + reactions:
- 2
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 72.0. Group: other: vehicle control. No with. + reactions: 2.0. Total no. in groups: 15.0.
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 4.1%
- No. with + reactions:
- 1
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 48.0. Group: test group. Dose level: 4.1%. No with. + reactions: 1.0. Total no. in groups: 15.0.
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 2.05%
- No. with + reactions:
- 2
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 48.0. Group: test group. Dose level: 2.05%. No with. + reactions: 2.0. Total no. in groups: 15.0.
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 0.41%
- No. with + reactions:
- 1
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 48.0. Group: test group. Dose level: 0.41%. No with. + reactions: 1.0. Total no. in groups: 15.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 72
- Group:
- test chemical
- Dose level:
- 4.1%
- No. with + reactions:
- 1
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 72.0. Group: test group. Dose level: 4.1%. No with. + reactions: 1.0. Total no. in groups: 15.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 72
- Group:
- test chemical
- Dose level:
- 2.05%
- No. with + reactions:
- 1
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 72.0. Group: test group. Dose level: 2.05%. No with. + reactions: 1.0. Total no. in groups: 15.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 72
- Group:
- test chemical
- Dose level:
- 0.41%
- No. with + reactions:
- 0
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 72.0. Group: test group. Dose level: 0.41%. No with. + reactions: 0.0. Total no. in groups: 15.0.
Any other information on results incl. tables
After challenge with 4.1 %, 2.05 % and 0.41 % of 2-aminoethanol, 3/15, 2/15 and 3/15 animals reacted positively after 72 hours. Two out of 15 animals showed a reaction to the vehicle. Of the 12 control animals, none reacted to 2-aminoethanol or the vehicle. Possible cross reactions to 5 % of triethanolamine and 7 % of diethanolamine occurred in 3 and 2 animals, respectively. In a 2nd test, only 1 or 2 animals showed a reaction to 4.1 % and 2.05 % of 2-aminoethanol, but none of the animals reacted to 0.41 % of 2-aminoethanol or the physiological saline solution used as a vehicle in this study. Moreover, reactions to 10 % of triethanolamine and 7 % of diethanolamine were only observed in 1 and 2 animals, respectively. Of the 12 control animals none reacted to one of the ethanolamines, and 1/12 animals reacted to the vehicle after 24 hours.
The test with monoethanolamine has been performed twice.
Applicant's summary and conclusion
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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