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EC number: - | CAS number: -
- 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
The assessment of skin sensitization property of the registration
substance is derived based on the read-across approach.
2,2'-(octadec-9-enylimino) bisethanol CAS 25307-17-9, was tested for its
skin sensitization property according to OECD 406 Test Guideline. No
significant skin sensitization property was found. Likewise, no skin
sensitization property is expected for the registration substance.
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.6 (Skin Sensitisation)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- The registration substance is a surfactant.
- Species:
- guinea pig
- Strain:
- Hartley
- Sex:
- male/female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Charles River Laboratories France, L'Arbresle, France.
- Age at study initiation: 1-2 months
- Weight at study initiation: males 361 +/- 18 g, females 339 +/- 25g
- Housing: Polycarbonate cages with stainless steel tops. Autoclaved sawdust bedding (SICA, Alfortville, France)
- Diet (e.g. ad libitum): ad libitum, 106 pelleted diet (SAFE, Villemoisson, Epiny-sur-Orge, France
- Water (e.g. ad libitum): ad libitum via polypropylene bottle. Water filtered by a FG Millipor membrane (0.22 micron)
- Acclimation period: At least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 +/- 2
- Humidity (%): 30 - 70
- Air changes (per hr): approximately 12 cycles of filtered, no-recycled air
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: From: 19th April 2005 To: 27th May 2005 - Route:
- intradermal and epicutaneous
- Vehicle:
- other: corn oil for intradermal induction. topical induction ethanol/water (80/20). Acetone for the challenge phase.
- Concentration / amount:
- Intradermal induction injections:
Freunds complete adjuvant (FCA) diluted to 50% (v/v) with 0.9% NaCl (both groups)
Test substance at a concentration of 0.1% in corn oil (treated group) of corn oil vehicle alone (control group)
Test substance at the concentration of 0.1% in a mixture of FCA/0.9% NaCl (50/50 w/w) (treated group) or corn oil vehicle at a concentration of
50% (w/v) in a mixture of FCA/0.9% NaCl (50/50, v/v)
Topical induction: 10% of the test substance in ethanol/water (80/20).
Challenge dosing:
1% (w/w) test substance in acetone - Route:
- epicutaneous, occlusive
- Vehicle:
- other: corn oil for intradermal induction. topical induction ethanol/water (80/20). Acetone for the challenge phase.
- Concentration / amount:
- Intradermal induction injections:
Freunds complete adjuvant (FCA) diluted to 50% (v/v) with 0.9% NaCl (both groups)
Test substance at a concentration of 0.1% in corn oil (treated group) of corn oil vehicle alone (control group)
Test substance at the concentration of 0.1% in a mixture of FCA/0.9% NaCl (50/50 w/w) (treated group) or corn oil vehicle at a concentration of
50% (w/v) in a mixture of FCA/0.9% NaCl (50/50, v/v)
Topical induction: 10% of the test substance in ethanol/water (80/20).
Challenge dosing:
1% (w/w) test substance in acetone - No. of animals per dose:
- 10 males and 10 females for the vehicle control group
20 males and 20 females for the test substance group - Details on study design:
- MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: Intradermal injection single exposure at six injection points. Cutaneous single application on day 8.
- Exposure period: For cutaneous application exposure was for 48 hours.
- Test groups: Backs of guinea pigs were clipped for an area of 4cm x 2cm in their interscapular area. 6 intradermal injections on day 1, 2 of FCA at 50 %( v/v) in 0.9% NaCl in the anterior part of the clipped area. 2 injections of the test substance at 0.1% (w/w) in corn oil in the middle of the area. 2 injections of the test substance at 0.1% (w/w) in a mixture of FCA/0.9% NaCl (50/50).
No topical application of sodium lauryl sulfate was necessary on day 7 due to test substance being irritant. On day 8 all test animals were exposed to 10% (w/w) test substance fully loaded on a 8cm2 filter paper applied under an occlusive dressing on the intrescapular area for 48 hours.
- Control group:
- Site: The clipped intrescapular are of the back
- Frequency of applications: Intradermal injections on day 1 followed by cutaneous application on day 8.
- Duration: Cutaneous application 48 hours
- Concentrations: For the intradermal injection 6 intradermal injections on day 1, 2 of FCA at 50 %( v/v) in 0.9% NaCl in the anterior part of the clipped area. 2 injections of the corn oil vehicle in the middle of the area. 2 injections of a mixture of FCA/0.9% NaCl (50/50).
On day 8 all animals were exposed to an 8cm2 filter paper fully loaded with the ethanol/water (80/20) vehicle applied under an occlusive dressing on the intrescapular area for 48 hours.
B. CHALLENGE EXPOSURE
- No. of exposures: On day 22 the treated and the test animals received a single application of the test substance and the vehicle control.
- Day(s) of challenge: Day 22
- Exposure period: 24 hours - Chamber held in contact with the skin by an adhesive anallergenic waterproof plaster.
- Test groups: The filter paper of a chamber (Finn Chamber) was full loaded with the test substance at a concentration of 1%(w/w) in acetone, applied to the shaved area of the posterior left flank. The acetone vehicle was applied under the same condition to the skin of the posterior left flank.
- Control group: They received the same challenge exposure with test substance and vehicle control as the test group.
- Site: The shaved left and right posterior flanks
- Concentrations: 1% test substance (w/w) in acetone or acetone vehicle control
- Evaluation (hr after challenge): 24 and 48 hours after removal of the dressing with the challenge application.
OTHER: - Positive control substance(s):
- yes
- Remarks:
- Mercaptobenzthiazole
- Positive control results:
- 1% (w/w) Mercaptobenzothiazole was used for the intradermal induction and 20% (W/W) for the cutaneous induction on day 8. followed by 22% (w/w) on the day 22 challenge. The vehicle was corn oil. There were 5 control animals and 10 treated animals.
Under the experimental conditions based on the Magnusson and Kligman method, the mercaptobenzthiazole positive control induced a positive skin sensitisation in 80% (8/10) guinea pigs. - Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- corn oil intradermal and ethanol/water cutaneous
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- No clinical signs
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- Corn oil intradermal, ethanol/water cutaneous
- No. with + reactions:
- 2
- Total no. in group:
- 10
- Clinical observations:
- Discrete erythema (grade 1)
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 0.1% intradermal and 10% for cutaneous induction
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Clinical observations:
- No clinical signs
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 0.1% for intradermal and 10% for cutaneous induction
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Clinical observations:
- No clinical signs
- Remarks on result:
- no indication of skin sensitisation
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The skin sensitization property of the registration substance is derived based on the read-across approach.
2,2'-(octadec-9-enylimino) bisethanol CAS 25307-17-9, was tested for its skin sensitization property according to OECD 406 Test Guideline. No significant skin sensitization property was found. - Executive summary:
The skin sensitization property of the registration substance is derived based on the read-across approach.
2,2'-(octadec-9-enylimino) bisethanol CAS 25307-17-9, was tested for its skin sensitization property according to OECD 406 Test Guideline. The applied induction doses were 0.1% for intradermal- and 10% for topical treatment and the applied challenge dose was 1%. No response was observed in twenty treated animals and in ten control animals. No significant skin sensitization property was found.
Reference
Preliminary Study | |||||
Administration by intradermal route | |||||
Animal | Concentration of the | Scoring after treatment | |||
number | test item % (w/w) | 24 hours | 48 hours | 6 days | |
male 301 | 25 + FCA | N | N | - | |
25 | N | N | - | ||
10 + FCA | N | N | - | ||
10 | I | N | - | ||
5 + FCA | I | N | - | ||
5 | I | N | - | ||
female 302 | 25 + FCA | N | N | - | |
25 | N | N | - | ||
10 + FCA | N | N | - | ||
10 | N | N | - | ||
5 + FCA | I | N | - | ||
5 | I | N | - | ||
male 305 | 2.5 + FCA | I | N | - | |
2.5 | I | N | - | ||
1 + FCA | I | N | - | ||
1 | I | I | - | ||
0.5 + FCA | I | I | - | ||
0.5 | LI | LI | - | ||
female 306 | 2.5 + FCA | I | N | - | |
2.5 | I | N | - | ||
1 + FCA | I | N | - | ||
1 | I | I | - | ||
0.5 + FCA | I | I | - | ||
0.5 | I | I | - | ||
male 309 | 0.5 + FCA | I | I | A | |
0.5 | LI | LI | I | ||
0.25 + FCA | I | I | I | ||
0.25 | LI | LI | LI | ||
0.1 + FCA | I | I | I | ||
0.1 | LI | LI | LI | ||
female 310 | 0.5 + FCA | I | I | A | |
0.5 | LI | LI | I | ||
0.25 + FCA | I | I | A | ||
0.25 | LI | LI | LI | ||
0.1 + FCA | I | I | I | ||
0.1 | LI | LI | LI | ||
FCA : mixture Freund's Complete Adjuvant/0.9% NaCl (50/50, v/v) | |||||
N : necrosis | |||||
I : irritation | |||||
LI : slight irritation | |||||
A : crusts | |||||
- : sacrificed animals | |||||
In order to respect the criteria for the selection of concentrations (the concentration | |||||
should be well-tolerated systemically and locally, intradermal injections should | |||||
cause moderate irritant effect but no necrosis or ulceration of the skin), | |||||
the concentration chosen for the main study was 0.1% (w/w). | |||||
Application by cutaneous route | |||||||
Results were as follows: | |||||||
Under the conditions of the induction phase | |||||||
Animal | Concentration of the | Scoring after removal of the dressing | |||||
number | test item % (w/w) | 24 hours | 48 hours | ||||
male 307 | 25 | 2 | 2 | ||||
female 308 | 10 | 1 | 1 | ||||
Under the conditions of the challenge phase | |||||||
Animal | Concentration of the | Scoring after removal of the dressing | |||||
number | test item % | 24 hours | 48 hours | ||||
male 301 | 100 | RF | LA | - | |||
50 (w/w) | LF | 3/A | - | ||||
female 302 | 100 | RF | LA | - | |||
50 (w/w) | LF | LA | - | ||||
male 305 | 25 (w/w) | RF | LN | - | |||
10 (w/w) | LF | 2/Oe | - | ||||
female 306 | 25 (w/w) | RF | LN | - | |||
10 (w/w) | LF | 2/Oe | - | ||||
male 309 | 5 (w/w) | RF | 2/Oe | 2/A | |||
2.5 (w/w) | LF | 0 | 0 | ||||
female 310 | 5 (w/w) | RF | 2/A | 3/A | |||
2.5 (w/w) | LF | 1 | 1 | ||||
male 311 | 1 (w/w) | RF | 0 | 0 | |||
0.5 (w/w) | LF | 0 | 0 | ||||
female 312 | 1 (w/w) | RF | 0 | 0 | |||
0.5 (w/w) | LF | 0 | 0 | ||||
RF : right flank | |||||||
LF : left flank | |||||||
LA : scoring masked by crusts | |||||||
A : crusts | |||||||
LN : scoring masked by necrosis | |||||||
Oe : oedema | |||||||
- : sacrificed animals | |||||||
On removal of the dressing, no residual test item was observed. | |||||||
In order to respect the criteria for the selection of concentrations (the concentrations should be | |||||||
well-tolerated systemically and locally, cutaneous application for the induction should cause at most | |||||||
weak or moderate skin reactions or be the maximal practicable concentration, cutaneous application | |||||||
for the challenge phase should be the highest concentration which does not cause irritant effect), the | |||||||
concentration chosen for the topical application of the induction phase (day 8) was 10% (w/w). | |||||||
For the challenge application (day 22), it was 1% (w/w). | |||||||
Application by cutaneous route | |||||||
Results were as follows: | |||||||
Under the conditions of the induction phase | |||||||
Animal | Concentration of the | Scoring after removal of the dressing | |||||
number | test item % (w/w) | 24 hours | 48 hours | ||||
male 307 | 25 | 2 | 2 | ||||
female 308 | 10 | 1 | 1 | ||||
Under the conditions of the challenge phase | |||||||
Animal | Concentration of the | Scoring after removal of the dressing | |||||
number | test item % | 24 hours | 48 hours | ||||
male 301 | 100 | RF | LA | - | |||
50 (w/w) | LF | 3/A | - | ||||
female 302 | 100 | RF | LA | - | |||
50 (w/w) | LF | LA | - | ||||
male 305 | 25 (w/w) | RF | LN | - | |||
10 (w/w) | LF | 2/Oe | - | ||||
female 306 | 25 (w/w) | RF | LN | - | |||
10 (w/w) | LF | 2/Oe | - | ||||
male 309 | 5 (w/w) | RF | 2/Oe | 2/A | |||
2.5 (w/w) | LF | 0 | 0 | ||||
female 310 | 5 (w/w) | RF | 2/A | 3/A | |||
2.5 (w/w) | LF | 1 | 1 | ||||
male 311 | 1 (w/w) | RF | 0 | 0 | |||
0.5 (w/w) | LF | 0 | 0 | ||||
female 312 | 1 (w/w) | RF | 0 | 0 | |||
0.5 (w/w) | LF | 0 | 0 | ||||
RF : right flank | |||||||
LF : left flank | |||||||
LA : scoring masked by crusts | |||||||
A : crusts | |||||||
LN : scoring masked by necrosis | |||||||
Oe : oedema | |||||||
- : sacrificed animals | |||||||
On removal of the dressing, no residual test item was observed. | |||||||
In order to respect the criteria for the selection of concentrations (the concentrations should be | |||||||
well-tolerated systemically and locally, cutaneous application for the induction should cause at most | |||||||
weak or moderate skin reactions or be the maximal practicable concentration, cutaneous application | |||||||
for the challenge phase should be the highest concentration which does not cause irritant effect), the | |||||||
concentration chosen for the topical application of the induction phase (day 8) was 10% (w/w). | |||||||
For the challenge application (day 22), it was 1% (w/w). | |||||||
MAIN STUDY
The test substance was not soluble in 0.9% NaCl: two phases were observed.
The vehicle chosen for intradermal injections was corn oil: a solution was obtained at the concentration of 25%; the dosage form preparation at the concentration of 25% (w/w) passed freely through a needle and into the dermis.
For topical applications, the vehicles used were a mixture ethanol/water (80/20) for the induction phase and acetone for the challenge application: solutions obtained whatever the proportion.
Clinical examinations
Marked local reactions at the intradermal injection sites were noted in a few animals of the treated group, between days 21 to 25.
No systemic clinical signs and no mortality were observed during the study.
Body weight
The body weight change of treated animals was similar to that of controls.
Challenge phase - Scoring of cutaneous reactions | |||||
Scoring of skin reactions was as follows | |||||
Control group | |||||
Sex | Animal | 24 hours | 48 hours | ||
number | LF | RF | LF | RF | |
Male | 81 | 0 | 0 | 0 | 0 |
82 | 0 | 0 | 0 | 0 | |
83 | 0 | 0 | 0 | 1 | |
84 | 0 | 0 | 0 | 0 | |
85 | 0 | 0 | 0 | 0 | |
Female | 96 | 0 | 0 | 0 | 1 |
97 | 0 | 0 | 0 | 0 | |
98 | 0 | 0 | 0 | 0 | |
99 | 0 | 0 | 0 | 0 | |
100 | 0 | 0 | 0 | 0 | |
LF : left flank (vehicle) | |||||
RF : right flank (test item at the concentration of 1% (w/w)) | |||||
Treated Group | |||||
Sex | Animal | 24 hours | 48 hours | ||
number | LF | RF | LF | RF | |
Male | 86 | 0 | 0 | 0 | 0 |
87 | 0 | 0 | 0 | 0 | |
88 | 0 | 0 | 0 | 0 | |
89 | 0 | 0 | 0 | 0 | |
90 | 0 | 0 | 0 | 0 | |
91 | 0 | 0 | 0 | 0 | |
92 | 0 | 0 | 0 | 0 | |
93 | 0 | 0 | 0 | 0 | |
94 | 0 | 0 | 0 | 0 | |
95 | 0 | 0 | 0 | 0 | |
Female | 101 | 0 | 0 | 0 | 0 |
102 | 0 | 0 | 0 | 0 | |
103 | 0 | 0 | 0 | 0 | |
104 | 0 | 0 | 0 | 0 | |
105 | 0 | 0 | 0 | 0 | |
106 | 0 | 0 | 0 | 0 | |
107 | 0 | 0 | 0 | 0 | |
108 | 0 | 0 | 0 | 0 | |
109 | 0 | 0 | 0 | 0 | |
110 | 0 | 0 | 0 | 0 | |
LF : left flank (vehicle) | |||||
RF : right flank (test item at the concentration of 1% (w/w)) | |||||
On removal of the dressing, no residual test item was observed. | |||||
After the challenge application, a discrete erythema (grade 1) was observed in 2/10 animals | |||||
of the control group at the 48-hour reading. | |||||
No cutaneous reactions were observed in the treated group. | |||||
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
- Additional information:
No data is available for the assessment of respiratory sensitization. Taking account that no significant skin sensitization can be reliably derived and that the registration is of low volatily, no significant hazard for the respiratory sensitization can be derived. No classification is justified for the endpoint respiratory sensitization.
Justification for classification or non-classification
The assessment of the skin sensitization property of the registration substance is based on the read-across approach.
2,2'-(octadec-9-enylimino) bisethanol CAS 25307-17-9, was tested for its skin sensitization property according to OECD 406 Test Guideline. No significant skin sensitization property was found. Likewise, no skin sensitization property is expected for the registration substance and no classification is justified for the endpoint skin sensitization.
No data is available for the assessment of respiratory sensitization. Taking account that no significant skin sensitization can be reliably derived and that the registration is of low volatily, no significant hazard for the respiratory sensitization can be derived. No classification is justified for the endpoint respiratory sensitization.
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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