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EC number: 205-476-5 | CAS number: 141-27-5
- 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 irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 05 Apr - 13 Apr 1978
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Basic data given; comparable to standards with restrictions.
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 978
- Report date:
- 1978
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Internal BASF-test: occlusive application of unspecified amount for 1 or 15 min, or 2 or 20 h, scoring at end of exposure and after 1, 2, 5, 7 and 8 d, internal scoring system
- GLP compliance:
- no
Test material
- Reference substance name:
- Citral
- EC Number:
- 226-394-6
- EC Name:
- Citral
- Cas Number:
- 5392-40-5
- IUPAC Name:
- 3,7-dimethylocta-2,6-dienal
- Reference substance name:
- (Z)-3,7-dimethylocta-2,6-dienal
- EC Number:
- 203-379-2
- EC Name:
- (Z)-3,7-dimethylocta-2,6-dienal
- Cas Number:
- 106-26-3
- Molecular formula:
- C10H16O
- IUPAC Name:
- 3,7-dimethylocta-2,6-dienal
- Details on test material:
- - Name of test material (as cited in study report): citral, 3,7-dimethyloctadien-2,6-al-1
Purity: >= 95 %
Constituent 1
Constituent 2
Test animals
- Species:
- rabbit
- Strain:
- Vienna White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Gaukler
- Weight at study initiation: 3.44 and 3.04 kg
- Sex: females
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- not specified
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- not specified
- Duration of treatment / exposure:
- 1 min, 15 min, 2 h and 20 h
- Observation period:
- 8 days
- Number of animals:
- 2
- Details on study design:
- TEST SITE
- Area of exposure: 2.5 x 2.5 cm
- Type of wrap if used: no data
OBSERVATIONS:
- observation of application site: after removal of the patch and on day 1, 2, 5, 7 and 8 after application
- at the end of the study: gross-pathology
REMOVAL OF TEST SUBSTANCE
- Washing: with Lutrol and Lutrol: water (1:1)
- Time after start of exposure: 1 min, 15 min, 2 h and 20 h
SCORING SYSTEM:
- Erythema: 1 = questionable, 2 = slight, 3 = moderate, 4 = severe
- Edema: 1 = very slight, 2 = slight, 3 = moderate, 4 = severe
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- other: 24 and 48 hrs
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 8 days
- Remarks on result:
- other: treatment time 1 min
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- other: 24 and 48 hrs
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 8 days
- Remarks on result:
- other: treatment time 1 min
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- other: 24 and 48 hrs
- Score:
- 2.25
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 8 days
- Remarks on result:
- other: treatment time 15 min
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- other: 24 and 48 hrs
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 8 days
- Remarks on result:
- other: treatment time 15 min
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- other: 24 and 48 hrs
- Score:
- 2.75
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 8 days
- Remarks on result:
- other: treatment time 2 hrs
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- other: 24 and 48 hrs
- Score:
- 2.75
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 8 days
- Remarks on result:
- other: treatment time 2 hrs
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- other: 24 and 48 hrs
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 8 days
- Remarks on result:
- other: treatment time 20 hrs- necroses observed
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- other: 24 and 48 hrs
- Score:
- 3
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 8 days
- Remarks on result:
- other: treatment time 20 hrs - necroses observed
- Irritant / corrosive response data:
- Exposures of 1 min, 15 min, and 2 hours lead in all animals to visible inflammation of treated skin areas which still persisted after the 8-day post-observation period. In addition, all animals showed desquamation from day 5 to the end of the observation period. (For details see Tables 1 to 3)
20-hr exposure: both animals showed enhanced inflammation which was not declining during the observation period. Additionally, both animals showed soft and parchment-like necroses indicating a severe irritating potential (for details see Table 4) - Other effects:
- Gross-pathology: the preliminary report about the skin was confirmed; organs without findings.
Any other information on results incl. tables
Remark: in all experiments the first reading is done immediately after the end of the exposure time, so the time points given for the readings are calculated starting with the onset of exposure.
Table 1: Skin reactions after a 1-min treatment
Readings |
Animal |
Exposure period: 1 min |
||
Erythema |
Edema |
Additional findings |
||
1 min |
1 |
2 |
0 |
|
2 |
1 |
0 |
||
24 h |
1 |
2 |
2 |
|
2 |
2 |
2 |
||
48 h |
1 |
2 |
2 |
|
2 |
2 |
2 |
||
5 d |
1 |
2 |
1 |
D |
2 |
2 |
1 |
Da |
|
7 d |
1 |
2 |
1 |
D |
2 |
2 |
1 |
D |
|
8 d |
1 |
2 |
1 |
D |
2 |
2 |
0 |
D |
|
Mean 24, 48h |
1 |
2 |
2 |
|
2 |
2 |
2 |
||
Mean 24, 48 h |
1-2 |
2 |
2 |
a = finding exceeding beyond area of exposure
D = desquamation
Table 2: Skin reactions after a 15-min treatment
Readings |
Animal |
Exposure period: 15 min |
||
Erythema |
Edema |
Additional findings |
||
15 min |
1 |
2 |
0 |
|
2 |
2 |
0 |
||
24 h |
1 |
2a |
2a |
|
2 |
3a |
2 |
||
48 h |
1 |
2a |
2a |
|
2 |
3a |
2 |
||
5 d |
1 |
2a |
2a |
Da |
2 |
3a |
2 |
Da |
|
7 d |
1 |
2 |
2 |
D |
2 |
2a |
2 |
Da |
|
8 d |
1 |
2 |
1 |
D |
2 |
2a |
1 |
Da |
|
Mean 24, 48h |
1 |
2 |
2 |
|
2 |
2.5 |
2 |
||
Mean 24, 48 h |
1-2 |
2.25 |
2 |
a = finding exceeding beyond the area of exposure
D = desquamation
Table 3: Skin reactions after a 2 -hr treatment
Readings |
Animal |
Exposure period: 2 h |
||
Erythema |
Edema |
Additional findings |
||
2 h |
1 |
2 |
2 |
|
2 |
2 |
2 |
||
24 h |
1 |
3a |
3a |
|
2 |
2 |
2 |
||
48 h |
1 |
3a |
3a |
|
2 |
3a |
3 |
||
5 d |
1 |
3a |
3a |
|
2 |
3a |
2a |
Da |
|
7 d |
1 |
2 |
3 |
D |
2 |
3 |
3 |
sDa |
|
8 d |
1 |
2 |
2 |
D |
2 |
2a |
2 |
sDa |
|
Mean 24, 48h |
1 |
3 |
3 |
|
2 |
2.5 |
2.5 |
||
Mean 24, 48 h |
1-2 |
2.75 |
2.75 |
a = finding exceeding beyond the area of exposure
D = desquamation
s=strong
Table 4: Skin reactions after a 20-hr treatment
Readings |
Animal |
Exposure period: 20 h |
||
Erythema |
Edema |
Additional findings (erythema / edema) |
||
20 h |
1 |
- |
- |
|
2 |
- |
- |
||
24 h |
1 |
4 |
3a |
Ns |
2 |
4 |
3 |
Ns |
|
48 h |
1 |
4 |
3a |
Np |
2 |
4a |
3a |
Np |
|
5 d |
1 |
4 |
3 |
Np |
2 |
4 |
2 |
Np |
|
7 d |
1 |
4a |
3 |
Np |
2 |
4 |
3 |
Np |
|
8 d |
1 |
4a |
2 |
Np |
2 |
4a |
2 |
Np |
|
Mean 24, 48h |
1 |
4 |
3 |
|
2 |
4 |
3 |
||
Mean 24, 48 h |
1-2 |
4 |
3 |
a = finding exceeding beyond the area of exposure
N = necrosis, s = soft, p = like parchment
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.