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EC number: 451-160-7 | CAS number: 17913-76-7
- 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
not irritating to skin
irritating, but not corrosive to the eyes
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:
- key study
- Study period:
- 2001
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Type of coverage:
- occlusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Duration of treatment / exposure:
- #1: 3 minutes 0,5 ml one animal
#2: 1 hour 0,5 ml three animals
#3: 4 hour 0,5 ml three animals - Observation period:
- 14 days
- Number of animals:
- three animals
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- mean
- Remarks:
- F8931, F8941, F8962
- Time point:
- other: day 14
- Score:
- ca. 2.17
- Max. score:
- 8
- Reversibility:
- fully reversible
- Remarks on result:
- other: normal
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- fully reversible
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 1.33
- Max. score:
- 4
- Reversibility:
- fully reversible
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- fully reversible
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0.67
- Max. score:
- 4
- Reversibility:
- fully reversible
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- fully reversible
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The substance is not classified as irritating to skin.
- Executive summary:
3 Minute exposure: There was no erythema or edema noted at 1 hour following patch removal.
1 hour exposure: Erythema was absent to barely perceptible at 1 hour following patch removal, barely perceptible at 24 hours. absent to barely perceptible at 48 hours, and absent to well defined at 72 hours. Erythema was absent by day 7 and 14. Edema was absent at 1 hour following patch removal and absent to barely perceptible at 24 hours. Edema was absent at 48 and 72 hours, and on days 7 and 14.
4 hour exposure: Erythema was barely perceptible at 1 hour following patch removal and barely perceptible to well defined at 24, 48, 72 hours. Erythema was absent on days 7 and 14. Edema was absent at 1 hour following patch removal, barely perceptible at 24 hours, and absent to barely perceptible at 48 and 72 hours. Edema was absent on days 7 and 14.
Systemic Observations: There were no abnormal physical signs noted during the observation period. All body weight changes were normal.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Eye irritation
Link to relevant study records
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 01.10.2001 - 15.10.2001
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Duration of treatment / exposure:
- 0,1 ml initial instillation
- Observation period (in vivo):
- 1, 24, 48, 72 hours and on days 7 and 14
- Number of animals or in vitro replicates:
- 3
- Details on study design:
- SCORING SYSTEM: Draize
TOOL USED TO ASSESS SCORE: mini-Maglite - Irritation parameter:
- cornea opacity score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- iris score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.3
- Max. score:
- 2
- Reversibility:
- fully reversible
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 3
- Reversibility:
- fully reversible
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- fully reversible
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 1.3
- Max. score:
- 4
- Reversibility:
- fully reversible
- Irritation parameter:
- iris score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- fully reversible
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 3
- Reversibility:
- fully reversible
- Irritation parameter:
- chemosis score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 2.7
- Max. score:
- 4
- Reversibility:
- fully reversible
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- fully reversible
- Irritation parameter:
- iris score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0.3
- Max. score:
- 2
- Reversibility:
- fully reversible
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 1.7
- Max. score:
- 3
- Reversibility:
- fully reversible
- Irritation parameter:
- chemosis score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 1.7
- Max. score:
- 4
- Reversibility:
- fully reversible
- Interpretation of results:
- Category 2 (irritating to eyes) based on GHS criteria
- Conclusions:
- 2,4,7,9-tetramethyldecane-4,7-diol is an ocular irritant, but not corrosive.
- Executive summary:
Ocular findings:
Corneal opacity was noted in 1/3 eyes, although fluorescein stain retention was noted in all the eyes.
The opacity cleared by day 7.
Iritis, noted in 3/3 eyes, cleared by day 7. Conjunctival irritation, noted in 3/3 eyes, cleared by day 14.
Reference
Score at time point / Reversibility |
Cornea |
Iris |
Conjunctivae |
Chemosis |
Discharge
|
Max. score: 4 |
Max. score: 2 |
Max. score: 3 |
Max. score: 4 |
Max. score: 3 |
|
60 min |
0h/0/0 |
0/0/0 |
1/2/2 |
2/3/3 |
2/2/2 |
24 h |
0h/0h/0h |
1/1/1 |
2/2/2 |
2/3/2 |
2/2/2 |
48 h |
0h/2/0h |
0/1/0 |
2/2/2 |
2/3/2 |
1/2/2 |
72 h |
0/2/0 |
0/1/0 |
2/2/1 |
2/2/1 |
1/2/1 |
7 d |
0/0/0 |
0/0/0 |
1/1/1 |
0/1/0 |
0/1/0 |
14 d |
0/0/0 |
0/0/0 |
0/0/0 |
0/0/0 |
0/0/0 |
Average 24h, 48h, 72h |
0/1.3/0 |
0.3/1/0.3 |
2/2/1.7 |
2/2.7/1.7 |
1.3/2/1.7 |
h = lack of normal luster
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Skin irritation
In a primary dermal irritation study according to OECD TG 404 young adult New Zealand White rabbits were dermally exposed to 0.5 mL 2,4,7,9-tetramethyldecane-4,7-diol (3 minutes exposure: one animal; 1 hour exposure: three animals; 4 hour exposure: three animals). Animals then were observed for 14 days. Irritation was scored by the method of Draize.
3 Minute exposure: There was no erythema or edema noted at 1 hour following patch removal.
1 hour exposure: Erythema was absent to barely perceptible at 1 hour following patch removal, barely perceptible at 24 hours. absent to barely perceptible at 48 hours, and absent to well defined at 72 hours. Erythema was absent by day 7 and 14. Edema was absent at 1 hour following patch removal and absent to barely perceptible at 24 hours. Edema was absent at 48 and 72 hours, and on days 7 and 14.
4 hour exposure: Erythema was barely perceptible at 1 hour following patch removal and barely perceptible to well defined at 24, 48, 72 hours. Erythema was absent on days 7 and 14. Edema was absent at 1 hour following patch removal, barely perceptible at 24 hours, and absent to barely perceptible at 48 and 72 hours. Edema was absent on days 7 and 14.
Systemic Observations: There were no abnormal physical signs noted during the observation period. All body weight changes were normal.
The substance is not irritating to skin.
Eye irritation
The purpose of this test was to determine the irritant and/or corrosive effects, if any, of a test article when instilled into the rabbit eye.
Three healthy New Zealand White rabbits (males), free from evidence of ocular irritation and corneal abnormalities, were dosed with 2,4,7,9-tetramethyldecane-4,7-diol. The test article (0.1 ml) was placed into the conjunctival sac of one eye of each rabbit. Sodium fluorescein dye procedures were used at the 24, 48, and 72-hour observation intervals and again on Days 7 and 14. The eyes were examined and scored by the Draize technique at 1,24,48, and 72 hours post-dose and on Days 7 and 14. The primary eye irritation score for each rabbit, each day, was calculated. Body weights were recorded pretest.
Corneal opacity was noted in 1/3 eyes (average score 1.3), although fluorescein stain retention was noted in all the eyes. The opacity cleared by Day 7. Iritis, noted in 3/3 eyes (average scores: 0.3/1/0.3), cleared by Day 7. Conjunctival redness, noted in 3/3 eyes (average scores: 2/2/1.7), cleared by Day 14. Chemosis noted in 3/3 eyes (average scores: 2/2.7/1.7), cleared by Day 14.
The substance is an ocular irritant, but not corrosive.
Respiratory irritation
No data on the respiratory irritation of 2,4,7,9-tetramethyldecane-4,7-diol are available.
There are no data gaps for the endpoint irritation/corrosion. No human information is available for this endpoint. However, there is no reason to believe that these results would not be applicable to humans.
Justification for classification or non-classification
According to the UN Globally Harmonized System of Classification and Labelling of Chemicals (GHS) Part 3 Chapter 3.3 it is classified to be irritating to eye.
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