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Diss Factsheets
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EC number: 310-290-3 | CAS number: 161907-80-8
- 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:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1990-02-26 to 1990-03-06
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study is well documented and performed according to generally valid and/or internationally accepted testing guidelines. The test material contained a high percentage of the test substance.
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 990
- Report date:
- 1990
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Principles of method if other than guideline:
- Deviating from OECD 404, six instead of 3 animals were used with a maximal observation period of 7 days.
- GLP compliance:
- no
Test material
- Reference substance name:
- Brake Fluid DOT 4 Super containing B-TTEGME
- IUPAC Name:
- Brake Fluid DOT 4 Super containing B-TTEGME
- Details on test material:
- - Name of test material (as cited in study report): Brake fluid DOT 4 Super
- Substance type: Borated Glycol Ether
- Physical state: Clear colourless liquid
- Analytical purity: 76% B-TTEGME
- Impurities (identity and concentrations): Confidential details on test material
- Composition of test material, percentage of components: Confidential details on test material
- Purity test date: Not provided
- Lot/batch No.: KSLA Ref. 7842/89 (0.0039); Toxicology ref. No. ST90/023
- Expiration date of the lot/batch: Not provided
- Stability under test conditions: Not provided
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Froxfield Farms U.K. Ltd.
- Age at study initiation: 3-5 monhts
- Weight at study initiation: 2.94-3.65 kg
- Housing: stainless steel cages 91x 66 x 45 cm.
- Diet: pelleted standard rabbit diet S.Q.C., Special Diets Services, Ltd., ad libitum
- Water: public supply, ad libitum
- Acclimation period: No data
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 15-20
- Humidity (%): 30-70
- Air changes (per hr): No data
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: From: 1990-02-26 To: 1990-03-06
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- 0.5 ml undiluted
- Duration of treatment / exposure:
- 4 hours
- Observation period:
- 0.5, 24, 48, 72 hours and 7 days
- Number of animals:
- 6
- Details on study design:
- TEST SITE
- On the day before dosing, the dorsal fur was removed using electric clippers.
- Area of exposure: a 6 cm2
- % coverage: 100% on lint patch covered with gauze
- Type of wrap if used: semi-occlusive elastic adhesive bandage
REMOVAL OF TEST SUBSTANCE
- Washing (if done): water
- Time after start of exposure: 4 hours
SCORING SYSTEM: Erythema and oedema were each scored on a five point scale
Erythema and Eschar Formation
- No erythema ...0
- Very slight erythema (barely perceptible) ...1
- Well defined erythema ...2
- Moderate to severe erythema ...3
- Severe erythema (beef redness) to eschar formation preventing grading of erythema...4
Oedema Formation
- No oedema...0
- Very slight oedema (barely perceptible) ...1
- Slight oedema (edges of area well defined by definite raising) ...2
- Moderate oedema (raised approximately 1 mm) ...3
- Severe oedema (raised more than 1 mm and extending beyond area of exposure) ...4
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24, 48, 72 hours
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: brake fluid
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24, 48, 72 hours
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: brake fluid
- Irritant / corrosive response data:
- No irritation or other dermal change.
Any other information on results incl. tables
Table 1. Dermal irritation testing in rabbits
Animal No. |
Sex |
Response |
0.5 hour |
24 hours |
48 hours |
72 hours |
7 days |
925 |
M |
Erythema |
0 |
0 |
0 |
0 |
0 |
Oedema |
0 |
0 |
0 |
0 |
0 |
||
926 |
M |
Erythema |
0 |
0 |
0 |
0 |
0 |
Oedema |
0 |
0 |
0 |
0 |
0 |
||
930 |
M |
Erythema |
0 |
0 |
0 |
0 |
0 |
Oedema |
0 |
0 |
0 |
0 |
0 |
||
957 |
F |
Erythema |
0 |
0 |
0 |
0 |
0 |
Oedema |
0 |
0 |
0 |
0 |
0 |
||
958 |
F |
Erythema |
0 |
0 |
0 |
0 |
0 |
Oedema |
0 |
0 |
0 |
0 |
0 |
||
959 |
F |
Erythema |
0 |
0 |
0 |
0 |
0 |
Oedema |
0 |
0 |
0 |
0 |
0 |
||
Mean Erythema score |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
||
Mean Oedema score |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
Table 2. Mean scores
Group mean 24, 48 & 72 hours |
|
Erythema |
0.0 |
Oedema |
0.0 |
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- No irritation or other dermal change.
- Executive summary:
Brake Fluid DOT 4 Super is considered to have a similar toxicological profile as B-TTEGME. Brake fluid DOT 4 Super was tested by semi-occluded topical application of 0.5 ml undiluted test material to the clipped dorsum of six rabbits for 4 hours. This corresponded to 0.375 ml B-TTEGME, assuming that Brake fluid DOT 4 and B-TTEGME have approximately the same density. No irritation or other dermal change was observed up to 7 days after administration.
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