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EC number: 250-418-4 | CAS number: 30989-05-0
- 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:
- key study
- Study period:
- 1995-03-07 to 1995-03-10
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 995
- Report date:
- 1995
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Version / remarks:
- 17 July 1992
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- Tris[2-[2-(2-methoxyethoxy)ethoxy]ethyl] orthoborate
- EC Number:
- 250-418-4
- EC Name:
- Tris[2-[2-(2-methoxyethoxy)ethoxy]ethyl] orthoborate
- Cas Number:
- 30989-05-0
- Molecular formula:
- C21H45BO12
- IUPAC Name:
- tris{2-[2-(2-methoxyethoxy)ethoxy]ethyl} borate
- Test material form:
- liquid
Constituent 1
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Lot/batch No.of test material: Partie 24, 05-Jan-1995; Product number / code: LP 1941
- Substance type: Borated Glycol Ether
- Expiration date of the lot/batch: stable until 05-Jul-1995
- Purity test date: Not provided
- Analytical purity: 97% (calculated after titration of boric acid)
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Chemical pharmaceutical factory Dr. K. Thomae, 88400 Biberach, Germany; SPF breed
- Age at study initiation: 3-5 months
- Weight at study initiation: 2.8-3.2 kg
- Housing: separate cages (arranged in a battery), air-conditioned rooms
- Diet: ssniff K-H (V2333) ad libitum and hay (approx. 15 g daily)
- Water: from automatic dispensers ad libitum
- Acclimation period: No data
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 17-23
- Humidity (%): 30-70
- Air changes (per hr): No data
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: From: 1995-03-07 To 1995-03-10
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 ml per patch (undiluted)
- Concentration (if solution): 100% (undiluted)
VEHICLE: not applicable - Duration of treatment / exposure:
- 4 hours
- Observation period:
- Examinations of the skin took place after 30-60 minutes as well as 24, 48 and 72 hours after removal of the patches.
- Number of animals:
- 3
- Details on study design:
- TEST SITE
- The dorsal region of the body was removed by an electric clipper over an area of 25 cm2.
- Area of exposure: 2.5 x 2.5 cm
- % coverage: 100% cellulose patch on a piece of surgical plaster
- Type of wrap used: semi-occlusive bandage.
REMOVAL OF TEST SUBSTANCE
- Washing (if done): all remnants of the test substance were carefully removed from the skin with warm tap water
- Time after start of exposure: 4 hours
SCORING SYSTEM: according to OECD 404
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
- Not assessable ...*
- Maximum possible: 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
- Not assessable ...*
- Maximum possible: 4
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritant / corrosive response data:
- No signs of irritation were observed during the study.
For further details, see table 1.
Any other information on results incl. tables
Table 1. Dermal irritation testing in rabbits
Animal No. |
Erythema |
Mean score |
Oedema |
Mean score |
||||||
30-60 minutes |
1 day |
2 days |
3 days |
30-60 minutes |
1 day |
2 days |
3 days |
|||
159 |
0 |
0 |
0 |
0 |
0.0 |
0 |
0 |
0 |
0 |
0.0 |
160 |
0 |
0 |
0 |
0 |
0.0 |
0 |
0 |
0 |
0 |
0.0 |
161 |
0 |
0 |
0 |
0 |
0.0 |
0 |
0 |
0 |
0 |
0.0 |
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Based upon the results of the study B-TEGME is not irritating to the skin.
- Executive summary:
In an acute dermal irritation/corrosion study according to OECD 404, three New Zealand White rabbits were dermally exposed with the test substance.
Semi-occlusive testing of 0.5 ml undiluted B-TEGME for 4 hours showed neither erythma nor oedema on any of the three rabbits after the exposure and observation time points.
It can be occluded that B-TEGME is not irritating to the skin.
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