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EC number: 226-685-8 | CAS number: 5451-76-3
- 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:
- 2013
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study was condcuted according to OECD TG 404, EPA TG OPPTS 870.2500 and in accordance with the Principles of Good Laboratory Practice (GLP).
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- reference to same study
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 013
- Report date:
- 2013
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 870.2500 (Acute Dermal Irritation)
- Deviations:
- no
- Principles of method if other than guideline:
- not applicable
- GLP compliance:
- yes
Test material
- Reference substance name:
- 2-butoxyethyl benzoate
- EC Number:
- 226-685-8
- EC Name:
- 2-butoxyethyl benzoate
- Cas Number:
- 5451-76-3
- Molecular formula:
- C13H18O3
- IUPAC Name:
- 2-butoxyethyl benzoate
- Test material form:
- other: variable colured liquid
- Details on test material:
- - Name of test material (as cited in study report): Butyl Cellosolve™ Benzoate
- Physical state: variable coloured liquid
- Analytical purity: 99.86%
- Lot/batch No.: 02112012-JLT
- Expiration date of the lot/batch: 11 February 2013
- Storage condition of test material: Ambient (+18 to +36 ºC)
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: inhouse bred (outbred)
- Age at study initiation: 7-8 months
- Weight at study initiation: 2.71 - 2.91 kg
- Housing: individually housed in rabbit cages (approx. size: L 65 x B 65 xH 45 cm) under standard laboaratory conditions
- Diet (ad libitum): The animals were offered rabbit feed manufactured by Pranav Agro Industries Ltd, Sangli, Maharashtra, India.
- Water (ad libitum): The animals were provided deep bore-well water passed through activated charcoal
filter and exposed to UV rays in Aquaguard on-line water filter-cum-purifier. The water was replenished once daily and the water bottles changed once a week.
- Acclimation period: 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 - 23°C
- Humidity (%): 64-67%
- Air changes (per hr): 12-15 air changes/hour
- Photoperiod (hrs dark / hrs light): 12 hour light and 12 hour dark cycle
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- clipped
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): A volume of 0.5 mL of the undiluted test substance was applied on to the test site of approximately 6 cm2 (2 x 3 cm) and covered by a 6-ply gauze pad. The entire trunk of each animal was then wrapped with non-irritating semi-occlusive adhesive tape to avoid dislocation of the patch. - Duration of treatment / exposure:
- 4-hour exposure period
- Observation period:
- 7 days
- Number of animals:
- 3 rabbits
- Details on study design:
- TEST SITE
- Area of exposure: Approximately 24 hours before treatment, the fur on the left side of the dorsolateral trunk surface [about 14 x 19 cm] was clipped with an electric clipper -Aesculap®- Germany. Care was taken to avoid abrading the skin. After clipping and prior to application, the animal’s skin (test site) was checked for any abnormalities according to the “Primary Skin Irritation Scoring System”, and the test site was found to be normal.
- % coverage: An approximately 6 cm2 intact test site was selected on each animal. The adjacent untreated skin of each animal served as the control site.
- Type of wrap if used: A volume of 0.5 mL of the undiluted test substance was applied on to the test site of approximately 6 cm2 (2 x 3 cm) and covered by a 6-ply gauze pad. The entire trunk of each animal was then wrapped with non-irritating semi-occlusive adhesive tape to avoid dislocation of the patch.
- The rabbits were restrained using an Elizabethan collar for 4 hours during the contact period of test substance.
REMOVAL OF TEST SUBSTANCE
- Washing: Following the exposure period, test patches were removed and the test sites were washed with de-ionised water to remove any residual test substance.
SCORING SYSTEM: The test sites were examined for signs of erythema and edema within 60 minutes and at intervals of approximately 24, 48 and 72 hours and on Day 7 after test patch removal according to the "Primary Skin Irritation Scoring System" developed by Draize, et.al (1944).
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- other: 24, 48 and 72 hours
- Score:
- 1
- Max. score:
- 1
- Reversibility:
- fully reversible within: 7 days
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- other: 24, 48 and 72 hours
- Score:
- 1
- Max. score:
- 1
- Reversibility:
- fully reversible within: 7 days
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- other: 24, 48 and 72 hours
- Score:
- 1
- Max. score:
- 1
- Reversibility:
- fully reversible within: 7 days
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- of all animals
- Time point:
- other: 24, 48 and 72 hours
- Score:
- 1
- Max. score:
- 1
- Reversibility:
- fully reversible within: 7 days
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- other: 24, 48 and 72 hours
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- other: not applicable
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- other: 24, 48 and 72 hours
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- other: not applicable
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- other: 24, 48 and 72 hours
- Score:
- 1
- Max. score:
- 1
- Reversibility:
- fully reversible within: 7 days
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- of all animals
- Time point:
- other: 24, 48 and 72 hours
- Score:
- 0.33
- Max. score:
- 1
- Reversibility:
- fully reversible within: 7 days
- Irritant / corrosive response data:
- Erythema score of 1 was observed in two rabbits (RB9663 & RB 9664) at 24, 48 and 72 hours post removal of the test patch. Erythema and Edema score of 1 was observed in the third rabbit (RB9665) at 24, 48 and 72 hours post removal of the test patch. The skin at the treated site of all the three rabbits was normal on the 7th day post removal of the test patch
- Other effects:
- There were no clinical signs of toxicity or mortality observed during the course of the study and the body weights of all the rabbits increased throughout the observation period.
Any other information on results incl. tables
None
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Under the testing conditions of this study, 2-butoxyethyl benzoate caused erythema (score of 1) in 3 rabbits and edema (score of 1) in one rabbit and these scores were completely reversed by day 7 post removal of the test patch and according to Guidance to regulation (EC) No. 1272/2008 on classification, labelling and packaging (CLP) of substances and mixtures, 2-butoxyethyl benzoate will be not classified for skin irritation.
- Executive summary:
The acute dermal irritation/corrosion study in rabbits was conducted to evaluate the skin irritation potential of 2-butoxyethyl benzoate. All the three rabbits were treated at the same time (4 hours only) as per sponsor’s request. A volume of 0.5 mL of the undiluted test substance was applied on to the test site of approximately 6 cm2 (2 x 3 cm) and covered by a 6-ply gauze pad. The patch was secured to the body of the animal by a non-irritating semi-occlusive adhesive tape. The patch was removed after 4 hours of skin contact. All test sites were evaluated for skin irritation according to the Draize (1944) evaluation method.
There were no clinical signs of toxicity or mortality observed during the course of the study and the body weights of all the rabbits increased throughout the observation period. Erythema score of 1 was observed in two rabbits (RB9663 & RB 9664) at 24, 48 and 72 hours post removal of the test patch. Erythema and Edema score of 1 was observed in the third rabbit (RB9665) at 24, 48 and 72 hours post removal of the test patch. The skin at the treated site of all the three rabbits was normal on the 7th day post removal of the test patch.
Under the testing conditions of this study, 2-butoxyethyl benzoate caused erythema (score of 1) in 3 rabbits and edema (score of 1) in one rabbit and these scores were completely reversed by day 7 post removal of the test patch and according to Guidance to regulation (EC) No. 1272/2008 on classification, labelling and packaging (CLP) of substances and mixtures, 2-butoxyethyl benzoate will be not classified for skin irritation.
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