Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 204-685-9 | CAS number: 124-17-4
- 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
Acute Toxicity: dermal
Administrative data
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1944
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- This is a very old study that does not meet the full requirements of current OECD guidelines (not all end points reported). Nevertheless, it is reported in some detail and the method followed forms the basis for current testing methods and provides the key required parameter of a trustworthy LD50. It is therefore considered a reliable contribution to understanding the acute dermal toxicity of this substance.
Cross-reference
- Reason / purpose for cross-reference:
- reference to other study
Data source
Referenceopen allclose all
- Reference Type:
- publication
- Title:
- Methods for the study of irritation and toxicity of substances applied topically to the skin and mucous membranes
- Author:
- Draize JH, Woodward G, Calvery HO
- Year:
- 1 944
- Bibliographic source:
- J Pharmac exp Ther, 82, 377
- Reference Type:
- publication
- Title:
- Toxicological investigations of compounds proposed for use as insect repellants
- Author:
- Draize JH, Alvarez, E, Whitesell MF, Woodward, G, Hagan EC, Nelson AA
- Year:
- 1 948
- Bibliographic source:
- J Pharmac Exper Ther, 43, 26
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 402 (Acute Dermal Toxicity)
- Deviations:
- yes
- Remarks:
- See below
- Principles of method if other than guideline:
- Study pre-dates guidelines but follows the basic principles of current methods
- GLP compliance:
- no
- Remarks:
- pre-dates guidelines
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- 2-(2-butoxyethoxy)ethyl acetate
- EC Number:
- 204-685-9
- EC Name:
- 2-(2-butoxyethoxy)ethyl acetate
- Cas Number:
- 124-17-4
- Molecular formula:
- C10H20O4
- IUPAC Name:
- 2-(2-butoxyethoxy)ethyl acetate
- Details on test material:
- No data on purity. Referred to as diethylene glycol monobutyl ether acetate
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 2.5-3.5kg
- Housing: no data during study but metabolism cages used to collect urine during observation period.
No further data
Administration / exposure
- Type of coverage:
- occlusive
- Vehicle:
- unchanged (no vehicle)
- Details on dermal exposure:
- TEST SITE
- Area of exposure: trunk
- % coverage: 10.7%
- Type of wrap if used: rubber sleeve made from rubber dam
REMOVAL OF TEST SUBSTANCE
- Washing (if done): no
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): sufficient to furnish a reservoir for the dose
OTHER
- Preparation of test site: clipping 24 hours prior to exposure. Half animals also subjected to epidermal abrasions 2 cm apart - Duration of exposure:
- 24 hours
- Doses:
- Not specified for main test but preliminary range finder doses 3.9, 6.0 and 9.4ml/kg
- No. of animals per sex per dose:
- Study states 'sufficient to calculate the fatal dose', but no specific numbers given. Total number of animals used in study 100.
- Control animals:
- other: concurrent testing of other substances effectively provided controls
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations and weighing: daily
- Necropsy of survivors performed: yes, but only on animals that died before end of observation period
- Other examinations performed: clinical signs, body weight, food consumption, organ weights, urine, blood morphology - Statistics:
- Method of Bliss (Quart. J. Pharm Pharmacol, 11, 192, 1938)
Results and discussion
Effect levelsopen allclose all
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 5.75 mL/kg bw
- Remarks on result:
- other: Results quoted in 1944 reference
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 5.5 mL/kg bw
- Remarks on result:
- other: Result quoted in 1948 reference
- Mortality:
- No data
- Clinical signs:
- other: No data
- Gross pathology:
- No data
- Other findings:
- No data
Any other information on results incl. tables
The 1948 reference is a compilation of results from this author's previous work. It is believed to be the quote the same results as from the 1944 reference, even though the quoted figures differ slightly.
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Executive summary:
In an old acute dermal toxicity study, 2 -(2 -butoxyethoxy)ethyl acetate was found to have an LD50 of around 5.5 -5.8ml/kg in rabbits. This study did not meet the full requirements of current OECD guideline (not all end points reported), but the method was reported in some detail and the results therefore considered reliable.
Synopsis
LD50 = 5.5 -5.8ml/kg (equivalent to 5400 - 5700mg/kg)
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.