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Diss Factsheets
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EC number: 203-846-0 | CAS number: 111-21-7
- 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
Acute Toxicity: other routes
Administrative data
- Endpoint:
- acute toxicity: other routes
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 984
- Report date:
- 1984
Materials and methods
- Principles of method if other than guideline:
- Single intratracheal injection of the test material in six rats.
- GLP compliance:
- no
Test material
- Reference substance name:
- 2,2'-[ethane-1,2-diylbis(oxy)]bisethyl diacetate
- EC Number:
- 203-846-0
- EC Name:
- 2,2'-[ethane-1,2-diylbis(oxy)]bisethyl diacetate
- Cas Number:
- 111-21-7
- Molecular formula:
- C10H18O6
- IUPAC Name:
- 2-[2-(2-acetyloxyethoxy)ethoxy]ethyl acetate
- Details on test material:
- - Name of test material (as cited in study report): Triethylene glycol diacetate
- Analytical purity: no data
- Physical state: liquid
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: A&E Farms, Altamont, USA
- Diet: Purina Laboratory Chow, either ground or pelleted
Administration / exposure
- Route of administration:
- other: intratracheal
- Vehicle:
- unchanged (no vehicle)
- Details on exposure:
- The animals were placed under deep ether anaesthesia and the hair of the ventral notch region was closely clipped and the skin washed with alcohol. A small incision was made through the skin and the underlying musculature was separated with muscle probes exposing the trachea. A bent needle was inserted into the trachea and the test material was injected. The skin incision was closed with adhesive (Eastman 910). After closure, the animals were held, head up, for a moment to facilitate flow into the lungs.
- Doses:
- 0.1 mL
- No. of animals per sex per dose:
- 6
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days
- Necropsy of all animals performed: yes
- Other examinations performed: histopathology of lungs and trachea
Results and discussion
Effect levels
- Sex:
- male
- Dose descriptor:
- other: tracheal and pulmonary lesions
- Effect level:
- 0.1 other: mL
- Based on:
- test mat.
- Mortality:
- 1/6 animals died 11 days after the surgery (animal #590)
- Clinical signs:
- 2/6 animals were weak, had rough coats, laboured respiration, avoided food and developed diarrhoea (animal #586 and #590).
- Body weight:
- 4/6 animals had normal weight gain. One animal lost weight (animal #586), one animal died at Day 11 (animal #590)
- Gross pathology:
- 1/6 animals had mottled lung (animal #590)
- Other findings:
- - Histopathology: The tracheas of two animals had massive aspiration pneumonia (animal #590 and 596). Of the four rats that survived, one had no inflammatory pulmonary lesions, two had mild to moderate chronic murine pneumonitis and one had patchy pulmonary edema and localized interstitial suppurative pneumonitis.
Any other information on results incl. tables
The tracheal lesions were those that occur routinely in rats and are not treatment related. The pulmonary lesions could be related to the introduction of foreign material into the airway and did not represent specific toxicologic effects.
Applicant's summary and conclusion
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.
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