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EC number: 246-131-9 | CAS number: 24293-43-4
Acute Toxicity: dermal
Administrative data
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP - Guideline study
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 008
- Report date:
- 2008
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 434 (Acute Dermal Toxicity - Fixed Dose Procedure)
- GLP compliance:
- yes (incl. QA statement)
- Test type:
- fixed dose procedure
- Limit test:
- yes
Test material
- Reference substance name:
- Bis(2-ethylhexyl) 2,2'-thiobisacetate
- EC Number:
- 246-131-9
- EC Name:
- Bis(2-ethylhexyl) 2,2'-thiobisacetate
- Cas Number:
- 24293-43-4
- Molecular formula:
- C20H38O4S
- IUPAC Name:
- 2-ethylhexyl 2-({2-[(2-ethylhexyl)oxy]-2-oxoethyl}sulfanyl)acetate
- Details on test material:
- - Name of test material (as cited in study report): Di(2-ethylhexyl) thiodiglycolate (Di-2-EHTDG)
- Physical state: slightly yellow to yellow, clear
- Analytical purity: 97.8%
- Main Impurities (identity and concentrations): Mono(2-ethylhexyl)thiodiglycolate; 2-ethylhexyl thioglycolate
- Lot/batch No.: 23015
- Storage condition of test material: at room temperature
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Harlan Winkelmann GmbH, D-33 178 Borchen.
- Age at study initiation: 8 - 12 weeks
- Weight at study initiation: 140 - 163 g
- Housing: Macrolon cages on Altromin saw fiber bedding
- Diet (e.g. ad libitum): Altromin 1324 maintenance diet for rats and mice
- Water (e.g. ad libitum): tap water
- Acclimation period: at least 5 d
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 +/-3
- Humidity (%): 45 - 65
- Air changes (per hr): 10
- Photoperiod (hrs dark / hrs light): 12 / 12
IN-LIFE DATES: From: 20 May 2008 To: 15 July 2008
Administration / exposure
- Type of coverage:
- semiocclusive
- Vehicle:
- unchanged (no vehicle)
- Details on dermal exposure:
- TEST SITE
- Area of exposure: dorsal trunk area
- % coverage: at least 10 % of the body surface
- Type of wrap if used: gauze-dressing and non-irritating tape, fixed with an additional dressing
REMOVAL OF TEST SUBSTANCE
- Washing (if done): residual test item was removed using tap water
- Time after start of exposure: 24 h
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 2.04 mL/kg bw. - Duration of exposure:
- 24 h
- Doses:
- single dose of 2000 mg/kg
- No. of animals per sex per dose:
- sighting study: 1
main study: 4 - Control animals:
- not required
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations and weighing:
The animals were weighed prior to the application and once a week thereafter.
Detailed clinical examinations were performed immediately after the dosing, at least once during the first 30 minutes, periodically during the first 24 hours, with special attention given during the first 4 hours, and daily thereafter.
Primary skin irritation was assessed 1, 2 and 3 days after removal of the test substance using the scoring system laid down in OECD guideline 404.
- Necropsy of survivors performed: yes
- Other examinations performed:
Cageside observations included changes in the skin and fur, eyes and mucous membranes. Also respiratory, circulatory, autonomic and central nervous systems and somatomotor activity and behaviour pattern were examined. Particular attention was directed to observations of tremor, convulsions, salivation, diarrhoea, lethargy, sleep and coma.
Results and discussion
- Preliminary study:
- No treatment related effects were observed
Effect levels
- Sex:
- female
- Dose descriptor:
- LD50
- Effect level:
- > 2 000 mg/kg bw
- Remarks on result:
- other: Wistar rat
- Mortality:
- No mortalities occured.
- Clinical signs:
- other: No clinical signs of toxicity were observed in all animals throughout the observation period.
- Gross pathology:
- No pathological abnormalities were noted.
Applicant's summary and conclusion
- Interpretation of results:
- practically nontoxic
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Based on the study results, no classification is required.
- Executive summary:
In an acute dermal toxicity study five female Wistar rats were dermally exposed to a single dose of 2000 mg/kg bw of the undiluted test substance Di(2-ethylhexyl) thiodiglycolate (Di-2-EHTDG) for 24 h under semiocclusive conditions. The application area comprised at least 10 % of the body surface area. The animals were observed for 14 days after application. No mortalities occured and no clinical signs of systemic toxicity were noted. The acute dermal LD(50) was calculated to be > 2000 mg/kg bw.
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