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Developmental toxicity of 2-ethylhexyl stearate
W Aulmann1, W Pittermann, F Bartnik
1Henkel KGaA, D-40191, Düsseldorf, Germany. Walter.Aulmann@Henkel.de
Summary
2-Ethylhexyl stearate showed no embryo-foetotoxicity or teratogenicity in rats. The No Observed Adverse Effect Level (NOAEL) for maternal toxicity was 1000 mg/kg, indicating safety at tested doses.
Area of Science:
- Toxicology
- Developmental Biology
- Chemical Safety Assessment
Background:
- 2-Ethylhexyl stearate is a chemical compound used in various applications.
- Assessing the potential risks of chemical substances to development is crucial for public health and environmental safety.
Purpose of the Study:
- To evaluate the embryo-foetal toxicity and teratogenicity of 2-Ethylhexyl stearate in a rat model.
- To determine the maternal and developmental No Observed Adverse Effect Level (NOAEL) for 2-Ethylhexyl stearate.
Main Methods:
- A study was conducted on pregnant rats following OECD guidelines for chemical testing (No. 414).
- Doses of 0, 100, 300, and 1000 mg/kg/day of 2-Ethylhexyl stearate were administered via gavage.
- Maternal toxicity, pre- and post-implantation loss, resorptions, and foetal malformations (skeletal and visceral) were assessed.
Main Results:
- Dams tolerated all tested dose levels without observable toxic effects.
- No significant differences were found in pre- and post-implantation loss or mean numbers of resorptions compared to the control group.
- No treatment-related skeletal or visceral malformations were detected in the offspring.
Conclusions:
- 2-Ethylhexyl stearate demonstrated no adverse effects on embryo-foetal development or teratogenicity in rats.
- The No Observed Adverse Effect Level (NOAEL) for maternal toxicity, embryo-foetal toxicity, and teratogenicity was determined to be 1000 mg/kg body weight/day.