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Acute Toxicity to Freshwater Invertebrates (OPPTS Harmonized Guideline 850.1010;<br />

OECD 202)<br />

Conclusion:<br />

The available acute toxicity data <strong>for</strong> freshwater invertebrates were judged inadequate to meet the<br />

endpoint. However, if the results <strong>of</strong> the study cited by IPCS (1998) (see below) are confirmed<br />

independently, the data might meet the endpoint given the high degree <strong>of</strong> agreement <strong>of</strong> the two<br />

available studies in freshwater invertebrates.<br />

Basis <strong>for</strong> Conclusion:<br />

The available data are summarized in Table 3-2. A flow-through study revealed a 48-hour LC 50<br />

<strong>of</strong> TDCPP with Daphnia magna <strong>of</strong> 3.8 mg/L (95% CI: 3.5-4.2 mg/L) and a NOEC <strong>of</strong> 1.6 mg/L<br />

(Unpublished study conducted in 1999, summarized in Akzo-Nobel, Inc., 2001a,b). Although<br />

some <strong>of</strong> the conditions <strong>of</strong> the study design (such as number <strong>of</strong> organisms, and water temperature<br />

and chemistry) appear to meet OPPTS Harmonized Guideline 850.1010, other aspects <strong>of</strong> the<br />

study, including compound purity and condition and fertility <strong>of</strong> the organisms in culture, were<br />

not reported in the summary. The amount <strong>of</strong> solvent used in the control group and the TDCPP<br />

treatments might have exceeded the recommended maximum solvent concentration, as per the<br />

OPPTS Guideline (100 mg/L), but this does not appear to have affected the study results. A 48hour<br />

LC 50 <strong>of</strong> 4.6 mg/L and a NOEC <strong>of</strong> 1.8 mg/L were reported <strong>for</strong> daphnia in a study by<br />

SafePharm (1993b), as cited in IPCS (1998). Although the results <strong>of</strong> the study by SafePharm<br />

(1993b) are in agreement with those <strong>of</strong> Akzo-Nobel, Inc. (2001a,b), the study by SafePharm<br />

(1993b), or a study summary, was not available to allow <strong>for</strong> an independent evaluation <strong>of</strong> these<br />

data. Confirmation <strong>of</strong> the results <strong>of</strong> the study by SafePharm (1993b) might allow the acute<br />

freshwater invertebrate toxicity endpoint to be satisfied.<br />

Acute Toxicity to Marine/Estuarine Invertebrates (OPPTS Harmonized Guideline<br />

850.1035)<br />

Conclusion:<br />

No available acute marine/estuarine invertebrate toxicity data.<br />

Basis <strong>for</strong> Conclusion:<br />

No acute toxicity studies in marine/estuarine invertebrate species were located.<br />

3-34

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