Sodium methanolate - ipcs inchem
Sodium methanolate - ipcs inchem
Sodium methanolate - ipcs inchem
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
OECD SIDS<br />
SODIUM METHANOLATE<br />
5. TOXICITY ID: 124-41-4<br />
DATE: 28.06.2006<br />
Remark : As the substance was tested in aqeous solution and sodium methylate<br />
hydrolyses rapidly to methanol and sodium hydroxide, in fact the hydrolysis<br />
products have been tested.<br />
Result : MORTALITY: No deaths occurred at either dose level<br />
CLINICAL SIGNS: irregular breathing and bad general condition. Skin:<br />
necrosis after the 24 hour application.<br />
NECROPSY FINDINGS:<br />
No macroscopic organ changes apart from the skin necrosis were<br />
observed.<br />
Test condition : TEST ORGANISMS: male and female Sprague-Dawley rats, SPF<br />
- Source: Hagemann, Extertal<br />
- Weight at study initiation: males: 220 g, females 190 g<br />
ADMINISTRATION: as 50% solution in water<br />
- Area covered: 50 cm2<br />
- Occlusion: yes, 24 hours<br />
- Vehicle: water<br />
- Concentration in vehicle: 50%<br />
- Doses: 1000 and 2000 mg/kg bw<br />
- Removal of test substance: after 24 hours with lukewarm water or<br />
water/lutrol<br />
EXAMINATIONS:<br />
Mortalitiy within 14 days<br />
Clinical symptoms<br />
Necropsy and macroscopic examination at termination.<br />
Test substance : <strong>Sodium</strong> methylate krist., BASF tested as 50% solution in water<br />
Reliability : (2) valid with restrictions<br />
Well documented study.<br />
Flag : Critical study for SIDS endpoint<br />
23.08.2005 (4)<br />
5.1.4 ACUTE TOXICITY, OTHER ROUTES<br />
Type : LD50<br />
Value : = 40 mg/kg bw<br />
Species : mouse<br />
Strain :<br />
Sex :<br />
Number of animals :<br />
Vehicle :<br />
Doses :<br />
Route of admin. : i.p.<br />
Exposure time :<br />
Method : other: not specified<br />
Year : 1979<br />
GLP : no<br />
Test substance : as prescribed by 1.1 - 1.4<br />
Result : Symptoms: uncharacteristic, in the beginning of the observation period<br />
body weight reduction. Deaths occurred within the whole of first week of<br />
the experiment.<br />
No macroscopic findings at necropsy.<br />
Source : BASF AG Ludwigshafen<br />
Test condition : Administration of 0.43 to 14.7 % (G/V) suspensions i.p.<br />
Observation period: 14 days.<br />
Test substance : Natriummethylat krist. 0,43 - 14,7 %ige Suspension in<br />
Lutrol (G/V).<br />
05.08.2005 (3)<br />
62<br />
UNEP PUBLICATIONS