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Sodium methanolate - ipcs inchem

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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 />

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