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AMMONIUM SULFATE CAS N°: 7783-20-2

AMMONIUM SULFATE CAS N°: 7783-20-2

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OECD SIDS<br />

<strong>AMMONIUM</strong> <strong>SULFATE</strong><br />

5. TOXICITY ID: <strong>7783</strong>-<strong>20</strong>-2<br />

DATE: 18.04.<strong>20</strong>06<br />

Species:<br />

Value:<br />

rat<br />

= 3000 - 4000 mg/kg bw<br />

Reliability: (4) not assignable<br />

secondary citation<br />

<strong>20</strong>-APR-<strong>20</strong>03 (114)<br />

Type:<br />

Species:<br />

Value:<br />

LD50<br />

mouse<br />

= 640 mg/kg bw<br />

Reliability: (4) not assignable<br />

secondary citation<br />

17-MAR-<strong>20</strong>03 (112)<br />

Type:<br />

Species:<br />

Strain:<br />

Sex:<br />

Vehicle:<br />

Doses:<br />

Value:<br />

LD50<br />

mouse<br />

other: ddy<br />

male/female<br />

water<br />

full LD50 test, 2670-3440mg/kg bw; screening test: <strong>20</strong>00 mg/kg<br />

bw (limit test)<br />

= 3040 mg/kg bw<br />

Method:<br />

other: according to TG 423 (screening) and TG 401 (full test)<br />

Year: 1984<br />

GLP:<br />

no data<br />

Test substance: other TS: ammonium sulfate, commercial grade<br />

Remark:<br />

Result:<br />

The study was undertaken to validate a screening test for<br />

the assessment of the acute oral toxicity with a view to<br />

minimizing the use of animals in the acute toxicity testing.<br />

Two laboratories cooperated in this study.<br />

Results from full LD50 test:<br />

LD50 = 3040 mg/kg bw (2670 - 3440 mg/kg bw)<br />

Results from the screening test:<br />

Approximative LD50 in males:<br />

in laboratory A > <strong>20</strong>00 mg/kg bw,<br />

in laboratory B > <strong>20</strong>00 mg/kg bw<br />

Approximative LD50 in females:<br />

in laboratory A > <strong>20</strong>00 mg/kg bw,<br />

in laboratory B > <strong>20</strong>00 mg/kg bw.<br />

Test condition:<br />

148<br />

Clinical signs, necropsy findings: not reported.<br />

The full LD50 test was performed according to the Toxicity<br />

Guidelines of Japan (Ministry of Health and Welfare in Japan<br />

1984)<br />

For the screening study, male and female ddy mice of 5-6<br />

weeks of age were treated with the test substance after at<br />

least 5 days of adaptation. The test substance was<br />

administered orally in a single dose after fasting for 16<br />

hours.<br />

Observation of animals, including body weight changes,<br />

mortality, gross lesion and behavioural and clinical<br />

abnormality, were performed for 14 days after exposure, and<br />

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