AMMONIUM SULFATE CAS N°: 7783-20-2
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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