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 />
Test substance:<br />
other TS: as prescribed by 1.1 - 1.4, "chemically pure"<br />
Result:<br />
The LD50 was determined to be 4250 mg/kg bw (95% confidence<br />
limits: 3788-4769).<br />
Mortality and time of death(s) per dose group:<br />
6400 mg/kg bw: 12 died within the first hour, 2 within 24<br />
hours, 4 within 48 hours; in total, 18/<strong>20</strong> died within 7<br />
days.<br />
5000 mg/kg bw: 8 died within the first hour, 1 within 24<br />
hours, 1 within 48 hours; in total 11/<strong>20</strong> died within 7 days.<br />
4000 mg/kg bw: 7 died within 24 hours, and 2 within 48<br />
hours; in total, 9/<strong>20</strong> died within 7 days.<br />
3<strong>20</strong>0 mg/kg bw: 1 animal died within the first hour, 1 within<br />
24 hours, 2 within 48 hours; in total, 4/<strong>20</strong> died within 7<br />
days.<br />
2500 mg/kg bw: no deaths occurred.<br />
Clinical signs observed were:<br />
4000-6400 mg/kg bw: immediately after application<br />
staggering, abdominal and lateral position, partly dorsal<br />
position, apathy, laboured and irregular breathing. On the<br />
next day, secretion out of eyes and mouth, reddened eyes and<br />
nose. In the post-exposure observation days the animals were<br />
without clinical symptoms.<br />
3<strong>20</strong>0 mg/kg bw: No symptoms on the application day. The next<br />
day, reddened eyes and nose, and irregular breathing were<br />
noted. Later without clinical signs.<br />
2500 mg/kg bw: No clinical signs noted.<br />
At necropsy, fluid in the thoracic cavity was observed in a<br />
few animals. In three animals, the stomach was filled with<br />
liquid, and bloody mouth and forelegs were noted. No<br />
pathological findings were noted with regard to the inner<br />
organs.<br />
Test condition: According to "Description of methods used in BASF acute<br />
toxicity and skin/eye irritation studies before pertinent<br />
OECD/EU test guidelines were in place" (BASF AG, <strong>20</strong>02)<br />
TEST ANIMALS: Rats of the Gassner strain, mean weight at the<br />
beginning of the study 131-148 g.<br />
EXPOSURE TO THE TEST SUBSTANCE:<br />
The test substance was given by single gavage to groups of<br />
rats at various dose levels as a 30% aqueous solution. 10<br />
male and 10 female rats were used per dose level.<br />
The LD50 was calculated according to the method described by<br />
Litchfield-Wilcoxon.<br />
Reliability: (2) valid with restrictions<br />
post exposure observation period only 7 days, no further<br />
information on purity, limited documentation<br />
Flag:<br />
Critical study for SIDS endpoint<br />
08-DEC-<strong>20</strong>03 (111)<br />
Type:<br />
Species:<br />
Value:<br />
LD50<br />
rat<br />
= 2840 mg/kg bw<br />
Reliability: (4) not assignable<br />
secondary citation<br />
17-MAR-<strong>20</strong>03 (112)<br />
Type:<br />
LD50<br />
146<br />
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