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 />
Type:<br />
LD100<br />
Species:<br />
rat<br />
Strain:<br />
Wistar<br />
Sex:<br />
male<br />
Route of admin.: i.p.<br />
Test substance:<br />
other TS: ammonium sulfate, reagent grade<br />
Result:<br />
The effect of ammonia intoxication has been studied after<br />
intraperitoneal injection of various ammonium salts to rats<br />
including ammonium sulfate. A standardized dose of<br />
10.6 mmol NH4-N/kg (1,4 g/kg bw) was lethal within 8-13<br />
minutes for all 13 ammonium salts tested including ammonium<br />
sulfate.<br />
Reliability: (2) valid with restrictions<br />
limited documentation. No further information on purity.<br />
18-NOV-<strong>20</strong>03 (109)<br />
Type:<br />
other: pulmonary oedema<br />
Species:<br />
rat<br />
Strain:<br />
Wistar<br />
Sex:<br />
male/female<br />
No. of Animals: 19<br />
Doses:<br />
6 % (600 mg/kg bw)<br />
Route of admin.: i.p.<br />
Method:<br />
other<br />
Year: 1969<br />
GLP:<br />
no data<br />
Test substance: other TS: ammonium sulfate<br />
Result:<br />
Test condition:<br />
160<br />
The major lesion was the formation of large blebs in<br />
endothelial cells, associated with a variable degree of oedema<br />
of the interstitium and of epithelial lining cells. These<br />
changes were present in every animal exposed to ammonium<br />
sulfate, irrespective of the time-interval after injection,<br />
the only difference being that the changes prominent in those<br />
exposed for longer intervals.<br />
The ultrastructural changes, produced by ammonium sulphate are<br />
similar to the changes in pulmonary oedema induced by methods<br />
other than by altered haemodynamics. The absence of<br />
carbon-marker leakage through intercellular junctions in this<br />
experiment suggest that the increased vascular permeability<br />
necessary for the formation of pulmonary oedema differs from<br />
leakage occurring in acute inflammation, in quality if not in<br />
mechanism.<br />
19 rats were used. A colloidal carbon suspension was injected<br />
into the tailveins of the rats in a dosage of 0.1 ml per 100 g<br />
bw. immediately after, a 6 % solution of ammonium sulfate was<br />
injected i.p. in a dosage of 10 ml/kg bw. Rats were killed at<br />
varying intervals (1.5, 5, 7.5, 10, 15, <strong>20</strong>, 30, 90 min) after<br />
injection of ammonium sulfate. 9 control animals were used.<br />
The lungs were prepared and examined by electron microscopes.<br />
Other organs like liver, spleen, kidney, heart and skeletal<br />
muscle were prepared and stained as a routine with<br />
haematoxylin and eosin, and in some instances with Weigert´s<br />
elastic tissue stain or by the periodic acid-Schiff method and<br />
examined microscopically or stained with uranyl acetate and<br />
examined by electron microscopy.<br />
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