No. 1031 - Miljøstyrelsen
No. 1031 - Miljøstyrelsen
No. 1031 - Miljøstyrelsen
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10<br />
CAS no Synonym<br />
Test Exposure<br />
route<br />
Species / model Conc. Exposure<br />
period<br />
Result/Effects NOAEL /<br />
LOAEL<br />
EPA DCN/Ref.<br />
556-67-2 D4 kinetics, effect on inhalation, human 10 ppm one hour mean deposition was 12%<br />
not relevant 86980000017<br />
immunologi-cal<br />
parameters, blood<br />
chemistry and pulmonary<br />
factors<br />
mouthpiece<br />
and nasal<br />
exposure<br />
peak plasma concentration was 78 ng/ml<br />
rapid elimination from plasma after exposure termination (25<br />
ng/ml; 6 hr and 4 ng/ml; 24 hr)<br />
no effect on blood chemistry<br />
no immunotoxic or proinflammatory/adjuvant effects<br />
1997<br />
556-67-2 D4 kinetics, 13C-D4 dermal human (3♀,3♂) 1.4 g (♂), 1 g (♀) 1, 2, 4, 6 and D4 levels significantly elevated above baseline in blood and not relevant 86010000007<br />
24 hours plasma at 1, 2, 4 and 6 hrs and in exhaled air at all time points<br />
female subjects had significantly higher blood and plasma<br />
levels compared to male subjects<br />
2000<br />
556-67-2 D4 kinetics, pilot study oral gavage, rat (♀) pre-treatment: PB: pre-treatment: Phenobarbital but not 3-MC pre-treatment increases the not relevant 86980000037<br />
to determine if inducing<br />
agents alter<br />
the metabolic profile<br />
of a single dose 14C-<br />
D4<br />
i.p. and i.v.<br />
80 mg/kg i.p.; 3-<br />
MC: 30 mg/kg i.p.<br />
14C-D4: 70 mg/kg<br />
i.v. or oral gavage<br />
once per day<br />
for 4 consecutive<br />
days;<br />
single administra-tion<br />
of<br />
14C-D4 the<br />
next day<br />
amount and rate of urinary excretion<br />
PB pre-treatment did not change urinary metabolic of D4<br />
profíle<br />
evidence that PB-inducible enzymes are involved in metabolism<br />
of D4 in rats<br />
1997<br />
556-67-2 D4 non-regulated study: intravenously rat (♀,♂), Fisher not stated no data ring opening and demethylation occurs (oxidation and hy- no data 86980000032<br />
identification of<br />
344<br />
drolysis)<br />
86980000072<br />
metabolites in urine<br />
(14C-D4)<br />
major metabolites constituting 75 - 85% of the total radioactivity<br />
were dimethylsilanediol, methylsilanetriol<br />
minor metabolites were tetramethyldisiloxane-1,3-diol<br />
[Me(2)Si(OH)-O-Si(OH)Me(2)], hexamethyltrisiloxane-1,5-diol<br />
[Me(2)Si(OH)-OSiMe(2)-OSi(OH)Me(2)], trimethyldisiloxane-1,3,3-triol<br />
[MeSi(OH)(2)-O-Si(OH)Me(2)], dimethyldisiloxane-1,1,3,3-tetrol<br />
[MeSi(OH)(2)-O-Si(OH)(2)Me], and dimethyldisiloxane-1,1,1,3,3-pentol<br />
[Si(OH)(3)-O-Si(OH)(2)Me].<br />
no parent D4 present in urine<br />
1997