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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

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