92890
1,3,5-三噁烷
purum, ≥99.0% (GC)
别名:
三氧杂环已烷, 三聚甲醛, 对称-三噁烷
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经验公式（希尔记法）:
C3H6O3
化学文摘社编号:
分子量:
90.08
EC Number:
203-812-5
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
102769
InChI
1S/C3H6O3/c1-4-2-6-3-5-1/h1-3H2
InChI key
BGJSXRVXTHVRSN-UHFFFAOYSA-N
SMILES string
C1OCOCO1
grade
purum
assay
≥99.0% (GC)
autoignition temp.
777 °F
expl. lim.
29 %
bp
112-115 °C
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Other Notes
This product has been replaced by 117854-ALDRICH | P(Oct)3 - Trioctylphosphine, technical grade, 90%
法规信息
新产品
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B Barański et al.
Medycyna pracy, 35(4), 245-255 (1984-01-01)
The study was aimed at evaluation of the effects of trioxane and dioxolane on the fertility and frequency of dominant lethal mutations in germ cells of male rats. In the first experiment each test compound was administered per os at
K Sitarek et al.
Polish journal of occupational medicine, 3(2), 209-213 (1990-01-01)
An aqueous solution of trioxane was administered by gavage to female rats, 5 days per week for 7 weeks, at doses of 0.19, 0.58 and 1.16 g/kg/day. A significant increase in the mean duration of the oestrous cycle, mainly due
Paweł Kaszycki et al.
Biodegradation, 13(2), 91-99 (2002-11-27)
Methylotrophic yeast Hansenula polymorpha were shown to cooperate with activated sludge from biological wastewater treatment stations, enhancing substantially its potential to biodegrade formaldehyde in industrial wastewater. After integration with yeast cells the modified sludge retained its original structure and activity
T Czajkowska et al.
Medycyna pracy, 38(4), 244-249 (1987-01-01)
The studies on the accumulation of toxic effects of TOX and DOX have been carried out with the Kagan and Stańkiewicz method. For 7 months the rats were intragastrically administered, with a tube, 20% water solutions of TOX and DOX
Axel G Griesbeck et al.
Bioorganic & medicinal chemistry letters, 15(3), 595-597 (2005-01-25)
A remarkable increase in antimalarial in vitro activity was achieved by integration of spiroadamantane motifs in 6-alkylidene 1,2,4-trioxanes 3a-h via diastereoselective photooxygenation of allylic alcohols and subsequent BF(3)-catalyzed peroxyacetalization with adamantanone to give the active compounds 3e-h.
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