T81108
1,3,5-Trioxane
≥99%
Synonym(s):
Metaformaldehyde, Trioxymethylene, sym.-Trioxane
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About This Item
Empirical Formula (Hill Notation):
C3H6O3
CAS Number:
Molecular Weight:
90.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-812-5
Beilstein/REAXYS Number:
102769
MDL number:
Product Name
1,3,5-Trioxane, ≥99%
InChI
1S/C3H6O3/c1-4-2-6-3-5-1/h1-3H2
InChI key
BGJSXRVXTHVRSN-UHFFFAOYSA-N
SMILES string
C1OCOCO1
assay
≥99%
autoignition temp.
777 °F
expl. lim.
29 %
mp
59-62 °C (lit.)
Quality Level
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Application
1,3,5-Trioxane is widely used as a source of anhydrous formaldehyde.
It can be used to synthesize:
It can be used to synthesize:
- Polyoxymethylene and hyperbranched polyesters.
- Calixarenes such as calix[4]resorcinarene, calix[6]resorcinarene and para-tert-butylcalix[8] and [9]arene.
- Various natural products including (−)-motuporin, (+)-sundiversifolide, (+)-lyconadin A and (−)-lyconadin B.
signalword
Danger
hcodes
Hazard Classifications
Flam. Sol. 1 - Repr. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
4.1B - Flammable solid hazardous materials
wgk
WGK 1
flash_point_f
113.0 °F - closed cup
flash_point_c
45 °C - closed cup
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Regulatory Information
危险化学品
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Hexahydro?1, 3, 5?tripropionyl?s?triazine.
Teeters WO and Gradsten MA.
Organic Syntheses, 51-51 (2003)
The Lyconadins: enantioselective total syntheses of (+)-lyconadin A and (−)-lyconadin B.
Beshore DC and Smith AB.
Journal of the American Chemical Society, 130(41), 13778-13789 (2008)
Single step synthesis of peripherally ?clickable? hyperbranched polyethers.
Saha A and Ramakrishnan S.
Macromolecules, 42(14), 4956-4959 (2009)
Total synthesis of (+)-sundiversifolide.
Yokoe H, et al.
Organic Letters, 9(6), 969-971 (2007)
Calix[6]resorcinarenes: the first examples of [1 6] metacyclophanes derived from resorcinols.
Konishi H, et al.
Journal of the Chemical Society. Chemical Communications, (3), 309-310 (1995)
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