1,4-Dioxane-2,5-diol

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Names

[ Name ]:
1,4-Dioxane-2,5-diol

[Synonym ]:
Glycolaldehyde dimer
hydroxyacetaldehyde dimer
G6805_ALDRICH
GLYCOALDEHYDE,DIMER
dimerized glycoaldehyde
2,5-Dihydroxy-1,4-dioxane
MFCD00012133
EINECS 205-484-9
2-hydroxyethanal dimer
1,4-Dioxane-2,5-diol,2,5-Dihydroxy-1,4-dioxane,Hydroxyacetaldehyde dimer

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
312.4±42.0 °C at 760 mmHg

[ Melting Point ]:
~85 °C

[ Molecular Formula ]:
C₄H₈O₄

[ Molecular Weight ]:
120.104

[ Flash Point ]:
142.8±27.9 °C

[ Exact Mass ]:
120.042259

[ PSA ]:
58.92000

[ LogP ]:
-0.75

[ Vapour Pressure ]:
0.0±1.5 mmHg at 25°C

[ Index of Refraction ]:
1.514

[ Storage condition ]:
2-8°C

[ Water Solubility ]:
H2O: 0.1 g/mL, clear, colorless

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2934999090

Precursor & DownStream

Precursor

DownStream

Ethanol,2,2'-(1,2-hydrazinediyl)bis-
4-hydroxybut-2-enal
(3S,3aR,6aS)-Hexahydrofuro[2,3-b]furan-3-ol
(3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-ol
(3S,3aS,6aR)-Hexahydrofuro[2,3-b]furan-3-ol
(3R,3aR,6aS)-Hexahydrofuro[2,3-b]furan-3-ol
2,2-Dimethoxyethanol
Glycolaldehyde
(1,2-dihydroxy-ethoxy)-acetaldehyde

Preparation

Customs

[ HS Code ]: 2934999090

[ Summary ]:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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Biomechanical strain imposed by age-related thickening of the basal lamina and augmented tissue stiffness in the prostate gland coincides with increased cancer risk. Here we hypothesized that the stru...

Trapping and desorption of complex organic molecules in water at 20 K.

J. Chem. Phys. 143 , 164704, (2015)

The formation, chemical, and thermal processing of complex organic molecules (COMs) is currently a topic of much interest in interstellar chemistry. The isomers glycolaldehyde, methyl formate, and ace...

One-step protecting-group-free synthesis of azepinomycin in water.

Org. Biomol. Chem. 13(11) , 3378-81, (2015)

We report an efficient, atom economical general acid-base catalyzed one-step multi-gram synthesis of azepinomycin from commercially available compounds in water. We propose that the described pH-depen...