Basic information Safety Supplier Related

3-Hydroxytetrahydrofuran

Basic information Safety Supplier Related

3-Hydroxytetrahydrofuran Basic information

Product Name:
3-Hydroxytetrahydrofuran
Synonyms:
  • 3-HYDROXYTETRAHYDROFURAN
  • 3-Furanol, tetrahydro-
  • 3-hydroxyoxolane
  • tetrahydro-3-furano
  • Tetrahydrofuran-3-ol
  • Tetrahydro-3-furanol
  • 3-HYDROXYTETRAHYDROFURAN 99%
  • 3-Hydroxytetrahydrofurane
CAS:
453-20-3
MF:
C4H8O2
MW:
88.11
EINECS:
207-219-2
Product Categories:
  • C4 to C7
  • Building Blocks
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Furans
  • Building Blocks
  • Heterocyclic Building Blocks
  • Alcohols and Derivatives
  • Heterocycles
Mol File:
453-20-3.mol
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3-Hydroxytetrahydrofuran Chemical Properties

Melting point:
25°C
Boiling point:
181 °C (lit.)
Density 
1.09 g/mL at 25 °C (lit.)
vapor pressure 
760 mm Hg ( 181 °C)
refractive index 
n20/D 1.45(lit.)
Flash point:
178 °F
storage temp. 
Sealed in dry,Room Temperature
pka
14.49±0.20(Predicted)
form 
Liquid
color 
Clear colorless to yellow
Specific Gravity
1.090
Water Solubility 
500g/L(room temperature)
Stability:
Stable. Incompatible with strong oxidizing agents, acid chlorides, acid anhydrides.
InChIKey
XDPCNPCKDGQBAN-UHFFFAOYSA-N
LogP
-0.830 (est)
CAS DataBase Reference
453-20-3(CAS DataBase Reference)
NIST Chemistry Reference
Tetrahydrofuran, 3-hydroxy-(453-20-3)
EPA Substance Registry System
3-Furanol, tetrahydro- (453-20-3)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-19
Safety Statements 
26-36-37/39
WGK Germany 
3
RTECS 
LU3450050
HS Code 
29321900

MSDS

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3-Hydroxytetrahydrofuran Usage And Synthesis

Chemical Properties

light yellow liquid

Synthesis

3068-00-6

453-20-3

The general procedure for the synthesis of 3-hydroxytetrahydrofuran from 1,2,4-butanetriol is as follows: 1,2,4-butanetriol is mixed with an equal volume of dioxane as a solvent in a batch reactor and a strongly acidic ion-exchange resin containing sulfonic acid groups (Amberlyst 15, in the H+ form) is added as a catalyst. The reaction was carried out at 100 °C for 20 h at atmospheric pressure. Upon completion of the reaction, the yield of 3-hydroxytetrahydrofuran was 96 mol%.

References

[1] Patent: WO2005/121111, 2005, A1. Location in patent: Page/Page column 33
[2] Patent: WO2005/121111, 2005, A1. Location in patent: Page/Page column 33
[3] Patent: WO2007/81065, 2007, A1. Location in patent: Page/Page column 6
[4] Patent: WO2005/121111, 2005, A1. Location in patent: Page/Page column 31; 34
[5] Patent: WO2005/121111, 2005, A1. Location in patent: Page/Page column 33-34

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