3-Hydroxytetrahydrofuran
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
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)
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
- Language:English Provider:3-Hydroxytetrahydrofuran
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
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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3-Hydroxytetrahydrofuran(453-20-3)Related Product Information
- 2-Methyltetrahydrofuran
- Tetrahydrofuran
- POLY(TETRAHYDROFURAN) STANDARD 15000
- (S)-(+)-3-Hydroxytetrahydrofuran
- α-Chloralose
- 1,2:3,5-Di-O-isopropylidene-alpha-D-xylofuranose
- beta-D-Ribofuranose 1-acetate 2,3,5-tribenzoate
- D-(-)-PANTOLACTONE
- 8-BROMOADENOSINE
- beta-D-Ribofuranose 1,2,3,5-tetraacetate
- D-GLUCOHEPTONO-1,4-LACTONE
- 2,2'-Cyclouridine
- D-RIBULOSE
- Span 60
- DIACETONE-D-GLUCOSE
- Span 20
- D-(-)-Gulonic acid gamma-lactone
- D-SACCHARIC ACID 1,4-LACTONE