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Tetrahydrofuran

SIGALD/178810 - ≥99.0%, contains 200-400 ppm BHT as inhibitor, ReagentPlus®

Synonym: THF; Butylene oxide; Oxolane; Tetramethylene oxide

CAS Number: 109-99-9
Empirical Formula (Hill Notation): C4H8O
Molecular Weight: 72.11
EC Number: 203-726-8
MDL Number: MFCD00005356
Linear Formula: C4H8O
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-178810-1L 1 L
$143.00
1/EA
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45-178810-4L 4 L
$318.00
1/EA
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45-178810-18L-CS 18 L
$861.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 178810-1L.

 

assay ≥99.0%
autoignition temp. 610 °F
bp 65-67 °C (lit.)
contains 200-400 ppm BHT as inhibitor
density 0.889 g/mL at 25 °C (lit.)
dilution (for general lab use)
expl. lim. 1.8-11.8 %
form liquid
InChI 1S/C4H8O/c1-2-4-5-3-1/h1-4H2
InChI key WYURNTSHIVDZCO-UHFFFAOYSA-N
mp −108 °C (lit.)
pH ~7
product line ReagentPlus®
Quality Level 100 
refractive index n20/D 1.407 (lit.)
SMILES string C1CCOC1
vapor density 2.5 (vs air)
vapor pressure 114 mmHg ( 15 °C)
  143 mmHg ( 20 °C)
Application: Tetrahydrofuran may be used for the dissolution of poly-ε-caprolactone (PCL) and 1,3-diaminopentane, during the preparation of poly-ε-caprolactone (PCL)-hydroxyapatite (HA) scaffolds and acrylate-terminated poly(5-amino-1-pentanol-co-1,4-butanediol diacrylate) (C32)- 1,3-diaminopentane (117) polymer, respectively.
General description: Tetrahydrofuran (THF) is a saturated cyclic ether mainly used as an organic solvent. On long term storage it forms organic peroxides. This process can be suppressed by adding butylated hydroxytoluene (BHT) as a stabilizer. BHT removes the free radicals required for the peroxide formation. THF constitutes the key fragment of various natural products (polyether antibiotics). THF can form a double hydrate with hydrogen sulfide. Crystal structure of this double hydrate has been investigated by three-dimensional single-crystal studies. Butane-1,4-diol is formed as an intermediate during the synthesis of THF. Hot THF is useful for the dissolution of polyvinylidene chloride (PVDV).
Legal Information: ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Other Notes: For information on tetrahydrofuran miscibility, please visit the following link:
Tetrahydrofuran Miscibility/Immiscibility Table 

Greener alternatives are available for many THF applications, 2-Methyltetrahydrofuran (155810 ) and Cyclopentyl methyl ether (675989 )

Read more about THF alternatives:
2-Methyltetrahydroun (2-MeTHF): A biomass-Derived solvent with Broad Applications in Organic Chemistry

The toxicological assessment of cyclopentyl methyl ether (CPME) as a green solvent
Packaging: 1, 4 L in glass bottle
Packaging: 18 L in steel drum
Purity ≥99.0%
bp 65-67 °C (lit.)
mp −108 °C (lit.)
Density 0.889 g/mL at 25 °C (lit.)
Refractive Index n20/D 1.407 (lit.)
UNSPSC 12191501

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