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Merck

178810-M

Sigma-Aldrich

Tetrahidrofuran

≥99.0%, reagent grade, contains 250 ppm BHT as inhibitor

Sinónimos:

Oxolano, Óxido de butileno, Óxido de tetrametileno

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About This Item

Fórmula empírica (notación de Hill):
C4H8O
Número de CAS:
Peso molecular:
72.11
Beilstein:
102391
Número CE:
Número MDL:
Código UNSPSC:
12191501
ID de la sustancia en PubChem:
NACRES:
NA.21

product name

Tetrahidrofuran, reagent grade, ≥99.0%, contains 250 ppm BHT as inhibitor

grado

reagent grade

densidad de vapor

2.5 (vs air)

presión de vapor

114 mmHg ( 15 °C)
143 mmHg ( 20 °C)

Análisis

≥99.0%

formulario

liquid

temp. de autoignición

610 °F

contiene

250 ppm BHT as inhibitor

lim. expl.

1.8-11.8 %

índice de refracción

n20/D 1.407 (lit.)

pH

~7

bp

65-67 °C (lit.)

mp

−108 °C (lit.)

densidad

0.889 g/mL at 25 °C (lit.)

cadena SMILES

C1CCOC1

InChI

1S/C4H8O/c1-2-4-5-3-1/h1-4H2

Clave InChI

WYURNTSHIVDZCO-UHFFFAOYSA-N

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Descripción general

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).

Aplicación

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.

Otras notas

For information on tetrahydrofuran miscibility, please visit the following link:
Tetrahydrofuran Miscibility/Immiscibility Table

Palabra de señalización

Danger

Clasificaciones de peligro

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

Órganos de actuación

Respiratory system

Riesgos supl.

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

1.4 °F - closed cup

Punto de inflamabilidad (°C)

-17.00 °C - closed cup


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Todd J Harris et al.
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Natural bone growth greatly depends on the precedent vascular network that supplies oxygen and essential nutrients and removes metabolites. Likewise, it is crucial for tissue-engineered bone to establish a vascular network that temporally precedes new bone formation, and spatially originates
An experimental and modeling study of the combustion of tetrahydrofuran.
Tran LS, et al.
Combustion and Flame, 162(5), 1899-1918 (2015)

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