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178810-M

Sigma-Aldrich

Tetrahydrofurane

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

Synonyme(s) :

Oxolane, Oxyde de butylène, Oxyde de tétraméthylène

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About This Item

Formule empirique (notation de Hill):
C4H8O
Numéro CAS:
Poids moléculaire :
72.11
Numéro Beilstein :
102391
Numéro CE :
Numéro MDL:
Code UNSPSC :
12191501
ID de substance PubChem :
Nomenclature NACRES :
NA.21

product name

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

Qualité

reagent grade

Densité de vapeur

2.5 (vs air)

Pression de vapeur

114 mmHg ( 15 °C)
143 mmHg ( 20 °C)

Pureté

≥99.0%

Forme

liquid

Température d'inflammation spontanée

610 °F

Contient

250 ppm BHT as inhibitor

Limite d'explosivité

1.8-11.8 %

Indice de réfraction

n20/D 1.407 (lit.)

pH

~7

Point d'ébullition

65-67 °C (lit.)

Pf

−108 °C (lit.)

Densité

0.889 g/mL at 25 °C (lit.)

Chaîne SMILES 

C1CCOC1

InChI

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

Clé InChI

WYURNTSHIVDZCO-UHFFFAOYSA-N

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Description générale

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).

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.

Autres remarques

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

Pictogrammes

FlameHealth hazardExclamation mark

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Respiratory system

Risques supp

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

1.4 °F - closed cup

Point d'éclair (°C)

-17.00 °C - closed cup


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Consulter la Bibliothèque de documents

An experimental and modeling study of the combustion of tetrahydrofuran.
Tran LS, et al.
Combustion and Flame, 162(5), 1899-1918 (2015)
Todd J Harris et al.
Biomaterials, 31(5), 998-1006 (2009-10-24)
The use of biomaterials for gene delivery can potentially avoid many of the safety concerns with viral gene delivery. However, the efficacy of polymeric gene delivery methods is low, particularly in vivo. One significant concern is that the interior and
Haiying Yu et al.
Biomaterials, 30(4), 508-517 (2008-11-01)
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

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