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Principaux documents

345296

Sigma-Aldrich

Poly(tetrahydrofuran)

average Mn ~1,000

Synonyme(s) :

α-Hydro-ω-hydroxypoly(oxy-1,4-butanediyl), Poly(1,4-butanediol), polyTHF

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About This Item

Formule linéaire :
H(OCH2CH2CH2CH2)nOH
Numéro CAS:
Numéro MDL:
Code UNSPSC :
12162002
ID de substance PubChem :
Nomenclature NACRES :
NA.23

Pression de vapeur

<0.01 mmHg ( 25 °C)
<1 mmHg ( 20 °C)

Niveau de qualité

Poids mol.

average Mn ~1,000

Contient

0.05-0.07% BHT as stabilizer

Pf

25-33 °C

Densité

0.974 g/mL at 25 °C

Chaîne SMILES 

OCCCCO

InChI

1S/C8H18O2/c1-3-5-6-10-8(4-2)7-9/h8-9H,3-7H2,1-2H3/t8-/m0/s1

Clé InChI

BJZYYSAMLOBSDY-QMMMGPOBSA-N

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Application

Poly(tetrahydrofuran) can be used as a starting material to prepare:
  • Thermally reversible urethane -epoxy networks.
  • Poly(hexamethylene 2,6-naphthalate)-block-poly(tetrahydrofuran) (PHN-b-N-pTHF) copolymers with shape memory effect via melt polycondensation.
  • Poly(3,4-ethylenedioxythiophene):poly(tetrahydrofuran) composite for the fabrication of memory organic electrochemical transistors.

Caractéristiques et avantages

  • High flexibility
  • Hydrolytic stability
  • Excellent abrasion resistance

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

>325.4 °F - Tag open cup

Point d'éclair (°C)

> 163 °C - Tag open cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves


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Consulter la Bibliothèque de documents

Jae Hyung Park et al.
Journal of biomaterials science. Polymer edition, 13(5), 527-542 (2002-08-17)
A multiblock copolymer composed of poly(ethylene oxide) (PEO) and poly(tetramethylene oxide) (PTMO) and which forms a physical hydrogel was blended with Pellethane, a commercial segmented polyurethane (SPU) developed for various biomedical devices, to provide a PEO-rich surface with improved stability.
H B Lin et al.
Journal of biomedical materials research, 28(3), 329-342 (1994-03-01)
In an attempt to improve endothelial cell adhesion and growth on a polyurethane copolymer, cell adhesive RGD-containing peptides were grafted to the polymer backbone. Two peptide grafting reaction schemes, including one-step and two-step approaches, were developed. FTIR and amino acid
G A Skarja et al.
Journal of biomedical materials research, 34(4), 439-455 (1997-03-15)
The adhesion of platelets to a series of segmented polyurethanes having sulfonate groups in the hard segment is reported. The polyurethanes were synthesized using sulfonated chain extenders of different structure. Analogous control materials without sulfonate groups also were studied. Adhesion
Jae Hyung Park et al.
Journal of biomedical materials research. Part A, 64(2), 309-319 (2003-01-11)
To investigate the effects of polymer chemistry and topology (linear or graft copolymer) on in vivo biocompatibility and biostability based on cage implant system, various hydrogels, composed of short hydrophilic [polyethylene oxide (PEO)] and hydrophobic block, were prepared by polycondensation
Mi-Young Koh et al.
Journal of materials science. Materials in medicine, 21(2), 385-392 (2009-09-17)
The osteoconduction potential of artificial materials is usually evaluated in vitro by apatite formation in a simulated body fluid (SBF) proposed by Kokubo and his colleagues. This paper reports the compositional dependence of apatite formation on organic-inorganic hybrids in the

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