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Sigma-Aldrich

Poly(tetrahydrofuran)

average Mn ~1,000

Synonym(s):

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

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About This Item

Linear Formula:
H(OCH2CH2CH2CH2)nOH
CAS Number:
25190-06-1
MDL number:
MFCD00148879
UNSPSC Code:
12162002
PubChem Substance ID:
24861307
NACRES:
NA.23

vapor pressure

<0.01 mmHg ( 25 °C)
<1 mmHg ( 20 °C)

mol wt

average Mn ~1,000

contains

0.05-0.07% BHT as stabilizer

mp

25-33 °C

density

0.974 g/mL at 25 °C

SMILES string

OCCCCO

InChI

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

InChI key

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.

Features and Benefits

  • High flexibility
  • Hydrolytic stability
  • Excellent abrasion resistance

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

>325.4 °F - Tag open cup

Flash Point(C)

> 163 °C - Tag open cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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R Nakaoka et al.
Journal of biomedical materials research, 49(1), 99-105 (1999-11-24)
Interaction of macrophages (Mos) with polyetherurethane (PEU) was investigated to clarify the role of the Mos in the early stage of tumorigenesis of PEUs. As for the inflammatory cytokines produced from Mos, the amount of tumor necrosis factor (TNF) produced
P Banu et al.
Journal of colloid and interface science, 277(2), 304-308 (2004-09-03)
Aqueous dispersions of poly(ester-imide)s [P(E-I)s] have been prepared by dispersing the P(E-I)s in water without any external solubilizing agents. P(E-I)s were prepared from anhydride-terminated polyester prepolymer and diisocyanate. The -COOH groups in the polymer were then neutralized using triethylamine and
M Renier et al.
Journal of biomaterials science. Polymer edition, 5(3), 231-244 (1993-01-01)
Poly(etherurethane urea) (PEUU) elastomers when employed as biomedical devices may be susceptible to extraction upon implantation. Four PEUU elastomers containing a single PEUU formulation, but varying in terms of their additives, were subjected to an in vitro extraction procedure. The
A Brandwood et al.
Journal of biomaterials science. Polymer edition, 6(1), 41-54 (1994-01-01)
A series of novel polyurethane elastomers based on methylenediphenyl diisocyanate, 1,4-butanediol and the macrodiols, poly(hexamethylene oxide), poly(octamethylene oxide), and poly(decamethylene oxide) were implanted subcutaneously in sheep for periods of 3 and 6 months. The specimens that were subjected to 3
K Y Chen et al.
Journal of biomaterials science. Polymer edition, 10(12), 1183-1205 (2000-02-15)
Two novel aliphatic polyurethaneurea anionomers were synthesized based on polydimethylsiloxane (PDMS)-polytetramethylene oxide (PTMO) soft segments. The hard segments consisted of either 4,4'-methylene dicyclohexyl diisocyanate (H12MDI), sulfonic acid-containing diol and 1,4-butandiol (BD) or H12MDI, carboxylic acid-containing diol and BD. The nonionic
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