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345288

Sigma-Aldrich

Poly(tetrahydrofuran)

average Mn ~650

Synonym(s):

Terathane® 650 polyether glycol, poly(tetramethylene ether), 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:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

vapor pressure

<0.01 mmHg ( 25 °C)
<1 mmHg ( 20 °C)

mol wt

average Mn ~650

contains

0.05-0.07% BHT as stabilizer

refractive index

n20/D 1.465

mp

11-19 °C

density

0.978 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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General description

Poly(tetrahydrofuran) (PTHF) is a highly flexible hydrophobic polymer widely used in the synthesis of thermoplastic elastomers such as polyesters and polyurethanes. The addition of PHTF imparts abrasion resistance, hydrolytic stability, and attractive dynamic properties to the material. This polymer can also be used to prepare block copolymers, end-functional star polymers, amphiphilic conetworks, and thermogels.

Application

Poly(tetrahydrofuran) can be used as a precursor to synthesize epoxy-urethane polymer networks. It can also be used as a diol comonomer to synthesize block copolymers, such as poly-(alkyleneterephthalаte-co-alkylenephosphate).

Legal Information

Terathane is a registered trademark of Invista North America S.a.r.l.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

474.8 °F - Cleveland open cup

Flash Point(C)

246 °C - Cleveland open cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Novel thermally-reversible epoxy-urethane networks
Viorica Gaina, et al.
Designed Monomers and Polymers, 15, 63-73 (2012)
Cross-linked poly(tetrahydrofuran) as promising sorbent for organic solvent/oil spill
Ilker Yati, et al.
Journal of Hazardous Materials, 309, 210-218 (2016)
A Takahara et al.
Journal of biomaterials science. Polymer edition, 5(3), 183-196 (1993-01-01)
The relationships among surface, bulk properties and lipid sorption behaviors of segmented polyurethanes (SPUs) with various polyol soft segments were investigated. The polyols used in this study were poly(ethylene oxide) (PEO), poly(tetramethylene oxide) (PTMO), and poly(dimethylsiloxane) (PDMS). The hard segment
Antony Memboeuf et al.
Journal of the American Society for Mass Spectrometry, 22(10), 1744-1752 (2011-09-29)
Collision induced dissociation tandem mass spectrometry experiments were performed to unequivocally separate compounds from an isobaric mixture of two products. The Survival Yield curve was obtained and is shown to consist in a linear combination of the curves corresponding to
W K Loke et al.
Biomaterials, 17(22), 2163-2172 (1996-11-01)
Hybrid biomaterials have been produced by the interaction of polyurethane oligomers with both fresh and glutaraldehyde-fixed porcine pericardium. The hybrid biomaterials so formed were translucent with occasional white streaks and/or spots, had increased stiffness (to touch) but remained pliable. No

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