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Merck
CN

345288

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:
25190-06-1
NACRES:
NA.23
PubChem Substance ID:
24861306
UNSPSC Code:
12162002
MDL number:
MFCD00148879

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InChI

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

SMILES string

OCCCCO

InChI key

BJZYYSAMLOBSDY-QMMMGPOBSA-N

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

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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
GHS07

signalword

Warning

hcodes

H302,H336

Hazard Classifications

Acute Tox. 4 Oral - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

474.8 °F - Cleveland open cup

flash_point_c

246 °C - Cleveland open cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCN5173
MKCH1246
MKCG2499
MKCC8528
MKBV1095V

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Synthesis of poly-(alkyleneterephthal?te-co-alkylenephosphate) s and their blends with a linear polyurethane
V Mitova, et al.
Bulgarian Chemical Communications, 129-129 (2020)
Cross-linked poly(tetrahydrofuran) as promising sorbent for organic solvent/oil spill
Ilker Yati, et al.
Journal of Hazardous Materials, 309, 210-218 (2016)
Novel thermally-reversible epoxy-urethane networks
Viorica Gaina, et al.
Designed Monomers and Polymers, 15, 63-73 (2012)
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
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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