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Merck
CN

345334

Poly(tetrahydrofuran)

average Mn ~2,900

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
NACRES:
NA.23
PubChem Substance ID:
24861311
UNSPSC Code:
12162002
MDL number:
MFCD00148879

Key Documents

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Product Name

Poly(tetrahydrofuran), average Mn ~2,900

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)

form

solid

mol wt

average Mn ~2,900

mp

30-43 °C

density

0.97 g/mL at 25 °C

Quality Level

200

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Application

PTHF can be used in the preparation of soft segment polyurethane for a variety of applications. It can also be used in the surface modification of cellulose fibers which can further be used as reinforcing polymerix materials.

General description

Poly(tetrahydrofuran) (PTHF) is a polyether that can be prepared by the cationic polymerization of tetrahydrofuran in the presence of a variety of initiator systems.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302,H336

Hazard Classifications

Acute Tox. 4 Oral - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

>325.4 °F - Tag open cup

flash_point_c

> 163 °C - Tag open cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCS9095
MKCN3155
MKCM7387
MKCK9733
MKCH7090

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Surface functionalization of cellulose by grafting oligoether chains
Bras J, et al.
Materials Chemistry and Physics, 120(2-3), 438-445 (2010)
Melting behavior of poly (tetrahydrofuran)-S and their blends
Tsuchiya M and Kojima T
Journal of Thermal Analysis and Calorimetry, 72(2), 651-655 (2003)
Mass spectral analysis of low-temperature pyrolysis products from poly (tetrahydrofuran)
Lattimer RP
Journal of Analytical and Applied Pyrolysis, 57(1), 57-76 (2001)
25. Polytetrahydrofuran
Sugar Series, 13, 186-204 (2000)
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
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