345326
Poly(tetrahydrofuran)
average Mn ~2,000, contains BHT as stabilizer
Synonym(s):
Terathane® 2000 polyether glycol, α-Hydro-ω-hydroxypoly(oxy-1,4-butanediyl), Poly(1,4-butanediol), polyTHF
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Linear Formula:
H(OCH2CH2CH2CH2)nOH
CAS Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
Recommended Products
vapor pressure
<0.01 mmHg ( 25 °C)
<1 mmHg ( 20 °C)
Quality Level
form
solid
mol wt
average Mn ~2,000
contains
BHT as stabilizer
mp
28-40 °C
density
0.972 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
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
Poly(tetrahydrofuran) (PTHF) can be used as a macroinitiator to prepare block copolymers via ring-opening polymerization.
Cross-linked PTHF can be used as a matrix to prepare thermally stable polymer electrolytes for lithium-ion batteries.
It can also be used as a starting material to prepare cyclodextrin-basedsupramolecular complexes for drug and gene delivery.
Cross-linked PTHF can be used as a matrix to prepare thermally stable polymer electrolytes for lithium-ion batteries.
It can also be used as a starting material to prepare cyclodextrin-basedsupramolecular complexes for drug and gene delivery.
Legal Information
Product of DuPont
Terathane is a registered trademark of Invista North America S.a.r.l.
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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
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
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
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.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service