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Merck
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Documenti

345326

Sigma-Aldrich

Poly(tetrahydrofuran)

average Mn ~2,000, contains BHT as stabilizer

Sinonimo/i:

Terathane® 2000 polyether glycol, α-Hydro-ω-hydroxypoly(oxy-1,4-butanediyl), Poly(1,4-butanediol), polyTHF

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About This Item

Formula condensata:
H(OCH2CH2CH2CH2)nOH
Numero CAS:
25190-06-1
Numero MDL:
MFCD00148879
Codice UNSPSC:
12162002
ID PubChem:
24861310
NACRES:
NA.23

Tensione di vapore

<0.01 mmHg ( 25 °C)
<1 mmHg ( 20 °C)

Forma fisica

solid

PM

average Mn ~2,000

contiene

BHT as stabilizer

Punto di fusione

28-40 °C

Densità

0.972 g/mL at 25 °C

Stringa SMILE

OCCCCO

InChI

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

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Categorie correlate

Applicazioni

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.

Note legali

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

Indicazioni di pericolo

H412

Consigli di prudenza

P273 - P501

Classi di pericolo

Aquatic Chronic 3

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

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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
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
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
R S Labow et al.
Journal of biomaterials science. Polymer edition, 8(10), 779-795 (1997-01-01)
Although biodegradation of model poly(ester-urethane)s and poly(ether-urethane)s has been demonstrated using a single enzyme system (cholesterol esterase (CE) in vitro, in vivo biodegradation most likely involves many processes acting together. In this study, the physical (film vs textured surface) and
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