Poly(tetrahydrofuran)

Poly(tetrahydrofuran) Basic information
Product Name:Poly(tetrahydrofuran)
Synonyms:4-butanediyl),.alpha.-hydro-.omega.-hydroxy-poly(oxy-1;alpha-hydro-omega-hydroxy-poly(oxy-4-butanediyl);b2000;glycols,polytetramethylene;hiprenemc532;polifurit;poly(butyleneoxide);poly(oxy-1,4-butylene)glycol
CAS:25190-06-1
MF:C16H33O5X2
MW:305.43
EINECS:607-637-9
Product Categories:Ethers;Hydrophobic Polymers;Materials Science;Polymer Science;Polymers;Tetrahydrofuran
Mol File:25190-06-1.mol
Poly(tetrahydrofuran) Structure
Poly(tetrahydrofuran) Chemical Properties
Melting point 33-36 °C
density 1 g/mL at 25 °C
vapor pressure <0.01 mm Hg ( 25 °C)
refractive index n20/D 1.465
Fp >230 °F
storage temp. Store below +30°C.
solubility <10g/l
Specific Gravity0.961
PH7 (H2O, 20℃)Aqueous solution
EPA Substance Registry SystemPoly(oxy-1,4-butanediyl), .alpha.-hydro-.omega.-hydroxy- (25190-06-1)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 1
RTECS MD0916000
HS Code 3907 20 20
ToxicityLD50 orally in Rabbit: > 5000 mg/kg
MSDS Information
ProviderLanguage
SigmaAldrich English
Poly(tetrahydrofuran) Usage And Synthesis
Chemical Propertiesmp 11 - 38 °C 100 - 4,400 mPa.s @ 40 °C
DefinitionChEBI: A macromolecule composed of repeating oxybutylene units.
PreparationLow molecular weight polymers of tetrahydrofuran were introduced commercially in 1955. The polymers were intended for use in the preparation of flexible polyurethane foams, being terminated by hydroxyl groups:

25190-06-1 synthesis_1


Although these polyethers produced good foams they were rather expensive and were soon displaced by the cheaper propylene oxide-based polyethers. However, these polymers of tetrahydrofuran (commonly called poly(oxytetramethylene)glycol) now find use in the preparation of polyamide, polyester and polyurethane thermoplastic elastomers.
Details of the manufacture of polytetrahydrofuran have not been disclosed. Polymerization of tetrahydrofuran can be effected only by cationic initiators. Combinations of metal halides with water are not effective but protic acids (e.g. HCl04) and oxonium salts (e.g. (C2H5£?3O+BF4-) are efficient initiators. Polymerization occurs by a ring-opening mechanism involving a tertiary oxonium ion, e.g.

25190-06-1 synthesis_2





Poly(tetrahydrofuran) Preparation Products And Raw materials
Tetrahydrofuran 1-Methoxy-2-propyl acetate POLY(TETRAHYDROFURAN) STANDARD 20000 POLY(1,4-BUTANEDIOL SUCCINATE) [LIQUID PHASE FOR GC] Allyloxypolyethyleneglycol 1,4-Butanediol 2,3-Butanediol Polyethylene Glycol Poly(tetrahydrofuran) Triton X-100 2-Ethoxyethanol 1,3-Butanediol Ethylene glycol 2-Methyltetrahydrofuran 2,2-Dimethyl-1,3-propanediol 2-Butoxyethanol 2-Butoxyethyl acetate 2-Phenoxyethanol

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