Tetrahydrofuran Inhibitor Free

Synonyms: Degassed and low oxygen tetrahydrofuran; Tetrahydrofuran ZerO2®; Butylene oxide; Oxolane; Tetramethylene oxide Molecular Formula: C4H8O Molecular Weight: 72.11 Linear Structural Formula: C4H8O MDL Number: MFCD00005356 Purity: >=99.9% Melting Point: -108 C (lit.) …

CAS Number: 109-99-9 Empirical Formula (Hill Notation): C₄H₈O Molecular Weight: 72.11 Beilstein Registry Number: 102391 EC Number: 203-726-88 MDL Number: MFCD00005356 Application Suitable for HPLC, spectrophotometry, environmental…

Chemical name: Tetrahydrofuran Product Brand: Chromasolv Material form: Solvent Density (g/cm3): 0.89 Flash Point (°C): 21 °C Molecular weight: 72.11 Molecular formula: C4H8O Chemical purity: =99.9% UN Number: UN 2056

Tetrahydrofuran (THF) is a saturated cyclic ether with a potential use as a biofuel. Its combustion studies have been investigated. Reports suggest that it is a better promoter than 1,3 dioxolane for CO2-hydrate formation. Synonyms: THF; Butylene oxide; Oxolane; Tetramethylene oxide …

anhydrous, ≥99.9%, inhibitor-free Empirical Formula: C₄H₈O Formula Weight: 72.11 Linear Formula: C₄H₈O MDL Number: MFCD00005356 Purity: ≥99.9% Boiling Point: 65-67 °C(lit.) Melting Point: …

For HPLC, ≥99.9%, inhibitor-free Empirical Formula: C₄H₈O Formula Weight: 72.11 Linear Formula: C₄H₈O MDL Number: MFCD00005356 Purity: ≥99.9% Boiling Point: 65-67 °C(lit.) Melting Point: …

Tetrahydrofuran (THF) is a saturated cyclic ether mainly used as an organic solvent. On long term storage it forms organic peroxides. This process can be suppressed by adding butylated hydroxytoluene (BHT) as a stabilizer. BHT removes the free radicals required for the peroxide formation. THF…

Tetrahydrofuran (THF) is a saturated cyclic ether mainly used as an organic solvent. On long term storage it forms organic peroxides. This process can be suppressed by adding butylated hydroxytoluene (BHT) as a stabilizer. BHT removes the free radicals required for the peroxide formation. It…

…• Preparation of tetrahydrofurans by oxidative cyclization of homoallylic alcohols • Preparation of isoxazoline N-Oxides from +ƒ-hydroxyketoximes via oxidative N-O coupling • Ring expansion in synthesis of aminopeptidase inhibitors • Oxidation and…