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product name
四氢呋喃, suitable for HPLC, ≥99.9%, inhibitor-free
蒸汽密度
2.5 (vs air)
品質等級
蒸汽壓力
114 mmHg ( 15 °C)
143 mmHg ( 20 °C)
化驗
≥99.9%
形狀
liquid
自燃溫度
610 °F
expl. lim.
1.8-11.8 %
技術
HPLC: suitable
雜質
≤0.015% peroxide (as H2O2)
<0.02% water
蒸發殘留物
<0.0005%
折射率
n20/D 1.407 (lit.)
bp
65-67 °C (lit.)
mp
−108 °C (lit.)
溶解度
H2O: soluble
密度
0.889 g/mL at 25 °C (lit.)
&lambda ;
H2O reference
紫外吸收
λ: 212 nm Amax: 1.0
λ: 250 nm Amax: 0.180
λ: 300 nm Amax: 0.020
λ: 350-400 nm Amax: 0.005
SMILES 字串
C1CCOC1
InChI
1S/C4H8O/c1-2-4-5-3-1/h1-4H2
InChI 密鑰
WYURNTSHIVDZCO-UHFFFAOYSA-N
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一般說明
Tetrahydrofuran (THF) is a saturated cyclic ether with a potential use as a biofuel. Its combustion studies have been reported. Reports suggest it is a better promoter than 1,3 dioxolane for CO2-hydrate formation. The effect of THF on the biological systems has been studied.
應用
Tetrahydrofuran may be used as a solvent in the following processes:
- Formation of diacetylinic polymers.
- RAFT polymerization of p-acetoxystyrene.
- Synthesis of di-tert-butyl-Phosphinoferrocene.
- As mobile phase solvent in high-performance liquid chromatography.
- As a solvent in the preparation of spin-coated poly(bisphenol A decane ether).
- Formation of butyrolactone (BTL) by green oxidation method.
- As a solvent for lignin depolymerization to isolate phenolic monomer.
訊號詞
Danger
危險分類
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
標靶器官
Central nervous system, Respiratory system
安全危害
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 1
閃點(°F)
-6.2 °F - closed cup
閃點(°C)
-21.2 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Journal of polymer science. Part A, Polymer chemistry, 48(12), 2517-2524 (2010-07-27)
The kinetics of the RAFT polymerization of p-acetoxystyrene using a trithiocarbonate chain transfer agent, S-1-dodecyl-S'-(α,α'-dimethyl-α″-acetic acid)trithiocarbonate, DDMAT, was investigated. Parameters including temperature, percentage initiator, concentration, monomer-to-chain transfer agent ratio and solvent were varied and their impact on the rate of
1,3 Dioxolane versus tetrahydrofuran as promoters for CO2-hydrate formation: Thermodynamics properties, and kinetics in presence of sodium dodecyl sulfate.
Chemical Engineering Science, 126, 688-697 (2015)
Oxidation of tetrahydrofuran to butyrolactone catalyzed by iron-containing clay.
Green Chemistry, 17(1), 435-441 (2015)
An efficient and economical process for lignin depolymerization in biomass-derived solvent tetrahydrofuran.
Bioresource Technology, 154, 10-17 (2014)
Novel Diacetylinic Aryloxysilane Polymers: A New Thermally Cross-Linkable High Temperature Polymer System.
Macromolecules, 46(11), 4370-4377 (2013)
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