437638
四氢呋喃
≥99.0%, ACS reagent, contains 250 ppm BHT as inhibitor, suitable for HPLC
别名:
THF, 丁烯氧化物, 四亚甲基氧化物, 氧杂环戊烷
产品名称
四氢呋喃, contains 250 ppm BHT as inhibitor, ACS reagent, ≥99.0%
等级
ACS reagent
质量水平
蒸汽密度
2.5 (vs air)
蒸汽压
114 mmHg ( 15 °C)
143 mmHg ( 20 °C)
方案
≥99.0%
表单
liquid
自燃温度
610 °F
包含
250 ppm BHT as inhibitor
expl. lim.
1.8-11.8 %
技术
HPLC: suitable
杂质
≤0.015% peroxide (as H2O2)
≤0.05% water
蒸发残留物
≤0.03%
颜色
APHA: ≤20
折射率
n20/D 1.407 (lit.)
pH值(酸碱度)
~7
沸点
65-67 °C (lit.)
mp
−108 °C (lit.)
溶解性
water: soluble
密度
0.889 g/mL at 25 °C (lit.)
SMILES字符串
C1CCOC1
InChI
1S/C4H8O/c1-2-4-5-3-1/h1-4H2
InChI key
WYURNTSHIVDZCO-UHFFFAOYSA-N
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应用
Tetrahydrofuran may be used used as a solvent in the following processes:
- Formation of diacetylinic polymers.
- RAFT polymerization of p-acetoxystyrene.
- Synthesis of di-tert-butyl-Phosphinoferrocene.
- Synthesis of n-TiO2-based amphiphilic polymer brushes.
- 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.
警示用语:
Danger
危险分类
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
靶器官
Respiratory system
补充剂危害
储存分类代码
3 - Flammable liquids
WGK
WGK 1
闪点(°F)
-6.2 °F - closed cup
闪点(°C)
-21.2 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
An efficient and economical process for lignin depolymerization in biomass-derived solvent tetrahydrofuran.
Long J, et al.
Bioresource Technology, 154, 10-17 (2014)
Oxidation of tetrahydrofuran to butyrolactone catalyzed by iron-containing clay.
Ausavasukhi A and Sooknoi T.
Green Chemistry, 17(1), 435-441 (2015)
1,3 Dioxolane versus tetrahydrofuran as promoters for CO2-hydrate formation: Thermodynamics properties, and kinetics in presence of sodium dodecyl sulfate.
Torre JP, et al.
Chemical Engineering Science, 126, 688-697 (2015)
Synthesis of NiO/TiO2 using amphiphilic diblock copolymer brushes (PMMA-b-PAA) by reversible addition fragmentation chain-transfer poltmerization.
Hojjati B and Charpentier PA.
Polymer Reviews, 50(2), 418-418 (2009)
Practical Synthesis of Di-tert-Butyl-Phosphinoferrocene.
Busacca CA, et al.
Organic Syntheses, 90, 316-326 (2013)
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