조직 및 계약 가격을 보려면 로그인를 클릭합니다.
크기 선택
보기 변경
제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
C5H10O
CAS 번호:
Molecular Weight:
86.13
UNSPSC Code:
12352005
NACRES:
NA.21
PubChem Substance ID:
EC Number:
202-507-4
Beilstein/REAXYS Number:
102448
MDL number:
Assay:
≥99%
Grade:
anhydrous
Bp:
78-80 °C (lit.)
Quality Level
grade
anhydrous
assay
≥99%
form
liquid
expl. lim.
0.34-6.3 % (lit.)
greener alternative product characteristics
Safer Solvents and Auxiliaries
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
impurities
≤0.002% water, ≤0.005% water (100 mL pkg)
evapn. residue
≤0.0003%
refractive index
n20/D 1.406 (lit.)
bp
78-80 °C (lit.)
mp
-136 °C (lit.)
density
0.86 g/mL at 25 °C (lit.)
greener alternative category
, Aligned
SMILES string
CC1CCCO1
InChI
1S/C5H10O/c1-5-3-2-4-6-5/h5H,2-4H2,1H3
InChI key
JWUJQDFVADABEY-UHFFFAOYSA-N
General description
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is a biorenewable and thus aligns with "Safer Solvents and Auxiliaries" and "Use of Renewable Feedstocks". Click here for more information.
2-Methyltetrahydrofuran (2-MTHF), a 2-methyl substituted tetrahydrofuran, is a biomass derived solvent. It is a potential greener solvent alternative for organic synthesis. It shows resistance to reduction by lithium making it a promising candidate as electrolytes in lithium batteries. Its polarity and Lewis base strength is intermediate between tetrahydrofuran (THF) and diethyl ether. The ring opening reaction of 2-MTHF has been studied using acid chloride and iodide.
2-Methyltetrahydrofuran (2-MTHF), a 2-methyl substituted tetrahydrofuran, is a biomass derived solvent. It is a potential greener solvent alternative for organic synthesis. It shows resistance to reduction by lithium making it a promising candidate as electrolytes in lithium batteries. Its polarity and Lewis base strength is intermediate between tetrahydrofuran (THF) and diethyl ether. The ring opening reaction of 2-MTHF has been studied using acid chloride and iodide.
Application
2-Methyltetrahydrofuran may be used as a solvent for phosphatidylserine synthesis.
It may be used as an alternative solvent to:
Organic Solar Cells
2-Methyltetrahydrofuran (2-MeTHF): A Biomass-Derived Solvent with Broad Application in Organic Chemistry
It may be used as an alternative solvent to:
- Dimethyl sulfoxide (DMSO) or methyl tert-butyl ether (MTBE) in the C-C bond forming reactions catalyzed by lyase enzyme.
- Tetrahydrofuran (THF) in the reaction between Grignard reagents and carbonyl compounds.
- Methylene chloride in some biphasic reactions.
Organic Solar Cells
2-Methyltetrahydrofuran (2-MeTHF): A Biomass-Derived Solvent with Broad Application in Organic Chemistry
Features and Benefits
Greener alternative for THF, DCM, DMSO, and MTBE
Still not finding the right product?
Explore all of our products under 2-Methyltetrahydrofuran
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Irrit. 2
supp_hazards
저장 등급
3 - Flammable liquids
wgk
WGK 2
flash_point_f
14.0 °F - closed cup
flash_point_c
-10.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Tatsuya Higaki et al.
Proceedings of the National Academy of Sciences of the United States of America, 116(27), 13215-13220 (2019-06-19)
Research on plasmons of gold nanoparticles has gained broad interest in nanoscience. However, ultrasmall sizes near the metal-to-nonmetal transition regime have not been explored until recently due to major synthetic difficulties. Herein, intriguing electron dynamics in this size regime is
Renxi Jin et al.
Nanoscale, 9(48), 19183-19190 (2017-12-01)
Doping metal nanoclusters with a second type of metal is a powerful method for tuning the physicochemical properties of nanoclusters at the atomic level and it also provides opportunities for a fundamental understanding of alloying rules as well as new
Dennis Weidener et al.
Molecules (Basel, Switzerland), 25(15) (2020-07-28)
Fractionation of lignocellulose into its three main components, lignin, hemicelluloses, and cellulose, is a common approach in modern biorefinery concepts. Whereas the valorization of hemicelluloses and cellulose sugars has been widely discussed in literature, lignin utilization is still challenging. Due


