추천 제품
Quality Level
Grade
analytical standard
vapor density
3.31 (vs air)
vapor pressure
13.5 mmHg ( 55 °C)
분석
≥98.5% (GC)
autoignition temp.
599 °F
유통기한
limited shelf life, expiry date on the label
expl. lim.
19.3 %
불순물
≤0.5% water
refractive index
n20/D 1.522-1.528
n20/D 1.525 (lit.)
bp
162 °C (lit.)
mp
−36 °C (lit.)
density
1.16 g/mL at 25 °C (lit.)
응용 분야
cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care
형식
neat
SMILES string
[H]C(=O)c1ccco1
InChI
1S/C5H4O2/c6-4-5-2-1-3-7-5/h1-4H
InChI key
HYBBIBNJHNGZAN-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Furfural is a furan derivative obtained from renewable biomass-derived carbohydrates.
애플리케이션
Furfural is a sustainable alternative for petroleum-based building blocks used in the production of fine chemicals, plastics, etc and also offers a promising, rich platform for lignocellulosic biofuels.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point (°F)
136.4 °F - closed cup
Flash Point (°C)
58 °C - closed cup
이미 열람한 고객
Sofia Tallarico et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 250, 119367-119367 (2021-01-06)
Chemocatalytic conversion of cellulose into lactic acid is a valuable alternative to simple sugar fermentation. Nevertheless, the procedures still need optimization to be translated to the industrial scale. Such translation would benefit by on-line monitoring of reaction parameters by fast
Production of 5-hydroxymethylfurfural and furfural by dehydration of biomass-derived mono-and poly-saccharides.
Chheda JN, et al.
Green Chemistry, 9(4), 342-350 (2007)
Jean-Paul Lange et al.
ChemSusChem, 5(1), 150-166 (2012-01-04)
Furfural offers a promising, rich platform for lignocellulosic biofuels. These include methylfuran and methyltetrahydrofuran, valerate esters, ethylfurfuryl and ethyltetrahydrofurfuryl ethers as well as various C(10)-C(15) coupling products. The various production routes are critically reviewed, and the needs for improvements are
T B Adams et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 35(8), 739-751 (1997-08-01)
The Expert Panel of the Flavor and Extract Manufacturers' Association (FEMA) has assessed the safety of furfural for its continued use as a flavour ingredient. The safety assessment takes into account the current scientific information on exposure, metabolism, pharmacokinetics, toxicology
Reetta Karinen et al.
ChemSusChem, 4(8), 1002-1016 (2011-07-06)
Furfurals are important intermediates in the chemical industry. They are typically produced by homogeneous catalysis in aqueous solutions. However, heterogeneously catalyzed processes would be beneficial in view of the principles of green chemistry: the elimination of homogeneous mineral acids makes
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