04623
糠醛
analytical standard
别名:
2-呋喃醛, 呋喃-2-甲醛
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关于此项目
经验公式（希尔记法）:
C5H4O2
化学文摘社编号:
分子量:
96.08
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
EC Number:
202-627-7
Beilstein/REAXYS Number:
105755
MDL number:
产品名称
糠醛, analytical standard
InChI key
HYBBIBNJHNGZAN-UHFFFAOYSA-N
InChI
1S/C5H4O2/c6-4-5-2-1-3-7-5/h1-4H
SMILES string
[H]C(=O)c1ccco1
grade
analytical standard
vapor density
3.31 (vs air)
vapor pressure
13.5 mmHg ( 55 °C)
assay
≥98.5% (GC)
autoignition temp.
599 °F
shelf life
limited shelf life, expiry date on the label
expl. lim.
19.3 %
impurities
≤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.)
application(s)
cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care
format
neat
Quality Level
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Application
糠醛是精细化工、塑料等生产中使用的石油基构件的可持续替代品 ，也为木质纤维素生物燃料提供了一个有前途的、丰富的平台。
General description
糠醛是一种呋喃衍生物，从生物质衍生的可再生碳水化合物中获得。
signalword
Danger
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
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
136.4 °F - closed cup
flash_point_c
58 °C - closed cup
法规信息
危险化学品
此项目有
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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