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W248908

Sigma-Aldrich

Furfural

≥98%, FCC, FG

Sinônimo(s):

2-Furaldehyde, Furan-2-carboxaldehyde

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About This Item

Fórmula empírica (Notação de Hill):
C5H4O2
Número CAS:
98-01-1
Peso molecular:
96.08
Número FEMA:
2489
Beilstein:
105755
Número CE:
202-627-7
Conselho da Europa nº:
2014
Número MDL:
MFCD00003229
Código UNSPSC:
12164502
ID de substância PubChem:
24900968
Número de Flavis:
13.018
NACRES:
NA.21

fonte biológica

synthetic

Nível de qualidade

400

grau

FG
Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines
meets purity specifications of JECFA

conformidade reg.

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
FDA 21 CFR 175.105

densidade de vapor

3.31 (vs air)

pressão de vapor

13.5 mmHg ( 55 °C)

Ensaio

≥98%

forma

liquid

temperatura de autoignição

599 °F

Lim. expl.

19.3 %

índice de refração

n20/D 1.525 (lit.)

pb

162 °C (lit.)

pf

−36 °C (lit.)

densidade

1.16 g/mL at 25 °C (lit.)

aplicação(ões)

flavors and fragrances

Documentação

see Safety & Documentation for available documents

alérgeno alimentar

no known allergens

alérgeno de fragrância

no known allergens

Organoléptico

almond; baked; bread; woody; sweet

cadeia de caracteres SMILES

[H]C(=O)c1ccco1

InChI

1S/C5H4O2/c6-4-5-2-1-3-7-5/h1-4H

chave InChI

HYBBIBNJHNGZAN-UHFFFAOYSA-N

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Aplicação


  • Intermolecular Diels-Alder Cycloadditions of Furfural-Based Chemicals from Renewable Resources.: Focuses on the regio- and diastereoselectivity of furfural in reactions with alkenes, highlighting its potential in developing bio-based polymers (Galkin and Ananikov, 2021).

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

136.4 °F - closed cup

Ponto de fulgor (°C)

58 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análise (COA)

Lot/Batch Number
SHBN9499
STBK3391
SHBN4189
STBJ9409
SHBM2104

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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Sigma-Aldrich

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5-Hidroximetil-2-furaldeído 99%

Sigma-Aldrich

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5-Hidroximetil-2-furaldeído

5-Hidroximetil-2-furaldeído analytical standard

Supelco

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5-Hidroximetil-2-furaldeído

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Sigma-Aldrich

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5-Methylfurfural

2-Furyl methyl ketone ≥99%, FG

Sigma-Aldrich

W316318

2-Furyl methyl ketone

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
Lilong Zhou et al.
Bioresource technology, 129, 450-455 (2012-12-26)
A new kind of bifunctional ionic liquid catalysts was synthesized to degrade microcrystalline cellulose in [BMIM]Cl at atmospheric pressure. The effects of reaction temperature, amount of catalysts, reaction time, ionic liquid purity and cellulose concentration on conversion were investigated. At
Gang Cao et al.
Food chemistry, 140(1-2), 273-279 (2013-04-13)
The aim of this study was to investigate the protective effect of 5-HMF on human umbilical vein endothelial cells (HUVECs) injured by high glucose in vitro, and the mechanism underlying this process. Our results demonstrated that high glucose-induced oxidative stress
Jianghua He et al.
ChemSusChem, 6(1), 61-64 (2012-12-12)
It's nano: Small and uniform chromium nanoparticles, either preformed or generated in situ, effectively catalyze the conversion of glucose into 5-hydroxymethyl furfural. The results compare favorably with those achieved by using a catalyst system based on divalent CrCl(2) in ionic
Arvind H Jadhav et al.
Bioresource technology, 132, 342-350 (2013-02-26)
Acidity modified silver exchanged silicotungstic acid (AgSTA) catalyst was prepared and characterized by X-ray diffraction, FT-IR spectroscopy, Raman spectroscopy, FT-IR pyridine adsorption, SEM imaging, EDX mapping, and antimicrobial activity was also tested. The catalytic activity was evaluated for the dehydration
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GC Analysis of Fermentation Compounds on a Packed Column (6.6% Carbowax® 20M on 80/120 Carbopack™ B AW)

Separation of Acetone; Acetic acid; Propionic acid; Ethyl butyrate; Ethanol; Isoamyl acetate; Isobutyric acid; 3-Methyl-2-butanol; Methyl acetate; 1-Propanol; Acetal, ≥98%, FG; 2-Methyl-1-pentanol; Butyl acetate; Ethyl propionate; 3-Pentanol; 2-Pentanol, 98%; Ethyl isobutyrate; Isobutyl acetate; Acetaldehyde; Furfural; Butyric acid; Methanol; Ethyl acetate

GC Analysis of Volatiles in Roasted Coffee Beans on Omegawax® after SPME using a 50/30 µm DVB/Carboxen/PDMS Fiber

-Cymene; 2,5-Dimethylpyrrole; Acetoin, ≥96%, FCC, FG; 2,5-Dimethylpyrazine; 2,6-Dimethylpyrazine; 2-Ethylpyrazine, ≥98%, FG; 2,3-Dimethylpyrazine; 4-Heptanone; 3-Ethylpyridine; 2,3,5-Trimethylpyrazine; Furfural; Pyrrole; Furfuryl acetate; Linalool; Linalyl acetate; 5-Methylfurfural; γ-Butyrolactone; 2-Acetyl-1-methylpyrrole; Furfuryl alcohol; 2-Acetylpyrrole; Pyrrole-2-carboxaldehyde

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