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Documentos Principais

W249106

Sigma-Aldrich

Furfuryl alcohol

≥97%, FG

Sinônimo(s):

2-(Hydroxymethyl)furan

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W249106-SAMPLE-K
R$ 384,00
1 KG
R$ 429,00
5 KG
R$ 786,00
25 KG
R$ 2.797,00

R$ 384,00


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W249106-SAMPLE-K
R$ 384,00
1 KG
R$ 429,00
5 KG
R$ 786,00
25 KG
R$ 2.797,00

About This Item

Fórmula empírica (Notação de Hill):
C5H6O2
Número CAS:
Peso molecular:
98.10
Número FEMA:
2491
Beilstein:
106291
Número CE:
Conselho da Europa nº:
2023
Número MDL:
Código UNSPSC:
12164502
ID de substância PubChem:
Número de Flavis:
13.019
NACRES:
NA.21

R$ 384,00


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fonte biológica

synthetic

Nível de qualidade

grau

FG
Halal
Kosher

Agency

meets purity specifications of JECFA

conformidade reg.

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

densidade de vapor

3.4 (vs air)

pressão de vapor

0.5 mmHg ( 20 °C)
1 mmHg ( 32 °C)
5.5 mmHg ( 55 °C)

Ensaio

≥97%

temperatura de autoignição

915 °F

Lim. expl.

16.3 %

índice de refração

n20/D 1.486 (lit.)

p.e.

170 °C (lit.)

pf

−29 °C (lit.)

densidade

1.135 g/mL at 25 °C (lit.)

aplicação(ões)

flavors and fragrances

Documentação

see Safety & Documentation for available documents

alérgeno alimentar

no known allergens

Organoléptico

bread; caramel; brown; sweet

cadeia de caracteres SMILES

OCc1ccco1

InChI

1S/C5H6O2/c6-4-5-2-1-3-7-5/h1-3,6H,4H2

chave InChI

XPFVYQJUAUNWIW-UHFFFAOYSA-N

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Categorias relacionadas

Descrição geral

Furfuryl alcohol is a volatile flavor compound identified in nonfat dry milk[1], rice cakes[2] and honey.[3]

Aplicação


  • Achmatowicz Rearrangement-Inspired Development of Green Chemistry, Organic Methodology, and Total Synthesis of Natural Products.: This study discusses innovative organic synthesis strategies inspired by the Achmatowicz rearrangement, focusing on green chemistry and the synthesis of natural products, which could include applications of furfuryl alcohol as a precursor or reagent (Liang et al., 2022).

  • Triplet Photochemistry of Dissolved Black Carbon and Its Effects on the Photochemical Formation of Reactive Oxygen Species.: This paper examines the triplet-state photochemistry of dissolved black carbon, which may implicate the photochemical behaviors of furfuryl alcohol in environmental matrices (Wang et al., 2020).

  • Production of Singlet Oxygen ((1)O(2)) during the Photochemistry of Aqueous Pyruvic Acid: The Effects of pH and Photon Flux under Steady-State O(2)(aq) Concentration.: Investigates singlet oxygen production in aqueous pyruvic acid, potentially relevant to understanding the photochemical properties of furfuryl alcohol (Eugene and Guzman, 2019).

  • Triplet-State Photochemistry of Dissolved Organic Matter: Triplet-State Energy Distribution and Surface Electric Charge Conditions.: Discusses the triplet-state energy of dissolved organic matter, which could relate to the behavior of furfuryl alcohol in various environmental conditions (Zhou et al., 2019).

Pictogramas

Skull and crossbonesHealth hazard

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 2 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - STOT RE 2 Inhalation - STOT SE 3

Órgãos-alvo

Nose, Respiratory system

Código de classe de armazenamento

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

149.0 °F - closed cup

Ponto de fulgor (°C)

65 °C - closed cup

Equipamento de proteção individual

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


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Optimized Likens-Nickerson methodology for quantifying honey flavors.
Bouseta A & Collin S.
Journal of Agricultural and Food Chemistry, 43(7), 1890-1897 (1995)
Hansruedi Glatt et al.
Mutagenesis, 27(1), 41-48 (2011-08-10)
5-Hydroxymethylfurfural (HMF) and furfuryl alcohol (FFA) are present in numerous foodstuffs at high levels. FFA is also used for the production of polymers. Both compounds had demonstrated some evidence of carcinogenic activity in 2-year bioassays. We tested these compounds and
Chun Kwan Tsang et al.
ACS nano, 6(12), 10546-10554 (2012-11-03)
A stable, label-free optical biosensor based on a porous silicon-carbon (pSi-C) composite is demonstrated. The material is prepared by electrochemical anodization of crystalline Si in an HF-containing electrolyte to generate a porous Si template, followed by infiltration of poly(furfuryl) alcohol
Organocatalytic synthesis of highly substituted furfuryl alcohols and amines.
J Stephen Clark et al.
Angewandte Chemie (International ed. in English), 51(48), 12128-12131 (2012-10-26)
Zehui Zhang et al.
ChemSusChem, 4(1), 112-118 (2011-01-13)
A clean, facile, and environment-friendly catalytic method has been developed for the conversion of furfuryl alcohol into alkyl levulinates making use of the novel solid catalyst methylimidazolebutylsulfate phosphotungstate ([MIMBS]₃PW₁₂O₄₀). The solid catalyst is an organic-inorganic hybrid material, which consists of

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