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W305618

Sigma-Aldrich

Tetrahydrofurfuryl alcohol

≥98%

Sinonimo/i:

NSC 15434, Tetrahydro-2-furanmethanol

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About This Item

Formula empirica (notazione di Hill):
C5H10O2
Numero CAS:
97-99-4
Peso molecolare:
102.13
Numero FEMA:
3056
Beilstein:
102723
Numero CE:
202-625-6
N° CoE:
2029
Numero MDL:
MFCD00005372
Codice UNSPSC:
12164502
ID PubChem:
24901453
Numero Flavis:
13.020
NACRES:
NA.21

Origine biologica

synthetic

Livello qualitativo

400

Grado

Kosher

Conformità normativa

FDA 21 CFR 117

Densità del vapore

3.52 (vs air)

Tensione di vapore

2.3 mmHg ( 39 °C)

Saggio

≥98%

Limite di esplosione

9.7 %

Indice di rifrazione

n20/D 1.452 (lit.)

P. eboll.

178 °C (lit.)

Punto di fusione

−80 °C (lit.)

Densità

1.054 g/mL at 25 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Organolettico

vegetable

Stringa SMILE

OCC1CCCO1

InChI

1S/C5H10O2/c6-4-5-2-1-3-7-5/h5-6H,1-4H2
BSYVTEYKTMYBMK-UHFFFAOYSA-N

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Descrizione generale

Tetrahydrofurfuryl alcohol is one of the aroma constituents of coffee.

Applicazioni


  • Electrochemical oxidation of tetrahydrofurfuryl alcohol on boron-doped diamond anode: Influence of current density and electrolyte solution.: Research into the electrochemical pathways of tetrahydrofurfuryl alcohol offers insights into its potential for energy storage applications, focusing on how varying electrical and solvent conditions affect its oxidation rates (Xiong Y et al., 2023).

  • Polar-Functionalized Polyethylenes Enabled by Palladium-Catalyzed Copolymerization of Ethylene and Butadiene/Bio-Based Alcohol-Derived Monomers.: This paper presents a novel approach to the synthesis of functionalized polymers using tetrahydrofurfuryl alcohol derivatives, which could revolutionize materials science with new, sustainable polymer blends (Jian Z et al., 2023).

Esclusione di responsabilità

For R&D or non-EU Food use. Not for retail sale.

Pittogrammi

Health hazardExclamation mark
GHS08,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H319,H360Df

Classi di pericolo

Eye Irrit. 2 - Repr. 1B

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

167.0 °F - closed cup

Punto d’infiammabilità (°C)

75 °C - closed cup

Dispositivi di protezione individuale

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

Certificati d'analisi (COA)

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Contribution of coffee aroma constituents to the mutagenicity of coffee.
Aeschbacher HU, et al.
Food And Chemical Toxicology, 27(4), 227-232 (1989)
G Zarnt et al.
Applied and environmental microbiology, 63(12), 4891-4898 (1997-12-24)
An organism tentatively identified as Ralstonia eutropha was isolated from enrichment cultures containing tetrahydrofurfuryl alcohol (THFA) as the sole source of carbon and energy. The strain was able to tolerate up to 200 mM THFA in mineral salt medium. The
S M Bellm et al.
The Journal of chemical physics, 136(24), 244301-244301 (2012-07-05)
Cross section data for electron scattering from DNA are important for modelling radiation damage in biological systems. Triply differential cross sections for the electron impact ionization of the highest occupied outer valence orbital of tetrahydrofurfuryl alcohol, which can be considered
G Zarnt et al.
Journal of bacteriology, 183(6), 1954-1960 (2001-02-27)
The quinohemoprotein tetrahydrofurfuryl alcohol dehydrogenase (THFA-DH) from Ralstonia eutropha strain Bo was investigated for its catalytic properties. The apparent k(cat)/K(m) and K(i) values for several substrates were determined using ferricyanide as an artificial electron acceptor. The highest catalytic efficiency was
Chung-Yi Chen
Natural product research, 24(19), 1830-1833 (2010-11-26)
Pressalanin A, a 2-functionalized tetrahydrofuranol, has been isolated from the leaves of Michelia compressa var. lanyuensis (Magnoliaceae), and the structure was determined on the basis of a spectroscopic analysis.
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