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Merck

W305618

Tetrahydrofurfuryl alcohol

≥98%

Synonyme(s) :

NSC 15434, Tetrahydro-2-furanmethanol

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A propos de cet article

Formule empirique (notation de Hill) :
C5H10O2
Numéro CAS:
97-99-4
Poids moléculaire :
102.13
FEMA Number:
3056
Council of Europe no.:
2029
UNSPSC Code:
12164502
PubChem Substance ID:
24901453
Flavis number:
13.020
EC Number:
202-625-6
NACRES:
NA.21
MDL number:
MFCD00005372
Beilstein/REAXYS Number:
102723
Organoleptic:
vegetable
Grade:
Kosher
Biological source:
synthetic
Food allergen:
no known allergens

Principaux documents

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SMILES string

OCC1CCCO1

InChI

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

InChI key

BSYVTEYKTMYBMK-UHFFFAOYSA-N

biological source

synthetic

grade

Kosher

reg. compliance

FDA 21 CFR 117

vapor density

3.52 (vs air)

vapor pressure

2.3 mmHg ( 39 °C)

assay

≥98%

expl. lim.

9.7 %

refractive index

n20/D 1.452 (lit.)

bp

178 °C (lit.)

mp

−80 °C (lit.)

density

1.054 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

vegetable

Quality Level

300, 400

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Catégories apparentées

General description

Tetrahydrofurfuryl alcohol is one of the aroma constituents of coffee.

Application


  • 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).

Disclaimer

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

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Repr. 1B

Classe de stockage

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

wgk

WGK 2

flash_point_f

167.0 °F - closed cup

flash_point_c

75 °C - closed cup

ppe

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

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Certificats d'analyse (COA)

Lot/Batch Number
SHBS3460
SHBR8469
SHBP8438
SHBM4428
SHBL9996

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Consulter la Bibliothèque de documents

Contribution of coffee aroma constituents to the mutagenicity of coffee.
Aeschbacher HU, et al.
Food And Chemical Toxicology, 27(4), 227-232 (1989)
T Schräder et al.
Journal of bacteriology, 183(24), 7408-7411 (2001-11-22)
Different aldehyde dehydrogenases (AlDHs) were formed during growth of Ralstonia eutropha Bo on tetrahydrofurfuryl alcohol (THFA). One of these enzymes, AlDH 4, was purified and characterized as a homodimer containing no prosthetic groups, showing a strong substrate inhibition, and having
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.
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
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
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