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145424

Sigma-Aldrich

5-Acetoxymethyl-2-furaldehyde

99%

Synonym(s):

(5-Formylfuran-2-yl)methyl acetate, 5-(Acetoxymethyl)-2-furaldehyde, 5-(Acetoxymethyl)-2-furancarboxaldehyde, 5-(Acetoxymethyl)furfural, 5-(Acetoxymethyl)furfuraldehyde

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About This Item

Empirical Formula (Hill Notation):
C8H8O4
CAS Number:
10551-58-3
Molecular Weight:
168.15
EC Number:
234-137-4
MDL number:
MFCD00003233
UNSPSC Code:
12352100
PubChem Substance ID:
24848725
NACRES:
NA.22
Pricing and availability is not currently available.

Assay

99%

form

solid

mp

53-55 °C (lit.)

SMILES string

[H]C(=O)c1ccc(COC(C)=O)o1

InChI

1S/C8H8O4/c1-6(10)11-5-8-3-2-7(4-9)12-8/h2-4H,5H2,1H3

InChI key

QAVITTVTXPZTSE-UHFFFAOYSA-N

General description

5-Acetoxymethyl-2-furaldehyde is a volatile flavor compound present in berrycactus[1]. It is a potential sweet modulator compound present in traditional balsamic vinegar of Modena[2].

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB0382
SDBB0675
STBL2784
STBK9965
STBJ8786

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Hedda Hillmann et al.
Journal of agricultural and food chemistry, 60(40), 9974-9990 (2012-09-14)
Sensory-directed fractionation of traditional balsamic vinegar of Modena (TBV) led to the identification of the sweet-bitter tasting hexose acetates 6-O-acetyl-α/β-d-glucopyranose and 1-O-acetyl-β-d-fructopyranose as well as the previously unknown sweetness modulator 5-acetoxymethyl-2-furaldehyde. Taste re-engineering experiments and sensory time-intensity studies confirmed 5-acetoxymethyl-2-furaldehyde
Moises Alejandro Vazquez-Cruz et al.
Journal of food science, 77(4), C366-C373 (2012-03-21)
Descriptive sensory analysis combined with a chemical analysis, provided insight regarding sensory significance for a better understanding of berrycactus' flavor. This study was based on the volatile components derived from the gas chromatography-olfactometry (GC-O) analysis. Four different ripening stages were
Pak Hin Chow et al.
Molecular pharmacology, 98(1), 38-48 (2020-05-22)
Aquaporin-1 (AQP1) dual water and ion channels enhance migration and invasion when upregulated in leading edges of certain classes of cancer cells. Work here identifies structurally related furan compounds as novel inhibitors of AQP1 ion channels. 5-Hydroxymethyl-2-furfural (5HMF), a component

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