137316
5-Methylfurfural
ReagentPlus®, 99%
Synonym(s):
5-Methyl-2-furaldehyde
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About This Item
Empirical Formula (Hill Notation):
C6H6O2
CAS Number:
Molecular Weight:
110.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-622-6
Beilstein/REAXYS Number:
106895
MDL number:
Assay:
99%
Form:
liquid
Product Name
5-Methylfurfural, ReagentPlus®, 99%
InChI key
OUDFNZMQXZILJD-UHFFFAOYSA-N
InChI
1S/C6H6O2/c1-5-2-3-6(4-7)8-5/h2-4H,1H3
SMILES string
[H]C(=O)c1ccc(C)o1
product line
ReagentPlus®
assay
99%
form
liquid
refractive index
n20/D 1.531 (lit.)
bp
187 °C (lit.)
density
1.107 g/mL at 25 °C (lit.)
functional group
aldehyde
Quality Level
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Application
5-Methylfurfural was used to investigate the volatile compounds isolated from Erica arborea and Calluna vulgaris unifloral honeys.
General description
5-Methylfurfural is formed during the photoexposition of ranitidine hydrochloride. It is employed as potential age marker for Madeira wine. It is a volatile compound present in Lavandula stoechas, Lavandula angustifolia and Lavandula angustifolia x latifolia unifloral honeys.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
flash_point_f
161.6 °F - closed cup
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_c
72 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Rosa Perestrelo et al.
Journal of agricultural and food chemistry, 59(7), 3186-3204 (2011-03-08)
The establishment of potential age markers of Madeira wine is of paramount significance as it may contribute to detect frauds and to ensure the authenticity of wine. Considering the chemical groups of furans, lactones, volatile phenols, and acetals, 103 volatile
Floral quality and discrimination of Lavandula stoechas, Lavandula angustifolia and Lavandula angustifolia x latifolia honeys.
Guyot-Declerck C, et al.
Food Chemistry, 79(4), 453-459 (2002)
Marzena Jamrógiewicz et al.
Journal of pharmaceutical and biomedical analysis, 76, 177-182 (2013-01-22)
Ranitidine (RAN) is on top of the list of prescribed drugs, due to its popularity as a selective H2-receptor antagonist, which efficiently decreases the amount of acid produced in the stomach. RAN is not stable both in a solid state
M Pitié et al.
Nucleic acids research, 28(24), 4856-4864 (2000-01-11)
Mechanisms of DNA oxidation by copper complexes of 3-Clip-Phen and its conjugate with a distamycin analogue, in the presence of a reductant and air, were studied. Characterisation of the production of 5-methylenefuranone (5-MF) and furfural, associated with the release of
S Uddin et al.
Biochemistry and molecular biology international, 35(1), 185-195 (1995-01-01)
Furfural and methylfurfural are dietary mutagens and are present in various food products and beverages. The alkaline-induced unwinding of calf thymus DNA permitted the measurement of the number of strand breaks formed by furfural and methylfurfural, as a function of
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