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Merck

V900723

Sigma-Aldrich

5-甲基糠醛

Vetec, reagent grade, 98%

别名:

5-甲基呋喃醛

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About This Item

经验公式(希尔记法):
C6H6O2
CAS号:
分子量:
110.11
Beilstein:
106895
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

等级

reagent grade

产品线

Vetec

方案

98%

折射率

n20/D 1.531 (lit.)

沸点

187 °C (lit.)

密度

1.107 g/mL at 25 °C (lit.)

SMILES字符串

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

InChI

1S/C6H6O2/c1-5-2-3-6(4-7)8-5/h2-4H,1H3

InChI key

OUDFNZMQXZILJD-UHFFFAOYSA-N

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法律信息

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

10 - Combustible liquids

WGK

WGK 2

闪点(°F)

161.6 °F - closed cup

闪点(°C)

72 °C - closed cup


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Shahabuddin et al.
Mutagenesis, 5(2), 131-136 (1990-03-01)
Methylfurfural (MF) or 5-methyl 2-furaldehyde is a dietary mutagen and is present in various food products and beverages. Alkaline unwinding of calf thymus DNA and the protection of cleavage sites in lambda phage DNA from the action of various restriction
E M Jouad et al.
Journal of inorganic biochemistry, 86(2-3), 565-571 (2001-09-22)
5-Methyl 2-furfuraldehyde thiosemicarbazone (M5HFTSC) with nickel(II) leads to three types of complexes: [Ni(M5HFTSC)(2)X(2)], [Ni(M5FTSC)(2)] and [Ni(M5FTSC)(2)] x 2DMF. In the first type the ligand remains in thione form, while in the two other, the anionic thiolato form is involved. The
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
Nick Wierckx et al.
Microbial biotechnology, 3(3), 336-343 (2011-01-25)
The formation of toxic fermentation inhibitors such as furfural and 5-hydroxy-2-methylfurfural (HMF) during acid (pre-)treatment of lignocellulose, calls for the efficient removal of these compounds. Lignocellulosic hydrolysates can be efficiently detoxified biologically with microorganisms that specifically metabolize the fermentation inhibitors

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