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382051

Sigma-Aldrich

4-Hydroxy-3-methoxycinnamaldehyde

98%

Sinónimos:

Coniferyl aldehyde

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About This Item

Fórmula lineal:
HOC6H3(OCH3)CH=CHCHO
Número de CAS:
458-36-6
Peso molecular:
178.18
EC Number:
207-278-4
MDL number:
MFCD00075811
UNSPSC Code:
12352100
PubChem Substance ID:
24863861
NACRES:
NA.22

assay

98%

bp

175 °C/5 mmHg (lit.)

mp

80-82 °C (lit.)

SMILES string

COc1cc(\C=C\C=O)ccc1O

InChI

1S/C10H10O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-7,12H,1H3/b3-2+

InChI key

DKZBBWMURDFHNE-NSCUHMNNSA-N

General description

4-Hydroxy-3-methoxycinnamaldehyde is an isoflavonoid. It has been isolated from the insecticidally active hot dichloromethane extract of heartwood of Gliricidia sepium, seed kernels of Melia azedarach L and barks of Cinnamomum cebuense.

Application

4-Hydroxy-3-methoxycinnamaldehyde is suitable for use in a study to investigate the antioxidant and antiradical activities of ferulates using a β-carotene-linoleate model system and a DPPH radical scavenging assay, respectively.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

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Isoflavonoids and a pterocarpan from< i> Gliricidia sepium</i>.
Herath HMTB, et al.
Phytochemistry, 47(1), 117-119 (1998)
Antioxidant and antiradical activity of ferulates.
Karamac M, et al.
Czech Journal of Food Sciences, 23(2), 469-475 (2005)
M Lisa Manier et al.
Journal of the American Society for Mass Spectrometry, 22(8), 1409-1419 (2011-09-29)
Isoniazid (INH) is an important component of front-line anti-tuberculosis therapy with good serum pharmacokinetics but unknown ability to penetrate tuberculous lesions. However, endogenous background interferences hinder our ability to directly analyze INH in tissues. Chemical derivatization has been successfully used
María C Carpinella et al.
Journal of agricultural and food chemistry, 53(8), 2922-2927 (2005-04-14)
In the continuous search for antifungal compounds from plants, the hydroxycoumarin scopoletin (1) was isolated from seed kernels of Melia azedarach L. from which three other compounds, vanillin (2), 4-hydroxy-3-methoxycinnamaldehyde (3), and (+/-) pinoresinol (4), have also been isolated. Guided
Consolacion Y Ragasa et al.
Chinese journal of natural medicines, 11(3), 264-268 (2013-06-04)
To investigate the chemical constituents of Cinnamomum cebuense, an endemic and critically endangered tree found only in Cebu, Philippines. The compounds were isolated by silica gel chromatography. The structures of the isolates were elucidated by NMR spectroscopy. The dichloromethane (DCM)
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