382051
4-Hydroxy-3-methoxycinnamaldehyde
98%
Synonym(s):
Coniferyl aldehyde
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About This Item
Linear Formula:
HOC6H3(OCH3)CH=CHCHO
CAS Number:
Molecular Weight:
178.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
207-278-4
MDL number:
Assay:
98%
InChI key
DKZBBWMURDFHNE-NSCUHMNNSA-N
InChI
1S/C10H10O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-7,12H,1H3/b3-2+
SMILES string
COc1cc(\C=C\C=O)ccc1O
assay
98%
bp
175 °C/5 mmHg (lit.)
mp
80-82 °C (lit.)
functional group
aldehyde
Quality Level
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
Seikwan Oh et al.
Archives of pharmacal research, 29(6), 469-475 (2006-07-13)
A series of yakuchinone B 1f and its analogs 1a-e was synthesized and evaluated for free radical scavenging, suppression of LPS-induced NO generation, cytotoxicity and anti-excitotoxicity in vitro. Compound 1c exhibited potent anti-excitotoxicity, while all compounds 1a-f showed considerable effects
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)
Linda Volpp et al.
Frontiers in pharmacology, 11, 74-74 (2020-03-17)
Ellagitannins are signature constituents of oak wood and their consumption has been associated with various health benefits. In vivo, they undergo metabolic degradation including gut microbial metabolism yielding urolithins. Only limited data is available about compounds being present in blood
Lei Xu et al.
Food chemistry, 286, 106-112 (2019-03-05)
An untargeted metabolomic method based on UPLC-QTOF were used to investigate the differences in coffee brewed by boiled, pour-over and cold-brew methods here. Distinctive separation among the three groups could be seen from principal component analysis and hierarchical clustering analysis.
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