coniferyl aldehyde structure
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Common Name | coniferyl aldehyde | ||
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CAS Number | 458-36-6 | Molecular Weight | 178.185 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 338.8±27.0 °C at 760 mmHg | |
Molecular Formula | C10H10O3 | Melting Point | 80-82ºC(lit.) | |
MSDS | Chinese USA | Flash Point | 136.8±17.2 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of coniferyl aldehydeConiferaldehyde (Ferulaldehyde), isolated from the ethanol extract of Vitex rotundifolia fruits, is an effective inducer of heme oxygenase-1 (HO-1). Coniferaldehyde exerts anti-inflammatory properties in response to LPS. Coniferaldehyde inhibits LPS-induced apoptosis through the PKCα/β II/Nrf-2/HO-1 dependent pathway in RAW264.7 macrophage cells[1]. |
Name | coniferyl aldehyde |
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Synonym | More Synonyms |
Description | Coniferaldehyde (Ferulaldehyde), isolated from the ethanol extract of Vitex rotundifolia fruits, is an effective inducer of heme oxygenase-1 (HO-1). Coniferaldehyde exerts anti-inflammatory properties in response to LPS. Coniferaldehyde inhibits LPS-induced apoptosis through the PKCα/β II/Nrf-2/HO-1 dependent pathway in RAW264.7 macrophage cells[1]. |
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Related Catalog | |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 338.8±27.0 °C at 760 mmHg |
Melting Point | 80-82ºC(lit.) |
Molecular Formula | C10H10O3 |
Molecular Weight | 178.185 |
Flash Point | 136.8±17.2 °C |
Exact Mass | 178.062988 |
PSA | 46.53000 |
LogP | 1.35 |
Vapour Pressure | 0.0±0.8 mmHg at 25°C |
Index of Refraction | 1.593 |
Storage condition | 2-8°C |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi: Irritant; |
Risk Phrases | 36/37/38 |
Safety Phrases | 26-37/39 |
RIDADR | NONH for all modes of transport |
HS Code | 2912499000 |
Precursor 7 | |
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DownStream 10 | |
HS Code | 2912499000 |
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Summary | 2912499000. other aldehyde-ethers, aldehyde-phenols and aldehydes with other oxygen function. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0% |
A derivatization and validation strategy for determining the spatial localization of endogenous amine metabolites in tissues using MALDI imaging mass spectrometry.
J. Mass Spectrom. 49(8) , 665-73, (2014) Imaging mass spectrometry (IMS) studies increasingly focus on endogenous small molecular weight metabolites and consequently bring special analytical challenges. Since analytical tissue blanks do not ... |
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Reagent precoated targets for rapid in-tissue derivatization of the anti-tuberculosis drug isoniazid followed by MALDI imaging mass spectrometry.
J. Am. Soc. Mass Spectrom. 22(8) , 1409-19, (2011) 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 ... |
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Antifungal synergistic effect of scopoletin, a hydroxycoumarin isolated from Melia azedarach L. fruits.
J. Agric. Food Chem. 53(8) , 2922-7, (2005) 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... |
Ferulaldehyde |
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(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enal |
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MFCD00075811 |
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coniferaldehyde |
4-hydroxy-3-methoxycinnamic aldehyde |
EINECS 207-278-4 |
4-HYDROXY-3-METHOXYCINNAMALDEHYDE |
(2E)-3-(4-Hydroxy-3-methoxyphenyl)acrylaldehyde |
coniferyl aldehyde |
Coniferylaldehyde |