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320617

Ethyl 4-hydroxy-3-methoxycinnamate

Name: Ethyl 4-hydroxy-3-methoxycinnamate
Brand: ALDRICH

98%

Synonym(s):

Ethyl ferulate

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About This Item

Linear Formula:

HOC₆H₃(OCH₃)CH=CHCO₂C₂H₅

CAS Number:

4046-02-0

Molecular Weight:

222.24

NACRES:

NA.22

PubChem Substance ID:

24859274

UNSPSC Code:

12352100

EC Number:

223-745-5

MDL number:

MFCD00009190

Assay:

98%

Form:

solid

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Properties

Quality Level

100

assay

98%

form

solid

bp

164-166 °C/0.5 mmHg (lit.)

mp

63-65 °C (lit.)

functional group

ester

SMILES string

CCOC(=O)\C=C\c1ccc(O)c(OC)c1

InChI

1S/C12H14O4/c1-3-16-12(14)7-5-9-4-6-10(13)11(8-9)15-2/h4-8,13H,3H2,1-2H3/b7-5+

InChI key

ATJVZXXHKSYELS-FNORWQNLSA-N

Description

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

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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Dual response surface-optimized process for feruloylated diacylglycerols by selective lipase-catalyzed transesterification in solvent free system.

Yan Zheng et al.

Bioresource technology, 100(12), 2896-2901 (2009-03-04)

Feruloylated diacylglycerol (FDAG) was synthesized using a selective lipase-catalyzed the transesterification between ethyl ferulate and triolein. To optimize the reaction conversion and purity of FDAG, dual response surface was applied to determine the effects of five-level-five-factors and their reciprocal interactions

Peroxidase-catalyzed oligomerization of ferulic acid esters.

Mirko Bunzel et al.

Journal of agricultural and food chemistry, 56(21), 10368-10375 (2008-10-10)

Valuable information about possible types of linkages, reaction mechanisms, and sequences for oxidative coupling of phenolic compounds in planta is available from in vitro model systems. Ferulate oligomers were generated in a system using ethyl ferulate, peroxidase, and hydrogen peroxide

Caffeic acid phenethyl ester and its related compounds limit the functional alterations of the isolated mouse brain and liver mitochondria submitted to in vitro anoxia-reoxygenation: relationship to their antioxidant activities.

Yun Feng et al.

Biochimica et biophysica acta, 1780(4), 659-672 (2008-01-31)

It is an important therapeutic strategy to protect mitochondria from oxidative stress, especially during ischemia-reperfusion. In the present study, an attempt has been made to evaluate the protective effects of caffeic acid phenethyl ester (CAPE) and its related phenolic compounds

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