Skip to Content
Merck
All Photos(1)

Documents

M13807

Sigma-Aldrich

4-Methoxycinnamic acid, predominantly trans

99%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3OC6H4CH=CHCO2H
CAS Number:
830-09-1
Molecular Weight:
178.18
EC Number:
212-594-0
MDL number:
MFCD00004398
UNSPSC Code:
12352103
PubChem Substance ID:
24896639
NACRES:
NA.23

Assay

99%

form

liquid crystal

mp

170-173 °C (lit.)

transition temp

crystalline phase to nematic phase 173.5 °C
nematic phase to isotropic phase 190 °C

SMILES string

COc1ccc(\C=C\C(O)=O)cc1

InChI

1S/C10H10O3/c1-13-9-5-2-8(3-6-9)4-7-10(11)12/h2-7H,1H3,(H,11,12)/b7-4+

InChI key

AFDXODALSZRGIH-QPJJXVBHSA-N

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

N Ikemoto et al.
Carbohydrate research, 239, 11-33 (1993-02-01)
The microscale analytical method that is being developed in this group for the structure determination of oligosaccharides yields monosaccharide derivatives bearing two types of chromophores suitable for exciton-coupling, namely, 4-bromobenzoate (lambda max 245 nm) and 4-methoxycinnamate (lambda max 311 nm).
Gunasekaran Sivagami et al.
Chemico-biological interactions, 196(1-2), 11-22 (2012-02-14)
We investigated the chemopreventive effect of p-methoxycinnamic acid (p-MCA), an active phenolic acid of rice bran, turmeric, and Kaemperfia galanga against 1,2-dimethylhydrazine-induced rat colon carcinogenesis. Male albino Wistar rats were randomly divided into six groups. Group 1 consisted of control
Sirichai Adisakwattana et al.
Life sciences, 78(4), 406-412 (2005-09-06)
We investigated the antihyperglycemic effect of p-methoxycinnamic acid (p-MCA), a cinnamic acid derivative, on plasma glucose and insulin concentrations, activities of hepatic glucose-regulating enzymes and hepatic glycogen content in normal and streptozotocin (STZ)-induced diabetic rats. p-MCA (10-100 mg/kg, PO) dose-dependently
So Ra Kim et al.
British journal of pharmacology, 135(5), 1281-1291 (2002-03-06)
1. We previously reported that four new phenylpropanoid glycosides and six known cinnamate derivatives isolated from roots of Scrophularia buergeriana Miquel (Scrophulariaceae) protected cultured cortical neurons from neurotoxicity induced by glutamate. Here, we have investigated the structure-activity relationships in the
Victor S Sobolev et al.
Journal of agricultural and food chemistry, 54(10), 3505-3511 (2006-05-17)
The peanut plant (Arachis hypogaea) is known to produce stilbene phytoalexins as a defensive response to fungal invasion; however, the distribution of phytoalexins among different organs of the peanut plant at early stages of growth under axenic conditions has not
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service