Key Documents

View All Documentation

133760

trans-Cinnamic acid

Name: <I>trans</I>-Cinnamic acid
Brand: ALDRICH

97%

Synonym(s):

trans-3-Phenylacrylic acid, Cinnamic acid

Select a Size

Change View

About This Item

Linear Formula:

C₆H₅CH=CHCOOH

CAS Number:

140-10-3

Molecular Weight:

148.16

NACRES:

NA.22

PubChem Substance ID:

24848120

eCl@ss:

39023931

UNSPSC Code:

12352100

EC Number:

205-398-1

MDL number:

MFCD00004369

Beilstein/REAXYS Number:

1905952

Assay:

97%

Form:

solid

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

200

assay

97%

form

solid

bp

300 °C (lit.)

mp

132-135 °C (lit.)

functional group

carboxylic acid, phenyl

SMILES string

OC(=O)\C=C\c1ccccc1

InChI

1S/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)/b7-6+

InChI key

WBYWAXJHAXSJNI-VOTSOKGWSA-N

Description

Application

trans-Cinnamic acid was used to establish library of phenolic compounds by liquid chromatography/ultraviolet and mass spectrometry/mass spectrometry.

Biochem/physiol Actions

trans-cinnamic acid has inhibitory effect on phorbol-12-myristate-13-acetate-induced invasion of human lung adenocarcinoma A549 cells. It is a potential agent which can prevent lung tumor cells from metastasizing. It induces intracellular release of Ca²⁺ from the vacuole to the cytoplasm which triggers phytotoxicity in cucumber.

Still not finding the right product?

Explore all of our products under trans-Cinnamic acid

pictograms

GHS07

signalword

Warning

hcodes

H319

pcodes

P264 - P280 - P305 + P351 + P338 - P337 + P313

Hazard Classifications

Eye Irrit. 2

wgk

WGK 1

flash_point_f

320.0 °F - closed cup

flash_point_c

160 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Storage Class

11 - Combustible Solids

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Selective trans-cinnamic acid uptake impairs [Ca2+]cyt homeostasis and growth in Cucumis sativus L.

Jingquan Yu et al.

Journal of chemical ecology, 35(12), 1471-1477 (2010-01-12)

To obtain insight into interspecies interactions mediated by allelochemicals, the response of cucumber (Cucumis sativus L. cv Jinyan No.4) and figleaf gourd (Cucurbita ficifolia Bouché) seedlings to trans-cinnamic acid (CA) (1) was investigated. While trans-CA is an autotoxin in cucumber

Molecular mechanism depressing PMA-induced invasive behaviors in human lung adenocarcinoma cells by cis- and trans-cinnamic acid.

Chiung-Man Tsai et al.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 48(3), 494-501 (2012-12-12)

Dietary polyphenols have been reported as an effective phytochemical for health protection and cinnamic acid (CA) is one of the polyphenols that has been demonstrated having chemopreventive potential. It was known that the early and distal metastasis might lead to

Screening non-colored phenolics in red wines using liquid chromatography/ultraviolet and mass spectrometry/mass spectrometry libraries.

Jianping Sun et al.

Molecules (Basel, Switzerland), 12(3), 679-693 (2007-09-14)

Liquid chromatography/ultraviolet (LC/UV) and mass spectrometry/mass spectrometry (MS/MS) libraries containing 39 phenolic compounds were established by coupling a LC and an ion trap MS with an electrospray ionization (ESI) source, operated in negative ion mode. As a result, the deprotonated

View All Related Papers

Global Trade Item Number

SKU	GTIN
133760-100G	04061838729644
133760-2KG	04061831828276
133760-500G	04061838729651