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Safety Information

65400

Sigma-Aldrich

2-Methoxycinnamic acid

≥97.0%

Synonym(s):

3-(2-Methoxyphenyl)acrylic acid

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About This Item

Empirical Formula (Hill Notation):
C10H10O3
CAS Number:
6099-03-2
Molecular Weight:
178.18
Beilstein:
2209714
EC Number:
228-047-4
MDL number:
MFCD00064238
UNSPSC Code:
12352100
PubChem Substance ID:
57652029
NACRES:
NA.22

Assay

≥97.0%

mp

182-186 °C

functional group

carboxylic acid

SMILES string

COc1ccccc1\C=C\C(O)=O

InChI

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

InChI key

FEGVSPGUHMGGBO-VOTSOKGWSA-N

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
STBF4082V

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Ninghui Ma et al.
Molecules (Basel, Switzerland), 23(9) (2018-09-12)
To rapidly clarify and quantify the chemical profiling of Cinnamomi cortex a reliable and feasible strategy of chromatographic fingerprinting with a suite of chemometrics methods was developed and validated by ultra-high performance liquid chromatography coupled with diode array detection. Furthermore
Sirichai Adisakwattana et al.
International journal of molecular sciences, 13(2), 1778-1789 (2012-03-13)
Cinnamic acid and its derivatives have shown a variety of pharmacologic properties. However, little is known about the antiglycation properties of cinnamic acid and its derivatives. The present study sought to characterize the protein glycation inhibitory activity of cinnamic acid

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