CINNAMIC ACID

PRODUCT IDENTIFICATION

CAS NO. 621-82-9

CINNAMIC ACID

EINECS NO. 205-398-1
FORMULA C6H5CH=CHCOOH
MOL WT. 148.16

H.S. CODE

2916.39.0600

TOXICITY

 
SYNONYMS 3-Phenyl-2-propenoic acid; 3-Phenylacrylic acid;
3-Phenylpropenoic acid; Phenylacrylic acid; Cinnamic acid; Phenylacrylic acid; tert-beta-Phenylacrylic acid; Zimtsaeure; Kyselina skoricove; Benzenepropenoic acid; Benzylideneacetic acid; Cinnamylic acid; trans-3-Phenylpropensaeure;
SMILES

c1(\C=C\C(O)=O)ccccc1

CLASSIFICATION

Carbocyclic carboxylic acid

EXTRA NOTES

FEMA No. 2288

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE white crystalline powder
MELTING POINT

132 - 135 C

BOILING POINT 300 C
SPECIFIC GRAVITY  
SOLUBILITY IN WATER slightly soluble
pKa 4.44
VAPOR DENSITY

 

AUTOIGNITION

 

NFPA RATINGS

Health hazard: 2, Fire: 1, Reactivity Hazard: 0

REFRACTIVE INDEX

 
FLASH POINT  
STABILITY

Stable under ordinary conditions

EXTERNAL LINKS & GENERAL DESCRIPTION

Wikipedia Linking

Google Scholar Search - Cinnamic acid

Drug Information Portal (U.S. National Library of Medicine) - Cinnamic acid

PubChem Compound Summary - Cinnamic acid

IPCS INCHEM - Cinnamyl Alcohol and Related Substances

Drug Bank -  Cinnamic acid

KEGG (Kyoto Encyclopedia of Genes and Genomes) - Cinnamic acid

http://www.ebi.ac.uk/ - Cinnamic acid

http://www.ncbi.nlm.nih.gov/ - Cinnamic acid

Material Safety Data Sheet

Local:
In biological chemistry, cinnamic acid  is a key intermediate in shikimate and phenylpropanoid pathways. Shikimic acid is a precursor of many alkaloids, aromatic amino acids, and indole derivatives. Phenylpropanoid are a class of plant metabolites based on phenylalanine. They are widely distributed in plants fulfilling many functions including plant defense mechanism, pigmentation and external signaling system. Phenylalanine is first converted to cinnamates, coumarines, caffeic acids, ferulic acids, and sinapic acids. Cinnamic acid is the precursor of these acids. Cinnamic acid is the parent compound of its esters which are more volatile to be transported to other parts easily. Commercial cinnamic acid, a phenylacrylic acid structure compound, is used in converting to its esters such as methyl, ethyl, and benzyl cinnamate for the perfume and flavour application. Cinnamic acid and Its derivatives including esters and carboxylic functional derivatives are used as important components in flavours, perfumes, synthetic indigo and pharmaceuticals. Cinnamate can act as optical filters or deactivate substrate molecules that have been excited by light for the protection polymers and organic substances. They, cosmetic grades, are used as sunscreen agents to reduce skin damage by blocking UV-A, B. Cinnamic acid is an odorless white crystalline powder; slightly soluble in water; melting point 133 C and boiling point 300 C.

SALES SPECIFICATION

APPEARANCE

white to yellowish crystals
ASSAY

99.0% min

MELTING POINT

132 - 135 C

LOSS ON DRYING

0.5% max

RESIDUE ON IGNITION

0.1% max

ARSENIC

2ppm max

HEAVY METALS

20ppm max

TRANSPORTATION
PACKING
 
HAZARD CLASS Not regulated
UN NO.  
SAFETY INFORMATION

HAZARD OVERVIEW

May cause eye, skin, and respiratory tract irritation. Target Organs: Respiratory system, eyes, skin.

GHS

 

SIGNAL WORD Warning

PICTOGRAMS

HAZARD STATEMENTS

H315-H319-H335

P STATEMENTS

P261-P305 + P351 + P338

EC DIRECTIVES

 

HAZARD CODES

RISK PHRASES

36/37/38

SAFETY PHRASES

26-36

PRICE INFORMATION