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Caffeic acid

CAS No.331-39-5
Chemical Name:Caffeic acid
Synonyms:Caffeic;NSC 623438;CAFFIC ACID;CAFFEIC ACID;AKOS B004050;Caffeic acid 0;Caffeicacid,96%;CaffeicAcidPure;CAFFEICACID(BULK;3,4-dihydroxyben
CBNumber:CB6281061
Molecular Formula:C9H8O4
Formula Weight:180.16
MOL File:331-39-5.mol
Caffeic acid Property
mp : 211-213 °C (dec.)(lit.)
storage temp. : Store at RT.
solubility : ethanol: 50 mg/mL
form : powder
color : yellow to tan
Water Solubility : soluble in hot water
Merck : 14,1635
BRN : 2210883
Stability:: Stable. Combustible. Incompatible with strong oxidizing agents, strong bases.
CAS DataBase Reference: 331-39-5(CAS DataBase Reference)
NIST Chemistry Reference: Cinnamic acid, 3,4-dihydroxy-(331-39-5)
EPA Substance Registry System: 2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-(331-39-5)
Safety
Hazard Codes : Xn,Xi
Risk Statements : 36/37/38-40-63-68
Safety Statements : 26-36/37/39-36
WGK Germany : 3
RTECS : GD8950000
Hazard Note : Irritant
HS Code : 29182990
Hazardous Substances Data: 331-39-5(Hazardous Substances Data)

Caffeic acid Chemical Properties,Usage,Production

Chemical Properties
Light yellow to greenish-yellow powder
Usage
antineoplastic, PGE2 synthase inhibitor, PK inhibitor
Usage
Caffeic Acid is a constituent of plants, probably occurs in plants only in conjugated forms. Caffeic acid is found in all plants because it is a key intermediate in the biosynthesis of lignin, one of the principal sources of biomass. Caffeic acid is one of the main natural phenols in argan oi.
General Description
Yellow prisms or plates (from chloroform or ligroin) or pale yellow granules. Alkaline solutions turn from yellow to orange.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
Caffeic acid is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in Caffeic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.
Health Hazard
ACUTE/CHRONIC HAZARDS: When heated to decomposition Caffeic acid emits acrid smoke and fumes.
Fire Hazard
Flash point data for Caffeic acid are not available; however, Caffeic acid is probably combustible.
Caffeic acid Preparation Products And Raw materials
Raw materials
Preparation Products
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331-39-5(Caffeic acid)Related Search:
RESCINNAMINE Caffeic acid 4-methyl ether 3,4-DIMETHOXYCINNAMIC ACID trans-2,4,5-Trimethoxycinnamic acid Caffeic acid 3-methyl ether Chlorogenic acid 3,4-dihydro-5,6,7-trimethoxy-2-naphthoic acid 4-Hydroxy-3,5-dimethoxycinnamic acid 3,4,5-TRIMETHOXYCINNAMIC ACID 3,4-(Methylenedioxy)cinnamic acid Caffeic acid Methyl cinnamate Ethyl cinnamate 2-HYDROXYCINNAMIC ACID ALPHA-CYANO-4-HYDROXYCINNAMIC ACID ASCORBICACID ACETIC ACID Caffeic acid methyl,CAFFEIC ACID METHYL ESTER
RARECHEM BK HC T335 TIMTEC-BB SBB006475 Organic Building Blocks (2E)-3-(3,4-Dihydroxyphenyl)-2-propenoic acid 2-Propenoic acid, 3-(3,4-dihydroxyphenyl)- 3-(3,4-dihydroxyphenyl)-2-propenoicaci 3-(3,4-Dihydroxyphenyl)propenoic acid 3,4-Dihydroxybenzeneacrylic acid 3,4-dihydroxybenzeneacrylicacid 3,4-dihydroxy-cinnamicaci 3,4-dihydroxycinnamicacid,predominantlytransisomer 4-(2’-carboxyvinyl)-1,2-dihydroxybenzene 4-(2-Carboxyethenyl)-1,2-dihydroxybenzene 4-(2'-Carboxyvinyl)-1,2-dihydroxybenzene CAFFEIC ACID LABOTEST-BB LT00233168 3-(3,4-DIHYDROXYPHENYL)-2-PROPENOIC ACID 3-(3,4-DIHYDROXYPHENYL)ACRYLIC ACID 331-39-5 Chemopreventive Agents C9 Cancer Research Carboxylic Acids Carbonyl Compounds Antioxidant and Free Radical Scavengers Building Blocks Analytical Reagents Analytical Chromatography Product Catalog BioChemical 3,4-DIHYDROXYCINNAMIC ACID AKOS B004050 Caffeicacid,96% CAFFEIC ACID, MATRIX SUBSTANCE FOR MALDI -MS 3,4-DIHYDROXYCINNAMIC ACID, 97%, PREDOMINANTLY TRANS 3,4-DIHYDROXYCINNAMIC ACID (CAFFEIC ACID) CaffeicAcidPure CAFFIC ACID 3,4-Dihydroxycinnamic acid, predominantly trans isomer, 99+% Caffeic CAFFEICACID(BULK CAFFEIC ACID(AHP) HO2C6H4CHCHCOOH OH2C6H3CHCHCOOH Pharmaceutical Intermediates CINNAMICACID,3,4-DIHYDROXY- Aromatic Cinnamic Acids, Esters and Derivatives Cinnamic acid Organic acids CAFFEIC ACID NATURAL CAFFEIC ACID SYNTHETIC Antioxidant Biochemistry HO2C6H3CHCHCO2H HO2C6H3CHCHCOOHH2O 3,4-Dihydroxycinnamic acid, 99+%, predominantly trans isomer (E)-3-(3,4-Dihydroxyphenyl)acrylic acid (E)-3,4-Dihydroxycinnamic acid 3,4-Dihydroxy-trans-cinnamic acid
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