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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 |
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Caffeic acid Property |
mp : |
211-213 °C (dec.)(lit.)
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storage temp. : |
Store at RT. |
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solubility : |
ethanol: 50 mg/mL
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Water Solubility : |
soluble in hot water |
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Stability:: |
Stable. Combustible. Incompatible with strong oxidizing agents, strong bases. |
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Caffeic acid Chemical Properties,Usage,Production |
Chemical Properties
Light yellow to greenish-yellow powder |
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Usage
antineoplastic, PGE2 synthase inhibitor, PK inhibitor |
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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. |
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General Description
Yellow prisms or plates (from chloroform or ligroin) or pale yellow granules. Alkaline solutions turn from yellow to orange. |
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Air & Water Reactions
Insoluble in water. |
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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. |
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Health Hazard
ACUTE/CHRONIC HAZARDS: When heated to decomposition Caffeic acid emits acrid smoke and fumes. |
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Fire Hazard
Flash point data for Caffeic acid are not available; however, Caffeic acid is probably combustible. |
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Caffeic acid Preparation Products And Raw materials |
Raw materials
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Preparation Products
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Caffeic acid Suppliers Global( 227)Suppliers |
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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
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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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