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CAS No.514-10-3
Chemical Name:ABIETIC ACID
Synonyms:OdoM;NSC 25149;ROSIN ACID;SYLVIC ACID;ABIETIC ACID;abietinicacid;l-abieticacid;colopholicacid;colophonic acid;AbieticAcid,75%
Molecular Formula:C20H30O2
Formula Weight:302.45
MOL File:514-10-3.mol
Melting point : 139-142 °C(lit.)
Boiling point : 440℃
density : 1.06
Fp : 208℃
storage temp. : 2-8°C
solubility : Soluble in alcohols, acetone and ethers
Water Solubility : Soluble in acetone, petroleum ether, diethyl ether and ethanol. Insoluble in water.
Sensitive : Air Sensitive
Merck : 14,7
BRN : 2221451
Stability:: Stable. Combustible. Incompatible with strong oxidizing agents.
CAS DataBase Reference: 514-10-3(CAS DataBase Reference)
Hazard Codes : Xi,N
Risk Statements : 36/37/38-50-50/53
Safety Statements : 26-36
RIDADR : UN 3077 9/PG 3
WGK Germany : 3
RTECS : TP8580000
F : 10-23
TSCA : Yes

ABIETIC ACID Chemical Properties,Usage,Production

Chemical Properties
yellow resinous powder, crystals or chunks
Abietic Acid is the primary component of resin acid found commonly in rosin. Abietic Acid exhibited potent testosterone 5α-reductase inhibitory activity in vitro.
ChEBI: An abietane diterpenoid that is abieta-7,13-diene substituted by a carboxy group at position 18.
General Description
Yellowish resinous powder.
Reactivity Profile
ABIETIC ACID reacts exothermically with bases, both organic (for example, the amines) and inorganic. Can react with active metals to form gaseous hydrogen and a metal salt. Such reactions are slow if the solid acid remains dry. Can react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slow 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: Slight fire hazard, slight explosive hazard as dust. Low toxicity.
Fire Hazard
ABIETIC ACID Preparation Products And Raw materials
Raw materials
Turpentine oil
Preparation Products
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514-10-3(ABIETIC ACID)Related Search:
POE ABIETIC ACID Abietic acid methyl Perilla oil 2-Butenedioic acid (E)-, reaction products with abietic acid, azelates, esters with glycerol HERCOLYN D Rosin 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, 2,2-bis[[[[1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenyl]carbonyl]oxy]methyl]-1,3-propanediyl ester, st HYDROGENATED GLYCERYL DEHYDROABIETATE/TETRAHYDROABIETATE Abietic acid, dehydro-6-sulfo- (6CI) CALCIUM RESINATE ABIETIC ACID SODIUM SALT 85+%,ABIETIC ACID SODIUM SALT,ABIETIC ACID SODIUM PENTAERYTHRITOL ABIETATE AMMONIUM ABIETATE calcium abietate POTASSIUM ABIETATE Cobalt abietate BARIUM ABIETATE TRIETHANOLAMINE ABIETATE
ABIETIC ACID 514-10-3 (1R,4AR,4BR,10AR)-7-ISOPROPYL-1,4A-DIMETHYL-1,2,3,4,4A,4B,5,6,10,10A-DECAHYDRO-PHENANTHRENE-1-CARBOXYLIC ACID Asymmetric Synthesis Chiral Building Blocks SYLVIC ACID ROSIN ACID (1r-(1alpha,4abeta,4balpha,10aalpha)-1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-d [1theta-(1alpha,4abeta,4balpha,10aalpha)]--7-(1-methylethyl) 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-,[1R-(1.alpha.,4a.beta.,4b.al1-Phenanthrenecarboxylicacid 13-isopropyl-podocarpa-13-dien-15-oicacid 13-isopropylpodocarpa-7,13-dien-15-oicacid 7,13-abietadien-18-oicacid abietinicacid imethyl-7-(1-methylethyl-)-1-phenanthrenecarboxylicacid kyselinaabietova l-abieticacid Complex Molecules Terpenes Terpenes (Others) abietic acid, technical 13-Isopropyodocarpa-7,13-dien-15-oic acid Abietic acid ;13-Isopropyodocarpa-7,13-dien-15-oic acid;Sylvic acid;13-iso-Propylpodocarpa-7,13-dien-15-oic acid colopholicacid colophonic acid ABIETIC ACID, TECH., 70% ABIETIC ACID MELTING POINT 153-167 C ABIETIC ACID, 90-95% Abieticacid,TechnicalGrade 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R,4aR,4bR,10aR)- ABIETIC ACID(SYLVIC ACID)(RG) C19H29COOH ABIETICACIDRESIN 514103 Biochemistry Terpenes (Others) Terpenes Asymmetric Synthesis Chiral Building Blocks Complex Molecules (-)-Abieta-7,13-dien-18-oic acid 1,2,3,4,4a,4bα,5,6,10,10aα-Decahydro-1β,4aβ-dimethyl-7-(1-methylethyl)phenanthrene-1α-carboxylic acid 13-Isopropylpodocarpa-7,13-dien-18-oic acid Abietic acid, 90+% Abietic acid,85% ABIETIC ACID, PRACT ABIETIC ACID(SYLVIC ACID)(P) 1,2,3,4,4a,4b,5,6,10,10a-cahydro-1,4a-diMethyl-7-(1-Methylethyl)-1-phenanthrenecarboxylic acid Abietic acid, 85% 25GR (1R,4aR,4bR,10aR)-1,2,3,4,4a,4b,5,6,10,10a-Decahydro-1,4a-diMethyl-7-(1-Methylethyl)-1-phenanthrenecarboxylic Acid NSC 25149 OdoM Rosin Acid Sylvic Acid ABIETIC ACID(SYLVIC ACID)(SH) Inhibitors Intermediates & Fine Chemicals Pharmaceuticals buildingblock
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