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ABIETIC ACID

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ABIETIC ACID Basic information

Product Name:
ABIETIC ACID
Synonyms:
  • ABIETIC ACID
  • (1R,4AR,4BR,10AR)-7-ISOPROPYL-1,4A-DIMETHYL-1,2,3,4,4A,4B,5,6,10,10A-DECAHYDRO-PHENANTHRENE-1-CARBOXYLIC ACID
  • 13-isopropyl-podocarpa-13-dien-15-oicacid
  • 13-isopropylpodocarpa-7,13-dien-15-oicacid
  • ABIETIC ACID, TECH., 70%
  • ABIETIC ACID MELTING POINT 153-167 C
  • ABIETIC ACID, 90-95%
  • Abieticacid,TechnicalGrade
CAS:
514-10-3
MF:
C20H30O2
MW:
302.45
EINECS:
208-178-3
Product Categories:
  • Biochemistry
  • Terpenes (Others)
  • Terpenes
  • Asymmetric Synthesis
  • Chiral Building Blocks
  • Complex Molecules
  • Inhibitors
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • buildingblock
Mol File:
514-10-3.mol
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ABIETIC ACID Chemical Properties

Melting point:
139-142 °C (lit.) 150-165 °C
Boiling point:
440℃
alpha 
D24 -106° (c = 1 in abs alc)
Density 
1.06
refractive index 
1.4800 (estimate)
Flash point:
208℃
storage temp. 
2-8°C
solubility 
Soluble in alcohols, acetone and ethers
pka
pK1:7.62 (25°C)
form 
Crystals and Chunks
color 
Yellow-brownish
Odor
at 100.00?%. mild acetic
optical activity
[α]20/D 85±10°, c = 1% in ethanol
Water Solubility 
Soluble in acetone, petroleum ether, diethyl ether and ethanol. Insoluble in water.
Sensitive 
Air Sensitive
Merck 
14,7
BRN 
2221451
Exposure limits
NIOSH: TWA 0.1 mg/m3
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents.
LogP
6.460
CAS DataBase Reference
514-10-3(CAS DataBase Reference)
EPA Substance Registry System
Abietic acid (514-10-3)
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Safety Information

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
10-23
TSCA 
Yes
HazardClass 
9
PackingGroup 
III
HS Code 
29162090
Toxicity
LD50 ivn-mus: 180 mg/kg

MSDS

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ABIETIC ACID Usage And Synthesis

odor

The pure abietic acid is virtually odorless. The mmmercial material has a faint, pleasant resinous odor.

Description

Abietic acid is probably a major allergen of colophony, by way of oxidation products. Its detection in a material indicates that allergenic components of colophony are present.

Chemical Properties

yellow resinous powder, crystals or chunks

Uses

Abietic Acid is the primary component of resin acid found commonly in rosin. Abietic Acid exhibited potent testosterone 5α-reductase inhibitory activity in vitro.

Uses

manufacture of esters (ester gums), e.g., methyl ester, vinyl and glyceryl esters for use in lacquers and varnishes; manufacture of "metal resinates", soaps, plastics, and paper sizes; assists growth of lactic and butyric acid bacteria; component in tall oil used as deodorizing agent in cooling fluids; major component of rosin used in the production of varnishes, printing inks, paper, soldering fluxes, greases, cutting fluids, glue tackifiers, adhesives, surface coatings, polish, shoes, insulations, waxes, cosmetics (mascara, rouge, eye shadow), topical medicaments, violin bow rosin, day, athletic grip aid, pine oil deansers; component in dental impression materials and periodontal packings

Uses

Abietic acid is used to make ester gums in lacquers, varnishes and soaps. It is also used in metal resonates and plastics. Further, it is utilized in musical instruments to make them less slippery. It acts as a precursor to natural product synthesis. In addition to this, it is used to depackage integrated circuits from their epoxy coatings.

Production Methods

by distillation of Rosin (from American Turpentine, e. g.) or by treatment with acid to isomenze the natural Levopimaric acid. Purification over the Diamylammonium salt.

Definition

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

Combustible.

Contact allergens

Abietic acid is probably the major allergen of colophony, along with dehydroabietic acid, by way of oxidation products. Its detection in a material indicates that allergenic components of colophony are present

Safety Profile

Poison by intravenous route.Combustible. Slight explosion hazard as dust. Whenheated to decomposition it emits acrid smoke andirritating fumes.

Solubility in organics

soluble in alcohol and oils. Also soluble in aqueous solution of Sodium hydroxide.

Purification Methods

Filter, dry it in a vacuum (over KOH or CaSO4) and store it in an O2-free atmosphere. It can also be purified via the anhydride, tritylabietate and the potassium, piperidine and brucine salts. max : nm(log ): 2343(4.3), 241(4.4), 2505(4.2), 235(4.34) and 240(4.36) in Et. [Harris & Sanderson Org Synth Coll Vol IV 1 1963, J Am Chem Soc 35 3736 1949, Lambard & Frey Bull Soc Chim Fr 1194 1948, Buchbauer et al. Monatsh Chem 116 1345 1985.] [Beilstein 9 IV 2175.]

ABIETIC ACID Preparation Products And Raw materials

Raw materials

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