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ABIETIC ACID

ABIETIC ACID Structure
CAS No.
514-10-3
Chemical Name:
ABIETIC ACID
Synonyms
Abietate;ROSIN ACID;ABIETIC ACID, TECH., 70%;OdoM;NSC 25149;abieticaci;SYLVIC ACID;ABIETIC ACID;abietinicacid;l-abieticacid
CBNumber:
CB1381555
Molecular Formula:
C20H30O2
Molecular Weight:
302.45
MOL File:
514-10-3.mol
MSDS File:
SDS
Modify Date:
2024/6/4 14:15:45

ABIETIC ACID Properties

Melting point 139-142 °C (lit.) 150-165 °C
alpha D24 -106° (c = 1 in abs alc)
Boiling point 440℃
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)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS09
Signal word  Warning
Hazard statements  H315-H319-H335-H400
Precautionary statements  P261-P264-P271-P273-P302+P352-P305+P351+P338
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
NFPA 704
0
2 1

ABIETIC ACID price More Price(6)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 00010 Abietic acid technical, ~75% (GC) 514-10-3 25G ₹8042.98 2022-06-14 Buy
Sigma-Aldrich(India) 00010 Abietic acid technical, ~75% (GC) 514-10-3 100G ₹15512.23 2022-06-14 Buy
ALFA India ALF-042582-MD Abietic acid, 90+% 514-10-3 250mg ₹8025 2022-05-26 Buy
TCI Chemicals (India) A0001 Abietic Acid min. 80.0 % 514-10-3 25G ₹2000 2022-05-26 Buy
ALFA India ALF-042582-03 Abietic acid, 90+% 514-10-3 1g ₹16054 2022-05-26 Buy
Product number Packaging Price Buy
00010 25G ₹8042.98 Buy
00010 100G ₹15512.23 Buy
ALF-042582-MD 250mg ₹8025 Buy
A0001 25G ₹2000 Buy
ALF-042582-03 1g ₹16054 Buy

ABIETIC ACID Chemical Properties,Uses,Production

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.

Definition

ChEBI: An abietane diterpenoid that is abieta-7,13-diene substituted by a carboxy group at position 18.

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.

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.]

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(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 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) ABIETICACIDRESIN SYLVIC 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 (-)-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% (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) 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 7,13-abietadien-18-oicacid abietinicacid imethyl-7-(1-methylethyl-)-1-phenanthrenecarboxylicacid kyselinaabietova l-abieticacid 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 technical, ~75% (GC) AbieticAcid,75% (1R,4aR,4bR,10aR)-1,4a-Dimethyl-7-(propan-2-yl)-1,2,3,4,4a,4b,5,6,10,10a-decahydrophenanthrene ABIETIC ACID 1-Phenanthrenecarboxylicacid, 1,2,3,4,4α,4β,5,6,10,10α-decahydro-1,4α-dimethyl-7-(1-methylethyl)-,(1R,4αR,4βR,10αR)- (1R,4AR,4BR,10AR)-1,4A-DIMETHYL-7-PROPAN-2-YL-2,3,4,4B,5,6,10,10A-OCTAHYDROPHENANTHRENE-1-CARBOXYLIC ACID abieticaci Abietic Acid, >95% 1-Phenanthrenecarboxylicacid, 1,2,3,4,4α,4β,5,6,10,10α-decahydro-1,4α-dimethyl-7-(1-methylethyl)-,(1R,4αR,4βR,10αR)- ABIETIC ACID, TECH., 70% ROSIN ACID Abietate ABIETIC ACID(SYLVIC ACID) 514-10-3 514103 C19H29COOH Chiral Building Blocks Asymmetric Synthesis Complex Molecules Terpenes Terpenes (Others)