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A9424

Sigma-Aldrich

Abietic acid

≥65% (GC)

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About This Item

Empirical Formula (Hill Notation):
C20H30O2
CAS Number:
514-10-3
Molecular Weight:
302.45
Beilstein:
2221451
EC Number:
208-178-3
MDL number:
MFCD03423567
UNSPSC Code:
12352000
PubChem Substance ID:
24891449

concentration

≥65% (GC)

mp

139-142 °C (lit.)

SMILES string

CC(C)C1=CC2=CC[C@@H]3[C@](C)(CCC[C@@]3(C)C(O)=O)[C@H]2CC1

InChI

1S/C20H30O2/c1-13(2)14-6-8-16-15(12-14)7-9-17-19(16,3)10-5-11-20(17,4)18(21)22/h7,12-13,16-17H,5-6,8-11H2,1-4H3,(H,21,22)/t16-,17+,19+,20+/m0/s1

InChI key

RSWGJHLUYNHPMX-ONCXSQPRSA-N

Gene Information

human ... TNF(7124)

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Description
Pricing

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H319,H335,H400

Hazard Classifications

Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
107K2501
086K2501
099F0767
092H0290
051K2611

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Alan Talevi et al.
Bioorganic & medicinal chemistry letters, 17(6), 1684-1690 (2007-01-20)
Linear discriminant analysis was performed to derive discriminant functions based on 2D descriptors and capable of classifying anticonvulsant from non-anticonvulsant compounds. Through application in virtual screening of the discriminant function which performed best in the validation steps, abietic acid was
Xian-Wen Yang et al.
Bioorganic & medicinal chemistry, 18(2), 744-754 (2009-12-22)
Twenty-five new (abiesadines A-Y, 1-25) and 29 known (26-54) diterpenes were isolated from the aerial parts of Abies georgei. Abiesadine A (1) is a novel 8,14-seco-abietane, while abiesadine B (2) is a novel 9,10-seco-abietane. The structures of the new compounds
Patrick Frank et al.
Analytical chemistry, 84(10), 4419-4428 (2012-05-02)
In 2008 the rostrum from an ancient warship was recovered from the Mediterranean near Acqualadrone, Sicily. To establish its provenance and condition, samples of black and brown rostrum wood were examined using sulfur K-edge X-ray absorption spectroscopy (XAS) and gas
Yi He et al.
Journal of pharmaceutical and biomedical analysis, 66, 345-348 (2012-04-10)
An herbal drug for the treatment of psoriasis showed severe clinical adverse reactions. The main component of adulterant was isolated from the drug and its chemical structure was elucidated as abietic acid using NMR, HR-MS, and HPLC-DAD-MS. Although abietic acid
Roberto E Di Paolo et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 9(15), 2214-2220 (2008-10-03)
The synthesis and photophysical properties of six new abietic acid based amine end-capped p-phenylenevinylene trimers (AECPV3) in their lowest excited singlet states are presented. The AECPV3 compounds show a large red-shift of both the absorption (25-30 nm) and emission (37-42
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