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Safety Information

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

A9424-100G:
A9424-BULK:
A9424-25G:
A9424-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
107K2501
086K2501
085K1265
071K2630
068H2507

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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
Simon Janocha et al.
Applied microbiology and biotechnology, 97(17), 7639-7649 (2013-06-25)
Cytochrome P450 enzymes exhibit a tremendous potential for biotechnological applications due to their ability to introduce oxygen into non-activated carbon atoms. Their catalytic diversity is complemented by a broad substrate range covering many natural compounds. Especially the functionalization of terpenoids
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
Simon Janocha et al.
Chembiochem : a European journal of chemical biology, 14(4), 467-473 (2013-02-02)
Cytochrome P450s are very versatile enzymes with great potential for biotechnological applications because of their ability to oxidize unactivated CH bonds. CYP105A1 from Streptomyces griseolus was first described as a herbicide-inducible sulfonylurea hydroxylase, but it is also able to convert
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
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