Methyl Abietate (CAS 127-25-3)
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Alternate Names:
Abietic Acid Methyl Ester (6CI,7CI); Methyl abietate; NSC 2141; (1R,4aR,4bR,10aR)-1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-1-Phenanthrenecarboxylic Acid Methyl Ester
CAS Number:
127-25-3
Molecular Weight:
316.48
Molecular Formula:
C21H32O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Methyl Abietate is an organic compound that belongs to the class of abietic acid derivatives. It is derived from abietic acid, which is a naturally occurring resin acid found in various coniferous trees. Methyl Abietate is used as a fragrance ingredient and flavoring agent due to its pleasant odor and taste. It is also employed in the manufacturing of cosmetics, soaps, and other personal care products. Additionally, Methyl Abietate has applications in the production of coatings, adhesives, and various chemical intermediates.
Methyl Abietate (CAS 127-25-3) References
- Loblolly pine abietadienol/abietadienal oxidase PtAO (CYP720B1) is a multifunctional, multisubstrate cytochrome P450 monooxygenase. | Ro, DK., et al. 2005. Proc Natl Acad Sci U S A. 102: 8060-5. PMID: 15911762
- Methyl jasmonate treatment of mature Norway spruce (Picea abies) trees increases the accumulation of terpenoid resin components and protects against infection by Ceratocystis polonica, a bark beetle-associated fungus. | Zeneli, G., et al. 2006. Tree Physiol. 26: 977-88. PMID: 16651247
- Chemical composition and biological activity of a new type of Brazilian propolis: red propolis. | Alencar, SM., et al. 2007. J Ethnopharmacol. 113: 278-83. PMID: 17656055
- Analysis of rosin and modified rosin esters in adhesives by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS). | Kumooka, Y. 2008. Forensic Sci Int. 176: 111-20. PMID: 17728087
- Synthesis and biological evaluation of abietic acid derivatives. | González, MA., et al. 2009. Eur J Med Chem. 44: 2468-72. PMID: 19217699
- Synthesis and biological evaluation of dehydroabietic acid derivatives. | González, MA., et al. 2010. Eur J Med Chem. 45: 811-6. PMID: 19892441
- Selective oxidation reactions of natural compounds with hydrogen peroxide mediated by methyltrioxorhenium. | Amato, ME., et al. 2013. Molecules. 18: 13754-68. PMID: 24213654
- Antioxidant Properties of Essential Oil Extracted from Pinus morrisonicola Hay Needles by Supercritical Fluid and Identification of Possible Active Compounds by GC/MS. | Cheng, MC., et al. 2015. Molecules. 20: 19051-65. PMID: 26492232
- Genetic and correlation analysis of oleoresin chemical components in slash pine. | Zhang, S., et al. 2016. Genet Mol Res. 15: PMID: 27706657
- Contact allergy due to colophony (III). Sensitizing potency of resin acids and some related products. | Hausen, BM., et al. 1989. Contact Dermatitis. 20: 41-50. PMID: 2914435
- Catalytic methyl esterification of colophony over ZnO/SFCCR with subcritical CO2: catalytic performance, reaction pathway and kinetics. | Wang, X., et al. 2018. R Soc Open Sci. 5: 172124. PMID: 29892399
- Crude Wood Rosin and Its Derivatives as Hydrophobic Surface Treatment Additives for Paper and Packaging. | Dal, AEB., et al. 2020. ACS Omega. 5: 31559-31566. PMID: 33344808
- Changes and bioactivities on volatile organic compounds of endophytic fungi Neurospora dictyophora 3ZF-02 in different ages. | Zhang, H., et al. 2023. J Basic Microbiol. 63: 104-115. PMID: 36470591
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Methyl Abietate, 1 g | sc-483050 | 1 g | $562.00 |