Cas no 13393-93-6 (Tetrahydroabietyl Alcohol)

Tetrahydroabietyl Alcohol is a hydrogenated derivative of abietyl alcohol, derived from rosin. It is a stable, high-purity tertiary alcohol with a fully saturated hydrophenanthrene ring structure, which enhances its resistance to oxidation and discoloration compared to non-hydrogenated rosin derivatives. This compound exhibits excellent solubility in organic solvents and compatibility with polymers, making it suitable for use in adhesives, coatings, and ink formulations. Its low volatility and thermal stability contribute to improved product durability. Additionally, it serves as a versatile intermediate in the synthesis of esters and other derivatives, offering enhanced performance in applications requiring light color and long-term stability.
Tetrahydroabietyl Alcohol structure
Tetrahydroabietyl Alcohol structure
Product Name:Tetrahydroabietyl Alcohol
CAS No:13393-93-6
MF:C20H36O
MW:292.49924659729
CID:187091
PubChem ID:114506
Update Time:2025-10-29

Tetrahydroabietyl Alcohol Chemical and Physical Properties

Names and Identifiers

    • 1-Phenanthrenemethanol,tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R,4aR,4bS,10aR)-
    • Hydroabietyl alcohol
    • Tetrahydroabietyl Al
    • TETRAHYDROABIETYL ALCOHOL
    • ABITOL
    • [(1R,4aR,4bS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,7,8,8a,9,10,10a-dodecahydrophenanthren-1-yl]methanol
    • 1-Phenanthrenemethanol,tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-
    • Abietyl alcohol, tetrahydro-(6CI)
    • (8X,13X)-Abietan-18-ol
    • HYDROABIETYL ALCOHOL PRIMARY ALCOHOL
    • tetradecahydro-7-isopropyl-1,4a-dimethylphenanthren-1-methanol
    • tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenemethano
    • tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-1-Phenanthrenemethanol
    • (1R,4aR,4bS,10aR)-Tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenemethanol
    • TETRAHYDROABIETYL ALCOHOL)
    • 1-Phenanthrenemethanol, tetradecahydro-1,4A-dimethyl-7-(1-methylethyl)-, (1R,4ar,4bs,10ar)-
    • UNII-2RMS84XMDF
    • 1-Phenanthrenemethanol, tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-
    • (1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,7,8,8a,9,10,10a-dodecahydrophenanthren-1-yl)methanol
    • EC 236-476-3
    • ABITOL(TM) E HYDROABIETYL ALCOHOL
    • DTXSID8027745
    • 13393-93-6
    • AI3-04505
    • SCHEMBL2843274
    • NS00007070
    • Abietyl alcohol, tetrahydro-
    • W-110333
    • 2RMS84XMDF
    • Q27255510
    • EINECS 236-476-3
    • [(1R,4ar,4bs,10ar)-7-isopropyl-1,4a-dimethyl-2,3,4,4b,5,6,7,8,8a,9,10,10a-dodecahydrophenanthren-1-yl]methanol
    • DB-215305
    • KBAYQFWFCOOCIC-GJTWTXHOSA-N
    • Tetrahydroabietyl Alcohol
    • Inchi: 1S/C20H36O/c1-14(2)15-6-8-17-16(12-15)7-9-18-19(3,13-21)10-5-11-20(17,18)4/h14-18,21H,5-13H2,1-4H3/t15?,16?,17-,18-,19-,20+/m0/s1
    • InChI Key: KBAYQFWFCOOCIC-GJTWTXHOSA-N
    • SMILES: OC[C@]1(C)CCC[C@]2(C)[C@H]3CCC(C(C)C)CC3CC[C@H]21

Computed Properties

  • Exact Mass: 292.27700
  • Monoisotopic Mass: 292.276616
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 21
  • Rotatable Bond Count: 2
  • Complexity: 376
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 4
  • Undefined Atom Stereocenter Count : 2
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 20.2
  • XLogP3: 6.7

Experimental Properties

  • Density: 0.93
  • Boiling Point: 375.5 °C at 760 mmHg
  • Flash Point: 175.8 °C
  • Refractive Index: 1.484
  • PSA: 20.23000
  • LogP: 5.27370

Tetrahydroabietyl Alcohol Pricemore >>

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Additional information on Tetrahydroabietyl Alcohol

Introduction to Tetrahydroabietyl Alcohol (CAS No: 13393-93-6)

Tetrahydroabietyl Alcohol, with the chemical formula C??H??O, is a significant compound in the field of organic chemistry and pharmaceutical research. Its CAS number, 13393-93-6, uniquely identifies it in scientific literature and industrial applications. This bicyclic alcohol is derived from abietic acid, a common component found in pine resin, and has garnered considerable attention due to its versatile chemical properties and potential applications in drug development and material science.

The structure of Tetrahydroabietyl Alcohol features a tetrahydropyran ring system, which contributes to its stability and reactivity. This structural motif makes it a valuable intermediate in the synthesis of various pharmacologically active molecules. The compound's ability to undergo selective functionalization allows chemists to modify its structure for tailored applications, particularly in the creation of chiral centers, which are crucial in many drug formulations.

In recent years, Tetrahydroabietyl Alcohol has been extensively studied for its role in enhancing the solubility and bioavailability of poorly water-soluble drugs. Its lipophilic nature facilitates the formulation of drugs that would otherwise exhibit poor oral absorption. This property has been particularly exploited in the development of novel drug delivery systems, where Tetrahydroabietyl Alcohol acts as a solvent or cosolvent to improve the dissolution rate of active pharmaceutical ingredients (APIs).

One of the most compelling applications of Tetrahydroabietyl Alcohol is in the field of medicinal chemistry. Researchers have leveraged its structural framework to design and synthesize new molecules with potential therapeutic benefits. For instance, derivatives of Tetrahydroabietyl Alcohol have been investigated for their anti-inflammatory, antioxidant, and anticancer properties. The compound's ability to form stable complexes with other molecules has also opened avenues for its use in targeted drug delivery systems, where it can enhance the specificity and efficacy of therapeutic agents.

The pharmaceutical industry has shown particular interest in Tetrahydroabietyl Alcohol due to its compatibility with various synthetic methodologies. Its role as a chiral auxiliary in asymmetric synthesis has been well-documented, enabling the production of enantiomerically pure compounds that are essential for many modern drugs. Additionally, its use as a stabilizer in liquid crystal displays (LCDs) and other electronic materials underscores its versatility beyond pharmaceutical applications.

Recent advancements in computational chemistry have further highlighted the importance of Tetrahydroabietyl Alcohol. Molecular modeling studies have revealed insights into how this compound interacts with biological targets, providing valuable information for drug design. These studies have not only enhanced our understanding of Tetrahydroabietyl Alcohol's mechanism of action but also identified new opportunities for its application in rational drug design.

The synthesis of Tetrahydroabietyl Alcohol itself is an area of active research. Traditional methods often involve catalytic hydrogenation of abietic acid or related precursors. However, newer approaches employing biocatalysis and green chemistry principles are being explored to improve yield and reduce environmental impact. These innovations align with the growing emphasis on sustainable practices in chemical manufacturing.

The safety profile of Tetrahydroabietyl Alcohol is another critical consideration. While it is not classified as a hazardous material under standard regulatory frameworks, proper handling procedures must be followed to ensure safe laboratory and industrial use. Its low toxicity makes it suitable for widespread application without significant health risks when handled under controlled conditions.

In conclusion, Tetrahydroabietyl Alcohol (CAS No: 13393-93-6) is a multifaceted compound with broad applications across pharmaceuticals, materials science, and organic synthesis. Its unique structural properties make it an indispensable tool for researchers developing new drugs and advanced materials. As scientific understanding evolves, the potential uses for Tetrahydroabietyl Alcohol are likely to expand further, reinforcing its importance as a cornerstone molecule in modern chemistry.

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