Cas no 71850-15-2 (Camaldulenic acid)

Camaldulenic acid structure
Camaldulenic acid structure
Product Name:Camaldulenic acid
CAS No:71850-15-2
MF:C30H46O4
MW:470.683849811554
CID:1080740
PubChem ID:10528366
Update Time:2025-07-09

Camaldulenic acid Chemical and Physical Properties

Names and Identifiers

    • Camaldulenic acid
    • Dehydromaslinic acid
    • (2alpha,3beta)-2,3-Dihydroxyoleana-11,13(18)-dien-28-oic acid
    • [ "" ]
    • 71850-15-2
    • AKOS032948942
    • FS-8610
    • (4aS,6aR,6aS,6bR,8aR,10R,11R,12aS)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid
    • (4aS,6aS,6bR,8aR,10R,11R,12aS,12bR)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b-dodecahydropicene-4a-carboxylic acid
    • Inchi: 1S/C30H46O4/c1-25(2)12-14-30(24(33)34)15-13-28(6)18(19(30)16-25)8-9-22-27(5)17-20(31)23(32)26(3,4)21(27)10-11-29(22,28)7/h8-9,20-23,31-32H,10-17H2,1-7H3,(H,33,34)/t20-,21+,22-,23+,27+,28-,29-,30+/m1/s1
    • InChI Key: YOLIZCATBHWOBV-JZQYXDLISA-N
    • SMILES: O[C@H]1[C@@H](C[C@@]2(C)[C@@H](CC[C@@]3(C)[C@]4(C)CC[C@@]5(C(=O)O)CCC(C)(C)CC5=C4C=C[C@@H]32)C1(C)C)O

Computed Properties

  • Exact Mass: 470.33960994g/mol
  • Monoisotopic Mass: 470.33960994g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 34
  • Rotatable Bond Count: 1
  • Complexity: 974
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 8
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 8.194
  • Topological Polar Surface Area: 77.8?2

Experimental Properties

  • Color/Form: Powder
  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 580.4±50.0 °C at 760 mmHg
  • Flash Point: 318.8±26.6 °C
  • Vapor Pressure: 0.0±3.7 mmHg at 25°C

Camaldulenic acid Security Information

Camaldulenic acid Pricemore >>

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Additional information on Camaldulenic acid

Camaldulenic Acid: A Comprehensive Overview

Camaldulenic acid, also known as Camaldulenic acid (CAS No. 71850-15-2), is a naturally occurring compound that has garnered significant attention in recent years due to its unique chemical properties and potential applications in various fields. This compound belongs to the class of triterpenoids, which are a large and diverse group of organic compounds found in plants. The Camaldulenic acid structure is characterized by a complex carbon skeleton, which contributes to its versatile biological activities and functional properties.

The Camaldulenic acid molecule is notable for its pentacyclic triterpene structure, which consists of five fused rings. This structural feature not only imparts stability to the molecule but also plays a crucial role in its interactions with biological systems. Recent studies have highlighted the potential of Camaldulenic acid as a bioactive compound with anti-inflammatory, antioxidant, and cytotoxic properties. These findings have opened new avenues for its use in pharmaceuticals, nutraceuticals, and cosmeceuticals.

One of the most promising applications of Camaldulenic acid is in the field of cancer research. Preclinical studies have demonstrated that this compound exhibits selective cytotoxicity against various cancer cell lines, making it a potential candidate for anticancer drug development. The mechanism behind this activity involves the modulation of key signaling pathways and the induction of apoptosis in malignant cells. These findings are particularly significant given the increasing need for novel therapeutic agents that can target cancer more effectively while minimizing side effects.

In addition to its anticancer properties, Camaldulenic acid has also shown potential as an anti-inflammatory agent. Chronic inflammation is a underlying factor in numerous diseases, including cardiovascular disorders, neurodegenerative conditions, and autoimmune diseases. The ability of Camaldulenic acid to suppress inflammatory pathways suggests its utility in developing new treatments for these conditions. Furthermore, its antioxidant properties make it a valuable ingredient in skincare products aimed at combating oxidative stress and promoting skin health.

The production of Camaldulenic acid traditionally relies on extraction from plant sources, particularly species belonging to the genus *Eucalyptus*. However, advancements in biotechnology have enabled the development of more efficient methods for synthesizing this compound. For instance, metabolic engineering of microbial systems has been explored as a sustainable approach to produce Camaldulenic acid on an industrial scale. These innovations not only enhance the availability of this compound but also reduce the environmental impact associated with its production.

From an environmental perspective, Camaldulenic acid has been studied for its role in plant defense mechanisms. It is believed to play a critical role in protecting plants from pathogens and environmental stressors. Understanding these mechanisms could provide insights into improving crop resilience and developing eco-friendly agricultural practices. Moreover, the ecological significance of Camaldulenic acid underscores its importance as a natural product with multifaceted applications.

Looking ahead, ongoing research into Camaldulenic acid is expected to uncover additional therapeutic applications and improve our understanding of its molecular mechanisms. Collaborative efforts between chemists, biologists, and pharmacologists are essential to fully harness the potential of this compound. As interest in natural products continues to grow, Camaldulenic acid stands out as a promising candidate for addressing some of the most pressing challenges in medicine and beyond.

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