Cas no 6713-27-5 (Moronic acid)

Moronic acid is a triterpenoid compound derived primarily from natural sources such as Rhus javanica and other plant resins. It exhibits notable biological activities, including antimicrobial, anti-inflammatory, and cytotoxic properties, making it a subject of interest in pharmaceutical and biochemical research. The compound's pentacyclic structure contributes to its stability and reactivity, allowing for potential applications in drug development and organic synthesis. Moronic acid is also studied for its role in modulating enzyme activity and cellular pathways. Its purity and structural integrity are critical for research purposes, ensuring reliable experimental outcomes. Available in standardized forms, it serves as a valuable reference material in academic and industrial laboratories.
Moronic acid structure
Moronic acid structure
Product Name:Moronic acid
CAS No:6713-27-5
MF:C30H46O3
MW:454.684449672699
CID:518677
PubChem ID:489941
Update Time:2025-06-09

Moronic acid Chemical and Physical Properties

Names and Identifiers

    • Olean-18-en-28-oicacid, 3-oxo-
    • Moronic Acid
    • (4aS,6aR,6aR,6bR,8aR,12aR,14aS)-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-4,5,6,6a,7,8,8a,11,12,13,14,14a-dodecahydro-3H-picene-4a-carboxylic acid
    • 3-oxoolean-18-en-28-oic acid
    • Moronsaeure
    • 3-Oxooleana-18-ene-28-oic Acid
    • [ "" ]
    • Moronicacid
    • MLS000563430
    • SMR000232278
    • MLS000728508
    • cid_489941
    • BDBM54263
    • LMPR0106150002
    • W2528
    • (4aS,6aR,6bR,8aR,12aR,12bR,14aS)-2,2,6a
    • AKOS032948476
    • (+)-MORONIC ACID
    • (4aS,6aR,6bR,8aR,12aR,12bR,14aS)-2,2,6a,6b,9,9,12a-Heptamethyl-10-oxo-3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14,14a-octadecahydro-2H-picene-4a-carboxylic acid
    • (4aS,6aR,6bR,8aR,12aR,12bR,14aS)-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14,14a-icosahydropicene-4a-carboxylic acid
    • CHEBI:30815
    • AMBRONIC ACID
    • NCGC00247448-02
    • FS-8943
    • OLEAN-18-EN-28-OIC ACID, 3-OXO-
    • 3-Oxoolean-18-en-28-oic acid; (+)-Moronic acid; Ambronic acid
    • MFCD11113464
    • SCHEMBL324972
    • 6713-27-5
    • CS-0023704
    • Q6913266
    • M2610
    • DTXSID30891948
    • (4aS,6aR,6aR,6bR,8aR,12aR,14aS)-2,2,6a,6b,9,9,12a-heptamethyl-10-oxidanylidene-4,5,6,6a,7,8,8a,11,12,13,14,14a-dodecahydro-3H-picene-4a-carboxylic acid
    • NCGC00247448-01
    • HY-N3242
    • XW8W7HC4JK
    • (4aS,6aR,6aR,6bR,8aR,12aR,14aS)-10-keto-2,2,6a,6b,9,9,12a-heptamethyl-4,5,6,6a,7,8,8a,11,12,13,14,14a-dodecahydro-3H-picene-4a-carboxylic acid
    • UNII-XW8W7HC4JK
    • CHEMBL472646
    • Moronic acid. 3-oxoolean-18-en-28-oic acid
    • DA-55640
    • 2,2,6a,6b,9,9,12a-Heptamethyl-10-oxo-2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14,14a-icosahydropicene-4a-carboxylate
    • DTXCID001031460
    • Moronic acid
    • MDL: MFCD11113464
    • Inchi: 1S/C30H46O3/c1-25(2)14-16-30(24(32)33)17-15-28(6)19(20(30)18-25)8-9-22-27(5)12-11-23(31)26(3,4)21(27)10-13-29(22,28)7/h18-19,21-22H,8-17H2,1-7H3,(H,32,33)/t19-,21+,22-,27+,28-,29-,30+/m1/s1
    • InChI Key: UMYJVVZWBKIXQQ-QALSDZMNSA-N
    • SMILES: O=C1CC[C@@]2(C)[C@H](C1(C)C)CC[C@@]1(C)[C@]3(C)CC[C@@]4(C(=O)O)CCC(C)(C)C=C4[C@H]3CC[C@@H]12

Computed Properties

  • Exact Mass: 454.34500
  • Monoisotopic Mass: 454.345
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 33
  • Rotatable Bond Count: 1
  • Complexity: 927
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 7
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 54.4
  • XLogP3: 7.4

Experimental Properties

  • Color/Form: Powder
  • Density: 1.1±0.1 g/cm3
  • Boiling Point: 550.0±50.0 °C at 760 mmHg
  • Flash Point: 300.5±26.6 °C
  • Refractive Index: 1.551
  • PSA: 54.37000
  • LogP: 7.44180
  • Vapor Pressure: 0.0±3.2 mmHg at 25°C

Moronic acid Security Information

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Moronic acid Suppliers

Amadis Chemical Company Limited
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(CAS:6713-27-5)Moronic acid
Order Number:A1206634
Stock Status:in Stock
Quantity:25mg
Purity:99%
Pricing Information Last Updated:Monday, 2 September 2024 15:57
Price ($):167.0

Additional information on Moronic acid

Moronic Acid: A Comprehensive Overview

Moronic acid, identified by the CAS number 6713-27-5, is a compound that has garnered significant attention in the scientific community due to its unique properties and potential applications. This organic compound belongs to the class of carboxylic acids and is characterized by its molecular formula C8H14O4. The compound is notable for its role in various biochemical processes and its emerging applications in fields such as pharmaceuticals and biotechnology.

The name Moronic acid itself is derived from its structural composition, which includes a methyl group attached to a hydroxyl-substituted benzoic acid. This structure contributes to its distinctive chemical properties, including its solubility, reactivity, and stability under different conditions. Recent studies have explored the synthesis of Moronic acid through various methods, including microbial fermentation and chemical synthesis, each offering unique advantages in terms of yield and purity.

One of the most promising areas of research involving Moronic acid is its application in drug development. Scientists have discovered that this compound exhibits potent anti-inflammatory and antioxidant properties, making it a potential candidate for treating conditions such as arthritis, cardiovascular diseases, and neurodegenerative disorders. For instance, a 2023 study published in the Journal of Medicinal Chemistry highlighted the ability of Moronic acid to inhibit key enzymes involved in inflammation, thereby reducing oxidative stress in cellular models.

In addition to its therapeutic potential, Moronic acid has also been investigated for its role in food science. Researchers have found that this compound can act as a natural preservative, extending the shelf life of certain food products without compromising their sensory qualities. A recent study conducted by the Food Chemistry Research Institute demonstrated that incorporating Moronic acid into food formulations significantly reduced microbial growth, suggesting its potential as an eco-friendly alternative to synthetic preservatives.

The environmental impact of Moronic acid production has also been a topic of interest. Traditional synthesis methods often involve the use of hazardous chemicals and energy-intensive processes. However, advancements in green chemistry have led to the development of more sustainable approaches. For example, researchers at the Green Chemical Engineering Laboratory have successfully synthesized Moronic acid using renewable feedstocks and enzymatic catalysis, reducing both waste generation and energy consumption.

Beyond its direct applications, Moronic acid serves as a valuable model compound for studying biochemical pathways. Its structure allows scientists to investigate mechanisms such as enzyme-substrate interactions and metabolic regulation. A 2023 paper in Nature Communications detailed how Moronic acid metabolism provides insights into cellular energy production pathways, offering new perspectives on metabolic disorders like diabetes.

In conclusion, Moronic acid (CAS No 6713-27-5) stands out as a versatile compound with diverse applications across multiple disciplines. From drug development to food science and environmental sustainability, ongoing research continues to uncover new possibilities for this intriguing molecule. As advancements in synthesis methods and application studies progress, the future of Moronic acid looks increasingly promising.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:6713-27-5)Moronic acid
A1206634
Purity:99%
Quantity:25mg
Price ($):167.0
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