Cas no 553-84-4 (Perilla ketone)

Perilla ketone (PK), chemically known as 4-(1-methylethenyl)-1-cyclohexen-1-yl methyl ketone, is a naturally occurring compound derived from Perilla frutescens. It is recognized for its role as a bioactive phytochemical with applications in flavoring, fragrance, and pharmaceutical research. PK exhibits notable insecticidal and antimicrobial properties, making it valuable in agrochemical formulations. Its structural similarity to other terpenoid ketones allows for versatility in synthetic chemistry, particularly in the development of derivatives with enhanced bioactivity. The compound’s stability and low toxicity profile further support its utility in industrial and research settings. Analytical methods for PK quantification, such as GC-MS, ensure precise characterization for quality control.
Perilla ketone structure
Perilla ketone structure
Product Name:Perilla ketone
CAS No:553-84-4
MF:C10H14O2
MW:166.216963291168
CID:367478
PubChem ID:68381
Update Time:2025-06-08

Perilla ketone Chemical and Physical Properties

Names and Identifiers

    • 1-Pentanone,1-(3-furanyl)-4-methyl-
    • Perilla Ketone
    • 1-(furan-3-yl)-4-methylpentan-1-one
    • 1-(3-Furanyl)-4-methyl-1-pentanone
    • 1-(3-Furyl)-4-methyl-1-pentanone
    • 1-(3-furyl)-4-methylpentan-1-one
    • 1-[3]Furyl-4-methyl-pentan-1-on
    • 1-furan-3-yl-4-methyl-pentan-1-one
    • 3-(3-Methylpentanoyl)furan
    • BRN 0114624
    • NSC348407
    • Purple mint plant extract
    • .BETA.-FURYL ISOAMYL KETONE
    • 1-(uran-3-yl)-4-methylpentan-1-one
    • 1-furan-3-yl-4-methylpentan-1-one
    • CHEBI:195771
    • Z1179940260
    • 1-Pentanone, 1-(3-furanyl)-4-methyl-
    • perillaketone
    • DTXSID10203828
    • NCI60_003097
    • MS-22906
    • CS-0182031
    • 553-84-4
    • Purple Mint Plant Isolate
    • AKOS012403470
    • HY-N9508
    • 1ST180092
    • 1-Pentanone, 1-(3-furyl)-4-methyl-
    • NSC 348407
    • beta-Furyl isoamyl ketone
    • BDBM50276352
    • NSC-348407
    • Q7168519
    • 5-17-09-00480 (Beilstein Handbook Reference)
    • CHEMBL469753
    • UNII-CV69S6Y94V
    • EN300-175722
    • WLN: T5OJ CV2Y1&1
    • CV69S6Y94V
    • PERILLA KETONE [MI]
    • 1-(3-furyl)-4-methyl-pentan-1-one
    • SCHEMBL4627614
    • 1-(3-Furanyl)-4-methyl-1-pentanone; 1-(3-Furyl)-4-methyl-1-pentanone; 3-(4-Methylpentanoyl)furan; NSC 348407;
    • DB-328913
    • G13090
    • Perilla ketone
    • Inchi: 1S/C10H14O2/c1-8(2)3-4-10(11)9-5-6-12-7-9/h5-8H,3-4H2,1-2H3
    • InChI Key: LVHLZMUFIYAEQB-UHFFFAOYSA-N
    • SMILES: O=C(C1=COC=C1)CCC(C)C

Computed Properties

  • Exact Mass: 166.09942
  • Monoisotopic Mass: 166.099
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 4
  • Complexity: 152
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.8
  • Topological Polar Surface Area: 30.2A^2

Experimental Properties

  • Density: d1515 0.9920
  • Boiling Point: bp 196°
  • Flash Point: 96.8°C
  • Refractive Index: nD20 1.4781
  • PSA: 30.21
  • LogP: 2.89850

Perilla ketone Security Information

  • Toxicity:LD50 in female, male mice, male rats (mg/kg): 2.5, 6, 10 i.p. (Wilson)

Perilla ketone Pricemore >>

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Additional information on Perilla ketone

Perilla ketone (CAS No. 553-84-4): A Comprehensive Overview of Its Applications and Recent Research Findings

Perilla ketone, with the chemical formula C10H10O, is a naturally occurring organic compound identified by its CAS number CAS No. 553-84-4. This compound is widely recognized for its distinctive aroma and has garnered significant attention in both the pharmaceutical and food industries due to its diverse biological activities. Over the years, extensive research has been conducted to elucidate its chemical properties, pharmacological effects, and potential applications in various fields.

The chemical structure of Perilla ketone features a menthone-like backbone with a ketone functional group, which contributes to its unique olfactory profile. This structural characteristic has made it a subject of interest in the development of natural fragrances and flavoring agents. Additionally, its role in traditional medicine, particularly in Asian cultures, has prompted modern scientific exploration into its therapeutic potential.

In recent years, studies have highlighted the antimicrobial and anti-inflammatory properties of Perilla ketone. Research published in peer-reviewed journals has demonstrated its effectiveness against various bacterial and fungal strains, making it a promising candidate for developing novel antimicrobial agents. Furthermore, preclinical studies have indicated that Perilla ketone exhibits significant anti-inflammatory effects by modulating key pro-inflammatory cytokines.

The pharmacological activity of Perilla ketone has also been explored in the context of neuroprotective and antioxidant therapies. Emerging research suggests that this compound may help mitigate oxidative stress and protect neuronal cells from damage caused by free radicals. These findings are particularly relevant in the context of neurodegenerative diseases such as Alzheimer's and Parkinson's, where oxidative stress plays a critical role in disease progression.

In the realm of food science, Perilla ketone is valued for its natural flavoring properties. It is commonly used in the production of beverages, snacks, and culinary dishes to impart a fresh, herbaceous aroma. The growing demand for natural and organic food additives has positioned Perilla ketone as a desirable alternative to synthetic flavor enhancers.

The synthesis of Perilla ketone can be achieved through various chemical pathways, including fermentation and enzymatic processes. These methods are increasingly being favored over traditional synthetic routes due to their environmental sustainability and higher yields. Advances in biotechnology have enabled the production of Perilla ketone on an industrial scale, making it more accessible for commercial applications.

The regulatory landscape for Perilla ketone varies across different regions, but it is generally considered safe for use in food and pharmaceutical products when within established guidelines. Regulatory bodies such as the FDA and EFSA have approved its use in various applications, reinforcing its safety profile. However, ongoing research is essential to ensure that its use remains within safe limits and to identify any potential long-term effects.

The future prospects of Perilla ketone are promising, with ongoing studies exploring its potential applications in personalized medicine and nanotechnology. For instance, researchers are investigating its role as a bioactive component in drug delivery systems, where it could enhance the efficacy of therapeutic agents by improving bioavailability.

In conclusion, Perilla ketone (CAS No. 553-84-4) is a multifaceted compound with significant implications across multiple industries. Its natural origin, coupled with its diverse biological activities, makes it a valuable asset in pharmaceuticals, food science, and beyond. As research continues to uncover new applications and benefits, the importance of this compound is likely to grow further.

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