Cas no 87827-55-2 (Lactiflorenol)

Lactiflorenol structure
Lactiflorenol structure
Product Name:Lactiflorenol
CAS No:87827-55-2
MF:C15H24O
MW:220.350464820862
CID:721945
PubChem ID:15934381
Update Time:2025-07-10

Lactiflorenol Chemical and Physical Properties

Names and Identifiers

    • 1-Azulenol,1,2,3,3a,4,5,6,8a-octahydro-1-methyl-4-methylene-7-(1-methylethyl)-,(1R,3aS,8aR)-
    • ALISMOL
    • (-)-Alismol
    • [ "(-)-Alismol" ]
    • Lactiflorenol
    • (1R,3aS,8aR)-1,2,3,3a,4,5,6,8a-Octahydro-1-methyl-4-methylene-7-(1-methylethyl)-1-azulenol (ACI)
    • 1-Azulenol, 1,2,3,3a,4,5,6,8a-octahydro-1-methyl-4-methylene-7-(1-methylethyl)-, [1R-(1α,3aβ,8aα)]- (ZCI)
    • (+)-Alismol
    • AKOS032948611
    • 87827-55-2
    • CID 15934381
    • 75556-47-7
    • 85404-63-3
    • 72646-96-9
    • 1-Azulenol, 1,2,3,3a,4,5,6,8a-octahydro-1-methyl-4-methylene-7-(1-methylethyl)-, (1R-(1alpha,3abeta,8abeta))-
    • DTXSID001007815
    • (1R,3aS,8aS)-1-methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,8a-hexahydroazulen-1-ol
    • BUPJOLXWQXEJSQ-QLFBSQMISA-N
    • 1-methyl-4-methylidene-7-(propan-2-yl)-1,2,3,3a,4,5,6,8a-octahydroazulen-1-ol
    • HY-N2838
    • CS-0023412
    • (1R,3aS,8aR)-1,2,3,3a,4,5,6,8a-Octahydro-1-methyl-4-methylene-7-(1-methylethyl)-1-azulenol; (+)-Alismol
    • (1R,3aS,8aR)-1-methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,8a-hexahydroazulen-1-ol
    • FS-9126
    • AKOS040760260
    • (1R,3aS,8aR)-7-isopropyl-1-methyl-4-methylene-2,3,3a,5,6,8a-hexahydroazulen-1-ol
    • BUPJOLXWQXEJSQ-RBSFLKMASA-N
    • 1.alpha.,5.beta.H-Guaia-6,10(14)-dien-4.beta.-ol
    • DA-50325
    • Inchi： 1S/C15H24O/c1-10(2)12-6-5-11(3)13-7-8-15(4,16)14(13)9-12/h9-10,13-14,16H,3,5-8H2,1-2,4H3/t13-,14-,15-/m1/s1
    • InChI Key： BUPJOLXWQXEJSQ-RBSFLKMASA-N
    • SMILES： C[C@]1(CC[C@@H]2C(CCC(=C[C@@H]12)C(C)C)=C)O

Computed Properties

  • Exact Mass: 220.18300
  • Monoisotopic Mass: 220.183
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 1
  • Complexity: 326
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 3
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Molecular Weight: 220.35
  • XLogP3: 2.7
  • Topological Polar Surface Area: 20.2

Experimental Properties

  • Color/Form: Oil
  • Density: 0.97
  • Boiling Point: 316.8°C at 760 mmHg
  • Flash Point: 131.2°C
  • Refractive Index: 1.513
  • PSA: 20.23000
  • LogP: 3.69600
  • Vapor Pressure: 0.0±1.5 mmHg at 25°C

Lactiflorenol Security Information

Lactiflorenol Pricemore >>

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Lactiflorenol Related Literature

Related Categories

Additional information on Lactiflorenol

Exploring Lactiflorenol (CAS No. 87827-55-2): A Comprehensive Guide to Its Properties and Applications

In the realm of bioactive compounds, Lactiflorenol (CAS No. 87827-55-2) has garnered significant attention for its unique structural and functional characteristics. This naturally derived molecule, often associated with microbial metabolites, is increasingly studied for its potential applications in cosmetics, pharmaceuticals, and biotechnology. Researchers and industry professionals alike are exploring its anti-inflammatory, antioxidant, and skin-barrier-enhancing properties, making it a hot topic in formulations targeting aging skin and microbiome balance.

The chemical structure of Lactiflorenol features a distinctive polyketide backbone, which contributes to its biological activity. With a molecular formula of C15H22O3, it belongs to a class of compounds known for their low toxicity and high biocompatibility. These traits align with the growing consumer demand for clean-label ingredients and sustainable skincare solutions. Recent studies highlight its role in modulating cutaneous microbiota, a key focus area in dermatological research linked to conditions like eczema and acne.

From a commercial perspective, Lactiflorenol is gaining traction in prebiotic skincare formulations. Brands emphasize its ability to support skin homeostasis by promoting beneficial bacteria while inhibiting pathogens—a mechanism resonating with the "skin-gut axis" trend. Analytical techniques such as HPLC and NMR spectroscopy confirm its purity, addressing quality concerns raised by manufacturers seeking standardized extracts. Notably, its stability under varying pH conditions makes it suitable for serums, creams, and even oral supplements.

Environmental considerations further enhance the appeal of Lactiflorenol. Derived through fermentation technology—a process lauded for its low carbon footprint—it aligns with the EU Green Deal objectives and clean beauty movements. Patent filings reveal innovative delivery systems like liposomal encapsulation to boost its bioavailability, answering frequent search queries about "how to improve ingredient penetration" in cosmetic science forums.

Ongoing clinical trials investigate Lactiflorenol's efficacy against oxidative stress, a primary culprit in photoaging. Preliminary data suggest synergistic effects when combined with vitamin C or niacinamide, topics frequently searched by formulators. Regulatory-wise, it holds GRAS (Generally Recognized As Safe) status in topical applications, though oral use requires further evaluation—a nuance often queried in FDA compliance discussions.

In conclusion, Lactiflorenol (CAS No. 87827-55-2) represents a convergence of cutting-edge science and market trends. Its multifunctionality bridges gaps between dermatology, microbiology, and green chemistry, offering actionable insights for brands navigating the "next-generation actives" landscape. As research unfolds, this compound may well redefine standards in personalized skincare and microbiome-friendly formulations.

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