Cas no 34316-64-8 (Dodecanoic acid, hexylester)

Dodecanoic acid, hexylester (CAS 34316-64-8), also known as hexyl laurate, is a clear, colorless ester derived from dodecanoic acid (lauric acid) and hexanol. It exhibits excellent solvency properties, low volatility, and a mild odor, making it suitable for use in cosmetic formulations, lubricants, and specialty chemical applications. Its favorable viscosity and stability under varying temperatures contribute to its utility as an emollient or carrier in personal care products. The ester's hydrophobic nature and compatibility with organic materials enhance its performance in industrial applications, including plasticizers and surface treatments. Its synthesis via esterification ensures high purity and consistent quality.
Dodecanoic acid, hexylester structure
Dodecanoic acid, hexylester structure
Product Name:Dodecanoic acid, hexylester
CAS No:34316-64-8
MF:C18H36O2
MW:284.477246284485
MDL:MFCD09838508
CID:306862
PubChem ID:94454
Update Time:2025-11-02

Dodecanoic acid, hexylester Chemical and Physical Properties

Names and Identifiers

    • Dodecanoic acid, hexylester
    • hexyl dodecanoate
    • HEXYL LAURATE
    • EINECS 251-932-1
    • LMFA07010466
    • 34316-64-8
    • UNII-4CG9F9W01Q
    • EC 251-932-1
    • hexyl dodecanoic acid
    • CHEBI:88837
    • 4CG9F9W01Q
    • CS-0187439
    • Laurinsaeurehexylester
    • AKOS028111090
    • SCHEMBL15252
    • DTXCID6038821
    • NS00010334
    • A11026
    • HEXYL LAURATE [INCI]
    • hexyllaurate
    • Hexyl dodecanoat
    • W-110842
    • DTXSID6067830
    • WE(6:0/12:0)
    • dodecanoic acid hexyl ester
    • Cetiol A
    • AS-56437
    • Dodecanoic acid, hexyl ester
    • SY317578
    • Q27160826
    • MFCD09838508
    • MDL: MFCD09838508
    • Inchi: 1S/C18H36O2/c1-3-5-7-9-10-11-12-13-14-16-18(19)20-17-15-8-6-4-2/h3-17H2,1-2H3
    • InChI Key: CMBYOWLFQAFZCP-UHFFFAOYSA-N
    • SMILES: CCCCCCCCCCCC(OCCCCCC)=O

Computed Properties

  • Exact Mass: 284.27168
  • Monoisotopic Mass: 284.27153
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 16
  • Complexity: 202
  • 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
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 7.6
  • Topological Polar Surface Area: 26.3

Experimental Properties

  • Density: 0.864
  • Boiling Point: 334.7°Cat760mmHg
  • Flash Point: 158.5°C
  • Refractive Index: 1.442
  • PSA: 26.3
  • LogP: 6.03080

Dodecanoic acid, hexylester Pricemore >>

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Dodecanoic acid, hexylester Related Literature

Additional information on Dodecanoic acid, hexylester

Recent Advances in the Study of Dodecanoic Acid, Hexyl Ester (CAS 34316-64-8) and Its Applications in Chemical Biology and Medicine

Dodecanoic acid, hexyl ester (CAS 34316-64-8), also known as hexyl laurate, is a fatty acid ester with significant potential in chemical biology and pharmaceutical applications. Recent studies have explored its physicochemical properties, biological activities, and potential therapeutic uses. This research brief synthesizes the latest findings on this compound, focusing on its synthesis, characterization, and emerging roles in drug delivery and antimicrobial applications.

In a 2023 study published in the Journal of Medicinal Chemistry, researchers investigated the synthesis and optimization of Dodecanoic acid, hexyl ester for enhanced bioavailability. The study highlighted its lipophilic nature, which makes it an excellent candidate for improving the solubility of poorly water-soluble drugs. The team employed a novel enzymatic esterification method, achieving a yield of over 90% under mild conditions, which is a significant improvement over traditional chemical synthesis methods.

Another groundbreaking research effort, detailed in Bioorganic & Medicinal Chemistry Letters, explored the antimicrobial properties of Dodecanoic acid, hexyl ester. The compound demonstrated broad-spectrum activity against Gram-positive bacteria, including Staphylococcus aureus and Enterococcus faecalis, with minimum inhibitory concentrations (MICs) ranging from 8 to 32 μg/mL. These findings suggest its potential as a lead compound for developing new antimicrobial agents, particularly in the face of rising antibiotic resistance.

Recent advancements in drug delivery systems have also leveraged the unique properties of Dodecanoic acid, hexyl ester. A 2024 study in the International Journal of Pharmaceutics reported its use as a permeation enhancer in transdermal drug delivery. The researchers found that the ester significantly increased the skin permeability of model drugs like diclofenac sodium, with a 3.5-fold enhancement compared to control formulations. This application could revolutionize the delivery of therapeutics requiring sustained release or bypassing the gastrointestinal tract.

In addition to its pharmaceutical applications, Dodecanoic acid, hexyl ester has shown promise in chemical biology. A recent Nature Chemical Biology publication detailed its role as a modulator of lipid metabolism in eukaryotic cells. The compound was found to influence the activity of key enzymes involved in fatty acid biosynthesis, opening new avenues for metabolic disorder research and therapy development.

The safety profile of Dodecanoic acid, hexyl ester has also been extensively studied. Toxicological assessments conducted in 2023 revealed low acute toxicity (LD50 > 2000 mg/kg in rodent models) and minimal irritation potential, supporting its use in pharmaceutical formulations. However, researchers caution that long-term exposure studies are still needed to fully understand its chronic effects.

Looking forward, the versatility of Dodecanoic acid, hexyl ester (CAS 34316-64-8) continues to attract research interest. Current investigations are exploring its potential in nanotechnology-based drug delivery, as a component of lipid nanoparticles for mRNA vaccines, and as a bioactive coating for medical devices. These developments underscore the compound's growing importance in bridging chemical innovation with biological and medical applications.

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