Cas no 62675-82-5 (rac 3-Hydroxydecanoic Acid Methyl Ester)

Technical Introduction: rac 3-Hydroxydecanoic Acid Methyl Ester rac 3-Hydroxydecanoic Acid Methyl Ester is a chiral ester derivative of 3-hydroxydecanoic acid, commonly utilized in organic synthesis and pharmaceutical research. Its racemic form provides versatility in stereochemical studies and intermediate applications. The compound features a hydroxyl group at the β-position, enabling further functionalization, while the methyl ester moiety enhances solubility and reactivity in various solvents. This makes it suitable for use in polymerization reactions, biodegradable materials, and as a precursor for bioactive molecules. Its well-defined structure and stability under standard conditions ensure consistent performance in laboratory and industrial settings. The product is typically characterized by GC-MS, NMR, and HPLC for purity verification.
rac 3-Hydroxydecanoic Acid Methyl Ester structure
62675-82-5 structure
Product Name:rac 3-Hydroxydecanoic Acid Methyl Ester
CAS No:62675-82-5
MF:C11H22O3
MW:202.290584087372
CID:435720
PubChem ID:521747
Update Time:2025-06-07

rac 3-Hydroxydecanoic Acid Methyl Ester Chemical and Physical Properties

Names and Identifiers

    • Decanoic acid, 3-hydroxy-, methyl ester
    • rac 3-Hydroxydecanoic Acid Methyl Ester
    • METHYL 3-HYDROXYDECANOATE
    • Methyl 3-hydroxydecanoate #
    • AKOS030524653
    • E89405
    • DL-2-HYDROXYDECANOICACIDMETHYLESTER
    • Methyl ester of 3-hydroxydecanoic acid
    • DTXSID90334720
    • SCHEMBL1271079
    • HY-W127538
    • SB50162
    • CS-0185764
    • 62675-82-5
    • FT-0695823
    • METHYL3-HYDROXYDECANOATE
    • 3-hydroxy Decanoic Acid methyl ester
    • 73634-77-2
    • BP-29857
    • PD077431
    • r-(3)-Hydroxydecanoic acid,methyl ester
    • FT-0669510
    • MFCD00133276
    • Inchi: 1S/C11H22O3/c1-3-4-5-6-7-8-10(12)9-11(13)14-2/h10,12H,3-9H2,1-2H3
    • InChI Key: UBVACUZVNTVHTE-UHFFFAOYSA-N
    • SMILES: OC(CC(=O)OC)CCCCCCC

Computed Properties

  • Exact Mass: 202.15700
  • Monoisotopic Mass: 202.15689456g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 9
  • Complexity: 146
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.8
  • Topological Polar Surface Area: 46.5?2

Experimental Properties

  • PSA: 46.53000
  • LogP: 2.27090

rac 3-Hydroxydecanoic Acid Methyl Ester Pricemore >>

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rac 3-Hydroxydecanoic Acid Methyl Ester Production Method

Additional information on rac 3-Hydroxydecanoic Acid Methyl Ester

Introduction to Rac 3-Hydroxydecanoic Acid Methyl Ester (CAS No. 62675-82-5)

Rac 3-Hydroxydecanoic Acid Methyl Ester (CAS No. 62675-82-5) is a versatile compound with significant applications in various fields, including pharmaceuticals, cosmetics, and chemical research. This ester is characterized by its unique molecular structure, which includes a hydroxyl group and a methyl ester group, making it an important intermediate in the synthesis of more complex molecules.

The chemical formula of Rac 3-Hydroxydecanoic Acid Methyl Ester is C12H24O3, and its molecular weight is approximately 216.31 g/mol. The compound is a colorless to pale yellow liquid with a mild, characteristic odor. It is soluble in most organic solvents but has limited solubility in water, which can be advantageous in certain chemical processes and formulations.

One of the key applications of Rac 3-Hydroxydecanoic Acid Methyl Ester is in the pharmaceutical industry. Recent studies have shown that this compound can serve as a building block for the synthesis of bioactive molecules with potential therapeutic properties. For instance, it has been used in the development of anti-inflammatory agents and anti-cancer drugs. The hydroxyl group in the molecule can undergo various chemical transformations, such as esterification, etherification, and oxidation, which can lead to the formation of diverse derivatives with different biological activities.

In the field of cosmetics, Rac 3-Hydroxydecanoic Acid Methyl Ester is valued for its emollient properties and its ability to enhance the texture and stability of cosmetic formulations. It can be used in creams, lotions, and other personal care products to improve their spreadability and moisturizing effects. Additionally, its low toxicity and good skin compatibility make it a safe and effective ingredient for use in cosmetic applications.

From a research perspective, Rac 3-Hydroxydecanoic Acid Methyl Ester has been extensively studied for its role in lipid metabolism and signaling pathways. Recent studies have explored its potential as a model compound for investigating the mechanisms of fatty acid metabolism and its implications for metabolic disorders such as diabetes and obesity. The compound's ability to modulate lipid signaling pathways has also been investigated for its potential therapeutic applications in these areas.

In terms of synthesis, Rac 3-Hydroxydecanoic Acid Methyl Ester can be prepared through various methods, including esterification reactions involving 3-hydroxydecanoic acid and methanol under acidic conditions. The racemic nature of the compound means that it contains equal amounts of both enantiomers, which can be important for certain applications where chirality plays a crucial role.

The safety profile of Rac 3-Hydroxydecanoic Acid Methyl Ester is generally favorable. It is considered to have low toxicity when used appropriately and has not been associated with significant environmental concerns. However, like any chemical compound, it should be handled with care, following standard laboratory safety protocols to ensure safe use.

In conclusion, Rac 3-Hydroxydecanoic Acid Methyl Ester (CAS No. 62675-82-5) is a valuable compound with a wide range of applications in pharmaceuticals, cosmetics, and chemical research. Its unique chemical properties make it an important intermediate in the synthesis of bioactive molecules and cosmetic formulations. Ongoing research continues to uncover new potential uses for this compound, further highlighting its significance in various scientific fields.

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