Cas no 22446-38-4 (Ethyl 3-Hydroxyphenylacetate)

Ethyl 3-Hydroxyphenylacetate structure
Ethyl 3-Hydroxyphenylacetate structure
Product Name:Ethyl 3-Hydroxyphenylacetate
CAS No:22446-38-4
MF:C10H12O3
MW:180.200483322144
MDL:MFCD07369387
CID:252537
PubChem ID:354334534
Update Time:2025-10-29

Ethyl 3-Hydroxyphenylacetate Chemical and Physical Properties

Names and Identifiers

    • Ethyl 2-(3-hydroxyphenyl)acetate
    • Ethyl (3-Hydroxyphenyl)acetate
    • Ethyl 3-Hydroxyphenylacetate
    • Benzeneaceticacid, 3-hydroxy-, ethyl ester
    • Ethyl-3-hydroxyphenylacetate
    • (3-hydroxyphenyl)acetic acid ethyl ester
    • 3-hydroxyphenylacetic acid ethyl ester
    • AC1LC9ZA
    • CTK4E9524
    • ethyl (3-hydroxyphenyl)pentanoate
    • ethyl 3-hydroxy-phenylacetate
    • ethyl m-hydroxyphenylacetate
    • Jsp004565
    • SureCN905142
    • Benzeneacetic acid, 3-hydroxy-, ethyl ester
    • NSQBADKMIYCCSC-UHFFFAOYSA-N
    • Acetic acid, (m-hydroxyphenyl)-, ethyl ester
    • ethyl 3-hydoxyphenylacetate
    • ethyl(3-hydroxyphenyl)acetate
    • Ethyl (3-hydroxyphenyl)acetate #
    • DS-8512
    • (3-Hydroxy phenyl)-acetic acid ethyl ester
    • (3-hydroxy-phenyl)-acetic acid ethyl ester
    • Benzeneaceticacid,3-hydroxy-,ethyl ester
    • 22446-38-4
    • SCHEMBL905142
    • 3-Hydroxy-benzeneacetic Acid Ethyl Ester
    • (3-hydroxyphenyl)-acetic acid ethyl ester
    • DTXSID20341346
    • SY234751
    • CS-0030409
    • FT-0668293
    • AKOS010659218
    • A910171
    • ethyl2-(3-hydroxyphenyl)acetate
    • MFCD07369387
    • E1242
    • DA-07958
    • MDL: MFCD07369387
    • Inchi: 1S/C10H12O3/c1-2-13-10(12)7-8-4-3-5-9(11)6-8/h3-6,11H,2,7H2,1H3
    • InChI Key: NSQBADKMIYCCSC-UHFFFAOYSA-N
    • SMILES: O(CC)C(CC1C=CC=C(C=1)O)=O

Computed Properties

  • Exact Mass: 180.07866
  • Monoisotopic Mass: 180.078644241g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 4
  • Complexity: 168
  • 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: 1.5
  • Topological Polar Surface Area: 46.5

Experimental Properties

  • Boiling Point: 179°C/12mmHg(lit.)
  • Refractive Index: 1.5220 to 1.5270
  • Stability/Shelf Life: Store in Freezer
  • PSA: 46.53

Ethyl 3-Hydroxyphenylacetate Security Information

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Ethyl 3-Hydroxyphenylacetate Suppliers

Amadis Chemical Company Limited
Gold Member
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(CAS:22446-38-4)Ethyl 3-Hydroxyphenylacetate
Order Number:A910171
Stock Status:in Stock
Quantity:100g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 12:37
Price ($):346.0

Additional information on Ethyl 3-Hydroxyphenylacetate

Ethyl 3-Hydroxyphenylacetate (CAS No. 22446-38-4): Properties, Applications, and Market Insights

Ethyl 3-Hydroxyphenylacetate (CAS No. 22446-38-4) is a versatile organic compound widely used in the fragrance, pharmaceutical, and specialty chemical industries. This ester derivative of 3-hydroxyphenylacetic acid is valued for its pleasant aroma and functional properties, making it a key ingredient in various formulations. With the growing demand for natural-like fragrances and bio-based chemicals, this compound has gained significant attention in recent years.

The chemical structure of Ethyl 3-Hydroxyphenylacetate features a phenyl ring with a hydroxyl group at the meta position and an ethyl ester functional group. This unique arrangement contributes to its solubility in organic solvents and moderate polarity, which are crucial for its applications in perfumery and organic synthesis. Researchers are increasingly exploring its potential as a flavor enhancer and intermediate for pharmaceutical compounds, aligning with current trends in green chemistry and sustainable manufacturing.

In the fragrance industry, Ethyl 3-Hydroxyphenylacetate CAS 22446-38-4 is prized for its floral and honey-like notes, often used as a middle note in premium perfumes and personal care products. The compound's stability under various pH conditions makes it particularly valuable for cosmetic formulations and aromatherapy products. Recent market analyses show growing demand for this ingredient in vegan cosmetics and clean beauty products, reflecting consumer preferences for eco-friendly ingredients.

The synthesis of 3-Hydroxyphenylacetic acid ethyl ester typically involves esterification reactions under controlled conditions. Modern production methods emphasize catalytic efficiency and waste reduction, responding to the chemical industry's focus on process intensification and circular economy principles. Analytical techniques like HPLC and GC-MS are commonly employed to ensure the purity of the final product, which is crucial for meeting the stringent requirements of pharmaceutical-grade materials.

Beyond its traditional uses, Ethyl 3-Hydroxyphenylacetate is being investigated for novel applications in material science and biodegradable polymers. Its aromatic structure and functional groups make it a potential building block for advanced materials with specific optical or mechanical properties. This aligns with current research trends in smart materials and functional coatings, where bio-derived compounds are gaining prominence.

The global market for phenylacetate derivatives including Ethyl 3-Hydroxyphenylacetate 22446-38-4 is experiencing steady growth, driven by expanding applications in personal care and fine chemicals. Regional markets in Asia-Pacific show particularly strong demand, correlating with the growth of premium cosmetic industries in these areas. Industry reports highlight opportunities in custom synthesis and specialty chemical manufacturing for this compound.

Quality control standards for Ethyl 3-hydroxyphenyl acetate have become more rigorous, with emphasis on traceability and sustainability certifications. Manufacturers are increasingly adopting green chemistry metrics to evaluate their production processes, responding to customer demands for environmentally responsible sourcing. This trend is particularly evident in European and North American markets, where regulatory compliance and eco-labeling significantly influence purchasing decisions.

Recent scientific literature has explored the potential biological activities of 3-hydroxyphenylacetic acid derivatives, including possible applications in nutraceuticals and functional foods. While not classified as pharmaceutical actives, these compounds are being studied for their antioxidant properties and metabolic effects, opening new avenues for research in food science and preventive health applications.

Storage and handling of Ethyl 3-Hydroxyphenylacetate CAS No. 22446-38-4 require standard precautions for organic esters. The compound should be kept in airtight containers away from strong oxidizers and excessive heat. Proper ventilation and personal protective equipment are recommended when working with this material in industrial settings, following general laboratory safety protocols for organic chemicals.

Future developments in Ethyl 3-Hydroxyphenylacetate applications may focus on biocatalytic production methods and derivative compounds with enhanced properties. The growing interest in bio-based aromatics and green solvents suggests expanding opportunities for this versatile chemical intermediate. Industry experts anticipate increased research into its use as a platform chemical for more complex specialty molecules in coming years.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:22446-38-4)Ethyl 3-Hydroxyphenylacetate
A910171
Purity:99%
Quantity:100g
Price ($):346.0
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