Cas no 88122-12-7 (Benzaldehyde, 3,4-dihydroxy-2-methyl-)

Benzaldehyde, 3,4-dihydroxy-2-methyl- structure
88122-12-7 structure
Product Name:Benzaldehyde, 3,4-dihydroxy-2-methyl-
CAS No:88122-12-7
MF:C8H8O3
MW:152.147322654724
CID:644354
PubChem ID:11263595
Update Time:2025-07-23

Benzaldehyde, 3,4-dihydroxy-2-methyl- Chemical and Physical Properties

Names and Identifiers

    • Benzaldehyde, 3,4-dihydroxy-2-methyl-
    • 3,4-dihydroxy-2-methylbenzaldehyde
    • 3,4-Dihydroxy-2-methylbenzaldehyde (ACI)
    • F74840
    • EN300-657217
    • DB-128131
    • SCHEMBL670303
    • 88122-12-7
    • Z1416171282
    • Methylprotocatechualdehyd
    • DTXSID40460427
    • Inchi: 1S/C8H8O3/c1-5-6(4-9)2-3-7(10)8(5)11/h2-4,10-11H,1H3
    • InChI Key: OSYMDNUEVGSSKZ-UHFFFAOYSA-N
    • SMILES: O=CC1C(C)=C(O)C(O)=CC=1

Computed Properties

  • Exact Mass: 152.047344113g/mol
  • Monoisotopic Mass: 152.047344113g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 146
  • 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
  • Topological Polar Surface Area: 57.5?2

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Benzaldehyde, 3,4-dihydroxy-2-methyl- Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:88122-12-7)Benzaldehyde, 3,4-dihydroxy-2-methyl-
Order Number:A1241495
Stock Status:in Stock
Quantity:250mg/1g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 18:45
Price ($):204/550

Additional information on Benzaldehyde, 3,4-dihydroxy-2-methyl-

Benzaldehyde, 3,4-dihydroxy-2-methyl- (CAS No. 88122-12-7): A Comprehensive Overview of Its Properties and Applications

Benzaldehyde, 3,4-dihydroxy-2-methyl-, with the CAS No. 88122-12-7, is a specialized organic compound that has garnered significant attention in the fields of pharmaceuticals, flavor and fragrance, and organic synthesis. This compound, also known as 2-methyl-3,4-dihydroxybenzaldehyde, belongs to the class of benzaldehyde derivatives, which are widely recognized for their versatile chemical properties and broad applications. The presence of hydroxyl groups and a methyl substituent on the benzene ring enhances its reactivity and functionality, making it a valuable intermediate in various industrial processes.

In recent years, the demand for natural and synthetic flavor compounds has surged, driven by consumer preferences for clean-label products and sustainable ingredients. Benzaldehyde, 3,4-dihydroxy-2-methyl- is often explored for its potential role in flavor enhancement and aroma profiling, particularly in the food and beverage industry. Its structural similarity to vanillin and other phenolic aldehydes makes it a candidate for natural flavor alternatives, aligning with the trend toward plant-based and eco-friendly formulations.

From a pharmaceutical perspective, this compound has been investigated for its bioactive properties. Researchers are particularly interested in its antioxidant and anti-inflammatory potential, which could be leveraged in nutraceuticals and cosmeceuticals. The 3,4-dihydroxy moiety is a hallmark of many polyphenols, which are known for their health benefits, including free radical scavenging and cellular protection. These attributes have spurred interest in Benzaldehyde, 3,4-dihydroxy-2-methyl- as a building block for drug discovery and functional food additives.

The synthetic versatility of Benzaldehyde, 3,4-dihydroxy-2-methyl- also makes it a key player in organic chemistry. It serves as a precursor for the synthesis of heterocyclic compounds, ligands for metal catalysis, and specialty polymers. Its ability to undergo electrophilic substitution and oxidation reactions allows chemists to tailor its properties for specific applications, such as advanced materials and agrochemicals. This adaptability is particularly relevant in the context of green chemistry, where atom efficiency and reduced waste are prioritized.

In the realm of analytical chemistry, CAS No. 88122-12-7 is often characterized using techniques like HPLC, GC-MS, and NMR spectroscopy. These methods ensure purity assessment and structural confirmation, which are critical for quality control in industrial settings. The compound's UV-visible absorption properties also make it suitable for sensor development and photochemical studies, further expanding its utility in research and development.

As the scientific community continues to explore sustainable and innovative solutions, Benzaldehyde, 3,4-dihydroxy-2-methyl- remains a compound of interest. Its multifunctional nature and compatibility with green synthesis protocols position it as a forward-looking ingredient in various industries. Whether in flavor science, pharmaceuticals, or material engineering, this compound exemplifies the intersection of chemistry and innovation, offering endless possibilities for future advancements.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:88122-12-7)Benzaldehyde, 3,4-dihydroxy-2-methyl-
A1241495
Purity:99%/99%
Quantity:250mg/1g
Price ($):204/550
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