Cas no 1112-33-0 ((2R)-2,4-dihydroxy-3,3-dimethylbutanoic acid)

(2R)-2,4-Dihydroxy-3,3-dimethylbutanoic acid is a chiral hydroxy acid characterized by its stereospecific (R)-configuration and two hydroxyl groups at the 2- and 4-positions, along with geminal dimethyl substitution at the 3-position. This structural motif imparts unique reactivity, making it valuable as a synthetic intermediate in pharmaceutical and fine chemical applications. The compound’s stereocenter and polyfunctional nature enable its use in asymmetric synthesis, particularly in constructing complex molecules with precise stereochemical control. Its stability under mild conditions and compatibility with diverse reaction environments further enhance its utility. The presence of both hydroxyl and carboxyl groups allows for selective derivatization, facilitating applications in peptidomimetics, chelating agents, or chiral auxiliaries.
(2R)-2,4-dihydroxy-3,3-dimethylbutanoic acid structure
1112-33-0 structure
Product Name:(2R)-2,4-dihydroxy-3,3-dimethylbutanoic acid
CAS No:1112-33-0
MF:C6H12O4
MW:148.157082557678
CID:143254
PubChem ID:439251
Update Time:2025-10-28

(2R)-2,4-dihydroxy-3,3-dimethylbutanoic acid Chemical and Physical Properties

Names and Identifiers

    • Butanoic acid,2,4-dihydroxy-3,3-dimethyl-, (2R)-
    • Dexpanthenol impurity B
    • D-pantoic acid
    • (R)-Pantoic acid
    • D-(+)-PANTOICACID
    • (R)-2,4-Dihydroxy-3,3-dimethylbutyric acid
    • [R,(+)]-2,4-Dihydroxy-3,3-dimethylbutyric acid
    • (2R)-2,4-dihydroxy-3,3-dimethylbutanoic acid
    • UNII-0J1TL6G6J9
    • DTXSID101016980
    • NS00068399
    • C00522
    • Butanoic acid, 2,4-dihydroxy-3,3-dimethyl-, (R)-
    • Q23054703
    • Pantoic acid, (R)-
    • pantoate
    • Pantoic acid
    • (R)-2,4-Dihydroxy-3,3-dimethylbutanoic acid
    • SCHEMBL213982
    • DEXPANTHENOL IMPURITY B [EP IMPURITY]
    • Butanoic acid, 2,4-dihydroxy-3,3-dimethyl-, (2R)-
    • 1112-33-0
    • (R)-pantoate
    • CHEMBL1794671
    • (R)-2,4-Dihydroxy-3,3-dimethylbutanoicacid
    • EN300-176271
    • (-)-Pantoic acid
    • 0J1TL6G6J9
    • CHEBI:18697
    • OTOIIPJYVQJATP-BYPYZUCNSA-N
    • AKOS006378584
    • Z1205493806
    • Inchi: 1S/C6H12O4/c1-6(2,3-7)4(8)5(9)10/h4,7-8H,3H2,1-2H3,(H,9,10)/t4-/m0/s1
    • InChI Key: OTOIIPJYVQJATP-BYPYZUCNSA-N
    • SMILES: O[C@@H](C(=O)O)C(C)(C)CO

Computed Properties

  • Exact Mass: 148.07355886g/mol
  • Monoisotopic Mass: 148.07355886g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 3
  • Complexity: 130
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 1
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: -0.3
  • Topological Polar Surface Area: 77.8?2

(2R)-2,4-dihydroxy-3,3-dimethylbutanoic acid Pricemore >>

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Additional information on (2R)-2,4-dihydroxy-3,3-dimethylbutanoic acid

Introduction to (2R)-2,4-Dihydroxy-3,3-Dimethylbutanoic Acid (CAS No. 1112-33-0)

(2R)-2,4-Dihydroxy-3,3-Dimethylbutanoic Acid is a naturally occurring organic compound with the CAS registry number 1112-33-0. This compound is a member of the family of hydroxyl acids and has gained significant attention in recent years due to its versatile applications in various industries. The molecule consists of a four-carbon chain with two hydroxyl groups at positions 2 and 4 and two methyl groups at position 3. Its structure makes it highly functional and capable of participating in a wide range of chemical reactions.

Recent studies have highlighted the potential of (1112-33-0) in the field of food additives. Researchers have explored its role as a natural preservative in food products, demonstrating its ability to inhibit microbial growth without altering the sensory properties of the food. This has led to increased interest in its application in the food industry as a safer alternative to synthetic preservatives.

In addition to its role in food preservation, (2R)-Dihydroxy-Dimethylbutanoic Acid has shown promise in the cosmetics industry. Its ability to penetrate the skin and deliver active ingredients has made it a valuable component in skincare products. Recent clinical trials have indicated that it can enhance skin hydration and reduce signs of aging when applied topically.

The pharmaceutical industry has also taken notice of this compound. Studies have shown that (CAS No. 1112-33-0) can act as a chelating agent, binding to metal ions and preventing their harmful effects on biological systems. This property has led to its exploration as a potential therapeutic agent in treating conditions related to metal toxicity.

Furthermore, (Dihydroxy-Dimethylbutanoic Acid) has been investigated for its role in biochemistry and metabolism. Researchers have found that it plays a critical role in energy production within cells by acting as an intermediate in certain metabolic pathways. This discovery has opened new avenues for understanding cellular energy dynamics and developing treatments for metabolic disorders.

Despite its numerous applications, the production and utilization of (CAS No. 1112-33-0) are not without challenges. One major concern is its stability under various environmental conditions, which can affect its efficacy in different applications. Ongoing research is focused on improving its stability through chemical modifications and advanced formulation techniques.

In conclusion, ((2R)-Dihydroxy-Dimethylbutanoic Acid) is a multifaceted compound with significant potential across multiple industries. Its unique chemical properties and versatile applications make it an area of active research interest. As advancements continue to be made, this compound is poised to play an even more prominent role in shaping innovative solutions across various sectors.

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