Cas no 7534-51-2 (N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide)

N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide is a multifunctional polyhydroxy compound characterized by its three hydroxyl groups and an acetamide moiety. This structure imparts high solubility in water and polar solvents, making it suitable for applications requiring hydrophilic compatibility. The compound’s stability under physiological conditions and its ability to participate in hydrogen bonding enhance its utility in pharmaceutical formulations, particularly as an excipient or intermediate. Its polyol backbone may also contribute to moisture retention in cosmetic or biomedical applications. The presence of both hydroxyl and amide functional groups allows for further chemical modifications, enabling tailored derivatization for specialized uses in organic synthesis or material science.
N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide structure
7534-51-2 structure
Product Name:N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide
CAS No:7534-51-2
MF:C6H13NO4
MW:163.171722173691
CID:981718
PubChem ID:285324
Update Time:2025-06-11

N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide Chemical and Physical Properties

Names and Identifiers

    • N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide
    • 2-acetamido-2-(hydroxymethyl)propane-1,3-diol
    • AC1L62U2
    • AC1Q1KGI
    • AC1Q5L8B
    • Acetamino-tris-hydroxymethyl-methan
    • AG-H-00261
    • AR-1K3478
    • CTK2H9150
    • N-(2-Hydroxy-1,1-bis-hydroxymethyl-aethyl)-acetamid
    • N-(2-hydroxy-1,1-bis-hydroxymethyl-ethyl)-acetamide
    • NSC142169
    • SCHEMBL9816463
    • N-(1,3-Dihydroxy-2-(hydroxymethyl)propan-2-yl)acetamide
    • DTXSID70301278
    • acetyl-tris(hydroxymethyl)aminomethane
    • NSC-142169
    • 7534-51-2
    • G68101
    • DS-011868
    • Inchi: 1S/C6H13NO4/c1-5(11)7-6(2-8,3-9)4-10/h8-10H,2-4H2,1H3,(H,7,11)
    • InChI Key: JGAAIGKMNGHHHI-UHFFFAOYSA-N
    • SMILES: OCC(CO)(CO)NC(C)=O

Computed Properties

  • Exact Mass: 163.08449
  • Monoisotopic Mass: 163.084
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 4
  • Complexity: 124
  • 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: -2.6
  • Topological Polar Surface Area: 89.8?2

Experimental Properties

  • Density: 1.294
  • Melting Point: 109-113 °C
  • Boiling Point: 506.2°C at 760 mmHg
  • Flash Point: 260°C
  • Refractive Index: 1.515
  • PSA: 89.79
  • LogP: -1.77090

N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
A2B Chem LLC
AC48884-100mg
N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide
7534-51-2 97%
100mg
$76.00 2024-04-19
A2B Chem LLC
AC48884-250mg
N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide
7534-51-2 97%
250mg
$129.00 2024-04-19

Additional information on N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide

N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide (CAS No. 7534-51-2): An Overview of Its Properties and Applications

N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide (CAS No. 7534-51-2) is a versatile compound with a wide range of applications in the fields of chemistry, biology, and pharmaceuticals. This compound, also known as N-(1,3-dihydroxy-2-hydroxymethylpropyl)acetamide, has gained significant attention due to its unique chemical structure and potential therapeutic properties. In this article, we will delve into the chemical properties, synthesis methods, and recent research findings related to this compound.

The chemical structure of N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide consists of an acetamide group attached to a 1,3-dihydroxy-2-hydroxymethylpropan-2-yl moiety. This structure confers the compound with several important functional groups, including hydroxyl groups and an amide group, which contribute to its reactivity and solubility in various solvents. The presence of multiple hydroxyl groups makes it highly polar and water-soluble, which is advantageous for its use in aqueous environments.

Recent studies have focused on the synthesis and characterization of N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide. One notable method involves the reaction of 1,3-dihydroxyacetone with acetic anhydride in the presence of a catalyst. This approach has been optimized to achieve high yields and purity levels, making it suitable for large-scale production. The synthesized compound can be further purified using techniques such as recrystallization or chromatography to ensure its quality for various applications.

In the field of medicinal chemistry, N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide has shown promise as a potential therapeutic agent. Research has indicated that this compound exhibits anti-inflammatory properties by inhibiting the production of pro-inflammatory cytokines such as TNF-alpha and IL-6. Additionally, it has been found to have antioxidant activity, which can help protect cells from oxidative stress and damage. These properties make it a candidate for the development of new drugs targeting inflammatory diseases and oxidative stress-related conditions.

Moreover, N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide has been studied for its potential use in drug delivery systems. Its hydrophilic nature allows it to be easily incorporated into hydrogels or other delivery vehicles, enhancing the bioavailability and efficacy of co-administered drugs. This property is particularly useful in the development of topical formulations for skin conditions or local treatments for other diseases.

Recent advancements in analytical techniques have also contributed to a better understanding of the behavior of N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide. High-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy have been employed to analyze its purity and structural integrity. These methods provide valuable insights into the compound's stability under different conditions and help ensure its consistency in various applications.

In conclusion, N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide (CAS No. 7534-51-2) is a multifaceted compound with a wide range of applications in chemistry, biology, and pharmaceuticals. Its unique chemical structure and properties make it a valuable component in various research and industrial settings. Ongoing research continues to uncover new potential uses for this compound, further highlighting its importance in the scientific community.

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