Cas no 996-78-1 (ETHYLENEDIAMINE DI-L-(+)-TARTRATE)

ETHYLENEDIAMINE DI-L-(+)-TARTRATE is a chiral salt derived from the reaction of ethylenediamine with L-(+)-tartaric acid. It is commonly utilized in asymmetric synthesis and resolution processes due to its ability to form diastereomeric complexes with racemic compounds. The product exhibits high enantiomeric purity, making it valuable for applications in pharmaceuticals and fine chemicals where stereoselectivity is critical. Its crystalline nature ensures ease of handling and purification. Additionally, the compound’s stability under standard conditions and solubility in polar solvents enhance its versatility in synthetic workflows. These properties make it a reliable reagent for chiral separations and catalyst preparation.
ETHYLENEDIAMINE DI-L-(+)-TARTRATE structure
996-78-1 structure
Product Name:ETHYLENEDIAMINE DI-L-(+)-TARTRATE
CAS No:996-78-1
MF:C10H20N2O12
MW:360.272004127502
MDL:MFCD00060266
CID:797542
PubChem ID:53384525
Update Time:2025-10-21

ETHYLENEDIAMINE DI-L-(+)-TARTRATE Chemical and Physical Properties

Names and Identifiers

    • ETHYLENEDIAMINE DI-L-(+)-TARTRATE
    • 996-78-1
    • Ethane-1,2-diamine bis((2R,3R)-2,3-dihydroxysuccinate)
    • MDL: MFCD00060266
    • Inchi: 1S/2C4H6O6.C2H8N2/c2*5-1(3(7)8)2(6)4(9)10;3-1-2-4/h2*1-2,5-6H,(H,7,8)(H,9,10);1-4H2/t2*1-,2-;/m11./s1
    • InChI Key: RWISDUHFHDEVCZ-STERTIEDSA-N
    • SMILES: O[C@@H](C(=O)O)[C@H](C(=O)O)O.O[C@@H](C(=O)O)[C@H](C(=O)O)O.NCCN

Computed Properties

  • Exact Mass: 360.10200
  • Monoisotopic Mass: 360.10162408g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 10
  • Hydrogen Bond Acceptor Count: 14
  • Heavy Atom Count: 24
  • Rotatable Bond Count: 7
  • Complexity: 262
  • 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
  • Topological Polar Surface Area: 60.2

Experimental Properties

  • Color/Form: Not determined
  • PSA: 282.16000
  • LogP: -3.94080
  • Solubility: Not determined

ETHYLENEDIAMINE DI-L-(+)-TARTRATE Pricemore >>

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Additional information on ETHYLENEDIAMINE DI-L-(+)-TARTRATE

ETHYLENEDIAMINE DI-L-(+)-TARTRATE and CAS No. 996-78-1: Applications and Research Insights

The compound ETHYLENEDIAMINE DI-L-(+)-TARTRATE, identified by the CAS number 996-78-1, is a significant chemical entity with diverse applications in pharmaceuticals, biotechnology, and material science. This introduction delves into the properties, synthesis, and recent research advancements associated with this compound.

ETHYLENEDIAMINE DI-L-(+)-TARTRATE is a chiral tartrate salt derived from ethylenediamine and L-tartaric acid. Its molecular structure imparts unique physicochemical properties, making it a valuable intermediate in organic synthesis. The presence of two stereocenters enhances its versatility in forming complex molecular architectures, which is particularly relevant in the development of enantioselective catalysts and chiral auxiliaries.

In pharmaceutical research, ETHYLENEDIAMINE DI-L-(+)-TARTRATE has been explored for its potential role in drug formulation and delivery systems. Its ability to form stable complexes with various pharmacophores has been leveraged to enhance drug solubility and bioavailability. Recent studies have highlighted its application in the synthesis of prodrugs, where its chiral environment can influence metabolic pathways, thereby improving therapeutic efficacy.

The compound's utility extends to biotechnology, where it serves as a precursor in the production of chiral ligands for asymmetric catalysis. These ligands are crucial in the synthesis of biologically active molecules, including pharmaceuticals and agrochemicals. The growing demand for enantiomerically pure compounds has spurred interest in innovative synthetic methodologies involving ETHYLENEDIAMINE DI-L-(+)-TARTRATE.

Recent advancements in computational chemistry have enabled more precise predictions of the behavior of ETHYLENEDIAMINE DI-L-(+)-TARTRATE in complex systems. Molecular dynamics simulations have revealed insights into its interactions with biological targets, aiding in the design of more effective drug candidates. Additionally, machine learning models have been employed to optimize synthetic routes, reducing waste and improving yield.

The environmental impact of synthesizing ETHYLENEDIAMINE DI-L-(+)-TARTRATE has also been a focus of recent research. Green chemistry principles have guided the development of more sustainable processes, emphasizing atom economy and minimal byproduct formation. For instance, catalytic hydrogenation techniques have been explored as an alternative to traditional acid-base neutralization methods.

In material science, ETHYLENEDIAMINE DI-L-(+)-TARTRATE has been investigated for its potential as a building block in polymer synthesis. Its chiral nature allows for the creation of polymers with tailored optical and mechanical properties. These materials are being explored for applications in optoelectronics and biomedical devices, where precise control over molecular architecture is essential.

The role of CAS No. 996-78-1 in standardizing the compound's identity and properties cannot be overstated. This unique numerical identifier ensures consistency across scientific literature and industrial applications. Regulatory agencies rely on such standards to ensure safety and efficacy in pharmaceutical products derived from this compound.

The future prospects for ETHYLENEDIAMINE DI-L-(+)-TARTRATE are promising, with ongoing research uncovering new applications and refining synthetic methodologies. Collaborative efforts between academia and industry are likely to drive innovation, particularly in areas such as personalized medicine and advanced materials.

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