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Catalog Number:
39460
CAS Number:
26549-65-5
(+)- N,N,N',N' -Tétraméthyl-L-tartardiamide
Purity:
≥ 98% (CG)
Synonym(s):
( R , R )-(+)-2,3-Dihydroxy- N,N,N',N' -tétraméthylsuccinamide
Documents
$76.51 /5G
Taille
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Informations sur le produit

(+)-N,N,N',N'-Tetramethyl-L-tartardiamide is a versatile compound recognized for its unique properties and applications in various fields, particularly in organic synthesis and pharmaceuticals. This chiral diamide serves as an effective chiral auxiliary, facilitating asymmetric synthesis processes. Its ability to enhance selectivity in reactions makes it invaluable for researchers aiming to develop enantiomerically pure compounds. Additionally, its solubility in organic solvents allows for easy integration into diverse chemical reactions, promoting efficiency and effectiveness in laboratory settings.

The compound is also noteworthy for its role in the synthesis of biologically active molecules, where it can help streamline the production of complex pharmaceuticals. Its application extends to the development of catalysts and ligands in coordination chemistry, showcasing its adaptability across different chemical disciplines. Researchers and industry professionals can leverage (+)-N,N,N',N'-Tetramethyl-L-tartardiamide to improve yields and optimize reaction conditions, making it an essential addition to any chemical toolkit.

Numéro CAS 
26549-65-5
Formule moléculaire
C8H16N2O4
Poids moléculaire 
204.23
Point de fusion 
185 - 189 °C
Rotation optique 
[α]20 D = 43 - 48 ° (C=1 dans EtOH)
Informations générales
Numéro CAS 
26549-65-5
Formule moléculaire
C8H16N2O4
Poids moléculaire 
204.23
Point de fusion 
185 - 189 °C
Rotation optique 
[α]20 D = 43 - 48 ° (C=1 dans EtOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

(+)-N,N,N',N'-Tetramethyl-L-tartardiamide is widely utilized in research focused on

  • Chiral Separation: This compound is effective in chiral chromatography, helping researchers separate enantiomers in pharmaceuticals, which is crucial for drug efficacy and safety.
  • Biochemical Studies: It serves as a stabilizing agent in biochemical assays, enhancing the reliability of results in enzyme activity studies and protein interactions.
  • Polymer Chemistry: In the production of specialty polymers, it acts as a chain extender, improving mechanical properties and thermal stability, making materials more durable for industrial applications.
  • Pharmaceutical Development: Used in the formulation of drug delivery systems, it enhances solubility and bioavailability of active pharmaceutical ingredients, leading to more effective treatments.
  • Analytical Chemistry: As a derivatizing agent, it aids in the analysis of amino acids and other compounds, providing clearer results in mass spectrometry and chromatography.

Citations