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Catalog Number:
39460
CAS Number:
26549-65-5
(+)-N,N,N',N'-Tetramethyl-L-tartardiamide
Purity:
≥ 98% (GC)
Synonym(s):
(R,R)-(+)-2,3-Dihydroxy-N,N,N',N'-tetramethylsuccinamide
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Product Information

(+)-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.

Synonyms
(R,R)-(+)-2,3-Dihydroxy-N,N,N',N'-tetramethylsuccinamide
CAS Number
26549-65-5
Purity
≥ 98% (GC)
Molecular Formula
C8H16N2O4
Molecular Weight
204.23
MDL Number
MFCD00025672
PubChem ID
551829
Melting Point
185 - 189 °C
Appearance
White or off-white crystalline powder
Optical Rotation
[α]20D = 43 - 48 ° (C=1 in EtOH)
Conditions
Store at RT
General Information
Synonyms
(R,R)-(+)-2,3-Dihydroxy-N,N,N',N'-tetramethylsuccinamide
CAS Number
26549-65-5
Purity
≥ 98% (GC)
Molecular Formula
C8H16N2O4
Molecular Weight
204.23
MDL Number
MFCD00025672
PubChem ID
551829
Melting Point
185 - 189 °C
Appearance
White or off-white crystalline powder
Optical Rotation
[α]20D = 43 - 48 ° (C=1 in EtOH)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
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