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Catalog Number:
36434
CAS Number:
726-42-1
1,3-Di-p-tolylcarbodiimide
Purity:
≥ 96% (GC)
Synonym(s):
1,3-Di-p-tolylcarbodiimide, Bis(4-methylphenyl)carbodiimide
Documents
$175.00 /1G
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Product Information

1,3-Di-p-tolylcarbodiimide is a versatile reagent widely utilized in organic synthesis, particularly in the formation of amides and peptide bonds. This compound is recognized for its ability to activate carboxylic acids, facilitating the coupling of amino acids and other nucleophiles, making it invaluable in peptide synthesis and pharmaceutical development. Its unique structure, featuring two p-tolyl groups, enhances its stability and reactivity, allowing for efficient reactions under mild conditions. Researchers appreciate its effectiveness in generating high-purity products, which is crucial in both academic and industrial settings.

In addition to its applications in peptide synthesis, 1,3-Di-p-tolylcarbodiimide is also employed in the preparation of various functionalized compounds, contributing to advancements in materials science and drug discovery. Its compatibility with a range of functional groups makes it a preferred choice for chemists looking to streamline their synthetic pathways. The compound's ability to minimize side reactions further distinguishes it from similar reagents, offering a more reliable option for complex organic transformations.

Synonyms
1,3-Di-p-tolylcarbodiimide, Bis(4-methylphenyl)carbodiimide
CAS Number
726-42-1
Purity
≥ 96% (GC)
Molecular Formula
C15H14N2
Molecular Weight
222.29
MDL Number
MFCD00010701
PubChem ID
69763
Melting Point
56 - 58 °C
Appearance
White to off-white or light yellow powder
Boiling Point
221 - 223 °C/20 mmHg
Conditions
Store at 2 - 8 °C
General Information
Synonyms
1,3-Di-p-tolylcarbodiimide, Bis(4-methylphenyl)carbodiimide
CAS Number
726-42-1
Purity
≥ 96% (GC)
Molecular Formula
C15H14N2
Molecular Weight
222.29
MDL Number
MFCD00010701
PubChem ID
69763
Melting Point
56 - 58 °C
Appearance
White to off-white or light yellow powder
Boiling Point
221 - 223 °C/20 mmHg
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

1,3-Di-p-tolylcarbodiimide is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a coupling agent in the synthesis of peptides and other organic molecules, enhancing reaction efficiency and yield.
  • Pharmaceutical Development: It plays a crucial role in drug formulation, particularly in creating stable intermediates for active pharmaceutical ingredients (APIs).
  • Polymer Chemistry: Used in the production of specialty polymers, it helps improve material properties such as strength and thermal stability.
  • Analytical Chemistry: It is employed in various analytical techniques, including chromatography, to improve separation and detection of compounds.
  • Bioconjugation: This compound is effective in linking biomolecules, facilitating the development of targeted therapies and diagnostic tools in biotechnology.

Citations