COMU丨CAS 1075198-30-9

COMU丨CAS 1075198-30-9
Product Introduction:
Catalog No.: SS122747
CAS No.: 1075198-30-9
Purity (HPLC): 99% min
Assay: 98%~102%
Product Name: COMU
Molecular Formula: C12H19N4O4.PF6
Molecular Weight: 428.27
Synonym(s): (1-Cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbenium hexafluorophosphate
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Technical Parameters
Description

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Specifications of COMU丨CAS 1075198-30-9

 

Appearance:

White crystalline powder

Purity (HPLC):

99% min

Assay:

98%~102%

Identification:

1HNMR

Melting point:

155.0~165.0 °C

Loss on drying:

0.5% max

Overview

 

COMU丨CAS 1075198-30-9 is a carbodiimide reagent widely used in peptide synthesis, protein conjugation, and other applications in organic chemistry. COMU is often considered a more efficient and less toxic alternative to traditional coupling agents like EDC (1-ethyl-3-(3-dimethylaminopropyl) carbodiimide) and DCC (dicyclohexylcarbodiimide).

 

Applications of COMU丨CAS 1075198-30-9

 

1. Peptide Synthesis
A. Coupling Reagent in Solid-Phase Peptide Synthesis
● COMU丨CAS 1075198-30-9 is widely used in solid-phase peptide synthesis (SPPS) as a coupling reagent for the synthesis of peptides. It facilitates the activation of carboxyl groups of amino acids, allowing for the efficient coupling of amino acids during peptide elongation.
● Unlike other reagents, COMU does not generate by-products such as ureas or ammonium salts, making it a cleaner choice for peptide synthesis.
B. Minimal Side Reactions
● COMU offers significant advantages over older reagents like DCC, particularly due to its low tendency to produce side reactions such as urea formation. This results in fewer purification steps and higher yield of the desired peptide.

2. Protein Conjugation
● COMU is also utilized in protein conjugation, where it activates carboxyl groups of proteins or peptides to facilitate their attachment to other molecules such as biotin, fluorescent tags, or drug molecules. This is especially useful in bioconjugation techniques for the development of diagnostic tools, therapeutic agents, and biosensors.

3. Pharmaceutical and Biotech Industry
A. Drug Development
● In the pharmaceutical industry, COMU is valuable in drug development and biotechnology, particularly for the synthesis of peptide-based drugs and biopharmaceuticals. It provides an efficient and reliable method to couple biologically active molecules, which is essential for developing peptidomimetics, vaccines, and protein therapeutics.
B. Synthesis of Bioconjugates
● The use of COMU in bioconjugate synthesis allows for the precise construction of conjugates that can be used for drug delivery, targeted therapies, and therapeutic proteins. This makes it an important tool in the design of targeted treatments in personalized medicine.

4. Peptoid Synthesis
● COMU is sometimes employed in the synthesis of peptoids, which are synthetic polymers that mimic peptides but with altered backbone structures. Peptoids are used in drug discovery and biosensing applications, and COMU's efficiency in coupling amines to activated carboxyls makes it suitable for their synthesis.

5. Biochemical Research
● COMU is used in biochemical research for applications that involve the synthesis and modification of peptides, proteins, and other bioactive molecules. It provides a reliable means for introducing functional groups into bioactive molecules, aiding in the exploration of protein interactions, enzyme activity, and cellular processes.

 

Benefits of COMU丨CAS 1075198-30-9

 

1. High Coupling Efficiency
● One of the main advantages of COMU over other coupling reagents is its high coupling efficiency. It significantly reduces the number of coupling cycles required in peptide synthesis, leading to faster reactions and higher yields of peptides with fewer impurities.
2. Reduced Side Reactions
● COMU丨CAS 1075198-30-9 minimizes common side reactions, such as urea formation, which is prevalent with traditional reagents like DCC. This results in fewer unwanted by-products and easier purification, ultimately improving the quality of the final product.
3. Compatibility with Sensitive Functional Groups
● COMU is known for being mild and compatible with a wide variety of functional groups in peptide synthesis. It does not interfere with sensitive residues like serine, threonine, or tyrosine, which are critical for the biological activity of peptides and proteins.
4. Reduced Toxicity
● COMU is considered to have lower toxicity compared to traditional reagents like DCC and EDC. This makes it safer to handle in laboratory and industrial environments, and is particularly important when working with biological systems or biotech applications where safety and regulatory compliance are essential.
5. Clean Reaction Mechanism
● The use of COMU results in a cleaner reaction mechanism, with minimal by-products or side reactions, leading to simplified purification steps. This is particularly beneficial for large-scale peptide production and for synthesis in biopharmaceutical manufacturing.

 

Conclusion
COMU丨CAS 1075198-30-9 is a highly efficient coupling reagent that plays a vital role in peptide synthesis, protein conjugation, and the development of biopharmaceuticals. Its main advantages include high coupling efficiency, low side reactions, compatibility with sensitive functional groups, and reduced toxicity, making it a preferred choice for organic chemists and biotechnologists. COMU's ability to produce high-quality peptides and bioconjugates with minimal purification efforts makes it a valuable tool in the fields of drug development, biochemical research, and peptide-based therapeutics. Despite its benefits, proper safety measures should be observed when handling this chemical in both laboratory and industrial settings.

 

 

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