Unlock Advanced Synthesis with (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3

Unlock Advanced Synthesis with (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3: A Comprehensive Guide

This article provides a comprehensive guide to (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3, a key reagent in advanced synthesis. We delve into its parameters, usage scenarios, case studies, solutions, expert guidance, and FAQs to help you understand and utilize this product effectively.

Abstract

This guide aims to provide a detailed overview of (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3, a crucial reagent in advanced synthesis. By exploring its parameters, usage scenarios, case studies, solutions, expert guidance, and FAQs, this guide aims to help users understand and effectively utilize this product in their research and development processes.

Product Parameters

(S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3 is a white crystalline solid with a melting point of 150-152°C. It is soluble in water and slightly soluble in organic solvents. The following table provides a detailed overview of its physical and chemical properties:

Property Description
Appearance White crystalline solid
Melting Point 150-152°C
Solubility Water: Soluble; Organic solvents: Slightly soluble
Storage Condition Store in a cool, dry place, away from light and heat

Usage Scenarios

(S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3 is widely used in the synthesis of peptides, peptidomimetics, and other bioactive molecules. It is particularly useful in the following scenarios:

  • Peptide synthesis: The reagent can be used as a protecting group in the synthesis of peptides, providing a stable and efficient way to introduce amino acids into the peptide chain.
  • Peptidomimetic synthesis: The reagent can be used to synthesize peptidomimetics, which are molecules that mimic the structure and function of peptides but have improved properties.
  • Bioactive molecule synthesis: The reagent can be used to synthesize various bioactive molecules, such as antibiotics, antivirals, and anticancer agents.

Case Studies

Here are two case studies showcasing the use of (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3 in real-world applications:

Case Study 1: Synthesis of a Peptide Inhibitor

Company A, a biotech firm specializing in the development of peptide-based therapeutics, used (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3 to synthesize a peptide inhibitor targeting a specific protein involved in cancer. The reagent was used as a protecting group in the synthesis of the peptide, allowing for efficient and stable introduction of amino acids into the peptide chain. The resulting peptide inhibitor was successfully tested in vitro and in vivo, demonstrating its potential as a novel cancer treatment.

Case Study 2: Synthesis of a Peptidomimetic

Company B, a pharmaceutical company focused on the development of novel drugs, utilized (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3 to synthesize a peptidomimetic with improved stability and bioactivity. The reagent was used to introduce modifications to the peptide backbone, resulting in a molecule with enhanced affinity for its target receptor. The synthesized peptidomimetic was further developed into a potential therapeutic candidate for a neurodegenerative disease.

Solutions

When using (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3, it is essential to consider the following solutions to ensure successful synthesis:

  • Optimize reaction conditions: Adjusting reaction temperature, pH, and solvent choice can significantly impact the efficiency and yield of the synthesis.
  • Choose appropriate protecting groups: Selecting the right protecting groups for each amino acid in the peptide sequence is crucial for achieving high purity and yield.
  • Utilize efficient purification techniques: Employing advanced purification methods, such as HPLC or preparative LC, can help obtain high-purity products.

Expert Guidance

For users who are new to the synthesis of peptides and peptidomimetics, it is advisable to seek expert guidance. Consulting with experienced chemists or researchers can help you navigate the complexities of the synthesis process and optimize your experimental conditions. Additionally, attending workshops or seminars on peptide synthesis can provide valuable insights and best practices.

FAQs

Here are some frequently asked questions about (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3:

  • Q: What is the shelf life of (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3?
  • A: The shelf life of the reagent is typically 2 years when stored under appropriate conditions.
  • Q: Can (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3 be used in large-scale synthesis?
  • A: Yes, the reagent can be used in large-scale synthesis, but it is essential to optimize reaction conditions and purification techniques to ensure high yields and purity.
  • Q: Are there any side effects or safety concerns associated with (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3?
  • A: The reagent is generally considered safe for use in the laboratory, but it is essential to follow proper handling and disposal procedures to minimize any potential risks.

Conclusion

In conclusion, (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate CAS 113231-05-3 is a valuable reagent in advanced synthesis, particularly in the fields of peptide and peptidomimetic research. By understanding its parameters, usage scenarios, case studies, solutions, expert guidance, and FAQs, users can effectively utilize this product in their research and development processes.

Keywords

(S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid Hydrate, CAS 113231-05-3, peptide synthesis, peptidomimetic synthesis, bioactive molecule synthesis, protecting group, purification technique

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