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TCI

CAS 5497-76-7

L-Proline tert-Butyl Ester Hydrochloride TCI P1729

L-Proline tert-Butyl Ester Hydrochloride TCI P1729

Chemical Identity

CAS No.
5497-76-7
PubChem
CID 6453107·SID 125308074
Formula
C9H18ClNO2
Molecular weight
207.70 g/mol
Purity
>98.0%(N)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
tert-butyl (2S)-pyrrolidine-2-carboxylate;hydrochloride
SMILES
CC(C)(C)OC(=O)[C@@H]1CCCN1.Cl
InChIKey
IUUYANMOEMBTBV-FJXQXJEOSA-N
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L-Proline tert-Butyl Ester Hydrochloride is a chemical compound widely used in laboratory settings for its versatility in chemical and biochemical applications. This compound is a key reagent in peptide chemistry, playing a crucial role in the synthesis of peptides and amino acid modifications. Its unique structure allows it to participate in controlled reactions, making it essential for researchers working on protein structure and function studies. Due to its stability and reactivity under specific conditions, it is a valuable tool in various biochemical processes.

The compound is preferred for its solubility in organic solvents such as ethyl acetate and acetone, which simplifies dissolution and reaction processes. Its ester form enables controlled deesterification, enhancing its stability during synthesis. These properties make it a reliable choice for laboratories that require precision in chemical reactions. Additionally, its chemical stability ensures consistent results in experiments, contributing to its popularity among researchers.

In Indonesian laboratories, L-Proline tert-Butyl Ester Hydrochloride is commonly used in biochemical, pharmacological, and materials science research. It supports experiments related to peptide synthesis and amino acid modification, aiding in the development of new drugs and materials. Its availability through suppliers like AMI Scientific ensures that researchers have access to this essential compound for their work.

TCI brochures (PDF)

  • Peptide Synthesis: This compound is ideal for synthesizing peptides due to its controlled reactivity and stability, allowing for precise chemical modifications.
  • Amino Acid Modification: Its ester form facilitates controlled deesterification, making it suitable for amino acid functional group modifications.
  • Protein Structure Studies: It supports research on protein structure and function by enabling the study of amino acid interactions in synthetic environments.
  • Biochemical Research: Its solubility in organic solvents makes it a preferred choice for experiments requiring efficient dissolution and reaction conditions.
  • Materials Science Development: It is used in the development of new materials by enabling controlled chemical reactions in synthetic processes.

Brand TCI
CAS number 5497-76-7
Molecular formula —
Purity —
Category Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes Available in standard laboratory quantities
Physical form Solid powder
Storage Store in a cool, dry place away from moisture and light

L-Proline tert-Butyl Ester Hydrochloride should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in airtight containers to prevent exposure to moisture and air, which can affect its reactivity. Due to its potential for chemical reactions under certain conditions, it should be handled in a well-ventilated area. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. Proper storage and handling ensure the compound remains effective for its intended applications in research and development.

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