N-(tert-Butoxycarbonyl)-L-pyroglutamic Acid TCI B4083

Chemical Identity

Other names: Boc-Pyr-OH
CAS No.: 53100-44-0
PubChem: CID 104412·SID 253659761
Formula: C10H15NO5
Molecular weight: 229.23 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-1-[(2-methylpropan-2-yl)oxycarbonyl]-5-oxopyrrolidine-2-carboxylic acid
SMILES: CC(C)(C)OC(=O)N1[C@@H](CCC1=O)C(=O)O
InChIKey: MJLQPFJGZTYCMH-LURJTMIESA-N

Rp 1.378.650,00

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N-(tert-Butoxycarbonyl)-L-pyroglutamic Acid is a chemical compound widely used in laboratory settings, particularly in the fields of organic chemistry and biochemical research. This compound plays a crucial role in peptide synthesis, where it serves as a protecting group for the amino terminus of peptides. Its ability to form stable amide bonds makes it an essential component in the construction of complex molecular structures. In the laboratory, it is frequently utilized as a reagent to facilitate controlled chemical reactions, enabling the synthesis of bioactive molecules with high specificity.

The compound's unique chemical properties make it a preferred choice for researchers. It exhibits high reactivity in deprotonation reactions, allowing for the precise formation of amide linkages with other amino acids. This specificity is vital in the development of peptides with desired biological functions. Additionally, its stability under controlled reaction conditions ensures consistent results in synthetic processes. These characteristics make it a reliable and efficient reagent for advanced chemical and biochemical applications.

In Indonesian laboratories, this compound is commonly used by researchers in biochemistry, pharmacology, and materials science. It is a key component in the development of new drugs and bioactive compounds. Its role in peptide synthesis supports various research initiatives aimed at understanding molecular mechanisms and creating innovative chemical solutions. The compound's versatility and reliability make it an essential tool in modern laboratory research.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 14

Related TCI products

Peptide synthesis for drug development due to its ability to form stable amide bonds in controlled environments.
Biochemical research to study molecular interactions and reaction mechanisms in biological systems.
Pharmaceutical research for the design and synthesis of bioactive compounds with specific therapeutic properties.
Materials science applications in the creation of functional polymers and biomaterials.
Analytical chemistry for the characterization of complex molecular structures and reaction pathways.

Brand	TCI
CAS number	53100-44-0
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid powder
Storage	Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled with care in a well-ventilated laboratory setting. Avoid contact with incompatible substances such as strong acids or bases. Proper personal protective equipment, including gloves and safety goggles, should be worn during handling. Regular monitoring of storage conditions ensures the compound remains suitable for use in laboratory applications.

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