cis-4-Azido-N-(tert-butoxycarbonyl)-L-proline TCI A3129

Chemical Identity

CAS No.: 132622-65-2
PubChem: CID 12094910·SID 354335139
Formula: C10H16N4O4
Molecular weight: 256.26 g/mol
Purity: >98.0%(HPLC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S,4S)-4-azido-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid
SMILES: CC(C)(C)OC(=O)N1C[C@H](C[C@H]1C(=O)O)N=[N+]=[N-]
InChIKey: JZEOWBJXFSZTJU-BQBZGAKWSA-N

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TCI A3129 132622-65-2 cis-4-Azido-N-(tert-butoxycarbonyl)-L-proline is a specialized chemical compound used in advanced research applications within chemical biology and conjugation chemistry. This compound plays a key role in click chemistry reactions, where its azido group enables efficient and selective coupling with other molecules. Its unique structure makes it an essential tool for researchers aiming to synthesize complex molecules with high specificity. This compound is widely utilized in laboratories for its versatility and reliability in various experimental setups.

The compound’s chemical properties, including its stability under controlled conditions and its reactivity that can be tailored through specific chemical reactions, make it a preferred choice for many scientific applications. The presence of both the azido and tert-butoxycarbonyl groups allows for precise molecular modifications and coupling reactions. Its high purity and solid form ensure consistent performance and accuracy in laboratory experiments, making it suitable for both small-scale and larger research projects.

In Indonesian laboratories, this compound is commonly used in scientific research related to chemical biology, pharmacology, and biotechnology. It supports studies in drug development, medical diagnostics, and biomedical research. Many research institutions and universities rely on this compound to advance their understanding of molecular reactivity and to develop new chemical compounds. Its reliability and effectiveness have made it a staple in the chemical research toolkit of Indonesian scientists.

TCI brochures (PDF)

Click Chemistry 2026-09-08 · p. 7
Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 12

Related TCI products

Molecular conjugation studies benefit from this compound's azido group, enabling efficient click chemistry reactions for biomolecule labeling and functionalization.
Drug development research utilizes its reactivity to synthesize complex pharmaceutical compounds with targeted biological activity.
Biomedical diagnostics leverage its chemical stability and specificity for creating probes and markers in diagnostic assays.
Bioconjugation projects rely on its ability to form stable linkages with other molecules, facilitating the creation of therapeutic agents and imaging agents.
Academic research in chemical biology uses this compound to explore molecular interactions and develop novel chemical structures for scientific innovation.

Brand	TCI
CAS number	132622-65-2
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Conjugation Chemistry/Click Chemistry
Pack sizes	—
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its reactivity. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. It is important to keep the compound in a secure location, away from incompatible substances. Regular inspection of storage conditions is advised to ensure the integrity of the material remains intact for research use.

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