N-(tert-Butoxycarbonyl)-L-prolinamide TCI B3756

Chemical Identity

CAS No.: 35150-07-3
PubChem: CID 7019053·SID 172089060
Formula: C10H18N2O3
Molecular weight: 214.26 g/mol
Purity: >98.0%(HPLC)(N)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: tert-butyl (2S)-2-carbamoylpyrrolidine-1-carboxylate
SMILES: CC(C)(C)OC(=O)N1CCC[C@H]1C(=O)N
InChIKey: PITJAAIPVBVRAO-ZETCQYMHSA-N

Rp 900.900,00

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N-(tert-Butoxycarbonyl)-L-prolinamide is a chemical compound widely used in laboratory experiments involving chemical and biochemical research. It belongs to the category of peptide chemistry and is commonly employed in the synthesis of peptides and proteins. This compound serves as a derivative of proline, which gives it a complex molecular structure and makes it essential in peptide bond formation reactions. Its presence in various research settings highlights its importance in advancing biochemical and pharmaceutical studies.

The compound’s chemical stability under specific conditions makes it a preferred choice for synthetic processes in the laboratory. The tert-Butoxycarbonyl (Boc) group on its molecule provides resistance to hydrolysis, thereby extending its active lifetime in chemical reactions. This stability ensures that the compound remains effective during synthesis and manipulation, making it a reliable reagent for researchers. Its unique structural properties also allow for controlled chemical modifications, enhancing its utility in complex synthetic pathways.

In Indonesian laboratories, N-(tert-Butoxycarbonyl)-L-prolinamide is frequently used in biochemical and pharmacological research. It plays a crucial role in the development of bioactive compounds and in studying complex chemical reaction mechanisms. Its availability in the local market ensures that researchers and educational institutions can easily access this essential reagent for their experiments.

Related TCI products

Peptide Synthesis: This compound is ideal for synthesizing peptides and proteins due to its stable Boc group, which protects the amino group during reaction sequences.
Biochemical Research: Its role in peptide bond formation makes it a key reagent in studying biochemical pathways and molecular interactions.
Pharmaceutical Development: It is used in the creation of bioactive compounds, supporting drug discovery and development efforts.
Organic Chemistry Experiments: The compound’s chemical stability allows it to be used in various organic synthesis reactions requiring controlled reactivity.
Educational Research: It is commonly used in academic settings to teach and demonstrate peptide chemistry and synthetic methodologies.

Brand	TCI
CAS number	35150-07-3
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 light

This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which could affect its integrity. Due to its chemical nature, it should be handled with appropriate laboratory safety measures, such as wearing gloves and using a fume hood when necessary. Avoid direct contact with skin or inhalation of vapors. Ensure that storage conditions are consistent with standard chemical safety protocols to preserve its effectiveness and ensure safe handling in the laboratory.

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