trans-N-(tert-Butoxycarbonyl)-4-hydroxy-L-proline TCI B1635

Chemical Identity

Other names: Boc-Hyp-OH
CAS No.: 13726-69-7
PubChem: CID 11138980·SID 87564536
Formula: C10H17NO5
Molecular weight: 231.25 g/mol
Purity: >98.0%(T)(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid
SMILES: CC(C)(C)OC(=O)N1CC(C[C@H]1C(=O)O)O
InChIKey: BENKAPCDIOILGV-MLWJPKLSSA-N

Rp 1.829.100,00

~~Rp 1.294.650,00~~ Rp 1.829.100,00

Sale Sold out

Shipping calculated at checkout.

Berat 5g

Pembayaran hanya melalui request quotation dan dilakukan setelah tim kami menghubungi Anda. Mohon cantumkan nomor WhatsApp aktif untuk konfirmasi pesanan & pembuatan invoice. Estimasi pengiriman 2-4 minggu setelah pembayaran.

Dokumen Keamanan & Mutu

↓ Unduh SDS / MSDS (PDF resmi TCI)

CoA (Certificate of Analysis)

Spesifik per batch produksi — diterbitkan dan dikirim bersama barang sesuai nomor lot yang Anda terima.

Contoh CoA segera tersedia.

💬 Minta CoA via WhatsApp

View full details

Trans-N-(tert-Butoxycarbonyl)-4-hydroxy-L-proline is a chemical compound widely used in chemical and biochemical experiments, particularly in peptide synthesis. This compound plays a crucial role in laboratories by serving as a protected amino acid derivative, enabling the controlled synthesis of complex peptide structures. Its unique structure allows for the selective protection of hydroxyl groups, making it essential in multi-step synthetic processes. In research settings, it supports the development of bioactive molecules with specific functional properties, enhancing the precision and efficiency of peptide-based experiments.

The compound’s chemical properties make it a preferred choice in synthetic chemistry. The tert-butyloxycarbonyl (Boc) group provides stability against unwanted side reactions, ensuring the integrity of the molecule during synthesis. This stability allows for easier manipulation and handling in laboratory conditions, reducing the risk of degradation. Additionally, its reactivity in deprotection and bond formation reactions makes it versatile for various synthetic strategies. These characteristics make it a reliable and efficient reagent for advanced chemical and biochemical applications.

In Indonesian laboratories, this compound is commonly used by chemists and biochemists for peptide synthesis and molecular structure studies. It is particularly relevant in research areas such as pharmacology and biotechnology, supporting both academic and industrial research efforts. Its application is essential for the development of new therapeutic agents and biochemical tools, contributing to the advancement of scientific knowledge in the region.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 12

Related TCI products

Peptide Synthesis: This compound is ideal for constructing bioactive peptides due to its protected hydroxyl group, enabling precise and controlled synthesis in laboratory settings.
Molecular Structure Studies: Its complex structure allows researchers to investigate molecular interactions and functional properties in biochemical experiments.
Bioactive Molecule Development: The compound supports the creation of molecules with specific biological activities, which is crucial for pharmaceutical and biotechnological research.
Chemical Reactivity Testing: Its reactivity in bond formation and deprotection reactions makes it suitable for studying chemical mechanisms and reaction pathways.
Educational Research: It is widely used in academic institutions for teaching and research in chemical biology and peptide chemistry.

Brand	TCI
CAS number	13726-69-7
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 direct 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 moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Avoid exposure to strong acids or bases to prevent degradation. In laboratory settings, it should be stored in a well-ventilated area to ensure safety. Proper labeling and storage conditions are essential to maintain its effectiveness and ensure safe handling during experiments.

—