O-Benzyl-L-serine TCI B0861

Chemical Identity

CAS No.: 4726-96-9
PubChem: CID 78457·SID 87563840
Formula: C10H13NO3
Molecular weight: 195.21 g/mol
Purity: >99.0%(T)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-2-amino-3-phenylmethoxypropanoic acid
SMILES: C1=CC=C(C=C1)COC[C@@H](C(=O)O)N
InChIKey: IDGQXGPQOGUGIX-VIFPVBQESA-N

Rp 795.900,00

~~Rp 572.250,00~~ Rp 795.900,00

Sale Sold out

Shipping calculated at checkout.

Berat 1g 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

O-Benzyl-L-serine is a chemical compound widely used in laboratory settings, particularly within the fields of chemistry and biochemistry. It plays a crucial role in peptide synthesis and organic molecule modification, serving as a key building block for more complex chemical structures. This compound is commonly utilized in research focused on drug development, biological compound synthesis, and the study of protein structure and function. Its importance lies in its ability to participate in various chemical reactions, making it an essential tool for researchers working on molecular-level transformations.

One of the main reasons O-Benzyl-L-serine is preferred is its stable chemical structure and reactivity. The presence of a benzoate group on the oxygen atom allows it to engage in nucleophilic substitution reactions and peptide bond formation. These properties make it highly suitable for controlled chemical modifications under specific laboratory conditions. Its reactivity also enables selective functionalization of molecular chains, which is vital for creating targeted chemical compounds in research and development.

In Indonesian laboratories, O-Benzyl-L-serine is frequently used in pharmacology, biochemical research, and organic chemistry studies. Its role in synthesizing bioactive compounds and modifying molecular structures makes it a valuable resource for scientists working on drug discovery and molecular biology projects. Its versatility and reliability in chemical reactions ensure its continued use across various scientific disciplines in the region.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 30
Reagents for Biological Research 2025-03-11 · p. 58

Related TCI products

Peptide Synthesis: O-Benzyl-L-serine is ideal for constructing peptide chains due to its ability to participate in peptide bond formation.
Organic Molecule Modification: The compound's reactivity allows for selective functionalization of molecular chains, making it suitable for organic synthesis.
Drug Development Research: It is frequently used in the synthesis of bioactive compounds, supporting pharmaceutical research efforts.
Protein Structure Studies: Its role in molecular modeling and structural analysis aids in understanding protein behavior and function.
Biochemical Compound Synthesis: O-Benzyl-L-serine contributes to the creation of complex biological molecules, supporting biochemical research applications.

Brand	TCI
CAS number	4726-96-9
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in standard laboratory quantities
Physical form	Solid or crystalline, depending on formulation
Storage	Store in a cool, dry place away from direct light

O-Benzyl-L-serine should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent moisture absorption and contamination. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn when working with it. Avoid exposure to heat or direct sunlight to preserve its integrity. Proper storage ensures the compound remains effective for its intended applications in laboratory research.

—