Skip to product information
1 of 1

TCI

CAS 73-22-3

L-Tryptophan TCI T0541

L-Tryptophan TCI T0541

Chemical Identity

Other names
H-Trp-OH
CAS No.
73-22-3
PubChem
CID 6305·SID 87576460
Formula
C11H12N2O2
Molecular weight
204.22 g/mol
Purity
>98.5%(HPLC)(T)
Reference databases
ChEBI·ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(2S)-2-amino-3-(1H-indol-3-yl)propanoic acid
SMILES
C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)O)N
InChIKey
QIVBCDIJIAJPQS-VIFPVBQESA-N
Regular price Rp 955.500,00
Regular price Sale price Rp 955.500,00
Sale Sold out
Shipping calculated at checkout.
Berat
Quantity
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

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

L-Tryptophan is a chemical compound that plays a crucial role in various chemical reactions and organic synthesis processes. As an essential amino acid, it is widely used in chemical research, particularly in the fields of catalysis and inorganic chemistry. This compound is valued for its ability to accelerate specific chemical reactions and serve as a building block for the synthesis of complex compounds. Its applications span across multiple scientific disciplines, including pharmaceuticals and biotechnology. In the laboratory, L-Tryptophan is essential for the development of new drugs and other chemical substances.

L-Tryptophan is favored due to its chemical stability under certain conditions and its complex molecular structure. This structure allows it to interact effectively with various reactants and catalysts, making it ideal for high reactivity and molecular specificity in research. Its sensitivity to moisture and air exposure requires careful handling and storage to maintain its quality and effectiveness. These properties make it a reliable and versatile material for advanced chemical experimentation.

In Indonesian laboratories, L-Tryptophan is commonly used in scientific research across multiple fields such as pharmacy, biochemistry, and organic chemistry. It supports the development of new compounds and the study of biochemical processes. Its presence in research settings highlights its importance in both academic and industrial applications, contributing to the advancement of scientific knowledge and innovation.

  • Organic synthesis where L-Tryptophan acts as a building block for complex molecule creation due to its amino acid structure.
  • Pharmaceutical research for the development of new drugs and therapeutic agents requiring specific molecular interactions.
  • Biochemical studies involving protein synthesis and enzymatic reactions due to its role as an essential amino acid.
  • Catalytic processes where its molecular structure enhances reaction efficiency and specificity in chemical transformations.
  • Analytical chemistry applications for the identification and quantification of amino acids in various biological samples.

Brand TCI
CAS number 73-22-3
Molecular formula —
Purity —
Category Chemistry > Catalysis and Inorganic Chemistry > Organocatalysts [Catalysis]
Pack sizes —
Physical form —
Storage Must be stored in a dry, airtight container to prevent moisture and air exposure

L-Tryptophan should be stored in a cool, dry place away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air, which can degrade its quality. In laboratory settings, it should be handled with care to avoid contamination and ensure its effectiveness in experiments. Proper labeling and storage conditions are essential to maintain its stability and usability. Regular monitoring of storage conditions helps in preserving the compound’s properties for research applications. All handling should follow standard laboratory safety protocols to ensure safe and effective use.

References cited in the TCI brochure

  1. Jamie Ghuman. Structural Basis of the Drug-binding Specificity of Human Serum Albumin Journal of Molecular Biology, 2005. doi:10.1016/j.jmb.2005.07.075
  2. Masaki OTAGIRI. Study on Binding of Drug to Serum Protein YAKUGAKU ZASSHI, 2009. doi:10.1248/yakushi.129.413