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TCI

CAS 153-94-6

D-Tryptophan TCI T0539

D-Tryptophan TCI T0539

Chemical Identity

Other names
H-D-Trp-OH
CAS No.
153-94-6
PubChem
CID 9060·SID 87576458
Formula
C11H12N2O2
Molecular weight
204.22 g/mol
Purity
>98.0%(HPLC)(T)
Reference databases
ChEBI·ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(2R)-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-SECBINFHSA-N
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D-Tryptophan is an organic compound widely used in chemical and biochemical experiments within laboratory settings. As one of the essential amino acids, it plays a crucial role in the synthesis of complex compounds, particularly in catalytic and organic reactions. Its unique chemical structure, featuring both an amino and a carboxyl group, allows for versatile participation in various chemical transformations. This compound is particularly valuable in research fields such as biochemistry, pharmacology, and synthetic chemistry due to its functional versatility and reactivity.

D-Tryptophan is preferred for its stability under controlled conditions and its ability to participate in a wide range of chemical reactions. Its chemical properties make it an ideal candidate for applications requiring precise molecular interactions. The compound is sensitive to moisture and air exposure, which necessitates careful handling and storage. Despite these sensitivities, its chemical reactivity and structural characteristics make it a reliable and essential material for many laboratory processes.

In Indonesian laboratories, D-Tryptophan is extensively used in chemical, biological, and pharmaceutical research. It is commonly found in experiments related to amino acid metabolism, drug synthesis, and biochemical pathways. Its availability in the local market ensures accessibility for researchers and academic institutions, supporting a wide range of scientific investigations. The compound's relevance across multiple scientific disciplines highlights its importance in both academic and industrial research settings.

TCI brochures (PDF)

  • Biochemical research benefits from D-Tryptophan as it is essential for studying amino acid metabolism and protein synthesis in biological systems.
  • Pharmaceutical development utilizes D-Tryptophan in the synthesis of various drugs and biologically active compounds due to its structural similarity to other amino acids.
  • Organic chemistry experiments rely on D-Tryptophan for its reactivity in catalytic and synthetic reactions, making it a key component in the creation of complex molecules.
  • Biotechnology applications incorporate D-Tryptophan in the production of enzymes and bioactive compounds, supporting advancements in molecular biology.
  • Nutritional and dietary research uses D-Tryptophan to analyze its role in human health and its effects on metabolic processes.

Brand TCI
CAS number 153-94-6
Molecular formula —
Purity —
Category Chemistry > Catalysis and Inorganic Chemistry > Organocatalysts [Catalysis]
Pack sizes Available in various quantities as per standard laboratory supply
Physical form White crystalline powder
Storage Must be stored in a dry, cool, and airtight container to prevent degradation

D-Tryptophan should be stored in a dry, cool environment to maintain its chemical integrity and prevent moisture-induced degradation. It is recommended to use airtight containers made of glass or high-density polyethylene to minimize exposure to air and humidity. Due to its sensitivity, the compound should be handled with care, ideally in a controlled laboratory setting with proper ventilation. Avoid direct contact with moisture and ensure that storage conditions are consistent to preserve its reactivity and effectiveness. Regular monitoring of storage conditions is advised to ensure the compound remains suitable for use in research applications.

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