Fmoc-D-tryptophan
Nanjing Finechem Holdings Co., LTD
Specifications
N/A
Packing & Storage
Packing
Storage Powder -20°C 3 years 4°C 2 years;In solvent -80°C 6 months, -20°C 1 month
Shipping Room temperature in continental US; may vary elsewhere
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General Information
Chemical & Physical Properties
Safety Information
Synthetic Route
Biological Activity
Common Names Fmoc-D-Trp-OH
Structure
CAS No. 86123-11-7 Boiling Point (℃) 711.9±60.0 °C at 760 mmHg
Molecular Weight 426.464 Melting Point (℃) 182-185ºC
Density 1.4±0.1 g/cm3 Vapor Specific Gravity N/A
Molecular Formula C26H22N2O4 Flash Point (℃) 384.3±32.9 °C
Solubility N/A Autoignition Temperature (℃) N/A
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes T+:Very toxic
Safety Phrases S1-S28-S45
RIDADR NONH for all modes of transport
WGK Germany  3
SYMPTOMS PREVENTION FIRST AID
Inhalation Cough. Sore throat. Use local exhaust or breathing protection. Fresh air, rest.
Skin Redness. Burning sensation. Itching. Protective gloves. Remove contaminated clothes. Rinse and then wash skin with water and soap.
Eyes Redness. Pain. Wear safety goggles. First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Ingestion Abdominal pain. Nausea. Vomiting. Do not eat, drink, or smoke during work. Wash hands before eating. Rinse mouth. Induce vomiting (ONLY IN CONSCIOUS PERSONS!). Refer for medical attention.
Description DL-Lysine (Lysine) is an α-amino acid that is used in the biosynthesis of proteins.
Target Km: 100-400 μM (amino acid transporter b0,+)[1]
In Vitro DL-Lysine (Lys) is a high affinity, basic amino acid substrate for amino acid transporter b0,+ with Km value ranging from 100-400 μM[1].
References [1]. Nguyen TV, et al. PEPT1 enhances the uptake of gabapentin via trans-stimulation of b0,+ exchange. Pharm Res. 2007 Feb;24(2):353-60.
Synonyms
FMOC-D-TRP
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-tryptophan
Na-(9-Fluorenylmethoxycarbonyl)-D-tryptophan
D-Tryptophan, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
Fmoc-D-Trp-OH
N-Fmoc-D-tryptophan
Nalpha-(9-Fluorenylmethoxycarbonyl)-D-tryptophan
MFCD00062954
Fmoc-D-tryptophan
N-Fmoc-D-Trp-OH
Product Description
Fmoc-D-Tryptophan is an innovative compound that plays a vital role in protecting amino acids during various chemical synthesis processes. With its exceptional properties and versatile applications in the field of chemical engineering, Fmoc-D-Tryptophan has gained significant recognition in the global market. This product introduction aims to showcase the key features, advantages, and potential applications of Fmoc-D-Tryptophan, emphasizing its crucial role in safeguarding amino acids and facilitating efficient synthesis in the ever-evolving chemical industry.

Optimal Amino Acid Protection: Fmoc-D-Tryptophan offers optimal protection for amino acids, ensuring their stability and preventing unwanted reactions during chemical synthesis. With its advanced protective group, Fmoc-D-Tryptophan effectively shields the amino acid moiety, preserving the reactivity of functional groups and minimizing side reactions. This precise protection enables the efficient synthesis of complex molecules and facilitates the production of high-quality amino acid derivatives.

Versatile Applications: Fmoc-D-Tryptophan finds extensive applications in a wide range of chemical synthesis processes. Its exceptional protection capabilities make it an indispensable tool in peptide synthesis, where it plays a critical role in preserving the integrity and reactivity of amino acids during peptide bond formation. Fmoc-D-Tryptophan is also widely used in the synthesis of pharmaceuticals, natural products, and bioactive compounds, enabling the efficient production of diverse molecules in the pharmaceutical and chemical industries.

Improved Solubility and Stability: Fmoc-D-Tryptophan exhibits improved solubility and stability, making it highly compatible with various solvents, reagents, and reaction conditions. Its enhanced solubility and stability properties facilitate seamless integration into different chemical processes, ensuring efficient and reliable synthesis. The use of Fmoc-D-Tryptophan enhances reaction efficiency, minimizes unwanted side reactions, and contributes to the production of high-quality amino acid derivatives.

Global Market Impact: Fmoc-D-Tryptophan has made a significant impact on the global chemical market, establishing itself as a leading solution for amino acid protection. Its exceptional performance, reliable quality, and cost-effectiveness have gained widespread recognition and trust from researchers, scientists, and industry professionals. The growing demand for Fmoc-D-Tryptophan reflects its effectiveness in optimizing synthetic processes and delivering high-quality amino acid derivatives.

Conclusion: Fmoc-D-Tryptophan represents a groundbreaking advancement in amino acid protection for chemical synthesis. Its optimal protection capabilities, versatile applications, and improved solubility and stability make it an invaluable asset in modern chemical engineering. By choosing Fmoc-D-Tryptophan, researchers and manufacturers can confidently protect amino acids, enhance synthetic efficiency, and accelerate the development of pharmaceuticals, natural products, and bioactive compounds. Fmoc-D-Tryptophan is driving progress in the global chemical industry, enabling efficient and reliable synthesis processes while ensuring superior product quality.

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