Fmoc-L-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
Free Quote
For samples, pricing, or more information, please call us at 0086-25-52397805 or mail to info@alchemist-chem.com or fill out the following form.
We will respond to you as soon as possible.

Tel: 0086-25-52397805

Email: info@alchemist-chem.com

General Information
Chemical & Physical Properties
Safety Information
Synthetic Route
Biological Activity
Common Names Fmoc-Trp-OH
Structure
CAS No. 35737-15-6 Boiling Point (℃) 711.9±60.0 °C at 760 mmHg
Molecular Weight 426.464 Melting Point (℃) 182-185 °C(lit.)
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-OH
FMOC-TRP
MFCD00037126
FMOC-TRYPTOPHAN
L-TRYPTOPHAN-N-FMOC
N-Fmoc-D-Trp-OH
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-tryptophan
Tryptophan, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
Nalpha-FMOC-L-Trypto
Fmoc-Trp-OH
FMOC-L-TRP-OH
N-Fmoc-L-Trp-OH
N-((9H-Fluoren-9-ylmethoxy)carbonyl)-L-tryptophan
EINECS 252-706-5
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]tryptophan
Nα-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-tryptophan
FMOC-L-TRP
N-Fmoc-D-tryptophan
Fmoc-L-tryptophan
Product Description
Fmoc-L-Tryptophan is a cutting-edge chemical compound specifically designed to provide superior protection for amino acids during various chemical processes. With its exceptional properties and versatile applications in the field of chemical synthesis, Fmoc-L-Tryptophan has gained significant recognition in the global market. This product introduction aims to highlight the key features, benefits, and potential applications of Fmoc-L-Tryptophan, emphasizing its crucial role in safeguarding amino acids and enabling efficient synthesis in the ever-evolving chemical industry.

Advancements in Chemical Engineering: Fmoc-L-Tryptophan represents a significant advancement in chemical engineering, offering enhanced protection and stability for amino acids during various synthetic procedures. Developed through cutting-edge research and innovative manufacturing techniques, this compound ensures the integrity of amino acids and prevents unwanted reactions, allowing for efficient and high-yielding chemical transformations.

Superior Amino Acid Protection: Fmoc-L-Tryptophan provides superior protection for amino acids by forming a robust and reversible bond. This protective group effectively shields the amino acid moiety, preserving the reactivity of functional groups and preventing unwanted side reactions. The precise control over chemical transformations facilitated by Fmoc-L-Tryptophan leads to improved synthetic efficiency, resulting in the production of high-quality amino acid derivatives with excellent yield and purity.

Wide Range of Applications: Fmoc-L-Tryptophan finds extensive utility in various chemical synthesis applications due to its exceptional protective properties. It is particularly valuable in peptide synthesis, pharmaceutical manufacturing, and the preparation of complex organic molecules. Fmoc-L-Tryptophan demonstrates compatibility with a wide range of solvents and reagents, making it an ideal choice for both traditional and advanced synthetic methodologies.

Global Market Impact: Fmoc-L-Tryptophan has made a significant impact on the global chemical market, establishing itself as a leading solution for amino acid protection. Its consistent quality, reliability, and cost-effectiveness have garnered a strong reputation among researchers, scientists, and industry professionals. The product has witnessed a substantial increase in demand, attracting a growing customer base across different regions. Fmoc-L-Tryptophan has become an essential tool for chemical manufacturers aiming to optimize their synthetic processes and deliver high-quality amino acid derivatives.

Conclusion: Fmoc-L-Tryptophan revolutionizes amino acid protection in chemical synthesis, offering enhanced stability, compatibility, and reliability. Its broad applications and positive impact on the global market position it as a key component of modern chemical engineering. By choosing Fmoc-L-Tryptophan, researchers and manufacturers can confidently protect amino acids, enhance synthetic efficiency, and accelerate the development of pharmaceuticals, specialty chemicals, and other complex organic compounds.

Leave A Message
Leave A Message ×
If you are interested in our products and want to know more details,please leave a message here,we will reply you as soon as we can.