Fmoc-L-phenylalanine
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-L-Phenylalanine
Structure
CAS No. 35661-40-6 Boiling Point (℃) 620.1±50.0 °C at 760 mmHg
Molecular Weight 387.428 Melting Point (℃) 180-187 °C(lit.)
Density 1.3±0.1 g/cm3 Vapor Specific Gravity N/A
Molecular Formula C24H21NO4 Flash Point (℃) 328.8±30.1 °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 Fmoc-Phe-OH is a phenylalanine derivative[1].
Target Km: 100-400 μM (amino acid transporter b0,+)[1]
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References [1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-816.
Synonyms
Fmoc-L-Phc-OH
N-FMOC-PHE-OH
EINECS 252-661-1
L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-Fmoc-(S)-phenylalanine
FMOC-L-PHE-OH
FMOC-L-PHE
N-Fmoc-L-Phe-OH
MFCD00037128
9-fluorenylmethyloxycarbonyl-Phe-OH
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanoic acid
N-FMOC-L-PHE
N-Fmoc-L-phenylalanine
FMOC-PHENYLALANINE
Product Description
Fmoc-L-Phenylalanine is a cutting-edge compound that revolutionizes the protection of amino acids in various chemical synthesis processes. With its exceptional properties and wide-ranging applications in the field of chemical engineering, Fmoc-L-Phenylalanine has emerged as a key player in the global market. This product introduction aims to highlight the key features, advantages, and potential applications of Fmoc-L-Phenylalanine, showcasing its crucial role in safeguarding amino acids and facilitating efficient synthesis in the dynamic chemical industry.

Superior Amino Acid Protection: Fmoc-L-Phenylalanine offers superior protection for amino acids, ensuring their stability and preventing undesired reactions during chemical synthesis. Equipped with an advanced protective group, Fmoc-L-Phenylalanine 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-L-Phenylalanine finds versatile applications in a wide array 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-L-Phenylalanine is also widely used in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals, enabling the efficient production of diverse compounds in the pharmaceutical and chemical industries.

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

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

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

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