Fmoc-L-valine
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-Val-OH
Structure
CAS No. 68858-20-8 Boiling Point (℃) 551.8±33.0 °C at 760 mmHg
Molecular Weight 339.385 Melting Point (℃) 143-147ºC
Density 1.2±0.1 g/cm3 Vapor Specific Gravity N/A
Molecular Formula C20H21NO4 Flash Point (℃) 287.5±25.4 °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-L-Val-OH is a valine 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):1793-1144.
Synonyms
L-Valine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-valine
N-Fmoc-Val-OH (N-Fmoc-L-valine)
FMco-Val-OH
N-FMOC-L-VAL
FMOC-L-VAL-OH
FMOC-VAL
FMOC-VAL-OH
MFCD00037124
N-((9H-Fluoren-9-ylmethoxy)carbonyl)-L-valine
FMOC-VALINE
FMOC-L-VALINE
N-Fmoc-L-valine
FMOC-L-VAL
N-FMOC-VAL-OH
Fmoc-Valine-OH
EINECS 272-515-0
Product Description
Fmoc-L-Valine is a cutting-edge chemical compound that offers superior protection for amino acids during various chemical synthesis processes. With its exceptional properties and wide-ranging applications in the field of chemical engineering, Fmoc-L-Valine has gained significant recognition in the global market. This product introduction aims to highlight the key features, benefits, and potential applications of Fmoc-L-Valine, emphasizing its crucial role in safeguarding amino acids and facilitating efficient synthesis in the ever-evolving chemical industry.

Advanced Amino Acid Protection: Fmoc-L-Valine provides advanced protection for amino acids, ensuring their stability and preventing undesired reactions during chemical synthesis. With its innovative protective group, Fmoc-L-Valine effectively shields the amino acid moiety, preserving the reactivity of functional groups and minimizing side reactions. This precise protection allows for efficient and high-yielding synthesis, leading to the production of high-quality amino acid derivatives.

Versatile Applications: Fmoc-L-Valine finds extensive use in a wide range of chemical synthesis applications. Its superior protection capabilities make it an indispensable tool in peptide synthesis, where it plays a vital role in maintaining the integrity and reactivity of amino acids during the formation of peptide bonds. Additionally, Fmoc-L-Valine is valuable in the synthesis of pharmaceutical intermediates, agrochemicals, and specialty chemicals, enabling the efficient production of diverse compounds in the pharmaceutical and chemical industries.

Enhanced Chemical Compatibility: Fmoc-L-Valine demonstrates excellent compatibility with various solvents, reagents, and reaction conditions commonly employed in chemical synthesis. This versatility allows for seamless integration into different synthetic methodologies, making Fmoc-L-Valine suitable for a wide range of applications. Its compatibility and reliability contribute to improved synthetic efficiency and consistent product quality.

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

Conclusion: Fmoc-L-Valine represents a significant advancement in amino acid protection for chemical synthesis. Its advanced properties, versatile applications, and enhanced chemical compatibility make it an essential component in modern chemical engineering. By choosing Fmoc-L-Valine, researchers and manufacturers can confidently protect amino acids, enhance synthetic efficiency, and accelerate the development of pharmaceuticals, agrochemicals, and specialty chemicals. Fmoc-L-Valine is a key driver of progress in the global chemical industry, enabling efficient and reliable synthesis processes while maintaining superior product quality.

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