Fmoc-L-serine
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-Ser-OH
Structure
CAS No. 73724-45-5 Boiling Point (℃) 599.3±50.0 °C at 760 mmHg
Molecular Weight 327.331 Melting Point (℃) 104-106°C
Density 1.4±0.1 g/cm3 Vapor Specific Gravity N/A
Molecular Formula C18H17NO5 Flash Point (℃) 316.2±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-Ser-OH is a serine 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
Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-Fmoc-L-serine-OH
Fmoc-Ser-OH
MFCD00051928
N-FMOC-L-SERINE
FMOC-SERINE
FMOC-SER
L-Serine-d3-N-FMOC
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]serine
N-Fmoc-L-serine allyl ester
Fmoc-L-Ser-OH
Product Description
Fmoc-L-Serine is a cutting-edge product that combines amino acid protection with the field of chemical synthesis. With its exceptional properties and wide range of applications, Fmoc-L-Serine has gained significant recognition in the international market. This product introduction aims to highlight the key features, advantages, and potential applications of Fmoc-L-Serine, showcasing its vital role in safeguarding amino acids and promoting efficient synthesis in the dynamic chemical industry.

Superior Amino Acid Protection: Fmoc-L-Serine offers superior protection for amino acids, ensuring their stability and preventing undesired reactions during chemical synthesis. Its advanced protective group shields the amino acid, preserving the reactivity of functional groups and minimizing side reactions. This precise protection allows for the synthesis of complex molecules and facilitates the production of high-quality amino acid derivatives.

Versatile Applications: Fmoc-L-Serine finds extensive applications in chemical synthesis processes. Its exceptional protection capabilities make it indispensable in peptide synthesis, safeguarding the amino acid backbone during peptide bond formation. Fmoc-L-Serine is also widely used in the synthesis of pharmaceuticals, cosmetics, and agrochemicals, contributing to the efficient production of various compounds in the global chemical industry.

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

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

Conclusion: Fmoc-L-Serine represents a significant advancement in amino acid protection for chemical synthesis. Its superior protection capabilities, versatile applications, and enhanced solubility and stability make it an invaluable tool in modern chemical engineering. By utilizing Fmoc-L-Serine, researchers and manufacturers can confidently protect amino acids, enhance synthetic efficiency, and accelerate the development of pharmaceuticals, cosmetics, and agrochemicals. Fmoc-L-Serine is driving progress in the global chemical industry, enabling efficient and reliable synthesis processes while ensuring superior product quality. Choose Fmoc-L-Serine for unparalleled amino acid protection and unlock new possibilities in chemical synthesis.

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