Fmoc-D-proline
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-Pro-OH
Structure
CAS No. 101555-62-8 Boiling Point (℃) 548.6±43.0 °C at 760 mmHg
Molecular Weight 337.369 Melting Point (℃) 110-116°C
Density 1.3±0.1 g/cm3 Vapor Specific Gravity N/A
Molecular Formula C20H19NO4 Flash Point (℃) 285.6±28.2 °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-D-Pro-OH is a proline 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
Fmoc-D-Pro-OH
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-proline
MFCD00065671
N-Fmoc-Pro-OH ( N-Fmoc-L-proline)
1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-proline
1,2-Pyrrolidinedicarboxylic acid, 1-(9H-fluoren-9-ylmethyl) ester, (2R)-
(2R)-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carboxylic acid
Fmoc-D-Proline
Product Description
Fmoc-D-Proline is a cutting-edge chemical compound that provides exceptional protection for amino acids during various chemical synthesis processes. With its superior properties and versatile applications in the field of chemical engineering, Fmoc-D-Proline has gained significant recognition in the global market. This product introduction aims to showcase the key features, benefits, and potential applications of Fmoc-D-Proline, emphasizing its crucial role in safeguarding amino acids and enabling efficient synthesis in the ever-evolving chemical industry.

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

Enhanced Chemical Compatibility: Fmoc-D-Proline demonstrates excellent compatibility with a wide range of solvents, reagents, and reaction conditions commonly used in chemical synthesis. This versatility allows for seamless integration into various synthetic methodologies, making Fmoc-D-Proline suitable for diverse applications, including peptide synthesis, pharmaceutical manufacturing, and the synthesis of complex organic molecules. Its compatibility and reliability contribute to improved synthetic efficiency and consistent product quality.

Global Market Impact: Fmoc-D-Proline 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-D-Proline is a testament to its effectiveness in optimizing synthetic processes and delivering high-quality amino acid derivatives.

Versatile Applications: Fmoc-D-Proline finds extensive use in a wide range of chemical synthesis applications. Its advanced protection capabilities make it an essential tool in peptide synthesis, where it ensures the integrity and reactivity of amino acids in the formation of peptide bonds. Additionally, Fmoc-D-Proline is valuable in the synthesis of pharmaceutical intermediates, specialty chemicals, and other complex organic molecules, enabling the efficient production of diverse compounds in the pharmaceutical and chemical industries.

Conclusion: Fmoc-D-Proline represents a significant advancement in amino acid protection for chemical synthesis. Its superior properties, enhanced compatibility, and versatile applications have positioned it as a crucial component in modern chemical engineering. By choosing Fmoc-D-Proline, researchers and manufacturers can confidently protect amino acids, enhance synthetic efficiency, and accelerate the development of pharmaceuticals, specialty chemicals, and other complex organic compounds. Fmoc-D-Proline is a key contributor to the advancement of the global chemical industry, enabling efficient and reliable synthesis processes while maintaining high product quality.

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