Fmoc-L-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
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-Pro-OH
Structure
CAS No. 71989-31-6 Boiling Point (℃) 548.6±43.0 °C at 760 mmHg
Molecular Weight 337.369 Melting Point (℃) 112-115ºC
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-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
MFCD00065670
Fmoc-L-Pro-OH
EINECS 276-259-0
Fmoc-L-proline
1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-proline
Fmoc-L-proline-OH
1,2-Pyrrolidinedicarboxylic acid, 1-(9H-fluoren-9-ylmethyl) ester, (2S)-
Fmoc-Pro-OH
Product Description
Fmoc-L-Proline is a cutting-edge product that combines amino acid protection with the field of chemical synthesis. With its unique features and wide range of applications, Fmoc-L-Proline has gained significant traction in the international market. This product introduction aims to highlight the key attributes, benefits, and potential applications of Fmoc-L-Proline, underscoring its pivotal role in safeguarding amino acids and promoting efficient synthesis in the dynamic chemical industry.

Optimal Amino Acid Protection: Fmoc-L-Proline offers optimal protection for amino acids, ensuring their stability and preventing unwanted 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 enables the synthesis of complex molecules and facilitates the production of high-quality amino acid derivatives.

Versatile Applications: Fmoc-L-Proline finds versatile applications in various chemical synthesis processes. Its exceptional protection capabilities make it a valuable component in peptide synthesis, safeguarding the amino acid backbone during peptide bond formation. Fmoc-L-Proline is also widely used in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals, enabling efficient production of diverse compounds in the global chemical industry.

Enhanced Solubility and Stability: Fmoc-L-Proline exhibits enhanced solubility and stability, making it compatible with a wide range of solvents, reagents, and reaction conditions. Its improved solubility and stability properties allow for seamless integration into different chemical processes, facilitating efficient and reliable synthesis. By utilizing Fmoc-L-Proline, researchers can enhance reaction efficiency, minimize undesired side reactions, and produce high-quality amino acid derivatives.

Global Market Impact: Fmoc-L-Proline 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 growing demand for Fmoc-L-Proline reflects its effectiveness in optimizing synthetic processes and delivering high-quality amino acid derivatives.

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

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.