Fmoc-L-Hydroxyproline
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-L-hydroxyproline
Structure
CAS No. 88050-17-3 Boiling Point (℃) 595.5±50.0 °C at 760 mmHg
Molecular Weight 353.369 Melting Point (℃) 189-193ºC
Density 1.4±0.1 g/cm3 Vapor Specific Gravity N/A
Molecular Formula C20H19NO5 Flash Point (℃) 314.0±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 DL-Lysine (Lysine) is an α-amino acid that is used in the biosynthesis of proteins.
Target Km: 100-400 μM (amino acid transporter b0,+)[1]
In Vitro DL-Lysine (Lys) is a high affinity, basic amino acid substrate for amino acid transporter b0,+ with Km value ranging from 100-400 μM[1].
References [1]. Nguyen TV, et al. PEPT1 enhances the uptake of gabapentin via trans-stimulation of b0,+ exchange. Pharm Res. 2007 Feb;24(2):353-60.
Synonyms
1,2-Pyrrolidinedicarboxylic acid, 4-hydroxy-, 1-(9H-fluoren-9-ylmethyl) ester, (2S,4R)-
(2S,4R)-1-(9H-fluoren-9-ylmethoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid
(4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-hydroxy-L-proline
MFCD00151929
Fmoc-Hyp-OH
Fmoc-L-4-hydroxyproline
Fmoc-L-hydroxyproline
Product Description
Fmoc-L-Hydroxyproline is an innovative compound that serves as an essential tool in protecting amino acids during various chemical synthesis processes. With its unique properties and versatile applications in the field of chemical engineering, Fmoc-L-Hydroxyproline has gained significant recognition in the global market. This product introduction aims to highlight the key features, benefits, and potential applications of Fmoc-L-Hydroxyproline, emphasizing its crucial role in safeguarding amino acids and enabling efficient synthesis in the ever-evolving chemical industry.

Enhanced Amino Acid Protection: Fmoc-L-Hydroxyproline offers enhanced protection for amino acids, ensuring their stability and preventing unwanted reactions during chemical synthesis. With its advanced protective group, Fmoc-L-Hydroxyproline effectively shields the amino acid moiety, preserving the reactivity of functional groups and minimizing side reactions. This precise protection facilitates efficient and high-yielding synthesis, resulting in the production of high-quality amino acid derivatives.

Versatile Applications: Fmoc-L-Hydroxyproline finds extensive use in a wide range of chemical synthesis applications. Its exceptional protection capabilities make it an indispensable tool in peptide synthesis, where it plays a critical role in maintaining the integrity and reactivity of amino acids during peptide bond formation. Fmoc-L-Hydroxyproline is also widely employed in the synthesis of pharmaceutical intermediates, natural products, and bioactive compounds, enabling the efficient production of diverse molecules in the pharmaceutical and chemical industries.

Improved Solubility and Stability: Fmoc-L-Hydroxyproline exhibits improved solubility and stability, making it suitable for a variety of synthetic methodologies. Its compatibility with different solvents, reagents, and reaction conditions allows for seamless integration into various chemical processes. The enhanced solubility and stability of Fmoc-L-Hydroxyproline contribute to improved synthetic efficiency and consistent product quality.

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

Conclusion: Fmoc-L-Hydroxyproline represents a significant advancement in amino acid protection for chemical synthesis. Its enhanced protection capabilities, versatile applications, and improved solubility and stability make it an invaluable component in modern chemical engineering. By choosing Fmoc-L-Hydroxyproline, researchers and manufacturers can confidently protect amino acids, enhance synthetic efficiency, and accelerate the development of pharmaceuticals, natural products, and bioactive compounds. Fmoc-L-Hydroxyproline is a catalyst for progress in the global chemical industry, enabling efficient and reliable synthesis processes while maintaining superior product quality.

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.