Fmoc-D-aspartic acid
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-Asp-OH
Structure
CAS No. 136083-57-3 Boiling Point (℃) 587.2±45.0 °C at 760 mmHg
Molecular Weight 355.341 Melting Point (℃) N/A
Density 1.4±0.1 g/cm3 Vapor Specific Gravity N/A
Molecular Formula C19H17NO6 Flash Point (℃) 308.9±28.7 °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-Asp-OH is an aspartic acid 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
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-aspartic acid
L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartic acid
N-Fmoc-L-aspartic acid
D-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-(9-fluorenylmethoxycarbonyl)-L-aspartic acid
Fmoc-D-aspartic acid
Fmoc-D-Asp-OH
(2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}succinic acid
N-Fmoc-D-aspartic Acid
Fmoc-aspartic acid
MFCD01318740
Product Description
Fmoc-D-Aspartic Acid is an innovative product that combines amino acid protection with the field of chemical synthesis. With its exceptional properties and versatile applications, Fmoc-D-Aspartic Acid has gained significant recognition and widespread use in the international market. This product introduction aims to showcase the key features, advantages, and potential applications of Fmoc-D-Aspartic Acid, highlighting its crucial role in protecting amino acids and enabling efficient synthesis in the dynamic world of chemical engineering.

Superior Amino Acid Protection: Fmoc-D-Aspartic Acid offers superior protection for amino acids, ensuring their stability and preventing unintended 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 enables the production of high-quality amino acid derivatives.

Versatile Applications: Fmoc-D-Aspartic Acid finds extensive applications in various chemical synthesis processes. Its exceptional protective properties make it an indispensable component in peptide synthesis, where it effectively safeguards the amino acid backbone during peptide bond formation. Fmoc-D-Aspartic Acid is widely utilized in the production of pharmaceuticals, agrochemicals, and specialty chemicals, facilitating efficient synthesis and the creation of diverse compounds in the global chemical industry.

Enhanced Solubility and Compatibility: Fmoc-D-Aspartic Acid exhibits enhanced solubility and compatibility, allowing for seamless integration into a wide range of solvents, reagents, and reaction conditions. Its improved solubility and compatibility properties enable effortless incorporation into various chemical processes, enhancing efficiency and reliability in synthesis. By utilizing Fmoc-D-Aspartic Acid, researchers can improve reaction outcomes, minimize undesired side reactions, and produce high-quality amino acid derivatives.

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

Conclusion: Fmoc-D-Aspartic Acid represents a remarkable advancement in amino acid protection for chemical synthesis. Its superior protective capabilities, versatile applications, and enhanced solubility and compatibility make it an invaluable asset in modern chemical engineering. By harnessing Fmoc-D-Aspartic Acid, researchers and manufacturers can confidently protect amino acids, enhance synthesis efficiency, and expedite the development of pharmaceuticals, agrochemicals, and specialty chemicals. Fmoc-D-Aspartic Acid is driving progress in the global chemical industry, enabling efficient and reliable synthesis processes while ensuring superior product quality. Choose Fmoc-D-Aspartic Acid for unmatched amino acid protection and unlock new possibilities in chemical synthesis.

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