Taiy Chemical
N-(9-Fluorenylmethyloxycarbonyl) oxysuccinimide
Product Name N-(9-Fluorenylmethoxycarbonyloxy)succinimide
Synonyms:89706 1-(9H-Fluorenylmethoxycarbonyloxy)-2,5-pyrrolidinedione; FMOC-ONSu; N-(9-fluorenylmethoxycarbonyloxy)-succinimide; N-(9-Fluorenylmethyloxycarbonyl) oxysuccinimide; N-(9H-Fluoren-2-ylmethoxycarbonyloxy)succinimide; FMOC-OSU; N-(9-Fluorenylmethoxy Carbonyloxy) succinimide; 9-Fluorenylmethyl succinimidyl carbonate; 1-{[(9H-fluoren-9-ylmethoxy)carbonyl]oxy}pyrrolidine-2,5-dione; N-(9-Fluorenylmethoxy-carbonyloxy)succinimide; N-(9-Fluorenylmethoxy Carbonyloxy)Succinimide; N-(9-FluorenylmethoxyCarbonyloxy) Succinimide
CAS RN. 82911-69-1
EINECS 433-520-5
Molecular Weight 337.3261
Molecular Formula C19H15NO5
Density 1.42g/cm3
Melting Point(℃) 150-153℃
Boiling Point(℃) 494.3°C at 760 mmHg
Flash Point(℃) 252.7°C
refractive_index 1.661
Hazard Symbols Xi Details
Xi
Risk Codes  R36/37/38;    Details
 R36/37/38;     Details
Safety Description  S24/25;Details
 S24/25; Details
FAQ
What is N-(9-Fluorenylmethyloxycarbonyl)oxysuccinimide (Fmoc-OSu)?

N-(9-Fluorenylmethyloxycarbonyl)oxysuccinimide, commonly known as Fmoc-OSu, is a reagent used in peptide synthesis. It is utilized for the protection and activation of amino groups in order to facilitate the coupling of amino acids during peptide bond formation.

How is Fmoc-OSu used in peptide synthesis?

Fmoc-OSu is typically utilized in solid-phase peptide synthesis, where peptides are assembled on a solid support. In this process, the Fmoc group is often employed to protect the N-terminal amino group of the growing peptide chain. Fmoc-OSu is then used to activate the carboxyl group of the incoming amino acid, allowing it to react with the N-terminal amine and form a peptide bond.

What are the advantages of using Fmoc-OSu in peptide synthesis?

Fmoc-OSu offers several advantages in peptide synthesis. It provides efficient protection of the N-terminal amine, allowing for selective activation of the carboxyl group of amino acids. This reagent also promotes high coupling yields and facilitates the synthesis of complex peptides. Additionally, Fmoc-OSu is relatively stable and easy to handle, making it a popular choice for peptide chemists.

How should Fmoc-OSu be stored and handled?

Fmoc-OSu should be stored in a cool, dry place away from light and moisture. It is important to handle this reagent with care, as it can be sensitive to air and moisture. Proper precautions should be taken to avoid exposure to skin, eyes, and clothing. Additionally, Fmoc-OSu should be used in a well-ventilated area, and personal protective equipment should be worn when handling this compound.

Are there any safety considerations when working with Fmoc-OSu?

When working with Fmoc-OSu, it is important to follow proper safety protocols to minimize the risk of exposure. This reagent should be handled in a fume hood to avoid inhalation of vapors. Gloves, safety glasses, and a lab coat should be worn at all times when working with Fmoc-OSu. In the event of skin or eye contact, immediate medical attention should be sought, and contaminated areas should be thoroughly rinsed with water.
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