Fmoc-2-Abz-OH | Fmoc-2-abz amino acid

Fmoc-2-Abz-OH | Fmoc-2-abz amino acid - Omizzur
* For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
Name

Fmoc-2-Abz-OH

TypeFmoc-2-abz amino acid
CAS

150256-42-1

Purity % (HPLC)> 98.0% (HPLC)
Pack size

CIF Price ( USD )

Inventory
25g$140.0
In stock
100gPlease inquire the lowest
In stock
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General Description

Fmoc is a commonly used amino acid protecting group that protects the amino groups of amino acids to prevent them from binding with other molecules. Fmoc groups have high chemical stability in peptide chain synthesis, so they can remain unchanged throughout the entire process of peptide chain synthesis. This makes Fmoc a highly effective amino acid protecting group.


Omizzur Fmoc-2-Abz-OH | 2-Abz amino acid

Fmoc-2-Abz-OH (CAS: 150256-42-1) is a derivative of Fmoc-2-Abz amino acid. It appears as a gray white powder and is commonly used in the synthesis of peptide products. Omizzur ltd is currently in stock supply and has fast global shipping.


Omizzur popular Fmoc-amino acid derivatives

Fmoc-Lys(Boc)-OHFmoc-Aib-OHFmoc-Cys(Acm)-OH
Fmoc-Arg(Pbf)-OHFmoc-Lys(Alloc)-OHFmoc-D-Allo-Ile-OH
Fmoc-Trp(Boc)-OHFmoc-Cys(CAM)-OHFmoc-Tyr(H2PO3)-OH
Fmoc-Asn(trt)-OHFmoc-Lys(Dde)-OHFmoc-tBu-Gly-OH
Fmoc-Cys(Trt)-OHFmoc-Pen(Acm)-OHFmoc-Orn(Boc)-OH
Fmoc-His(Trt)-OH(Fmoc-Cys-OH)2Fmoc-Glycinol
Fmoc-Tyr(tBu)-OHFmoc-Arg(Mts)-OHFmoc-Lys(Me3)-OH.HCl
Fmoc-Thr(tbu)-OHFmoc-Arg(Pbf)-OpfpFmoc-Glu-OtBu
Fmoc-Met-OHFmoc-Asn-OPfp
Fmoc-Val-OHFmoc-D-Arg(pbf)-OH

** Omizzur provides a wide range of fmoc amino acids, with over 800 different types currently available. Please contact our customer service for the latest product catalog. | web: www.omizzur.com



Amino acids and Derivatives

Amino acids and their derivatives are a class of compounds that contain both amino and carboxyl groups in their molecules. Appears in a free or bound state within an organism. Free amino acids are distributed in all animal cells and body fluids, while bound amino acids are mainly the basic components of proteins and peptides.


At present, Omizzur can artificially synthesize thousands of amino acid derivatives, including natural amino acids and various derivatives of non natural amino acids. Omizzur offers nearly 300 different types of modifications and protective groups to choose from.


Fast links:

>> Fmoc amino acids                                                                              >> Unnatural amino acids

>> Boc amino  acids                                                                                >> N-methyl amino acids

>> Cbz amino acids                                                                                 >> Activated amino acids

>> Amino acids derivatives                                                                     >> Reagents & Resins


Product Data Sheet

Fmoc-2-abz amino acid | Fmoc-2-Abz-OH Supply


NameFmoc-2-Abz-OH
TypeFmoc-2-abz amino acid
Synonym(s)2-(Fmoc-amino)benzoic acid, N-Fmoc-anthranilic acid
CAS150256-42-1
Size20g / 50g / 100g
Molecular FormulaC22H17NO4
Molecular Weight359.4
Applicationspeptide synthesis
AppearanceWhite to off white powder
Boiling point537.6±33.0 °C at 760 mmHg
Density1.4±0.1 g/cm3
Melting point216-218 °C(lit.)
StabilityStable at room temperature and pressure, avoid contact with strong oxidants.
InventoryIn stock


Shipping & Storage

Storage conditions: Sealed storage, stored in a cool and dry warehouse. The storage temperature is 2-8 º C.

Shipping: By Fedex door to door or by air / Worldwide Fast Shipping



Omizzur Daily Peptide Tip: How to choose a protective group for peptide liquid-phase synthesis?


Peptide liquid-phase synthesis is a method of peptide synthesis carried out in solution, mainly used to prepare peptides with specific biological activities. In this process, the selection of protecting groups is very important, as it can protect the amino acids in the polypeptide chain from non-specific reactions and ensure the correct synthesis of peptides.


4 Main Tips for Selecting Protective Group :

1. Selectivity: The protecting group should be able to be specifically removed under specific conditions (such as acidic or alkaline) without affecting other formed peptide bonds.


2. Stability: The protecting group should be stable throughout the entire synthesis process and will not be removed under inappropriate conditions (such as solvent or reaction conditions).


3. Compatibility: The protecting group should be compatible with other reagents and conditions used in the synthesis process. For example, if the protecting group reacts with certain reagents, then this protecting group is not suitable for this synthesis.


4. Removability: The protecting group should be easily removed after synthesis to obtain the final target peptide. Otherwise, it may cause damage to the structure of the polypeptide.


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