Product Details
| Product Name: FMOC-Glycine | CAS No.: 29022-11-5 |
| EC-No.: 249-373-3 | Min. Order: 1kg |
| Purity: 98%min | Supply Ability: 1000kg |
| Release date: 2026/01/22 | |
| Type: SZ01 |
FMOC-Glycine Cas 29022-11-5
Specification
Items | Specifications | Results |
Appearance | White to off-white powder | White powder |
Purity(HPLC) | ≥99% | 99.71% |
TLC | ≥98% | >98% |
Melting Point | 165-185 ℃ | 175.3-175.7 ℃ |
Clarity of solution | 0.3 gram in 2ml DMF clear solution | Complies |
Water Content(K.F.) | ≤1.0% | 0.19% |
Element analysis(C、H、N) | ≤5.0% | <5.0% |
Loss on drying | ≤1.0%(60 ℃,2h) | 0.10% |
Kaiser Test | <0.05% | <0.05% |
IR Spectrum | In accordance with the structure | Complies |
Mass Spectrum | In accordance with the structure | Complies |
NMR Spectrum | In accordance with the structure | Complies |
Conclusion | It meets the quality inspection standards. | |
Welcome to contact with us to get more information.
Fmoc-Gly-OH is a protected amino acid derivative used primarily in solid-phase peptide synthesis (SPPS). Its name breaks down as follows:
Gly: This is the standard three-letter abbreviation for the amino acid Glycine. It is the simplest amino acid, with a hydrogen atom as its side chain.
Fmoc: Stands for Fluorenylmethyloxycarbonyl. This is a protecting group that blocks the amine group (-NH₂) of the glycine molecule.
-OH: Indicates that the carboxylic acid group (-COOH) of the glycine is free and reactive.
Primary Function and Use
In peptide synthesis, amino acids are linked together by forming a bond between the amine group of one and the carboxylic acid group of another. To prevent unwanted reactions, the amine group must be "protected."
Fmoc-Gly-OH is the building block for incorporating glycine into a growing peptide chain. The Fmoc group protects Glycine's amine functionality during the coupling process. Once the glycine is attached to the chain, the Fmoc group can be easily and selectively removed using a mild base (like piperidine), exposing the amine group so it can react with the next protected amino acid.
Key Characteristics
Orthogonal Protection: The Fmoc group is stable to acids but easily removed by base. This allows it to be used alongside other acid-labile protecting groups, offering chemists flexibility in synthesizing complex peptides.
Crystallinity: Fmoc-Gly-OH is typically a white, crystalline solid, making it easy to handle, store, and measure accurately in the lab.
Essential Reagent: It is a fundamental and widely used reagent in pharmaceuticals, biochemistry, and research for creating custom peptides and peptide-based drugs.
In summary, Fmoc-Gly-OH is not a drug or a supplement, but a crucial tool for chemists to manually construct peptide molecules, one amino acid at a time.
Packages
Delivery
Payment term
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Contact information
Spring Zhang
Email: export@fortunachem.com
Skype: Fortunachem201304
QQ:3169620873
Tel: +86-27-59207892
Website: www.fortunachem.com
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