Fmoc-Gly-OH

Fmoc-Gly-OH Suppliers list

Company Name:	GenChem & GenPharm (Changzhou) Co., Ltd. Gold
Tel:	0519-85720003 18861157602
Email:	410649415@qq.com

Company Name:	Zepeptide Biotechnology (Shijiazhuang) Co., LTD Gold
Tel:	13383293380 18032131480
Email:	649498984@qq.com

Fmoc-Gly-OH manufacturers

Fmoc-Gly-OH: Tool for Amino Group Quantification in TiO2@SiO2 Core-Shell Materials
Fmoc-Gly-OH is a peptide synthesis reagent, and modifies TiO2@SiO2 core-shells to enable UV-based amino group quantification.
Dec 16，2025

Fmoc-Gly-OH Basic information

Product Name:	Fmoc-Gly-OH
Synonyms:	9-FLUORENYLMETHOXYCARBONYL-GLYCINE;FMOC-GLY-OH;F-FMOC-GLYCINE;N-alpha-(9-fluorenylmethyloxycarbonyl)-L-glycine;FMOC-Glycine,98%;Fmoc-glycine N-(9-Fluorenylmethoxycarbonyl)-glycine;N-Fmoc-glycine Fmoc-Gly-OH;FMoc-DL-Glycine
CAS:	29022-11-5
MF:	C17H15NO4
MW:	297.31
EINECS:	249-373-3
Product Categories:	Glycine [Gly, G];Fmoc-Amino Acids and Derivatives;Amino Acids (N-Protected);Biochemistry;Fmoc-Amino Acids;Fmoc-Amino acid series;Protected Amino Acids;Fluorenes, Flurenones;AMINOACIDS DERIVATIVES;Amino Acid Derivatives;Azepanes/Diazepanes;Amino Acids
Mol File:	29022-11-5.mol

Fmoc-Gly-OH Chemical Properties

Melting point	174-175 °C(lit.)
Boiling point	438.82°C (rough estimate)
density	1.1671 (rough estimate)
refractive index	1.4500 (estimate)
storage temp.	2-8°C
solubility	almost transparency in Methanol
form	Powder
pka	3.89±0.10(Predicted)
color	White
BRN	2163967
Major Application	peptide synthesis
InChI	InChI=1S/C17H15NO4/c19-16(20)9-18-17(21)22-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15H,9-10H2,(H,18,21)(H,19,20)
InChIKey	NDKDFTQNXLHCGO-UHFFFAOYSA-N
SMILES	C(O)(=O)CNC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O
CAS DataBase Reference	29022-11-5(CAS DataBase Reference)

Safety Information

MSDS Information

Fmoc-Gly-OH Usage And Synthesis

Chemical Properties	white to light yellow crystal powde
Uses	Fmoc-Gly-OH is an N-Fmoc-protected form of Glycine (G615990). Glycine is a nonessential amino acid that acts as an inhibitory neyrotransmitter in the vertebrate central nervous system. Glycine also posesses cytoprotective against oxidant damage in the kidney.
Preparation	Glycine (Gly) (0.5 g, 6.66 mmol) was dissolved in 10% NaCO₃ (14 ml) under stirring in a 50-ml flask. To the resulting solution, which had been put into an ice bath, 9-fluorenylmethoxycarbonyl chloride (Fmoc-Cl) (1.72 g, 6.66 mmol) in dioxane (12 ml) was gradually added. The reaction mixture was stirred at room temperature for 4 hours. Then added water (150 ml) to the mixture. The aqueous phase layer was separated from the reaction mixture and stripped with ether three times (75 ml×3). The stripped aqueous layer was acidified with 2N HCl aqueous solution to a pH=2, followed by extraction with ethyl acetate three times (75 ml×3). The organic phase layer was recovered and concentrated to obtain crude product of 1.70 g. The crude product was recrystallized in a mixed solvent of ethyl acetate hexane=1:2 (30 ml), and white solid denoted as Fmoc-Gly-OH was obtained after filtration at a reduced pressure.
General Description	Fmoc-Gly-OH is used for fmoc solid-phase peptide synthesis.
reaction suitability	reaction type: Fmoc solid-phase peptide synthesis

Fmoc-Gly-OH Preparation Products And Raw materials

Preparation Products

Tag:Fmoc-Gly-OH(29022-11-5) Related Product Information

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