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4429-05-4

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4429-05-4 Usage

General Description

Fructosyl-glycine is a chemical compound formed by the reaction between fructose and glycine, an amino acid. It is a type of Amadori product, which are formed in the early stages of the Maillard reaction, a series of complex chemical reactions between amino acids and reducing sugars. Fructosyl-glycine is often used as a model compound to study the Maillard reaction in food chemistry and has been implicated in the browning and flavor development of various food products. Additionally, fructosyl-glycine has been studied for its potential role in advanced glycation end products (AGEs) formation, which are implicated in various age-related diseases such as diabetes and Alzheimer's.

Check Digit Verification of cas no

The CAS Registry Mumber 4429-05-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,2 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4429-05:
(6*4)+(5*4)+(4*2)+(3*9)+(2*0)+(1*5)=84
84 % 10 = 4
So 4429-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO7/c10-3-5(12)8(16)7(15)4(11)1-9-2-6(13)14/h5,7-10,12,15-16H,1-3H2,(H,13,14)/t5-,7-,8-/m1/s1

4429-05-4Relevant articles and documents

Analysis of Amadori compounds by high-performance cation exchange chromatography coupled to tandem mass spectrometry

Davidek, Tomas,Kraehenbuehl, Karin,Devaud, Stephanie,Robert, Fabien,Blank, Imre

, p. 140 - 147 (2007/10/03)

High-performance cation exchange chromatography coupled to tandem mass spectrometry or electrochemical detection was found to be an efficient tool for analyzing Amadori compounds derived from hexose and pentose sugars. The method allows rapid separation and identification of Amadori compounds, while benefiting from the well-known advantages of mass spectrometry, such as specificity and sensitivity. Glucose- and xylose-derived Amadori compounds of several amino acids, such as glycine, alanine, valine, leucine/isoleucine, methionine, proline, phenylalanine, and glutamic acid, were separated or discriminated using this new method. The method is suitable for the analysis of both model reaction mixtures and food products. Fructosylglutamate was found to be the major Amadori compound in dried tomatoes (~1.5 g/100 g) and fructosylproline in dried apricots (~0.2 g/100 g). Reaction of xylose and glycine at 90 °C (pH 6) for 2 h showed rapid formation of xylulosylglycine (~12 mol %, 15 min) followed by slow decrease over time. Analysis of pentose-derived Amadori compounds is shown for the first time, which represents a major breakthrough in studying occurrence, formation, and decomposition of these labile Maillard intermediates.

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