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75762

Sigma-Aldrich

3-Desoxyglucoson

≥75% (TLC)

Synonym(e):

3-Desoxy-D-erythro-hexosulose

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About This Item

Empirische Formel (Hill-System):
C6H10O5
CAS-Nummer:
4084-27-9
Molekulargewicht:
162.14
UNSPSC-Code:
12352201
PubChem Substanz-ID:
329766689
NACRES:
NA.25

Qualitätsniveau

100

Assay

≥75% (TLC)

Form

solid

Farbe

faintly yellow to orange

Lagertemp.

room temp

SMILES String

OC[C@H]1OC(O)C(=O)C[C@@H]1O

InChI

1S/C6H10O5/c7-2-5-3(8)1-4(9)6(10)11-5/h3,5-8,10H,1-2H2/t3-,5+,6?/m0/s1

InChIKey

UHPMJDGOAZMIID-OPAZFOKUSA-N

Anwendung

3-Desoxyglucoson wird als Referenzstandard für die Analyse und den Nachweis von Glucoseabbauprodukten, Glycationsmitteln, die durch Prozesse wie Hitzesterilisation erzeugt werden, eingesetzt.

Sonstige Hinweise

Für einen umfassenden Überblick über unser vielfältiges Angebot an Monosacchariden für Ihre Forschung empfehlen wir Ihnen den Besuch unserer Seite zur Kategorie Kohlenhydrate.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Hydroxyaceton contains ≤500 ppm sodium carbonate as stabilizer, technical grade, 90%

Sigma-Aldrich

138185

Hydroxyaceton

2-Furaldehyd 99%

Sigma-Aldrich

185914

2-Furaldehyd

Acetaldehyd puriss. p.a., anhydrous, ≥99.5% (GC)

Sigma-Aldrich

00070

Acetaldehyd

Michael Hellwig et al.
Journal of agricultural and food chemistry, 58(19), 10752-10760 (2010-09-09)
1,2-Dicarbonyl compounds are formed in food during Maillard and caramelization reactions. 3-Deoxy-D-threo-hexos-2-ulose (3-deoxygalactosone, 3-DGal) and galactosone, two 1,2-dicarbonyl compounds originating from the degradation of galactose, were synthesized and converted to the respective quinoxalines, which were characterized by NMR spectroscopy. Analytical
He Li et al.
Journal of agricultural and food chemistry, 67(32), 9050-9059 (2019-07-25)
The control of 2,3-dihydro-3,5-dihydroxy-6-methyl-4(H)-pyran-4-one (DDMP) formation in the Maillard reaction is important to improve the thermally treated food quality as a result of its intense bitterness and potential toxicity. In this work, phenolic acids, such as gallic, protocatechuic, caffeic, and
Danielle T Loughlin et al.
Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society, 17(5), 739-749 (2009-09-23)
The interaction of fibroblasts with the extracellular matrix is critical for wound healing. Advanced glycation end products (AGEs) occur through nonenzymatic glycation of long-lived proteins such as collagens. One precursor to these modifications, 3-deoxyglucosone (3DG), is elevated in patients with
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Molecular nutrition & food research, 51(4), 473-478 (2007-03-29)
Peritoneal dialysis (PD) is commonly performed by using preprepared dialysis solutions containing glucose, which are thermally treated to achieve commercial sterilization. A series of glucose degradation products (GDPs) are being formed, which react with the tissue during the dialysis procedure
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Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis, 28(3), 277-282 (2008-05-14)
Glucose degradation products (GDPs) are important in the outcome of peritoneal dialysis (PD) treatment. 3,4-dideoxyglucosone-3-ene (3,4-DGE) is the most cytotoxic GDP found in conventionally manufactured fluids and may, in addition, be recruited from 3-deoxyglucosone (3-DG). It is not known what
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