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L-Erythrose

Catalog No. T20229   CAS 533-49-3
Synonyms: L-(+)-Erythrose

L(+)-Erythrose is an aldotetrose rare sugar. It may be used in glycation studies and as a reference compound in tetrose carbohydrate separation and quantitation analysis. It also can be used to help identify and characterize erythrose reductase(s) and to study the mechanisms of mutarotation in mono sugars.

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L-Erythrose Chemical Structure
L-Erythrose, CAS 533-49-3
Pack Size Availability Price/USD Quantity
10 mg 35 days $ 78.00
25 mg 35 days $ 150.00
50 mg 35 days $ 215.00
100 mg 35 days $ 293.00
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Biological Description
Chemical Properties
Storage & Solubility Information
Description L(+)-Erythrose is an aldotetrose rare sugar. It may be used in glycation studies and as a reference compound in tetrose carbohydrate separation and quantitation analysis. It also can be used to help identify and characterize erythrose reductase(s) and to study the mechanisms of mutarotation in mono sugars.
Synonyms L-(+)-Erythrose
Molecular Weight 120.1
Formula C4H8O4
CAS No. 533-49-3

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: Soluble

TargetMolReferences and Literature

1. Draskovits M, Stanetty C, Baxendale IR, Mihovilovic MD. Indium- and Zinc-Mediated Acyloxyallylation of Protected and Unprotected Aldotetroses-Revealing a Pronounced Diastereodivergence and a Fundamental Difference in the Performance of the Mediating Metal. J Org Chem. 2018 Mar 2;83(5):2647-2659. doi: 10.1021/acs.joc.7b03063. Epub 2018 Feb 9. PubMed PMID: 29369620; PubMed Central PMCID: PMC5838623. 2. Zou X, Lin J, Mao X, Zhao S, Ren Y. Biosynthesis of L-Erythrose by Assembly of Two Key Enzymes in Gluconobacter oxydans. J Agric Food Chem. 2017 Sep 6;65(35):7721-7725. doi: 10.1021/acs.jafc.7b02201. Epub 2017 Aug 24. PubMed PMID: 28707464. 3. Zweckmair T, Böhmdorfer S, Bogolitsyna A, Rosenau T, Potthast A, Novalin S. Accurate analysis of formose reaction products by LC-UV: an analytical challenge. J Chromatogr Sci. 2014 Feb;52(2):169-75. doi: 10.1093/chromsci/bmt004. Epub 2013 Feb 1. PubMed PMID: 23377653. 4. Jasiński M, Lentz D, Reissig HU. Carbohydrate-auxiliary assisted preparation of enantiopure 1,2-oxazine derivatives and aminopolyols. Beilstein J Org Chem. 2012;8:662-74. Epub 2012 Apr 30. PubMed PMID: 23015812; PubMed Central PMCID: PMC3388852.

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Keywords

L-Erythrose 533-49-3 L Erythrose LErythrose L-(+)-Erythrose inhibitor inhibit

 

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