15075-50-0 Purity
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Specification
3,4-Dihydroxybutanoic acid (3,4-DHBA) is a platform four-carbon (C4) compound that can be used as a precursor to several of the chemicals most important to the commercial industry: antibiotics, chiral molecules, HIV inhibitors, cholesterol-lowering chirals, etc.
This is a dual substrate biosynthetic system for the generation of 3,4-DHBA using a synthetic pathway constructed in engineered E.coli, where synthetic substrate is xylose and growth substrate is glucose.
More precisely, the new approach for synthesising 3,4-DHBA from xylose and glucose via a reengineered Weimberg pathway heterologously expressed in engineered E. coli was developed. The pathway requires four or five reaction steps namely dehydrogenation, dehydration, decarboxylation and oxidation, each of which was catalyzed by a xylose dehydrogenase, a xylonate dehydratase, a 2-keto acid decarboxylase and an ALDH or a coenzyme A-acylating aldehyde dehydrogenase (CoA-acylating ALDH) with a thiolase.
The molecular formula is C4H8O4.
The synonyms for 3,4-dihydroxybutanoic acid are 2-Deoxytetronic acid and 3,4-dihydroxybutyric acid.
The molecular weight is 120.10 g/mol.
The IUPAC name is 3,4-dihydroxybutanoic acid.
The InChI is InChI=1S/C4H8O4/c5-2-3(6)1-4(7)8/h3,5-6H,1-2H2,(H,7,8).
The InChIKey is DZAIOXUZHHTJKN-UHFFFAOYSA-N.
The canonical SMILES is C(C(CO)O)C(=O)O.
The CAS number is 1518-61-2.
The XLogP3-AA value is -1.6.
It is a solid.