L-(+)-Erythrose - ≥90%, 40% aqueous solution , CAS No.533-49-3

CAS: 533-49-3 Cat. No.: E759680 Summenformel: C4H8O4 Molekulargewicht: 120.10 Beilstein Registry Number: 1721697 EG-Nummer: 208-567-8
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GRADE & PURITY ≥90% 40% aqueous solution
Synonyms
(2S,3S)-2,3,4-trihydroxy-butanal | L-Erythrose | L-Erythrose
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
Size
Deutschland (EU)
USA*
Price
Qty
5mg
E759680-5mg
6 Auf Lager
69,33€
25mg
E759680-25mg
2 Auf Lager
242,88€
100mg
E759680-100mg
Auf Bestellung · 8–12 Wochen
780,88€
Enter a quantity for the sizes you want to add.
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Why this grade

≥90%, 40% aqueous solution for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

L-Erythrose is a monosaccharide that contains an hydroxyl group on the second carbon atom. It can be synthesized by a synthetic scheme involving glycolaldehyde and hydroxylamine. L-Erythrose has been shown to inhibit the enzyme phosphoglycerate kinase, which converts 2-phosphoglycerate into phosphoenolpyruvate. L-Erythrose has also been shown to inhibit dehydroascorbic acid reductase, which converts dehydroascorbic acid into ascorbic acid, and galactitol reductase, which converts galactitol into D-tagatose. The mutant strain of Escherichia coli K12 that was engineered to produce L-erythrose showed a decreased susceptibility to phage infection and an increased resistance to oxidative stress. In addition, the polyol pathway in E. coli was induced by L-erythrose treatment.

Application:

L-Erythrose is a rare aldotetrose that have been used as a chirality factor used in QSAR studies of chiral molecules.

Specifications

Synonyme
(2S,3S)-2,3,4-trihydroxy-butanal | L-Erythrose | L-Erythrose
Spezifikationen & Reinheit
≥90%, 40% aqueous solution
Storage
Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Reinheit
≥90%
Namen und Kennungen
Pubchem Sid528765247
Kanonisches LächelnC(C(C(C=O)O)O)O
IUPAC Name(2S,3S)-2,3,4-trihydroxybutanal
InChIKeyYTBSYETUWUMLBZ-DMTCNVIQSA-N
INCHI1S/C4H8O4/c5-1-3(7)4(8)2-6/h1,3-4,6-8H,2H2/t3-,4+/m1/s1
Isomere SMILES C([C@@H]([C@@H](C=O)O)O)O
WGK Deutschland 3
Molekulargewicht 120.10
Beilstein 1721697
Reaxy-Rn 1751758
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1751758&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
KlasseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Not available
Direct ParentMonosaccharides
Alternative Parents Beta-hydroxy aldehydes  Alpha-hydroxyaldehydes  Secondary alcohols  Polyols  Short-chain aldehydes  Primary alcohols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Monosaccharide - Beta-hydroxy aldehyde - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Short-chain aldehyde - Primary alcohol - Carbonyl group - Aldehyde - Alcohol - Aliphatic acyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as monosaccharides. These are compounds containing one carbohydrate unit not glycosidically linked to another such unit, and no set of two or more glycosidically linked carbohydrate units. Monosaccharides have the general formula CnH2nOn.
External Descriptors erythrose
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot NumberCertificate TypeDatumArtikel
D2518334Certificate of AnalysisMar 25, 2025 E759680
D2518335Certificate of AnalysisMar 25, 2025 E759680
D2518336Certificate of AnalysisMar 25, 2025 E759680
D2518337Certificate of AnalysisMar 25, 2025 E759680
Chemische und physikalische Eigenschaften
Flammpunkt (°F)>235.4 °F
Flammpunkt (°C)>113 °C
Molekulargewicht120.100 g/mol
XLogP3-2.200
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Exact Mass120.042 Da
Monoisotopic Mass120.042 Da
Topological Polar Surface Area77.800 Ų
Heavy Atom Count8
Formal Charge0
Complexity72.400
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Lösungsrechner
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