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220477

Sigma-Aldrich

D-(−)-Lyxose

99%

Synonym(s):

D-Lyxopyranose

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About This Item

Empirical Formula (Hill Notation):
C5H10O5
CAS Number:
Molecular Weight:
150.13
Beilstein:
1723083
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

optical activity

[α]25/D -15.8°, c = 4 in H2O

mp

108-112 °C (lit.)

SMILES string

O[C@@H]1COC(O)[C@@H](O)[C@H]1O

InChI

1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3+,4+,5?/m1/s1

InChI key

SRBFZHDQGSBBOR-AGQMPKSLSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Laura K Jennings et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(36), 11353-11358 (2015-08-28)
Biofilm formation is a complex, ordered process. In the opportunistic pathogen Pseudomonas aeruginosa, Psl and Pel exopolysaccharides and extracellular DNA (eDNA) serve as structural components of the biofilm matrix. Despite intensive study, Pel's chemical structure and spatial localization within mature
Judit E Sponer et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(32), 9990-9998 (2008-09-24)
Recent experimental studies suggest that complexation with borate minerals stabilizes ribose, and that the borate complex of ribose is more stable than those of related aldopentoses, that is, arabinose, lyxose, and xylose. These findings have revived the debate on the
Michal Letek et al.
PLoS genetics, 6(9), e1001145-e1001145 (2010-10-14)
We report the genome of the facultative intracellular parasite Rhodococcus equi, the only animal pathogen within the biotechnologically important actinobacterial genus Rhodococcus. The 5.0-Mb R. equi 103S genome is significantly smaller than those of environmental rhodococci. This is due to
Álvaro Vázquez-Mayagoitia et al.
Astrobiology, 11(2), 115-121 (2011-03-12)
The RNA-world theory hypothesizes that early Earth life was based on the RNA molecule. However, the notion that ribose, the sugar in RNA, is unstable still casts a serious doubt over this theory. Recently, it has been found that the
Carsten Hofmann et al.
Chemistry & biology, 12(10), 1137-1143 (2005-10-26)
The oligosaccharide antibiotic avilamycin A is composed of a polyketide-derived dichloroisoeverninic acid moiety attached to a heptasaccharide chain consisting of six hexoses and one unusual pentose moiety. We describe the generation of mutant strains of the avilamycin producer defective in

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