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Merck
CN

220477

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
UNSPSC Code:
12352201
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-212-8
Beilstein/REAXYS Number:
1723083
MDL number:
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InChI key

SRBFZHDQGSBBOR-AGQMPKSLSA-N

InChI

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

SMILES string

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

assay

99%

optical activity

[α]25/D -15.8°, c = 4 in H2O

mp

108-112 °C (lit.)

Quality Level

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

涉药品监管产品
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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
Kei-Ichi Kitahara et al.
Journal of chromatography. A, 1216(44), 7415-7421 (2009-04-14)
Using an HPLC column packed with monodispersed vinylbenzeneboronic acid-divinylbenzene (V-D) copolymer resins, the elution behaviors of the mono- and disaccharides were studied under different pH mobile phases. The monodispersed V-D copolymer resins were prepared by the copolymerization of 4-vinylbenzeneboronic acid
Johanna Schulten et al.
Carbohydrate research, 346(13), 1767-1775 (2011-07-26)
Excess di(tert-butyl)silylene (DTBS) bis(trifluoromethanesulfonate) formed bis-DTBS derivatives with the four aldopentoses (arabinose, lyxose, ribose and xylose). The structure of the bis-chelates was affected by the bulk of the DTBS groups and the requirement of flat silacycles in the case of
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

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