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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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
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
M T Migawa et al.
Journal of medicinal chemistry, 41(8), 1242-1251 (1998-05-09)
Several 2-substituted alpha-D- and alpha-L-lyxofuranosyl and 5-deoxylyxofuranosyl derivatives of 5,6-dicholro-2-(isopropylamino)-1-(beta-L-ribofuranosyl) benzimidazole (1263W94) and 2,5,6-trichloro-1(beta-D-ribofuranosyl)benzimidazole (TCRB) were synthesized and evaluated for activity against two herpesviruses (HSV-1 and HCMV) and for their cytotoxicity against HFF and KB cells. Condensation of 1,2,3,5-tetra-O-acetyl-L-lyxofuranose (2a)

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