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M5878

Sigma-Aldrich

Methyl β-D-xylopyranoside

≥99% (GC)

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25 G
CHF 468.00

About This Item

Formula empirica (notazione di Hill):
C6H12O5
Numero CAS:
612-05-5
Peso molecolare:
164.16
Numero CE:
210-289-7
Numero MDL:
MFCD00047532
Codice UNSPSC:
12352201
ID PubChem:
24897051
NACRES:
NA.25

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Origine biologica

synthetic (organic)

Saggio

≥99% (GC)

Stato

powder

Attività ottica

[α]20/D -66.5 to -64.5, c = 10% (w/v) in water

tecniche

gas chromatography (GC): suitable

Colore

white to off-white

Punto di fusione

155-158 °C (lit.)

Solubilità

water: 100 mg/mL, clear to hazy, colorless to light yellow

Temperatura di conservazione

room temp

Stringa SMILE

CO[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O

InChI

1S/C6H12O5/c1-10-6-5(9)4(8)3(7)2-11-6/h3-9H,2H2,1H3/t3-,4+,5-,6-/m1/s1
ZBDGHWFPLXXWRD-JGWLITMVSA-N

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Applicazioni

Methyl β-D-xylopyranoside has been used in a study to assess tetraisopropyldisiloxane-1,3-diyl as a versatile protecting group for pentopyranosides. [1] It has also been used in a study that investigated transacetylations to carbohydrates catalyzed by acetylxylan esterase in the presence of an organic solvent. [2]

Altre note

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
MKCV6022
MKCS8852
MKCR2399
MKCP7604
MKCL5784

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D-(+)-Xylose ≥99% (GC)

Sigma-Aldrich

X1500

D-(+)-Xylose

Peter Biely et al.
Biochimica et biophysica acta, 1622(2), 82-88 (2003-07-26)
Streptomyces lividans acetylxylan esterase removes the 2- or 3-O-acetyl groups from methyl 2,4-di-O-acetyl- and 3,4-di-O-acetyl beta-D-xylopyranoside. When the free hydroxyl group was replaced with a hydrogen or fluorine, the rate of deacetylation was markedly reduced, but regioselectivity was not affected.
Mária Mastihubová et al.
Carbohydrate research, 339(12), 2101-2110 (2004-07-29)
Four modified substrates for acetylxylan esterases, 2-deoxy, 3-deoxy, 2-deoxy-2-fluoro, and 3-deoxy-3-fluoro derivatives of di-O-acetylated methyl beta-D-xylopyranoside were synthesized via 2,3-anhydropentopyranoside precursors. Methyl 2,3-anhydro-4-O-benzyl-beta-D-ribopyranoside was transformed into methyl 2,3-anhydro-4-O-benzyl-beta-D-lyxopyranoside in three steps. The epoxide ring opening of 2,3-anhydropentopyranosides was accomplished either
Marìa Eugenia Hidalgo-Lara et al.
Journal of industrial microbiology & biotechnology, 32(8), 345-348 (2005-06-30)
Synthesis of extracellular xylanase in Cellulomonas flavigena is induced in the presence of xylan and sugarcane bagasse as substrates. The essential factors for efficient production of xylanase are the appropriate medium composition and an inducing substrate. The increase in xylanase
Tran N Pham et al.
Journal of the American Chemical Society, 126(40), 13100-13110 (2004-10-08)
We have developed methodology for the determination of solution structures of small molecules from residual dipolar coupling constants measured in dilute liquid crystals. The power of the new technique is demonstrated by the determination of the structure of methyl beta-d-xylopyranoside
P B Gordon et al.
Carbohydrate research, 151, 121-134 (1986-08-15)
The influence of methyl beta-D-xylopyranoside on human endothelial cell proteoglycans isolated from the medium and extracellular matrix was investigated. Confluent cultures of human endothelial cells incorporate significant amounts of heparan sulfate (78%), chondroitin sulfate (10%), and dermatan sulfate (12%) into
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