Skip to Content
Merck
CN

V000763

D-(+)-Xylose

puriss., 98.5%

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C5H10O5
CAS Number:
Molecular Weight:
150.13
EC Number:
200-400-7
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1562108
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


grade

puriss.

assay

98.5%

mp

154-158 °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-IOVATXLUSA-N



Still not finding the right product?

Explore all of our products under D-(+)-Xylose


Storage Class

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

新产品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



Thu V Vuong et al.
PloS one, 9(4), e95170-e95170 (2014-04-17)
The xylan-binding module Clostridium thermocellum CBM22A was successfully fused to a gluco-oligosaccharide oxidase, GOOX-VN, from Sarocladium strictum via a short TP linker, allowing the fused protein to effectively bind different xylans. The presence of the CtCBM22A at the N-terminal of
S Kilaru et al.
Fungal genetics and biology : FG & B, 79, 166-173 (2015-06-21)
Development of new fungicides, needed for sustainable control of fungal plant pathogens, requires identification of novel anti-fungal targets. Essential fungal-specific proteins are good candidates, but due to their importance, gene deletion mutants are not viable. Consequently, their cellular role often
Jose Serate et al.
Biotechnology for biofuels, 8, 180-180 (2015-11-20)
Microbial conversion of lignocellulosic feedstocks into biofuels remains an attractive means to produce sustainable energy. It is essential to produce lignocellulosic hydrolysates in a consistent manner in order to study microbial performance in different feedstock hydrolysates. Because of the potential