Skip to Content
Merck

C8286

Cellotetraose

≥85% (HPLC)

Synonym(s):

(β-D-Glc-[1→4])3-D-Glc, D-(+)-Cellotetraose

Slide 1 of 1
Sign In to View Organizational & Contract Pricing.

Select a Size

2 MG

PLN 612.00

10 MG

PLN 2,060.00

PLN 612.00

Please contact Customer Service for Availability
​
Request a Bulk Order

About This Item

Empirical Formula (Hill Notation):
C24H42O21
CAS Number:
38819-01-1
Molecular Weight:
666.58
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
24893043
MDL number:
MFCD00079079
Beilstein/REAXYS Number:
78869

Key Documents

View All Documentation

Skip To

Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

biological source

synthetic (organic)

Quality Level

200

assay

≥85% (HPLC)

form

powder

color

white

solubility

water: 25 mg/mL, clear, colorless to faintly yellow

storage temp.

−20°C

SMILES string

OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)[C@@H](O[C@@H]2CO)O[C@H]3[C@H](O)[C@@H](O)[C@@H](O[C@@H]3CO)O[C@H]4[C@H](O)[C@@H](O)C(O)O[C@@H]4CO)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C24H42O21/c25-1-5-9(29)10(30)15(35)22(40-5)44-19-7(3-27)42-24(17(37)12(19)32)45-20-8(4-28)41-23(16(36)13(20)33)43-18-6(2-26)39-21(38)14(34)11(18)31/h5-38H,1-4H2/t5-,6-,7-,8-,9-,10+,11-,12-,13-,14-,15-,16-,17-,18-,19-,20-,21?,22+,23+,24+/m1/s1

InChI key

LUEWUZLMQUOBSB-YQGOCCRESA-N

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
C725222150M4295
Cellotetraose ≥85% (HPLC)

Sigma-Aldrich

C8286

Cellotetraose

D-(+)-Cellobiose ≥98% (HPLC)

Sigma-Aldrich

C7252

D-(+)-Cellobiose

D-(+)-Cellobiose ≥99.0%, suitable for microbiology, Reducing sugar disaccharide

Millipore

22150

D-(+)-Cellobiose

Maltotriitol ≥95%

Sigma-Aldrich

M4295

Maltotriitol

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

100

Application

Cellotetraose is a 4-glucose polymer cellulodextrin derived from cellulose degradation. Cellotetraose and other cellulodextrins, such as cellulobiose, cellulotriose and cellopentaose are used by cellulosic bacteria as sources of energy. Cellotetraose is used to help identify, differentiate and characterize oligosaccharide metabolizing enzymes.[1][2]

Biochem/physiol Actions

Cellotetraose is a substrate for many cellulases and for 1,4-β-D-glucan glucohydrolases. It is also the end product of some cellulases, such as Cel9R from Clostridium thermocellum.

Other Notes

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SLCQ4671
SLCR4055
SLCQ8594
SLCQ6432
SLCG2602

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Takuji Oyama et al.
PloS one, 8(11), e80448-e80448 (2013-11-28)
CpMan5B is a glycoside hydrolase (GH) family 5 enzyme exhibiting both β-1,4-mannosidic and β-1,4-glucosidic cleavage activities. To provide insight into the amino acid residues that contribute to catalysis and substrate specificity, we solved the structure of CpMan5B at 1.6 Å
Hitoshi Suzuki et al.
Applied and environmental microbiology, 76(18), 6164-6170 (2010-07-27)
The wood decay basidiomycete Phanerochaete chrysosporium produces a variety of cellobiohydrolases belonging to glycoside hydrolase (GH) families 6 and 7 in the presence of cellulose. However, no inducer of the production of these enzymes has yet been identified. Here, we
Yuko Yoneda et al.
Journal of the American Chemical Society, 130(49), 16678-16690 (2009-06-26)
Hydrogen bonding is important in cellulosic and other carbohydrate structures, but the role of interactions between nonpolar groups is less understood. Therefore, we synthesized cyclohexyl 4'-O cyclohexyl beta-D-cellobioside (8), a molecule that has two glucose rings and two nonpolar cyclohexyl
Elizabeth A Znameroski et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(16), 6012-6017 (2012-04-05)
Neurospora crassa colonizes burnt grasslands in the wild and metabolizes both cellulose and hemicellulose from plant cell walls. When switched from a favored carbon source such as sucrose to cellulose, N. crassa dramatically upregulates expression and secretion of a wide
Tzu-Hui Wu et al.
Biochimica et biophysica acta, 1814(12), 1832-1840 (2011-08-16)
The hyperthermophilic endoglucanase Cel5A from Thermotoga maritima can find applications in lignocellulosic biofuel production, because it catalyzes the hydrolysis of glucan- and mannan-based polysaccharides. Here, we report the crystal structures in apo-form and in complex with three ligands, cellotetraose, cellobiose
View All Related Papers

Global Trade Item Number

SKUGTIN
C8286-10MG04061832628783
C8286-25MG04061832628790
C8286-2MG04061833522097

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service