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P-NITROPHENYL B-D-CELLOTETRAOSIDE

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P-NITROPHENYL B-D-CELLOTETRAOSIDE Basic information

Product Name:
P-NITROPHENYL B-D-CELLOTETRAOSIDE
Synonyms:
  • P-NITROPHENYL BETA-D-CELLOTETRAOSIDE
  • P-NITROPHENYL B-D-CELLOTETRAOSIDE
  • 4-Nitrophenyl β-D-cellotetraoside
  • P-nitrophenyl β-D-celloteraoside
  • 4-Nitrophenyl O-β-D-Glucopyranosyl-(14)-O-β-D-glucopyranosyl-(14)-O-β-D-glucopyranosyl-(14)-β-D-glucopyranoside
  • P-nitrophenyl B-D-celloteraoside
  • 4-Nitrophenylb-D-cellotetraoside
  • p-Nitrophenyl -D-Cellotetraoside
CAS:
129411-62-7
MF:
C30H45NO23
MW:
787.67
EINECS:
1533716-785-6
Product Categories:
  • Oligosaccharides
Mol File:
129411-62-7.mol
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P-NITROPHENYL B-D-CELLOTETRAOSIDE Chemical Properties

Melting point:
>266°C dec.
Boiling point:
1123.2±65.0 °C(Predicted)
Density 
1.79±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
DMSO (Slightly), Water (Slightly)
form 
Solid
pka
12.43±0.70(Predicted)
color 
Off-White
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Safety Information

HS Code 
29389090
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P-NITROPHENYL B-D-CELLOTETRAOSIDE Usage And Synthesis

Description

4-Nitrophenyl β-D-cellotetraoside is small molecule cellulose mimic that consists of a tetramer of D-glucose units joined by β-1-4-glycosidic bonds. An aglycosidic bond links a 4-nitrophenyl moiety to the anomeric carbon of the first glucose unit. 4-Nitrophenyl β-D-cellotetraoside is employed in cellulose degradation studies to determine the specificity of cellulases. The defined, small, and soluble structure of 4-nitrophenyl β-D-cellotetraoside makes it well suited for these studies. Its fragmentation pattern after enzymatic digestion can be analyzed by TLC or by release of 4-nitrophenol which exhibits strong absorbance at 395 nm in alkaline solution.

Chemical Properties

Off-White Solid

Uses

p-Nitrophenyl β-D-Cellotetraoside (cas# 129411-62-7) is a compound useful in organic synthesis.

References

[1] YOSHIHIRO HAKAMADA . Enzymatic properties, crystallization, and deduced amino acid sequence of an alkaline endoglucanase from Bacillus circulans[J]. Biochimica et biophysica acta. General subjects, 2002, 1570 3: Pages 174-180. DOI: 10.1016/s0304-4165(02)00194-0
[2] YUKI HAYASHI. Transcellobiosylation Reactions Catalyzed by Different Exoglucanase Components of a Trichoderma viride Cellulase in Aqueous Organic Solvent[J]. Biocatalysis and Biotransformation, 2003, 21 1: 25-31. DOI: 10.1080/1024242031000088555
[3] V. ZVERLOV W S G Velikodvorskaya. A newly described cellulosomal cellobiohydrolase, CelO, from Clostridium thermocellum: investigation of the exo-mode of hydrolysis, and binding capacity to crystalline cellulose.[J]. Microbiology-Sgm, 2002, 148 Pt 1 1: 247-255. DOI: 10.1099/00221287-148-1-247

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