A chromogenic substrate for endoglucanases and cellobiohydrolases
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4-Nitrophenyl β-D-Cellotrioside

Item No. 19523

Technical Information
Formal Name
4-nitrophenyl O-β-D-glucopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→4)-β-D-glucopyranoside
CAS Number
106927-48-4
Synonyms
  • p-Nitrophenyl β-D-Cellotrioside
Molecular Formula
C24H35NO18
Formula Weight
Purity
≥98%
A crystalline solid
λmax
221, 296 nm
SMILES
OC[C@H]([C@@H](O[C@@]1([H])[C@H](O)[C@@H](O)[C@H](O[C@]2([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](CO)O1)[C@H](O)[C@H]3O)O[C@H]3OC4=CC=C([N+]([O-])=O)C=C4
InChi Code
InChI=1S/C24H35NO18/c26-5-10-13(29)14(30)17(33)23(39-10)42-21-12(7-28)41-24(19(35)16(21)32)43-20-11(6-27)40-22(18(34)15(20)31)38-9-3-1-8(2-4-9)25(36)37/h1-4,10-24,26-35H,5-7H2/t10-,11-,12-,13-,14+,15-,16-,17-,18-,19-,20-,21-,22-,23+,24+/m1/s1
InChi Key
BETIRLUWOMCBBJ-ZENQEEDISA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    4-Nitrophenyl β-D-cellotrioside is a chromogenic substrate for endoglucanases and cellobiohydrolases.1 Hydrolysis of this substrate by these enzymes liberates 4-nitrophenol, which generates a yellow color that is measured by monitoring absorbance at 405 nm.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Hitomi, J., Hatada, Y., Kawaminami, S., et alAmino acid sequence and stereoselective hydrolytic reaction of an endo-1,4-β-glucanase from a Bacillus strain. Biosci. Biotech. Bioch. 61(12), 2004-2009 (2016).