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N3378

Sigma-Aldrich

4-Nitrophenyl β-D-fuco­pyran­oside

≥98% (TLC), powder

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About This Item

Empirical Formula (Hill Notation):
C12H15NO7
CAS Number:
1226-39-7
Molecular Weight:
285.25
Beilstein:
1291394
MDL number:
MFCD00040651
UNSPSC Code:
12352204
PubChem Substance ID:
24897639
NACRES:
NA.32

product name

4-Nitrophenyl β-D-fuco­pyran­oside, ≥98% (TLC)

Quality Level

200

Assay

≥98% (TLC)

form

powder

solubility

ethanol: soluble 25 mg/mL, clear, colorless to faintly yellow

storage temp.

−20°C

SMILES string

C[C@H]1O[C@@H](Oc2ccc(cc2)[N+]([O-])=O)[C@H](O)[C@@H](O)[C@H]1O

InChI

1S/C12H15NO7/c1-6-9(14)10(15)11(16)12(19-6)20-8-4-2-7(3-5-8)13(17)18/h2-6,9-12,14-16H,1H3/t6-,9+,10+,11-,12+/m1/s1

InChI key

YILIDCGSXCGACV-BVWHHUJWSA-N

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Application

4-Nitrophenyl β-D-fucopyranoside has been used as a chromogenic substrate to study substrate specificity and kinetic parameters of β-galactosidase.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Identification, purification and characterization of a novel glycosidase (BgLm1) from Leuconostoc mesenteroides
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New alkalophilic beta-galactosidase with high activity in alkaline pH region from Teratosphaeria acidotherma AIU BGA-1
Yamada M, et al.
Journal of Bioscience and Bioengineering, 123(1), 15-19 (2017)
Regioselective synthesis of alpha-L-fucosyl-containing disaccharides by use of alpha-L-fucosidases of various origins.
K Ajisaka et al.
Carbohydrate research, 224, 291-299 (1992-02-07)
M H Tomassi et al.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas, 43(1), 8-12 (2009-12-23)
The manner by which effects of simultaneous mutations combine to change enzymatic activity is not easily predictable because these effects are not always additive in a linear manner. Hence, the characterization of the effects of simultaneous mutations of amino acid
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