2-Naphthyl-α- L-fucopyranoside (β-Naphthyl-α-L-fucoside)

Description

2-Naphthyl-α- L-fucopyranoside is a chromogenic substrate for α-L-Fucosidase. 2-naphthol is released upon hydrolyzation. By simultaneous coupling with a suitable staining reagent, such as hexazonium p-rosaniline, the corresponding azo-dye is formed. Naphthols can also be detected by fluorescence analysis.

Product Specifications
2-Naphthyl-α- L-fucopyranoside
β-Naphthyl-α-L-fucoside
β-Nap-α-L-Fuc

MOLECULAR BIOLOGY GRADE

Formula: C16H18O5

MW: 290.32 g/mol

Storage/Handling: Store at -20°C. Protect from light.

PubChem Chemical ID: 6454626














2-Naphthyl-α- L-fucopyranoside (β-Naphthyl-α-L-fucoside)

View Sizes & Pricing

Catalog Number:
N-110-100
CAS Number:
63503-05-9
$331.00

For research use only. Not for food, drug, household, or cosmetic use.
Availability:
2-3 Weeks
Shipping:
$14.99 Ground shipping (In continental US only.)

    Description

    2-Naphthyl-α- L-fucopyranoside is a chromogenic substrate for α-L-Fucosidase. 2-naphthol is released upon hydrolyzation. By simultaneous coupling with a suitable staining reagent, such as hexazonium p-rosaniline, the corresponding azo-dye is formed. Naphthols can also be detected by fluorescence analysis.

    Product Specifications
    2-Naphthyl-α- L-fucopyranoside
    β-Naphthyl-α-L-fucoside
    β-Nap-α-L-Fuc

    MOLECULAR BIOLOGY GRADE

    Formula: C16H18O5

    MW: 290.32 g/mol

    Storage/Handling: Store at -20°C. Protect from light.

    PubChem Chemical ID: 6454626














    Product Specifications

    Catalog ID: N-110
    CAS #: 63503-05-9
    Formula: C16H18O5
    MW: 290.32 g/mol
    Grade: MOLECULAR BIOLOGY GRADE
    Storage/handling: Store at -20°C. Protect from light.
    PubChem Chemical ID: 6454626
    IUPAC Name: (2S,3S,4R,5S,6S)-2-methyl-6-naphthalen-2-yloxyoxane-3,4,5-triol
    InChI: InChI=1S/C16H18O5/c1-9-13(17)14(18)15(19)16(20-9)21-12-7-6-10-4-2-3-5-11(10)8-12/h2-9,13-19H,1H3/t9-,13+,14+,15-,16-/m0/s1
    InChIKey: HFJUQSUBZOKELZ-FITDYDNJSA-N
    SMILES: CC1C(C(C(C(O1)OC2=CC3=CC=CC=C3C=C2)O)O)O

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