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38153

Sigma-Aldrich

8-Hydroxyquinoline-β-D-glucuronide sodium salt

≥98.0% (HPLC)

Synonym(s):

8-Hydroxyquinoline-β-D-glucuronic acid sodium salt, 8-Quinolyl-β-D-glucopyranosiduronic acid sodium salt

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About This Item

Empirical Formula (Hill Notation):
C15H14NNaO7
CAS Number:
207728-71-0
Molecular Weight:
343.26
MDL number:
MFCD02683911
UNSPSC Code:
12352204
PubChem Substance ID:
329755745
NACRES:
NA.83

Assay

≥98.0% (HPLC)

form

powder

optical activity

[α]/D -84.0±4.0°, c = 1 in H2O

impurities

≤12% water

storage temp.

−20°C

SMILES string

[Na+].O[C@@H]1[C@@H](O)[C@@H](O[C@@H]([C@H]1O)C([O-])=O)Oc2cccc3cccnc23

InChI

1S/C15H15NO7.Na/c17-10-11(18)13(14(20)21)23-15(12(10)19)22-8-5-1-3-7-4-2-6-16-9(7)8;/h1-6,10-13,15,17-19H,(H,20,21);/q;+1/p-1/t10-,11-,12+,13-,15+;/m0./s1

InChI key

QYRMLNFJXNJXLO-KSOKONAESA-M

Application

Substrate for detection of β-D-glucuronidase, yields a brown precipitate upon cleavage; E. coli detection

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

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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A L James et al.
Zentralblatt fur Bakteriologie, Mikrobiologie, und Hygiene. Series A, Medical microbiology, infectious diseases, virology, parasitology, 267(3), 316-321 (1988-01-01)
The use of 8-hydroxyquinoline-beta-D-glucuronide for the demonstration of beta-glucuronidase activity within the family Enterobacteriaceae has been investigated. The compound has been shown to be an effective substrate for the bacterial enzyme and the Michaelis constant for the association has been
R D Reinders et al.
Letters in applied microbiology, 30(5), 411-414 (2000-05-03)
8-hydroxyquinoline-beta-D-glucuronide (HQG) was used to improve the presumptive identification of Shiga toxin-producing Escherichia coli O157 (STEC O157) on sorbitol MacConkey agars (SMAC). Advantages of HQG are (i) that it is less expensive than 5-bromo-4-chloro-3-indoxyl-glucuronide; (ii) that it is visible in

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