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43073

Paracetamol β-D-glucuronide potassium salt

analytical standard

Synonym(s):

p-Acetamidophenyl β-D-glucuronide, Acetaminophen glucuronide

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About This Item

Empirical Formula (Hill Notation):
C14H16KNO8
Molecular Weight:
365.38
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756303
MDL number:
MFCD03094680
Beilstein/REAXYS Number:
46644

Key Documents

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InChI key

IPROLSVTVHAQLE-BYNIDDHOSA-N

SMILES string

O[C@@H]1[C@@H](O)[C@H](OC2=CC=C(NC(C)=O)C=C2)O[C@H](C(O)=O)[C@H]1O

InChI

1S/C14H17NO8/c1-6(16)15-7-2-4-8(5-3-7)22-14-11(19)9(17)10(18)12(23-14)13(20)21/h2-5,9-12,14,17-19H,1H3,(H,15,16)(H,20,21)/t9-,10-,11+,12-,14+/m0/s1

grade

analytical standard

assay

≥98.5% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

impurities

≤12.0% water

application(s)

forensics and toxicology
pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

Quality Level

100

Related Categories

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM2421
BCCH6221
BCCG3564
BCCF0007
BCCC7383

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María L Ruiz et al.
Drug metabolism and disposition: the biological fate of chemicals, 35(11), 2060-2066 (2007-08-10)
The effect of spironolactone (SL) administration on 17alpha-ethynylestradiol (EE)-induced cholestasis was studied, with emphasis on expression and activity of Mrps. Adult male Wistar rats were divided into the following groups: EE (5 mg/kg daily for 5 days, s.c.), SL (200
Jialin Xu et al.
Drug metabolism and disposition: the biological fate of chemicals, 40(2), 259-266 (2011-10-28)
UDP-glucuronosyltransferases (Ugt) catalyze phase II conjugation reactions with glucuronic acid, which enhances chemical polarity and the elimination from the body. Few studies have addressed whether Ugt expression and activity are affected by liver disease, such as steatosis. The purpose of
Lúcia H M L M Santos et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 930, 75-81 (2013-06-04)
Paracetamol is among the most worldwide consumed pharmaceuticals. Although its occurrence in the environment is well documented, data about the presence of its metabolites and transformation products is very scarce. The present work describes the development of an analytical method
Cristina Barosa et al.
Magnetic resonance in medicine, 70(2), 315-319 (2012-10-02)
Plasma glucose (2) H-enrichment in positions 5 ((2) H5) and 2 ((2) H2) from deuterated water ((2) H2 O) provides a measure of the gluconeogenic contribution to endogenous glucose production. Urinary glucuronide analysis can circumvent blood sampling but it is
Qin-you Tan et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 893-894, 162-167 (2012-03-27)
A specific, sensitive and rapid method based on high performance liquid chromatography coupled to tandem mass spectrometry (HPLC-MS/MS) was developed for the simultaneous determination of paracetamol (APAP) and its glucuronide conjugate (PG) in human plasma and urine. Plasma samples were
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