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Paracetamol β-D-glucuronide

analytical standard

Synonyme(s) :

p-Acetamidophenyl β-D-glucuronide, Acetaminophen glucuronide

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About This Item

Formule empirique (notation de Hill):
C14H17NO8
Numéro CAS:
16110-10-4
Poids moléculaire :
327.29
Numéro Beilstein :
46644
Numéro MDL:
MFCD03094680
Code UNSPSC :
41116107
ID de substance PubChem :
329756303
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Pureté

≥98.5% (HPLC)

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Impuretés

≤12.0% water

Application(s)

forensics and toxicology
pharmaceutical (small molecule)

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

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

Clé InChI

IPROLSVTVHAQLE-BYNIDDHOSA-N

Catégories apparentées

Application

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

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Choose from one of the most recent versions:

Certificats d'analyse (COA)

Lot/Batch Number
BCCG3564
BCCF0007
BCCC7383
BCBZ4567
BCBT9425

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Sigma-Aldrich

N1627

4-Nitrophenyl β-D-glucuronide

Acétaminophène European Pharmacopoeia (EP) Reference Standard

Y0001781

Acétaminophène

Acétaminophène European Pharmacopoeia (EP) Reference Standard

P0300000

Acétaminophène

Acétaminophène analytical standard

Sigma-Aldrich

A3035

Acétaminophène

Acétaminophène British Pharmacopoeia (BP) Reference Standard

BP371

Acétaminophène

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
Drugs, bugs, and personalized medicine: pharmacometabonomics enters the ring.
Ian D Wilson
Proceedings of the National Academy of Sciences of the United States of America, 106(34), 14187-14188 (2009-08-27)
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