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80317

Supelco

Paracetamol-(ring-d4)

analytical standard

Synonym(e):

N-(4-Hydroxyphenyl-2,3,5,6-d4)-acetamid, Acetaminophen-(ring-d4), Acetaminophen-d4, [2H4]-Acetaminophen, [2H4]-Acetoaminophenol, [2H4]-Paracetamol

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About This Item

Empirische Formel (Hill-System):
C8D4H5NO2
CAS-Nummer:
64315-36-2
Molekulargewicht:
155.19
MDL-Nummer:
MFCD01317366
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329768785
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Assay

≥97.0% (HPLC)

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

Format

neat

Lagertemp.

−20°C

InChI

1S/C8H9NO2/c1-6(10)9-7-2-4-8(11)5-3-7/h2-5,11H,1H3,(H,9,10)/i2D,3D,4D,5D

InChIKey

RZVAJINKPMORJF-QFFDRWTDSA-N

Anwendung

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

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H302

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

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Analysenzertifikate (COA)

Lot/Batch Number
BCCC8346
BCCC3074
BCBX4586
BCBV3021
BCBS4429V

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4-Acetamidophenol analytical standard

Sigma-Aldrich

A3035

4-Acetamidophenol

2-Aminophenol 99%

Sigma-Aldrich

A71301

2-Aminophenol

4-Acetamidophenol Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1005

4-Acetamidophenol

Ibuprofen ≥98% (GC)

Sigma-Aldrich

I4883

Ibuprofen

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Xenobiotica; the fate of foreign compounds in biological systems, 51(3), 316-323 (2020-11-13)
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Landfill leachate could be a significant source of emerging contaminants (ECs) and antibiotic resistance genes (ARGs) into the environment. This study provides the first information on the occurrence of selected ECs and ARGs in raw leachate from 16-year old closed
Lei Xia et al.
Journal of applied toxicology : JAT, 36(2), 320-329 (2015-07-23)
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In vitro models based on primary human hepatocytes (PHH) have been advanced for clearance (CL) prediction of metabolically stable compounds, representing state-of-the-art assay systems for drug discovery and development. Yet, limited cell availability and large interindividual variability of metabolic profiles
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