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N-923

Supelco

Norfluoxetine oxalate solution

1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®

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About This Item

Empirical Formula (Hill Notation):
C18H18F3NO5
CAS Number:
Molecular Weight:
385.33
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

certified reference material

form

liquid

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 1 mL

manufacturer/tradename

Cerilliant®

concentration

1.0 mg/mL in methanol (as free base)

technique(s)

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

application(s)

clinical testing

format

single component solution

storage temp.

2-8°C

SMILES string

NCCC(C1=CC=CC=C1)OC2=CC=C(C(F)(F)F)C=C2.OC(C(O)=O)=O

InChI

1S/C16H16F3NO.C2H2O4/c17-16(18,19)13-6-8-14(9-7-13)21-15(10-11-20)12-4-2-1-3-5-12;3-1(4)2(5)6/h1-9,15H,10-11,20H2;(H,3,4)(H,5,6)

InChI key

FDWJCEPFCGIDPF-UHFFFAOYSA-N

General description

Norfluoxetine is a primary blood metabolite of the selective serotonin reuptake inhibitor (SSRI) fluoxetine, an antidepressant, sold under the trade name Prozac®. This Snap-N-Spike® Reference Solution is applicable to use in urine drug testing, clinical toxicology, or forensic analysis by LC-MS/MS or GC/MS.

Application


  • Forensic Detection of Cocaine and Antidepressants: Norfluoxetine is utilized in the development of an innovative analytical method using magnetic nanoparticles for the forensic detection of cocaine, antidepressants, and their metabolites in postmortem blood samples. This method represents a significant advance in forensic toxicology, providing rapid, sensitive, and reliable results essential for criminal investigations and legal proceedings (de Souza Schwarz et al., 2024).

  • Ion Channel Research in Dermatology: Research involving Norfluoxetine investigates its effects on selected ion channels, highlighting its potential implications in skin physiology. This study explores the multifaceted roles of serotonin reuptake inhibitors like Norfluoxetine in dermatological applications, contributing to better understanding and treatment of skin-related disorders (Kim et al., 2023).

  • Therapeutic Drug Monitoring: Norfluoxetine is featured in the simultaneous determination of serotonin selective reuptake inhibitors using an advanced UPLC MS-MS method. This method is used in clinical settings for therapeutic drug monitoring, ensuring proper dosage and optimizing treatment outcomes for patients undergoing antidepressant therapy (Eloisa Chávez-Castillo et al., 2022).

  • Pharmacological Research on TREK and TRESK Channels: Studies involving Norfluoxetine examine its interaction with TREK and TRESK K2P channels, important for understanding the pharmacological properties of drugs affecting the central nervous system. Such research aids in the development of new therapeutic agents for neurological conditions (Walsh et al., 2021).

  • Placental Aromatase Influence by SSRIs: Norfluoxetine is investigated for its impact on placental aromatase, a crucial enzyme in steroid hormone biosynthesis. Understanding how SSRIs affect this enzyme can improve safety profiles and therapeutic strategies during pregnancy, especially concerning fetal development (Hudon Thibeault et al., 2019).

Legal Information

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Prozac is a registered trademark of Eli Lilly and Co.
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup


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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