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Quinoclamine

PESTANAL®, analytical standard

Synonyme(s) :

2-Amino-3-chloro-1,4-naphthoquinone

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About This Item

Formule empirique (notation de Hill):
C10H6ClNO2
Numéro CAS:
2797-51-5
Poids moléculaire :
207.61
Numéro CE :
220-529-2
Numéro MDL:
MFCD00001680
Code UNSPSC :
41116107
ID de substance PubChem :
329754296
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

NC1=C(Cl)C(=O)c2ccccc2C1=O

InChI

1S/C10H6ClNO2/c11-7-8(12)10(14)6-4-2-1-3-5(6)9(7)13/h1-4H,12H2

Clé InChI

OBLNWSCLAYSJJR-UHFFFAOYSA-N

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Catégories apparentées

Description générale

Quinoclamine belongs to the class of naphthoquinone compounds.

Application

Quinoclamine may be used as an analytical reference standard for the determination of the analyte in:
  • Honeybees by dispersive solid-phase extraction (dSPE), followed by liquid and gas chromatography coupled with tandem mass spectrometry (LC-MS/MS and GC-MS/MS).
  • Chlorophyll-containing matrix by dSPE and GC-MS/MS.

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

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Informations légales

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogrammes

Health hazardExclamation markEnvironment
GHS08,GHS07,GHS09

Mention d'avertissement

Warning

Classification des risques

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Sens. 1A - STOT RE 2

Organes cibles

Blood,Kidney

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

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
BCCJ5950
BCCD2396
BCBW0886
SZBE343XV
SZBE133XV

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Si vous avez besoin d'une version particulière, vous pouvez rechercher un certificat spécifique par le numéro de lot.

Rechercher un(e) COA

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Two-step dispersive-solid phase extraction strategy for pesticide multiresidue analysis in a chlorophyll-containing matrix by gas chromatography-tandem mass spectrometry.
Walorczyk S, et al.
Journal of Chromatography A, 1412(2), 22-32 (2015)
Application of bioactivity database of Chinese herbal medicine on the therapeutic prediction, drug development, and safety evaluation.
Cheng HM, et al.
Journal of Ethnopharmacology, 132(2), 429-437 (2010)
K A Bae et al.
Biological & pharmaceutical bulletin, 19(6), 824-827 (1996-06-01)
There are some highly cytotoxic anticancer compounds inducing differentiation of cancer cells to normal cells at below highly cytotoxic concentration. Naphthoquinone derivatives having cytotoxic effects on cancer cell were tested to learn whether they have differentiation inducing activity in human
H Kwon et al.
Research communications in molecular pathology and pharmacology, 97(2), 215-227 (1997-08-01)
Naphthoquinone compounds have various pharmacological effects such as antiviral, antifungal and anticancer activities. We demonstrated the differentiation of the inducing effect of a naphthoquinone derivative, 2-chloro-3-amino-1,4-nahpthoquinone (NQCA) on the human leukemia cell line U-937. When U-937 cells were treated with
Lijie Hou et al.
Dalton transactions (Cambridge, England : 2003), 48(25), 9234-9242 (2019-06-05)
Green and renewable organic redox molecules are greatly advantageous over conventional inorganic intercalation electrode materials in terms of electrochemical reversibility and cycling stability. However, their electrical insulation prevents them from being used alone as electrode materials for supercapacitors. Herein, 2-amino-3-chloro-1,4-naphthoquinone
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