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Cyanophos

PESTANAL®, analytical standard

Synonyme(s) :

O-(4-Cyanophenyl) O,O-dimethyl phosphorothioate

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About This Item

Formule empirique (notation de Hill):
C9H10NO3PS
Numéro CAS:
Poids moléculaire :
243.22
Numéro Beilstein :
2695901
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

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

Température de stockage

2-8°C

Chaîne SMILES 

COP(=S)(OC)Oc1ccc(cc1)C#N

InChI

1S/C9H10NO3PS/c1-11-14(15,12-2)13-9-5-3-8(7-10)4-6-9/h3-6H,1-2H3

Clé InChI

SCKHCCSZFPSHGR-UHFFFAOYSA-N

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Catégories apparentées

Description générale

Cyanophos is an organophosphate insecticide, which is effectively used against various root-parasitic nematodes such as Diaspididae, Lepidoptera, Coccidae, Aphididae and other insects on various fruits and vegetables.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support. Cyanophos may be used as an analytical reference standard for the quantification of the analyte in biological samples using liquid chromatography coupled to mass spectrometry (LC-MS).

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

Skull and crossbonesEnvironment

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Code de la classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

>212.0 °F

Point d'éclair (°C)

> 100 °C

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

Enhancing agents for phytoremediation of soil contaminated by cyanophos
Romeh AA
Ecotoxicology and Environmental Safety, 117(2), 124-131 (2015)
W C Mullié et al.
Ecotoxicology and environmental safety, 43(1), 1-10 (1999-05-20)
Seven roosts of red-billed quelea, Quelea quelea, in the Senegal River Valley and Delta were visited during and after aerial or terrestrial treatments with either Cyanox (cyanophos 500 g a.i. liter-1, five roosts) or Queletox (fenthion 640 g a.i. liter-1
Matthieu Menager et al.
Photochemistry and photobiology, 86(2), 247-254 (2009-12-02)
Photodegradation in aqueous solutions is an important pathway for many agrochemicals such as pesticides. In the present work, the photochemical transformation of cyanophos (CYA) was investigated in aqueous solutions using UV light within the 254-313 nm range as well as
T Katami et al.
Journal of agricultural and food chemistry, 48(6), 2499-2501 (2000-07-11)
Bags impregnated with the organophosphorus pesticides prothiofos and cyanophos in three levels were used to cover Japanese apple-pears to protect them from insects. The amounts of prothiofos residue in the bags collected 4 months after application ranged from 0 to
Rapid simultaneous determination for organophosphorus
pesticides in human serum by LC-MS
Inoue S, et al.
Journal of Pharmaceutical and Biomedical Analysis, 44(2), 258-264 (2007)

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