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Merck

46279

Supelco

Cyanophos

PESTANAL®, analytical standard

Synonim(y):

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

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About This Item

Wzór empiryczny (zapis Hilla):
C9H10NO3PS
Numer CAS:
Masa cząsteczkowa:
243.22
Beilstein:
2695901
Numer WE:
Numer MDL:
Kod UNSPSC:
41116107
Identyfikator substancji w PubChem:
NACRES:
NA.24

klasa czystości

analytical standard

Poziom jakości

linia produktu

PESTANAL®

okres trwałości

limited shelf life, expiry date on the label

metody

HPLC: suitable
gas chromatography (GC): suitable

Zastosowanie

agriculture
environmental

format

neat

temp. przechowywania

2-8°C

ciąg 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

Klucz InChI

SCKHCCSZFPSHGR-UHFFFAOYSA-N

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Opis ogólny

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.

Zastosowanie

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).

Polecane produkty

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.

Informacje prawne

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

Piktogramy

Skull and crossbonesEnvironment

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

Klasyfikacja zagrożeń

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

Kod klasy składowania

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

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

>212.0 °F

Temperatura zapłonu (°C)

> 100 °C

Środki ochrony indywidualnej

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


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Certyfikaty analizy (CoA)

Lot/Batch Number

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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

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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