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45696

Supelco

Triazophos

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (Notação de Hill):
C12H16N3O3PS
Número CAS:
24017-47-8
Peso molecular:
313.31
Beilstein:
682554
Número CE:
245-986-5
Número MDL:
MFCD00055327
Código UNSPSC:
41116107
ID de substância PubChem:
329756908
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

agriculture
environmental

formato

neat

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

CCOP(=S)(OCC)Oc1ncn(n1)-c2ccccc2

InChI

1S/C12H16N3O3PS/c1-3-16-19(20,17-4-2)18-12-13-10-15(14-12)11-8-6-5-7-9-11/h5-10H,3-4H2,1-2H3

chave InChI

AMFGTOFWMRQMEM-UHFFFAOYSA-N

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Aplicação

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

Informações legais

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

Pictogramas

Skull and crossbonesEnvironment
GHS06,GHS09

Palavra indicadora

Danger

Frases de perigo

H301,H312,H330,H410

Classificações de perigo

Acute Tox. 1 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1

Código de classe de armazenamento

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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

Choose from one of the most recent versions:

Certificados de análise (COA)

Lot/Batch Number
BCCL8295
BCCK9763
BCCK7166
BCCJ3688
BCCD2400

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Shaonan Li et al.
Journal of environmental sciences (China), 23(5), 852-859 (2011-07-28)
In vivo activity of cholinesterase (ChE) in Daphnia magna was measured at different time points during 21-day exposure to triazophos and chlorpyrifos ranging from 0.05 to 2.50 microg/L and 0.01 to 2.00 microg/L, respectively. For exposure to triazophos, ChE was
Yan-Yuan Bao et al.
Journal of insect physiology, 56(9), 1087-1094 (2010-03-13)
The widespread use of insecticides has caused the resurgence of the brown planthopper, Nilaparvata lugens, in Asia. In this study, we investigated an organo-phosphorous insecticide, triazophos, and its ability to induce gene expression variation in female N. lugens nymphs just
Lin-Quan Ge et al.
Journal of proteome research, 10(10), 4597-4612 (2011-08-02)
The brown planthopper, Nilaparvata lugens (Stål) (Hemiptera: Delphacidae), is a classic example of a resurgent pest induced by insecticides. It has been demonstrated that triazophos treatment causes an increase in the content of male accessory gland proteins (Acps) that can
Mubeena Akhtar et al.
Colloids and surfaces. B, Biointerfaces, 69(1), 63-70 (2008-12-19)
The sorption efficiency of chickpea husk of black gram variety (BGH), for the removal of organophosphorous pesticides (OPPs), i.e. triazophos (TAP) and methyl parathion (MP) from aqueous media has been investigated. Optimization of operating sorption parameters, i.e. particle size, sorbent
Huaifen Li et al.
Colloids and surfaces. B, Biointerfaces, 89, 175-181 (2011-10-01)
An electrochemical sensor for pesticide triazophos (TAP) was prepared by deposition of gold nanoparticles (AuNPs) on carbon nanotubes (CNTs) modified glassy carbon (GC) electrode surface using a potentiostatic method, followed by electropolymerizing of o-hydroxyphenol at the AuNP/CNT/GC electrode surface in
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