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45696

Supelco

Triazophos

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C12H16N3O3PS
Número de CAS:
24017-47-8
Peso molecular:
313.31
Beilstein/REAXYS Number:
682554
EC Number:
245-986-5
MDL number:
MFCD00055327
UNSPSC Code:
41116107
PubChem Substance ID:
329756908
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

storage temp.

2-8°C

SMILES string

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

Inchi Key

AMFGTOFWMRQMEM-UHFFFAOYSA-N

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Application

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

Legal Information

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

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCL8295
BCCK9763
BCCK7166
BCCJ3688
BCCD2400

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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
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
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
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
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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