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45487

Supelco

Fenitrothion

PESTANAL®, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C9H12NO5PS
Numero CAS:
122-14-5
Peso molecolare:
277.23
Beilstein:
8983553
Numero CE:
204-524-2
Numero MDL:
MFCD00055407
Codice UNSPSC:
41116107
ID PubChem:
329756779
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

COP(=S)(OC)Oc1ccc(c(C)c1)[N+]([O-])=O

InChI

1S/C9H12NO5PS/c1-7-6-8(4-5-9(7)10(11)12)15-16(17,13-2)14-3/h4-6H,1-3H3
ZNOLGFHPUIJIMJ-UHFFFAOYSA-N

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Applicazioni

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

Note legali

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

Pittogrammi

Skull and crossbonesEnvironment
GHS06,GHS09

Avvertenze

Danger

Indicazioni di pericolo

H301,H312,H330,H410

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
BCCJ6185
BCCF3724
BCBW2030
SZBD022XV
SZB9029XV

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Amandine Guidez et al.
Memorias do Instituto Oswaldo Cruz, 115, e200313-e200313 (2021-02-04)
Aedes aegypti is the sole vector of urban arboviruses in French Guiana. Overtime, the species has been responsible for the transmission of viruses during yellow fever, dengue, chikungunya and Zika outbreaks. Decades of vector control have produced resistant populations to
A Larki
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 173, 1-5 (2016-09-03)
In this work, the intrinsic colorimetric property of carbon dots (CDs) was utilized for the determination of fenitrothion by applying dispersive liquid-liquid microextraction (DLLME) method. Label free CDs are extracted into carbon tetrachloride via assistance of trioctylmethylammonium chloride (Aliquat 336)
Roberto Sanchirico et al.
Journal of hazardous materials, 199-200, 390-400 (2011-12-06)
The thermal decomposition of Fenitrothion [phosphorothioic acid O,O-diethyl O-(3-methyl-4-nitrophenyl) ester] was investigated. Results obtained by different scale calorimetric techniques show that the thermal decomposition of Fenitrothion involves two main steps. Intermediate and final thermal degradation products formed during isothermal and
Fatma M El-Demerdash
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 47(4), 262-268 (2012-03-21)
A mixture of pyrethroids plus organophosphates was assessed for their potential effects on lipid peroxidation, the antioxidant defense system and lactate dehydrogenase (LDH) in rat kidney in vitro. Various insecticide concentrations were incubated with kidney homogenate at 37°C for different
Ai Okamura et al.
Toxicology letters, 210(2), 220-224 (2011-10-27)
The measurement of blood cholinesterase (ChE) activities is adopted worldwide for biological monitoring of exposure to organophosphorus insecticides (OPs). Recent development of analytical chemistry has made sensitive quantification possible of non-specific OP metabolites, dialkylphosphates, in urine as a biomarker of
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