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45487

Supelco

Fenitrothion

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C9H12NO5PS
CAS Number:
122-14-5
Molecular Weight:
277.23
Beilstein:
8983553
EC Number:
204-524-2
MDL number:
MFCD00055407
UNSPSC Code:
41116107
PubChem Substance ID:
329756779
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

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

InChI key

ZNOLGFHPUIJIMJ-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

Signal Word

Danger

Hazard Statements

H301,H312,H330,H410

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (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
Debasish Mandal et al.
The journal of physical chemistry. A, 116(10), 2536-2546 (2012-02-22)
Ab initio and density functional theory (DFT) calculations have been performed to understand the destruction chemistry of an important organophosphorus insecticide O,O-dimethyl O-(3-methyl-4-nitrophenyl) phosphorothioate, fenitrothion (FN), toward nucleophilic attack. Breaking of the P-OAr linkages through nucleophilic attack is considered to
Kuppusamy Kanagaraj et al.
Biosensors & bioelectronics, 35(1), 452-455 (2012-03-20)
A unique, efficient, highly sensitive and selective fluorescent chemosensor for fenitrothion has been reported for the first time using per-6-amino-β-cyclodextrin:Eu(III) complex. Among the various pesticides, the sensitivity response is found to be in the order, fenitrothion>quinalphos>methylparathion>parathion>methylparaoxon>paraoxon>fenchlorphos>profenofos>malathion. A detection limit as
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