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36552

Supelco

Fenthion

PESTANAL®, analytical standard

Synonym(s):

O,O′-Dimethyl O″-[3-methyl-4-(methylthio)phenyl] thiophosphate

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About This Item

Empirical Formula (Hill Notation):
C10H15O3PS2
CAS Number:
55-38-9
Molecular Weight:
278.33
Beilstein:
1974129
EC Number:
200-231-9
MDL number:
MFCD00055449
UNSPSC Code:
41116107
PubChem Substance ID:
329755394
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
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

storage temp.

2-8°C

SMILES string

COP(=S)(OC)Oc1ccc(SC)c(C)c1

InChI

1S/C10H15O3PS2/c1-8-7-9(5-6-10(8)16-4)13-14(15,11-2)12-3/h5-7H,1-4H3

InChI key

PNVJTZOFSHSLTO-UHFFFAOYSA-N

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General description

Fenthion is an organophosphorous pesticide, which can find applications in agriculture.It can serve as a potent anti-androgenic inhibitor of dihydrotestosterone.

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

Signal Word

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Muta. 2 - STOT RE 1 Oral

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ5059
BCCJ1089
BCBW6887
BCBT4329
SZBF252XV

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Antiandrogenic activity and metabolism of the organophosphorus pesticide fenthion and related compounds
Kitamura S, et al.
Environmental Health Perspectives, 111, 503-503 (2003)
Hapten heterology for a specific and sensitive indirect enzyme-linked immunosorbent assay for organophosphorus insecticide fenthion
Zhang Q, et al.
Analytica Chimica Acta, 596, 303-311 (2007)
Determination of ethoprop, diazinon, disulfoton and fenthion using dynamic hollow fiber-protected liquid-phase microextraction coupled with gas chromatography?mass spectrometry
Chen S-P and Huang D-S
Talanta, 69, 669-675 (2006)
Ramon Lavado et al.
Toxicology and applied pharmacology, 235(2), 143-152 (2008-12-30)
Previous studies in rainbow trout have shown that acclimation to hypersaline environments enhances the toxicity to thioether organophosphate and carbamate pesticides. In order to determine the role of biotransformation in this process, the metabolism of the thioether organophosphate biocide, fenthion
Nevin Uner et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 150(1), 33-38 (2009-05-16)
N-Acetyl-L-cysteine, a low-molecular weight thiol compound, with two different doses was used to prevent fenthion, an organophosphorus insecticide and acaricide, related oxidative stress in the brain of a model organism, Cyprinus carpio. Fish were exposed to sub-lethal and nominal concentration
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