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Merck
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Principaux documents

33587

Supelco

Fonofos solution

100 μg/mL in acetonitrile, PESTANAL®, analytical standard

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About This Item

Formule empirique (notation de Hill):
C10H15OPS2
Numéro CAS:
Poids moléculaire :
246.33
Beilstein:
1958949
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
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Qualité

analytical standard

Niveau de qualité

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Concentration

100 μg/mL in acetonitrile

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

single component solution

Température de stockage

2-8°C

Chaîne SMILES 

CCOP(=S)(CC)Sc1ccccc1

InChI

1S/C10H15OPS2/c1-3-11-12(13,4-2)14-10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3

Clé InChI

KVGLBTYUCJYMND-UHFFFAOYSA-N

Application

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

Informations légales

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

Pictogrammes

FlameExclamation mark

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

35.6 °F - closed cup

Point d'éclair (°C)

2 °C - closed cup

Équipement de protection individuelle

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


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Consulter la Bibliothèque de documents

John E Elliott et al.
Environmental toxicology and chemistry, 27(2), 452-460 (2008-03-20)
From 1994 to 1999 in the Lower Fraser Valley region of southwest Canada, fonofos (Dyfonate G) was recommended for control of introduced wireworm (Agriotes spp.) pests on potato and other root crops. As part of a wildlife-monitoring program, we collected
Khawja A Usmani et al.
Drug metabolism and disposition: the biological fate of chemicals, 34(9), 1606-1614 (2006-06-23)
Cytochromes P450 (P450s) are major catalysts in the metabolism of xenobiotics and endogenous substrates such as estradiol (E2). It has previously been shown that E2 is predominantly metabolized in humans by CYP1A2 and CYP3A4 with 2-hydroxyestradiol (2-OHE2) the major metabolite.
F Quadri et al.
Schweizerische medizinische Wochenschrift, 120(6), 153-154 (1990-02-10)
A 32-year-old woman who had ingested 300 ml of a potent cholinesterase inhibitor insecticide (Fonofos) with suicidal intent became progressively comatose and finally suffered respiratory arrest. Tracheal intubation, mechanical ventilation, vigorous gastric lavage and intravenous administration of atropine and obidoxime
A Hirashima et al.
Bioorganic & medicinal chemistry, 8(3), 653-656 (2000-03-25)
Molecular interaction between enantiomeric fonofos oxon (O-ethyl S-phenyl ethylphosphonothiolate) and acetylcholinesterase (AChE) of Torpedo californica was evaluated by using the Cerius2 program. It was suggested that the difference in the inhibitory activity of the two enantiomers of fonofos oxon on
W O Cook et al.
Veterinary and human toxicology, 27(4), 281-282 (1985-08-01)
An organophosphate toxicosis due to fonofos was diagnosed in an Iowa Dairy herd. Fonofos was detected in the feed source and in the rumen contents, liver, and kidney tissue of one cow that died acutely. Bulk tank milk contained detectable

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