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Merck
CN

33587

Supelco

Fonofos solution

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

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About This Item

Empirical Formula (Hill Notation):
C10H15OPS2
CAS Number:
944-22-9
Molecular Weight:
246.33
Beilstein:
1958949
MDL number:
MFCD00055421
UNSPSC Code:
41116107
PubChem Substance ID:
329754591

Key Documents

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grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

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

storage temp.

2-8°C

SMILES string

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

InChI key

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.

Legal Information

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

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

35.6 °F - closed cup

Flash Point(C)

2 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品
剧毒化学品
农药列管产品
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Kathryn Hughes Barry et al.
Environmental health perspectives, 119(12), 1726-1732 (2011-08-04)
Previous research indicates increased prostate cancer risk for pesticide applicators and pesticide manufacturing workers. Although underlying mechanisms are unknown, evidence suggests a role of oxidative DNA damage. Because base excision repair (BER) is the predominant pathway involved in repairing oxidative
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
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.
Organophosphate (fonofos) poisoning.
H E Amstutz
Modern veterinary practice, 62(8), 601-601 (1981-08-01)
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