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Merck
CN

33587

地虫磷 溶液

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

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经验公式(希尔记法):
C10H15OPS2
化学文摘社编号:
分子量:
246.33
PubChem Substance ID:
UNSPSC Code:
41116107
Beilstein/REAXYS Number:
1958949
MDL number:
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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

grade

analytical standard

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

Quality Level

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

wgk

WGK 2

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

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

存储类别

3 - Flammable liquids

flash_point_f

35.6 °F - closed cup

flash_point_c

2 °C - closed cup

ppe

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

法规信息

危险化学品
剧毒化学品
农药列管产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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.
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
I Ferrer et al.
Journal of chromatography. A, 778(1-2), 161-170 (1997-08-22)
The stability of four pesticides (desethylatrazine, fenamiphos, fenitrothion and fonofos) was examined under different storage conditions after preconcentration in disposable solid-phase extraction (SPE) cartridges containing new polymer sorbent materials (Hysphere-1, IST EnviroLut and LiChrolut). Complete recovery for all the compounds
Organophosphate (fonofos) poisoning.
H E Amstutz
Modern veterinary practice, 62(8), 601-601 (1981-08-01)

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