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Key Documents

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45305

Supelco

Dicrotophos

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C8H16NO5P
Número de CAS:
141-66-2
Peso molecular:
237.19
Beilstein/REAXYS Number:
1880084
EC Number:
205-494-3
MDL number:
MFCD00072499
UNSPSC Code:
41116107
PubChem Substance ID:
329756631
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(=O)(OC)O\C(C)=C\C(=O)N(C)C

InChI

1S/C8H16NO5P/c1-7(6-8(10)9(2)3)14-15(11,12-4)13-5/h6H,1-5H3/b7-6+

InChI key

VEENJGZXVHKXNB-VOTSOKGWSA-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.

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Legal Information

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

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCM0143
BCCH2359
BCBV7705
SZBE094XV
SZBB117XV

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Dietrich E Lorke et al.
Current pharmaceutical design, 23(23), 3432-3439 (2016-11-02)
Reversible cholinesterase inhibitors, when given prophylactically before exposure to organophosphates, are able to decrease organophosphate-induced mortality. However, the efficacy of pyridostigmine, the only pre-treatment substance approved by the US Federal Drug Administration, is unsatisfactory. In search of a better prophylactic
J E Snawder et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 24(3), 205-218 (1989-06-01)
Four organophosphorus insecticides and the active metabolites of two phosphorothionate insecticides were tested for their toxic and teratogenic effects on embryos of Xenopus laevis. All compounds caused dose-dependent developmental defects, such as abnormal pigmentation, abnormal gut development, notochordal defects and
J C Garrison et al.
The Anatomical record, 213(3), 464-472 (1985-11-01)
White Leghorn chicken eggs, specific pathogen free, were treated with the organophosphate insecticide dicrotophos and the early defects thus induced were characterized histologically. Eggs were incubated for 24, 48, 72, or 96 hr, injected with doses of dicrotophos ranging from
Facile gas chromatographic method for the determination of residues of bidrin in pecan.
P C Bardalaye et al.
Journal of chromatography, 369(1), 231-234 (1986-11-07)
P Glynn Tillman et al.
Journal of economic entomology, 97(3), 800-806 (2004-07-29)
Susceptibility of the brown stink bug, Euschistus serous (Say), and the spined soldier bug, Podisus maculiventris (Say), to acetamiprid, cyfluthrin, dicrotophos, indoxacarb, oxamyl, and thiamethoxam, was compared in residual and oral toxicity tests. Generally, susceptibility of P. maculiventris to insecticides
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