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Merck
CN

45305

Dicrotophos

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C8H16NO5P
CAS Number:
Molecular Weight:
237.19
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
205-494-3
Beilstein/REAXYS Number:
1880084
MDL number:
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InChI key

VEENJGZXVHKXNB-VOTSOKGWSA-N

InChI

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

SMILES string

COP(=O)(OC)O\C(C)=C\C(=O)N(C)C

grade

analytical standard

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

Quality Level

Related Categories

Application

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

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

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

pictograms

Skull and crossbonesEnvironment

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Regulatory Information

剧毒化学品
危险化学品
农药列管产品
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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 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
I C Maxwell et al.
Neurotoxicology, 3(1), 1-10 (1982-07-01)
Groups of rats were fed chlorfenvinphos (at two dose levels) or dicrotophos. Whole blood and plasma cholinesterase activity was markedly reduced. Compared with control animals there was no change in muscle action potential amplitude (M response) to a single stimulus

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