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Phosphamidon

PESTANAL®, analytical standard

Synonym(s):

2-Chloro-N,N-diethyl-3-(dimethylphosphono)crotonic amide

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About This Item

Empirical Formula (Hill Notation):
C10H19ClNO5P
CAS Number:
Molecular Weight:
299.69
Beilstein:
8323501
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
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grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

storage temp.

2-8°C

SMILES string

CCN(CC)C(=O)\C(Cl)=C(\C)OP(=O)(OC)OC

InChI

1S/C10H19ClNO5P/c1-6-12(7-2)10(13)9(11)8(3)17-18(14,15-4)16-5/h6-7H2,1-5H3/b9-8+

InChI key

RGCLLPNLLBQHPF-CMDGGOBGSA-N

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General description

Phosphamidon is a neurotoxic organophosphorus insecticide.[1][2]

Application

Phosphamidon may be used as a reference standard in the analysis of phosphamidon in tobacco samples using gas chromatography coupled with triple quadrupole mass spectrometry (GC-MS/MS).[3]
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

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Male reproductive toxicity of phosphamidon: histopathological changes in epididymis.
Akbarsha MA and P Sivasamy
Indian Journal of Experimental Biology, 36(1), 34-38 (1998)
Comparative study of pesticide multi-residue extraction in tobacco for gas chromatography-triple quadrupole mass spectrometry.
Lee M-J, et al.
Journal of Chromatography A, 1187(1-2), 25-33 (2008)
Vikas Joshi et al.
Naunyn-Schmiedeberg's archives of pharmacology, 382(4), 311-320 (2010-08-26)
Phosphamidon (PHOS) has been shown to affect nervous system adversely. The present study was designed to explore the modulation of the effects of PHOS on convulsions by neurosteroids, progesterone (PROG), and 4'-chlorodiazepam (4'-CD), in both acute and chronic seizure models.
Somayeh Koupaei Malek et al.
Journal of separation science, 41(14), 2934-2941 (2018-06-08)
The precise control of pesticide residues in foodstuffs depends significantly on the clean extraction of analytes using specifically designed separation methods. In this study, a one-pot sol-gel process was used for the preparation of a magnetic hybrid silica gel tetraethylortho
P Thangavel et al.
Chemosphere, 61(8), 1083-1092 (2005-05-11)
The endocrine response in a freshwater teleost, Sarotherodon mossambicus (Peters) under dimecron (an organophosphate pesticide) toxicity was investigated by estimating the serum levels of T3 (triiodothyronine), T4 (thyroxine), cortisol, prolactin and insulin in control and sub-lethal (0.001 ml l(-1)) dimecron-exposed

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