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32058

Supelco

Pirimiphos-methyl

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C11H20N3O3PS
CAS Number:
29232-93-7
Molecular Weight:
305.33
Beilstein:
755726
EC Number:
249-528-5
MDL number:
MFCD00055366
UNSPSC Code:
41116107
PubChem Substance ID:
329753990
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

CCN(CC)c1nc(C)cc(OP(=S)(OC)OC)n1

InChI

1S/C11H20N3O3PS/c1-6-14(7-2)11-12-9(3)8-10(13-11)17-18(19,15-4)16-5/h8H,6-7H2,1-5H3

InChI key

QHOQHJPRIBSPCY-UHFFFAOYSA-N

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General description

Pirimiphos-methyl (PMM) is an organophosphorous pesticide.

Application

PMM may have been used as reference standard for identification of possible intermediate products formed during photocatalytic degradation of PMM using different chromatographic methods, like GC, HPLC, GC-MS, TOC and LC-MS.
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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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

Signal Word

Danger

Hazard Statements

H302,H370,H372,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 1 - STOT SE 1

Target Organs

Nervous system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF9905
BCBT5775
SZBC010XV
SZBB103XV
SZE7151X

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Photocatalytic degradation of pesticide pirimiphos-methyl: Determination of the reaction pathway and identification of intermediate products by various analytical methods.
Herrmann, Jean Marie, et al.
Catalysis Today, 54.2, 353-367 (1999)
Cédric Pennetier et al.
Malaria journal, 6, 38-38 (2007-03-31)
To manage the kdr pyrethroid-resistance in Anopheline malaria vectors, new compounds or new strategies are urgently needed. Recently, mixing repellents (DEET) and a non-pyrethroid insecticide (propoxur) was shown to be as effective as deltamethrin, a standard pyrethroid, under laboratory conditions
Cédric Pennetier et al.
Emerging infectious diseases, 14(11), 1707-1714 (2008-11-04)
The spread of resistance to pyrethroids in the major Afrotropical malaria vectors Anopheles gambiae s.s. necessitates the development of new strategies to control resistant mosquito populations. To test the efficacy of nets treated with repellent and insecticide against susceptible and
Darjaniva Molina et al.
Biomedica : revista del Instituto Nacional de Salud, 29(4), 604-615 (2010-05-05)
A study of insecticide resistance was undertaken at focal level in the localities Catuaro, Guayana, Platanito and Rio de Agua, Libertador County, Sucre State, Venezuela, a region with malaria transmission, where Anopheles aquasalis is the main vector. Insecticide resistance was
Young-Su Jang et al.
Journal of the American Mosquito Control Association, 21(4), 400-403 (2006-03-02)
Mosqutio larvicidal activity of Chamaecyparis obtusa leaf-derived materials against the 4th-stage larvae of Aedes aegypti (L.), Ochlerotatus togoi (Theobald), and Culex pipiens pallens (Coquillett) was examined in the laboratory. A crude methanol extract of C. obtusa leaves was found to
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