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Piperophos

PESTANAL®, analytical standard

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About This Item

Formule empirique (notation de Hill):
C14H28NO3PS2
Numéro CAS:
Poids moléculaire :
353.48
Numéro Beilstein :
8395577
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

CCCOP(=S)(OCCC)SCC(=O)N1CCCCC1C

InChI

1S/C14H28NO3PS2/c1-4-10-17-19(20,18-11-5-2)21-12-14(16)15-9-7-6-8-13(15)3/h13H,4-12H2,1-3H3

Clé InChI

UNLYSVIDNRIVFJ-UHFFFAOYSA-N

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Description générale

Piperophos belongs to the class of organophosphorus insecticides, commonly present as an endocrine disrupting chemical with anti-androgenic activity.

Application

Piperophos may be used as an analytical reference standard for the quantification of the analyte in environmental samples, bovine milk samples and paprika using different chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Informations légales

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

Pictogrammes

Skull and crossbonesEnvironment

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

>212.0 °F

Point d'éclair (°C)

> 100 °C

Équipement de protection individuelle

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


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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

Determination of chloramphenicol, enrofloxacin and 29 pesticides residues in bovine milk by liquid chromatography-tandem mass spectrometry
Tian H
Chemosphere, 83(3), 349-355 (2011)
Gunda Viswanath et al.
The Journal of steroid biochemistry and molecular biology, 120(1), 22-29 (2010-03-10)
The present work describes the screening and characterization of some common endocrine disrupting chemicals for their (anti)androgenic activities. Various chemicals (mostly pesticides and pharmaceuticals) were screened with the NIH3T3 cell line stably expressing human androgen receptor (hAR) and luciferase reporter
Acute toxicity of pesticides to Gobius sp., Palaemonetes africanus, and Desmocaris trispimosa.
A G Ebere et al.
Bulletin of environmental contamination and toxicology, 49(4), 588-592 (1992-10-01)
Nasser Mokhtari et al.
Journal of the science of food and agriculture, 100(6), 2364-2371 (2019-12-20)
A new type of deep eutectic solvent based on three components using phosphate salts has been synthesized, characterized, and applied in the extraction of eight organothiophosphate pesticides from honey samples. In this study, the deep eutectic solvent was prepared from
Simultaneous determination of 64 pesticides in river water by stir bar sorptive extraction and thermal desorption-gas chromatography-mass spectrometry
Nakamura S and Daishima S
Analytical and Bioanalytical Chemistry, 382(1), 99-107 (2005)

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