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Merck
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Supelco

Piperophos

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (Notação de Hill):
C14H28NO3PS2
Número CAS:
Peso molecular:
353.48
Beilstein:
8395577
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

agriculture
environmental

formato

neat

temperatura de armazenamento

2-8°C

cadeia de caracteres 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

chave InChI

UNLYSVIDNRIVFJ-UHFFFAOYSA-N

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Descrição geral

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

Aplicação

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.

Informações legais

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

Pictogramas

Skull and crossbonesEnvironment

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

>212.0 °F

Ponto de fulgor (°C)

> 100 °C

Equipamento de proteção individual

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


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Certificados de análise (COA)

Lot/Batch Number

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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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