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46011

Supelco

Piperophos

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C14H28NO3PS2
CAS Number:
24151-93-7
Molecular Weight:
353.48
Beilstein:
8395577
MDL number:
MFCD00210346
UNSPSC Code:
41116107
PubChem Substance ID:
329757052
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

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

InChI key

UNLYSVIDNRIVFJ-UHFFFAOYSA-N

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General description

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.

Legal Information

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

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H302,H330,H410

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

>212.0 °F

Flash Point(C)

> 100 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL4842
BCCJ8717
BCCG0856
BCCF5067
BCBZ3339

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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
Development of a new QuEChERS method based on dry ice for the determination of 168 pesticides in paprika using tandem mass spectrometry.
Lee SW
Journal of Chromatography A, 1218(28), 4366-4377 (2011)
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