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Isoproturon-d6

PESTANAL®, analytical standard

Synonyme(s) :

3-(4-Isopropylphenyl)-1,1-dimethylurea-d6

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About This Item

Formule empirique (notation de Hill):
C12H12D6N2O
Numéro CAS:
217487-17-7
Poids moléculaire :
212.32
Numéro MDL:
MFCD01632296
Code UNSPSC :
41116107
ID de substance PubChem :
329754761
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

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

Changement de masse

M+6

Chaîne SMILES 

[2H]C([2H])([2H])N(C(=O)Nc1ccc(cc1)C(C)C)C([2H])([2H])[2H]

InChI

1S/C12H18N2O/c1-9(2)10-5-7-11(8-6-10)13-12(15)14(3)4/h5-9H,1-4H3,(H,13,15)/i3D3,4D3

Clé InChI

PUIYMUZLKQOUOZ-LIJFRPJRSA-N

Description générale

Isoproturon-d6 is an isotopically labeled standard of the phenylurea herbicide isoproturon, which is used for the pre- or post-emergence control of weeds in fruits, cotton and other crops.

Application

Isoproturon-d6 may be used as internal standard in the analysis of pesticides in fine airborne particulate matter, using liquid extraction under pressure and liquid chromatographic–tandem mass spectrometric method (HPLC-MS-MS).
Isoproturon-d6 may be used as an internal standard for the quantification of isoproturon in:
  • Soil samples using pressurized liquid extraction (PLE) followed by liquid chromatography coupled to mass chromatography (LC-MS) and electrospray ionization-tandem mass spectrometry (LC-ESI+-MS/MS).
  • Surface water samples using online solid phase extraction–liquid chromatography–tandem mass spectrometry (SPE–LC–MS/MS).

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

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

Pictogrammes

Health hazardEnvironment
GHS08,GHS09

Mention d'avertissement

Warning

Mentions de danger

H351,H373,H410

Classification des risques

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - STOT RE 2

Organes cibles

Blood

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
BCCH3101
BCCG0674
BCCF3015
BCBS6966V
SZBF224XV

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Microbial degradation of isoproturon and related phenylurea herbicides in and below agricultural fields.
Sorensen RB, et al.
FEMS Microbiology Ecology, 45(1), 1-11 (2003)
Elvio D Amato et al.
Chemosphere, 236, 124400-124400 (2019-09-24)
Recently, a new sampling device combining active and passive sampling (APS) was developed for the measurement of time-averaged concentrations of metal species and both polar and non-polar organic contaminants in water. By coupling a diffusion cell (loaded with a set
Aurélie Berthet et al.
Archives of toxicology, 91(11), 3529-3542 (2017-05-05)
Methylchloroisothiazolinone (MCI) and methylisothiazolinone (MI) are biocides used in many types of products such as cosmetics, paints, and cleaning agents. Skin contact is often encountered when using these products. Although MCI and MI are strong allergens and cause skin irritation
Frank David et al.
Talanta, 165, 201-210 (2017-02-06)
Two low-pressure columns (Bio-Beads SX-3) and three high-pressure GPC columns were compared for clean-up of a wide range of pesticides in fatty matrices of vegetable or animal origin. The GPC fractions were analyzed by GC-MS/MS and LC-MS/MS without additional clean-up.
Determination of chloroacetanilides, triazines and phenylureas and some of their metabolites in soils by pressurised liquid extraction, GC-MS/MS, LC-MS and LC-MS/MS.
Dagnac T, et al.
Journal of Chromatography A, 1067(1-2), 225-233 (2005)
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