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Alachlor-d13

PESTANAL®, analytical standard

Synonym(s):

2-Chloro-2′,6′-diethyl-N-(methoxymethyl)acetanilide-d13

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About This Item

Empirical Formula (Hill Notation):
C14H7D13ClNO2
CAS Number:
1015856-63-9
Molecular Weight:
282.85
MDL number:
MFCD06658594
UNSPSC Code:
41116107
PubChem Substance ID:
329754803
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

mass shift

M+13

SMILES string

[2H]c1c([2H])c(c(N(COC)C(=O)CCl)c(c1[2H])C([2H])([2H])C([2H])([2H])[2H])C([2H])([2H])C([2H])([2H])[2H]

InChI

1S/C14H20ClNO2/c1-4-11-7-6-8-12(5-2)14(11)16(10-18-3)13(17)9-15/h6-8H,4-5,9-10H2,1-3H3/i1D3,2D3,4D2,5D2,6D,7D,8D

InChI key

XCSGPAVHZFQHGE-PTKGBVOGSA-N

General description

Alachlor-d13 is a deuterated analog of the herbicide, alachlor which is a persistent contaminant in ground and surface waters.

Application

Alachlor-d13 may be used as an internal standard for the estimation of alachlor in water samples using accelerated solvent extraction (ASE), followed by size exclusion chromatography (SEC).
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

related product

Product No.
Description
Pricing

Signal Word

Warning

Hazard Statements

H302,H317,H351,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK0667
BCCD2520
BCBW0072
BCBV2077
SZBE099XV

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Determination of 10 particle-associated multiclass polar and semi-polar pesticides from small streams using accelerated solvent extraction.
Schafer BR, et al.
Chemosphere, 70(11), 1952-1960 (2008)
Jérémy Masbou et al.
Journal of hazardous materials, 353, 99-107 (2018-04-13)
Chiral pesticides are often degraded enantioselectively in soils, leading to disparity among enantiomers that may display different toxicity levels. Monitoring pesticide degradation extents and processes remains out of reach in the field using conventional bulk and enantiomer concentration analyses. Enantioselective
P Palma et al.
The Science of the total environment, 488-489, 208-219 (2014-05-20)
The purpose of this study was to evaluate the potential impact of the pesticides detected in the Alqueva reservoir (Guadiana Basin, South Iberian Peninsula) on the aquatic organisms belonging to this ecosystem. For this purpose, the occurrence and risk assessment

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