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Dicamba-d3

PESTANAL®, analytical standard

Synonym(s):

3,6-Dichloro-2-(methoxy-d3)benzoic acid

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About This Item

Empirical Formula (Hill Notation):
C8D3H3Cl2O3
CAS Number:
Molecular Weight:
224.06
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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+3

SMILES string

[2H]C([2H])([2H])Oc1c(Cl)ccc(Cl)c1C(O)=O

InChI

1S/C8H6Cl2O3/c1-13-7-5(10)3-2-4(9)6(7)8(11)12/h2-3H,1H3,(H,11,12)/i1D3

InChI key

IWEDIXLBFLAXBO-FIBGUPNXSA-N

General description

Dicamba-d3 is a metabolite of the pesticide dicamba, used for food, environmental, and toxicology analyses.

Application

Dicamba-d3 may be used as an analytical reference standard for the determination of the analyte in fresh water and air samples by hydrophilic interaction liquid chromatography coupled with tandem mass spectrometry and gas chromatography-mass spectrometry, respectively.
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

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Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 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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Pesticides measured in air and precipitation in the Yamaska Basin (Quebec): Occurrence and concentrations in 2004.
Aulagnier F, et al.
The Science of the Total Environment, 394(2-3), 338-348 (2008)
Manoj Ghaste et al.
Molecules (Basel, Switzerland), 25(16) (2020-08-17)
Dicamba is a moderately volatile herbicide used for post-emergent control of broadleaf weeds in corn, soybean, and a number of other crops. With increased use of dicamba due to the release of dicamba-resistant cotton and soybean varieties, growing controversy over
Hydrophilic interaction liquid chromatography coupled with tandem mass spectrometry for acidic herbicides and metabolites analysis in fresh water.
Fauvelle V, et al.
Environmental Science and Pollution Research International, 22(6), 3988-3996 (2015)

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