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45426

Supelco

Desmedipham

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C16H16N2O4
CAS Number:
13684-56-5
Molecular Weight:
300.31
Beilstein:
2395716
EC Number:
237-198-5
MDL number:
MFCD00055462
UNSPSC Code:
41116107
PubChem Substance ID:
329756722
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

SMILES string

CCOC(=O)Nc1cccc(OC(=O)Nc2ccccc2)c1

InChI

1S/C16H16N2O4/c1-2-21-15(19)18-13-9-6-10-14(11-13)22-16(20)17-12-7-4-3-5-8-12/h3-11H,2H2,1H3,(H,17,20)(H,18,19)

InChI key

WZJZMXBKUWKXTQ-UHFFFAOYSA-N

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Application

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

Health hazardEnvironment
GHS08,GHS09

Signal Word

Warning

Hazard Statements

H361d,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2

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
BCCG7177
BCCG7175
BCBV2741
BCBV2021
SZBD302XV

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W R Streber et al.
Plant molecular biology, 25(6), 977-987 (1994-09-01)
Tobacco plants were genetically engineered to express a detoxifying pathway for the herbicide phenmedipham. A gene from Arthrobacter oxidans strain P52 that encodes an enzyme catalysing the hydrolytic cleavage of the carbamate compound phenmedipham has recently been cloned and sequenced.
D Perret et al.
Journal of AOAC International, 84(5), 1407-1412 (2001-10-17)
A simple method is described for the simultaneous determination of residues of 2 carbamate herbicides (phenmedipham and desmedipham) and related metabolites (m-aminophenol, aniline, and m-toluidine) in soil. The analytes are extracted from spiked soils with methanol. The solvent/soil suspension is
Majid Abbaspoor et al.
Pest management science, 63(6), 576-585 (2007-04-18)
Desmedipham, phenmedipham and a 50% mixture of the two decreased the maximum quantum efficiency of photosystem II (F(v)/F(m)) and the relative changes at the J step (F(vj)) immediately after spraying in both sugar beet and black nightshade grown in the
Microbial degradation of the carbamate pesticides desmedipham, phenmedipham, promecarb, and propamocarb.
C O Knowles et al.
Bulletin of environmental contamination and toxicology, 27(4), 529-533 (1981-10-01)
Tânia Vidal et al.
Environmental toxicology, 27(9), 537-548 (2011-03-05)
As a way to improve the efficacy to target organisms, new pesticide generation is based on technologically advanced coformulations of two or more active ingredients. One example is Betanal(®)Expert, a postemergence herbicide composed of an Advanced Micro Droplet coformulation of

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