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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.
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
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
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
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)

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