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Merck

45463

Diuron

PESTANAL®, analytical standard

Synonym(e):

3-(3,4-Dichlorphenyl)-1,1-dimethyl-harnstoff

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Über diesen Artikel

Empirische Formel (Hill-System):
C9H10Cl2N2O
CAS-Nummer:
Molekulargewicht:
233.09
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
206-354-4
Beilstein/REAXYS Number:
2215168
MDL number:

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InChI key

XMTQQYYKAHVGBJ-UHFFFAOYSA-N

InChI

1S/C9H10Cl2N2O/c1-13(2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)

SMILES string

CN(C)C(=O)Nc1ccc(Cl)c(Cl)c1

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

Quality Level

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Dieser Artikel
340184540036574
Diuron PESTANAL®, analytical standard

Supelco

45463

Diuron

Diuron-d6 PESTANAL®, analytical standard

Supelco

34018

Diuron-d6

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

format

neat

format

neat

format

neat

format

neat

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

grade

analytical standard

grade

analytical standard

grade

analytical standard

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

product line

PESTANAL®

product line

PESTANAL®

product line

PESTANAL®

product line

PESTANAL®

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

target_organs

Blood

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - STOT RE 2 Inhalation

Lagerklasse

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects


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Die Dokumentenbibliothek aufrufen

S Giacomazzi et al.
Chemosphere, 56(11), 1021-1032 (2004-07-28)
Diuron is a biologically active pollutant present in soil, water and sediments. A synthesis of literature data on its physicochemical properties, partitioning behaviour, abiotic and biotic transformations, toxicological and ecotoxicological impacts has been here performed. Data have shown that diuron
Ezequiel Petrillo et al.
Science (New York, N.Y.), 344(6182), 427-430 (2014-04-26)
Light is a source of energy and also a regulator of plant physiological adaptations. We show here that light/dark conditions affect alternative splicing of a subset of Arabidopsis genes preferentially encoding proteins involved in RNA processing. The effect requires functional
Martin Dolezal et al.
European journal of medicinal chemistry, 43(5), 1105-1113 (2007-09-18)
Unsubstituted, halogenated and/or alkylated pyrazine-2-carboxylic acid amides connected via -CONH- bridge with substituted anilines were synthesized using currently known synthetic pathways. The synthetic approach, analytical, spectroscopic, lipophilicity and biological data of 20 newly synthesized compounds are presented. Structure-activity relationships among
Arne S Kristoffersen et al.
Applied spectroscopy, 66(10), 1216-1225 (2012-10-04)
In vivo fluorescence lifetimes of chlorophyll-a (chl-a) and nicotinamide adenine dinucleotide phosphate (NADPH) were obtained from the green microalgae Haematococcus pluvialis under normal and nutrient-stressed conditions (green stage and red stage, respectively), using two-photon excitation provided by a laser generating
Lijin Tian et al.
Physical chemistry chemical physics : PCCP, 15(9), 3146-3154 (2013-01-24)
Photosystems I (PSI) and II (PSII) are two major pigment-protein complexes of photosynthetic organisms that function in series to convert sunlight energy into chemical energy. We have studied the picosecond fluorescence behaviour of the core of both photosystems in vivo

Protokolle

-methylcarbamate 10 μg/mL; Diuron; Propham; Siduron; Methiocarb, analytical standard; Linuron 10 μg/mL; Swep 10 μg/mL; Chlorpropham 10 μg/mL; Barban; Neburon

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