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Merck
CN

45463

敌草隆

PESTANAL®, analytical standard

别名:

3-(3,4-二氯苯)-1,1-二甲基脲

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关于此项目

经验公式（希尔记法）:
C9H10Cl2N2O
化学文摘社编号:
330-54-1
分子量:
233.09
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756756
EC Number:
206-354-4
Beilstein/REAXYS Number:
2215168
MDL number:
MFCD00018136

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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

100

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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

存储类别

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

法规信息

农药列管产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCN0071
BCCJ0691
BCCF0588
BCBZ5361
BCBS1743

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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
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实验方案

US EPA Method 632: HPLC Analysis of Pesticides on Ascentis® C18

-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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