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Anilazin

PESTANAL®, analytical standard

Synonym(e):

6-(2-Chloranilino)-2,4-dichlor-1,3,5-triazin

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About This Item

Empirische Formel (Hill-System):
C9H5Cl3N4
CAS-Nummer:
101-05-3
Molekulargewicht:
275.52
Beilstein:
223133
EG-Nummer:
202-910-5
MDL-Nummer:
MFCD00041815
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329753777
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Produktlinie

PESTANAL®

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

agriculture
environmental

Format

neat

Lagertemp.

2-8°C

SMILES String

Clc1nc(Cl)nc(Nc2ccccc2Cl)n1

InChI

1S/C9H5Cl3N4/c10-5-3-1-2-4-6(5)13-9-15-7(11)14-8(12)16-9/h1-4H,(H,13,14,15,16)

InChIKey

IMHBYKMAHXWHRP-UHFFFAOYSA-N

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Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Rechtliche Hinweise

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Piktogramme

Exclamation markEnvironment
GHS07,GHS09

Signalwort

Warning

Gefahreneinstufungen

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
BCCM0755
BCCH3427
BCCC1816
BCBV3221
SZBE133XV

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J F Lawrence et al.
Journal - Association of Official Analytical Chemists, 63(6), 1300-1303 (1980-11-01)
Anilazine (2,4-dichloro-6-(2-chloroanilino)-1,3,5-triazine), a triazine fungicide, is extracted from potatoes or tomatoes with acetonitrile. An aliquot of the filtered extract is partitioned between methylene chloride and water. The organic phase is concentrated and passed through a 3% deactivated Florisil column for
J Liebich et al.
Journal of agricultural and food chemistry, 47(9), 3905-3910 (1999-12-20)
Humic substance fractions obtained from a degraded loess soil taken from a long-term lysimeter experiment with the fungicide anilazine were incubated in aerated liquid cultures together with native soil microorganisms. Biomineralization, remobilization of [U-phenyl-(14)C]anilazine, respectively, its metabolites, and changes of
F C Garg et al.
Zentralblatt fur Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene. Zweite naturwissenschaftliche Abteilung: Mikrobiologie der Landwirtschaft der Technologie und des Umweltschutzes, 136(6), 505-508 (1981-01-01)
The effect of anilazine on growth, respiration and enzyme activity of E. coli has been studied. Anilazine delays the growth of E. coli by prolonging the lag period. It inhibits glucose oxidation by 60% and succinate oxidation by 100%. It
J Lewalter et al.
Toxicology letters, 107(1-3), 131-144 (1999-07-22)
The modern environmental awareness leads to the realisation that the human metabolism is stressed by a huge number of chemical substances. Generally, these background exposures, consisting predominantly from natural and partly from industrial as well as life style sources, are
Dyrene dermatitis.
S H Schuman et al.
Lancet (London, England), 2(8206), 1252-1252 (1980-12-06)
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