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Merck
CN

31464

Anilazine

PESTANAL®, analytical standard

Synonym(s):

6-(2-Chloroanilino)-2,4-dichloro-1,3,5-triazine

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About This Item

Empirical Formula (Hill Notation):
C9H5Cl3N4
CAS Number:
Molecular Weight:
275.52
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
202-910-5
Beilstein/REAXYS Number:
223133
MDL number:
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InChI key

IMHBYKMAHXWHRP-UHFFFAOYSA-N

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)

SMILES string

Clc1nc(Cl)nc(Nc2ccccc2Cl)n1

grade

analytical standard

product line

PESTANAL®

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

storage temp.

2-8°C

Quality Level

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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

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Warning

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Regulatory Information

农药列管产品
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Dyrene dermatitis.
S H Schuman et al.
Lancet (London, England), 2(8206), 1252-1252 (1980-12-06)
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
C G Mathias
American journal of contact dermatitis : official journal of the American Contact Dermatitis Society, 8(1), 47-48 (1997-03-01)
Lawn care chemicals are frequently blamed when skin rashes occur in lawn care workers, although proof of a cause-and-effect relationship is often lacking. A lawn care worker developed severe dermatitis of the hands, arms, face, and neck shortly after his

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