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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:
101-05-3
Molecular Weight:
275.52
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329753777
EC Number:
202-910-5
Beilstein/REAXYS Number:
223133
MDL number:
MFCD00041815

Key Documents

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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

100

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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

Exclamation markEnvironment
GHS07,GHS09

signalword

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCM0755
BCCH3427
BCCC1816
BCBV3221

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D E Breithaupt et al.
Chemosphere, 41(9), 1401-1406 (2000-11-01)
Photoreactions, initiated by sunlight irradiation, between organochlorine pesticides and olefinic compounds of plant cuticles have been postulated. Concerning the formation of bound residues, which so far have not been detectable by common analytical techniques, photoaddition reactions are of main interest.
Triazines.
R Loosli
Toxicology, 91(1), 59-62 (1994-06-17)
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
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
Dyrene dermatitis.
S H Schuman et al.
Lancet (London, England), 2(8206), 1252-1252 (1980-12-06)
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