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31464

Supelco

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
Beilstein:
223133
EC Number:
202-910-5
MDL number:
MFCD00041815
UNSPSC Code:
41116107
PubChem Substance ID:
329753777
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

storage temp.

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)

InChI key

IMHBYKMAHXWHRP-UHFFFAOYSA-N

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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

Signal Word

Warning

Hazard Statements

H315 - H319 - H410

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH3427
BCCC1816
BCBV3221
SZBE133XV
SZBC102XV

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Triazines.
R Loosli
Toxicology, 91(1), 59-62 (1994-06-17)
S H Schuman et al.
Journal of the American Academy of Dermatology, 13(2 Pt 1), 220-223 (1985-08-01)
Fourteen of twenty-six migrant workers developed contact dermatitis at a single tomato-strawberry farm in Tennessee. Investigation identified one of eleven pesticides used by the farmer, 2,4-dichloro-6-(o-chloroanilino)-s-triazine anilazine; Dyrene), as the cause of the dermatitis in six of seven workers who
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.
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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