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Merck

36628

Supelco

Atrazine-desisopropyl

PESTANAL®, analytical standard

Sinónimos:

2-Amino-4-chloro-6-ethylamino-1,3,5-triazine

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About This Item

Fórmula empírica (notación de Hill):
C5H8ClN5
Número de CAS:
Peso molecular:
173.60
Beilstein/REAXYS Number:
8150
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable
solid phase extraction (SPE): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CCNc1nc(N)nc(Cl)n1

InChI

1S/C5H8ClN5/c1-2-8-5-10-3(6)9-4(7)11-5/h2H2,1H3,(H3,7,8,9,10,11)

InChI key

IVENSCMCQBJAKW-UHFFFAOYSA-N

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General description

Atrazine-desisopropyl is commonly used herbicide, which belongs to the class of triazines and is found to be a metabolite of atrazine.
Standard for Supelco MIP SPE cartridges. For more information request Supelco Literature T407075, T706023

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 mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Determination of atrazine, desethyl atrazine and desisopropyl atrazine in environmental water samples using hollow fiber-protected liquid-phase microextraction and high performance liquid chromatography
Peng J, et al.
Microchimica Acta, 158(1), 181-186 (2007)
D Q Tran et al.
Biochemical and biophysical research communications, 227(1), 140-146 (1996-10-03)
The chloro-S-triazine derived compounds atrazine, atrazine desisopropyl, cyanazine, and simazine are commonly used herbicides. These compounds do not have estrogenic activity in yeast expressing human estrogen receptor (hER) and an estrogen-sensitive reporter. In the presence of a concentration of estradiol
R Ikonen et al.
Toxicology letters, 44(1-2), 109-112 (1988-11-01)
Rats were given atrazine (2-chloro-4-ethylamino-6-(isopropylamino)-s-triazine) in drinking water for 1 or 3 weeks at 0.1 (0.45 mM), 0.2 (0.9 mM) or 0.5 g/l (2.3 mM) concentrations of the commercial agent. They excreted at both time points as the principal metabolite
Z Q Shao et al.
Journal of bacteriology, 177(20), 5748-5755 (1995-10-01)
We used degenerate oligodeoxyribonucleotides derived from the N-terminal sequence of the s-triazine hydrolase from Rhodococcus corallinus NRRL B-15444R in an amplification reaction to isolate a DNA segment containing a 57-bp fragment from the trzA gene. By using the nucleotide sequence
M L Magnuson et al.
Journal of chromatography. A, 868(1), 115-119 (2000-02-17)
Deethylatrazine (DEA), an atrazine degradation product, has been added to the US Environmental Protection Agency's Drinking Water Contaminant Candidate List (CCL). In its gas chromatographic analysis, DEA can coelute with deisopropylatrazine (DIA), another degradation product. The present work demonstrates that

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