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Merck

36628

Supelco

Atrazine-desisopropyl

PESTANAL®, analytical standard

Synonim(y):

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

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About This Item

Wzór empiryczny (zapis Hilla):
C5H8ClN5
Numer CAS:
Masa cząsteczkowa:
173.60
Beilstein:
8150
Numer MDL:
Kod UNSPSC:
41116107
Identyfikator substancji w PubChem:
NACRES:
NA.24

klasa czystości

analytical standard

Poziom jakości

linia produktu

PESTANAL®

okres trwałości

limited shelf life, expiry date on the label

metody

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

Zastosowanie

agriculture
environmental

format

neat

ciąg SMILES

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)

Klucz InChI

IVENSCMCQBJAKW-UHFFFAOYSA-N

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Opis ogólny

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

Zastosowanie

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

Informacje prawne

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

Piktogramy

Exclamation mark

Hasło ostrzegawcze

Warning

Zwroty wskazujące rodzaj zagrożenia

Klasyfikacja zagrożeń

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

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Środki ochrony indywidualnej

dust mask type N95 (US), Eyeshields, Gloves


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Certyfikaty analizy (CoA)

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Atrazine certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

90935

Atrazine

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)
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
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
K Wenger et al.
Journal of environmental quality, 34(6), 2187-2196 (2005-11-09)
DIMBOA (3,4-dihydro-2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3-one), a major benzoxazinone of Poaceae plants, was isolated and purified from corn seedlings. The effect of isolated and purified DIMBOA on the degradation of atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine], and its toxic breakdown products, desethylatrazine [2-chloro-4-amino-6-(isopropylamino)-s-triazine; DEA] and desisopropylatrazine [2-chloro-4-(ethylamino)-6-amino-s-triazine; DIA]
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

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