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Merck
CN

36654

Atrazine-desisopropyl solution

100 ng/μL in methanol, PESTANAL®, analytical standard

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About This Item

CAS Number:
EC Number:
200-659-6
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
8150
MDL number:
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InChI key

IVENSCMCQBJAKW-UHFFFAOYSA-N

InChI

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

SMILES string

CCNc1nc(N)nc(Cl)n1

grade

analytical standard

product line

PESTANAL®

concentration

100 ng/μL in methanol

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture

format

single component solution

storage temp.

2-8°C

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

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

51.8 °F

flash_point_c

11 °C

ppe

Eyeshields, Faceshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

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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
Soil leaching column chromatographic technique for estimation of leaching behavior of atrazine, deethylatrazine, deisopropylatrazine, and hydroxyatrazine on soil.
F Xu et al.
Bulletin of environmental contamination and toxicology, 63(1), 87-93 (1999-07-29)

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