36654
Atrazine-desisopropyl solution
100 ng/μL in methanol, PESTANAL®, analytical standard
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About This Item
CAS Number:
Beilstein:
8150
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
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
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
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
51.8 °F
Flash Point(C)
11 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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
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
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]
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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